nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
181 Aberrant Wnt signaling activation in human cancers: In vitro and in vivo models to facilitate Wnt targeted drug development
|
Liu, G. |
|
2014 |
50 |
S6 |
p. 60- 1 p. |
artikel |
2 |
537 Absolute quantitation of MET using mass spectrometry for clinical application: assay precision, stability, and correlation with MET gene amplification in FFPE tumor tissue
|
Cecchi, F. |
|
2014 |
50 |
S6 |
p. 175- 1 p. |
artikel |
3 |
Acknowledgement
|
|
|
2014 |
50 |
S6 |
p. xii- 1 p. |
artikel |
4 |
251 A combined in vitro and mathematical modelling approach for understanding the impact of an inhibitor of ATR on DNA damage and repair after ionising radiation
|
Yates, J. |
|
2014 |
50 |
S6 |
p. 84- 1 p. |
artikel |
5 |
78 A comprehensive in vitro screen to identify therapeutic candidates for inclusion with etoposide/platin combinations to improve treatment of SCLC
|
Evans, D. |
|
2014 |
50 |
S6 |
p. 30- 1 p. |
artikel |
6 |
83 Acquired resistance to BET bromodomain inhibitors is associated with modulation of the apoptotic signaling network
|
Sandy, P. |
|
2014 |
50 |
S6 |
p. 31-32 2 p. |
artikel |
7 |
4 Activity of galeterone in castrate-resistant prostate cancer (CRPC) with C-terminal AR loss: Results from ARMOR2
|
Taplin, M.E. |
|
2014 |
50 |
S6 |
p. 8- 1 p. |
artikel |
8 |
53 Adeno-associated virus (AAV) carrying diphtheria toxin a gene for pancreatic cancer therapy
|
Chen, M. |
|
2014 |
50 |
S6 |
p. 22- 1 p. |
artikel |
9 |
135 AD-O64.3: IFN-γ–TRAIL fusion protein. Use of two independent signaling pathways for a strong synergistic antitumor effect
|
Zerek, B. |
|
2014 |
50 |
S6 |
p. 47- 1 p. |
artikel |
10 |
519 AD-O53.2 – novel biological anticancer therapeutic agent with a dual mechanism of action
|
Poleszak, K. |
|
2014 |
50 |
S6 |
p. 169- 1 p. |
artikel |
11 |
590 A dose dense schedule improves antitumor activity of trabectedin in myxoid liposarcoma with type III FUS-CHOP chimera
|
Uboldi, S. |
|
2014 |
50 |
S6 |
p. 190- 1 p. |
artikel |
12 |
296 A first-in-Asian phase I dose escalation study to evaluate the safety and pharmacokinetics of VS-6063 (defactinib), a focal adhesion kinase inhibitor in subjects with non-hematologic malignancies
|
Shimizu, T. |
|
2014 |
50 |
S6 |
p. 97-98 2 p. |
artikel |
13 |
378 A first-in-human (FIH) safety and pharmacological study of SAR405838, a novel HDM2 antagonist, in patients with solid malignancies
|
de Weger, V. |
|
2014 |
50 |
S6 |
p. 121-122 2 p. |
artikel |
14 |
329 A first-in-human study evaluating the safety and pharmacology of MM-151, a novel oligoclonal anti-EGFR antibody combination in patients with refractory solid tumors
|
Beeram, M. |
|
2014 |
50 |
S6 |
p. 107- 1 p. |
artikel |
15 |
291 Aflibercept has anti-tumor activity in bevacizumab-escaping tumors of colorectal cancer: Molecular profiles and mechanisms
|
Dib, C. |
|
2014 |
50 |
S6 |
p. 96- 1 p. |
artikel |
16 |
406 Aflibercept (Zaltrap) directly attenuates the migration and invasion of colorectal cancer cells
|
Bouygues, A. |
|
2014 |
50 |
S6 |
p. 130- 1 p. |
artikel |
17 |
3 Afuresertib (GSK2110183), an oral AKT kinase inhibitor, in combination with carboplatin and paclitaxel in recurrent ovarian cancer
|
Blagden, S. |
|
2014 |
50 |
S6 |
p. 7- 1 p. |
artikel |
18 |
195 A humanized mouse model for preclinical testing of molecules targeting immune checkpoints
|
Baia, G. |
|
2014 |
50 |
S6 |
p. 63- 1 p. |
artikel |
19 |
280 A hybrid drug design approach to overcome imatinib resistance for treating leukemia
|
Wei, Y.M. |
|
2014 |
50 |
S6 |
p. 93- 1 p. |
artikel |
20 |
69 AKT3 activation mediates resistance to HER2-targeted therapies in HER2-amplified breast cancer
|
Sanz, F. Carmona |
|
2014 |
50 |
S6 |
p. 27-28 2 p. |
artikel |
21 |
373 AKT2 gene amplification is a marker for sensitivity to allosteric but not ATP-competitive AKT inhibitors
|
Abe, T. |
|
2014 |
50 |
S6 |
p. 120- 1 p. |
artikel |
22 |
16 Allografting improves the feasibility of genetically engineered mouse models (GEMM) for anti-cancer drug development
|
Kukuk, K. |
|
2014 |
50 |
S6 |
p. 11-12 2 p. |
artikel |
23 |
355 Altiratinib (DCC-2701): a balanced inhibitor of MET, TIE2, and VEGFR2 kinases that exhibits broad anti-tumor and anti-angiogenic activities
|
Flynn, D. |
|
2014 |
50 |
S6 |
p. 115- 1 p. |
artikel |
24 |
121 A modified double-deleted vaccinia virus combining viral oncolysis and potential gene therapy as a novel therapeutic for atypical teratoid/rhabdoid tumors
|
Ruan, Y. |
|
2014 |
50 |
S6 |
p. 42-43 2 p. |
artikel |
25 |
507 Amplification of D-type cyclin genes CCND2 and CCND3 confers an oncogene addiction phenotype in tumor cells and hypersensitivity to the CDK4/6 inhibitor LY2835219
|
Buchanan, S. |
|
2014 |
50 |
S6 |
p. 165- 1 p. |
artikel |
26 |
525 Analysing Src and phosphoinositide 3-kinase pathway inhibition in a radiotherapy context – pathway interplay and therapeutic response
|
Rowling, E. |
|
2014 |
50 |
S6 |
p. 170-171 2 p. |
artikel |
27 |
420 Analysis of genomic alterations in Ewing sarcoma (German cohort) reveals cooperating mutations and novel therapy targets
|
Richter, G.H.S. |
|
2014 |
50 |
S6 |
p. 134- 1 p. |
artikel |
28 |
133 Analysis of immune microenvironment in resectable NSCLC: Prognostic value of regulatory and conventional T cell markers proportion
|
Uso, M. |
|
2014 |
50 |
S6 |
p. 46- 1 p. |
artikel |
29 |
122 Analysis of immune-response markers in resectable NSCLC
|
Usó, M. |
|
2014 |
50 |
S6 |
p. 43- 1 p. |
artikel |
30 |
233 Analytical validation and application of the MPACT assay, a next generation sequencing based targeted mutation detection assay for treatment selection
|
Lih, C. |
|
2014 |
50 |
S6 |
p. 78- 1 p. |
artikel |
31 |
285 A nanomolar-potency small molecule inhibitor of the STAT5 protein
|
Cumaraswamy, A.A. |
|
2014 |
50 |
S6 |
p. 94- 1 p. |
artikel |
32 |
308 Androgen deprivation therapy sensitizes prostate cancer cells to T-cell killing through androgen receptor dependent modulation of the apoptotic pathway
|
Gameiro, S. |
|
2014 |
50 |
S6 |
p. 101- 1 p. |
artikel |
33 |
24 Androgen receptor (AR) expression in triple negative breast cancer (TNBC): results from a phase II neoadjuvant trial with carboplatin and eribulin mesylate in TNBC patients
|
Siziopikou, K. |
|
2014 |
50 |
S6 |
p. 14- 1 p. |
artikel |
34 |
272 8-(1-Anilino)ethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxamides as PI3Kbeta/delta inhibitors: structure–activity relationships and identification of AZD8186, a clinical candidate for the treatment of PTEN deficient tumours
|
Barlaam, B. |
|
2014 |
50 |
S6 |
p. 90-91 2 p. |
artikel |
35 |
25 An ING1b-derived peptide that inhibits cancer cell viability and promotes apoptosis
|
Boyko, A. |
|
2014 |
50 |
S6 |
p. 14- 1 p. |
artikel |
36 |
147 An integrated approach for identifying E-cadherin synthetic lethality networks
|
Bajrami, I. |
|
2014 |
50 |
S6 |
p. 50- 1 p. |
artikel |
37 |
388 An integrated molecular analysis of lung adenocarcinomas identifies potential therapeutic targets among TTF1-negative tumors
|
Cardnell, R.J. |
|
2014 |
50 |
S6 |
p. 124-125 2 p. |
artikel |
38 |
132 A novel anti-PDL1 antibody-based bifunctional protein with enhanced immunological activity
|
Wu, Y. |
|
2014 |
50 |
S6 |
p. 46- 1 p. |
artikel |
39 |
549 A novel cancer marker and potential therapeutic target
|
Parri, M.P. |
|
2014 |
50 |
S6 |
p. 178- 1 p. |
artikel |
40 |
403 A novel dielectrophoretic microwell array system for detection and single cell analysis of circulating tumor cells from breast cancer patients
|
Sawada, T. |
|
2014 |
50 |
S6 |
p. 129- 1 p. |
artikel |
41 |
326 A novel non-ligand competing anti-EGFR antibody for cancer treatment
|
Wang, X. |
|
2014 |
50 |
S6 |
p. 106- 1 p. |
artikel |
42 |
112 A novel primary human tumor explant platform provides a preclinical translational link from tissue culture to the clinic
|
Juan, G. |
|
2014 |
50 |
S6 |
p. 40- 1 p. |
artikel |
43 |
211 A novel synthetic lethal interaction between the histone mark H3K36me3 and checkpoint kinases
|
Pfister, S.X. |
|
2014 |
50 |
S6 |
p. 71- 1 p. |
artikel |
44 |
171 Antagonistic interaction between gemcitabine and erlotinib is influenced by EGR1 (early growth response 1) transcription factor expression
|
Hose, C.D. |
|
2014 |
50 |
S6 |
p. 57- 1 p. |
artikel |
45 |
556 Antagonizing microRNA mediated epigenetic reprogramming as therapeutic strategy for aggressive prostate cancer
|
Dallavalle, C. |
|
2014 |
50 |
S6 |
p. 180- 1 p. |
artikel |
46 |
530 Anti-angiogenic therapy induces T-lymphocyte infiltration associated with poor survival in metastatic renal cell carcinoma patients
|
Liu, X.D. |
|
2014 |
50 |
S6 |
p. 172- 1 p. |
artikel |
47 |
115 Anti-metastatic activity via co-blockade of PD-1 and adenosine A2A receptor
|
Mittal, D. |
|
2014 |
50 |
S6 |
p. 40-41 2 p. |
artikel |
48 |
9 Antineoplastic effects of auranofin in canine lymphoma
|
Thamm, D. |
|
2014 |
50 |
S6 |
p. 9-10 2 p. |
artikel |
49 |
523 Antitumor activity of mTOR kinase and DNA-PK inhibitor CC-115 in a mouse model of glioblastoma
|
Raymon, H. |
|
2014 |
50 |
S6 |
p. 170- 1 p. |
artikel |
50 |
70 Antitumor activity of S116836, a novel tyrosine kinase inhibitor, against imatinib-resistant FIP1L1-PDGFRa-expressing cells
|
Pan, J. |
|
2014 |
50 |
S6 |
p. 28- 1 p. |
artikel |
51 |
62 Antitumor and temozolomide-sensitizing effects of sodium metaarsenite in an orthotopic glioblastoma xenograft model
|
Kang, W.Y. |
|
2014 |
50 |
S6 |
p. 25- 1 p. |
artikel |
52 |
276 An X-ray crystal structure-based understanding of the inhibition of the MDM2–p53 protein–protein interaction by isoindolinones
|
Anil, B. |
|
2014 |
50 |
S6 |
p. 91-92 2 p. |
artikel |
53 |
435 A pan-cancer tumor-derived epithelial-to–mesenchymal transition (EMT) signature determines patterns of drug sensitivity and enrichment in immune target expression following EMT
|
Mak, M.P. |
|
2014 |
50 |
S6 |
p. 143- 1 p. |
artikel |
54 |
11 A panel of patient derived xenograft models of different haematological malignancies suitable for preclinical drug screening campaigns
|
Oswald, E. |
|
2014 |
50 |
S6 |
p. 10- 1 p. |
artikel |
55 |
61 A panel of pediatric liver cancer patient-derived xenografts to improve stratification of children with hepatoblastoma
|
Fabre, M. |
|
2014 |
50 |
S6 |
p. 25- 1 p. |
artikel |
56 |
389 A phase 1, dose-escalation, first-in-human study of ARQ 087, an oral pan-FGFR inhibitor, in adult subjects with advanced solid tumors
|
Papadopoulos, K. |
|
2014 |
50 |
S6 |
p. 125- 1 p. |
artikel |
57 |
508 A phase Ib trial of AMG386 and temsirolimus in patients with advanced sold tumors (PJC-008/NCI#9041)
|
Chiu, J.W. |
|
2014 |
50 |
S6 |
p. 165-166 2 p. |
artikel |
58 |
213 A phase I dose-finding study of BI 853520, a potent and selective inhibitor of focal adhesion kinase (FAK), in Japanese and Taiwanese patients with advanced or metastatic solid tumors
|
Doi, T. |
|
2014 |
50 |
S6 |
p. 72- 1 p. |
artikel |
59 |
526 A Phase I study of the dual, intravenous (IV) phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) inhibitor PF-05212384 in combination with irinotecan in patients (pts) with colorectal cancer (CRC) and other advanced solid tumors
|
Wainberg, Z. |
|
2014 |
50 |
S6 |
p. 171- 1 p. |
artikel |
60 |
461 A phase I trial of dabrafenib (BRAF inhibitor) and pazopanib in BRAF mutated advanced malignancies
|
Haraldsdottir, S. |
|
2014 |
50 |
S6 |
p. 151- 1 p. |
artikel |
61 |
342 A phase 1/2 study evaluating the safety, pharmacokinetics and efficacy of ABT-414 in subjects with advanced solid tumors likely to over-express the epidermal growth factor receptor (EGFR)
|
Tolcher, A. |
|
2014 |
50 |
S6 |
p. 111- 1 p. |
artikel |
62 |
210 A phase 1 study of KTN3379, a human anti-ErbB3 monoclonal antibody in patients with advanced cancers
|
LoRusso, P. |
|
2014 |
50 |
S6 |
p. 71- 1 p. |
artikel |
63 |
105 A platform to test multiple therapy options simultaneously in a patient's own tumor
|
Caffo, N. |
|
2014 |
50 |
S6 |
p. 38- 1 p. |
artikel |
64 |
334 Aplidin: first in class compound targeting EEF1A in tumor cells
|
Losada, A. |
|
2014 |
50 |
S6 |
p. 108- 1 p. |
artikel |
65 |
268 A potent and highly efficacious bivalent Smac Mimetic APG-1387 in Phase I clinical development
|
Lu, J. |
|
2014 |
50 |
S6 |
p. 89- 1 p. |
artikel |
66 |
408 A potent and selective small molecule inhibitor of MCL-1 sensitizes DLBCL cell lines to the BCL-2 selective inhibitor ABT-199
|
Phillips, D.C. |
|
2014 |
50 |
S6 |
p. 130- 1 p. |
artikel |
67 |
528 A procaspase activator shows preclinical promise for glioblastoma therapy
|
Riggins, G. |
|
2014 |
50 |
S6 |
p. 171-172 2 p. |
artikel |
68 |
557 A rational approach for discovery of inhibitors of YAP-TEAD interaction
|
Chene, L. |
|
2014 |
50 |
S6 |
p. 180- 1 p. |
artikel |
69 |
117 “Arming” the chimeric oncolytic adenovirus enadenotucirev to deliver checkpoint inhibitors and other therapeutics directly to tumours
|
Champion, B. |
|
2014 |
50 |
S6 |
p. 41- 1 p. |
artikel |
70 |
145 ARQ 087, a novel pan FGFR-inhibitor crosses the BBB (blood–brain barrier) and distributes to the brain of rats
|
Savage, R. |
|
2014 |
50 |
S6 |
p. 50- 1 p. |
artikel |
71 |
144 Association between interleukin 17/interleukin 17 receptor gene polymorphism and papillary thyroid cancer
|
Eun, Y. |
|
2014 |
50 |
S6 |
p. 50- 1 p. |
artikel |
72 |
93 A stress induced early innate response causes multi-drug tolerance in melanoma
|
Menon, D.R. |
|
2014 |
50 |
S6 |
p. 34- 1 p. |
artikel |
73 |
164 Augmentation of NAD+ by NQO1 activation attenuates cisplatin-mediated hearing impairment
|
Yang, S. |
|
2014 |
50 |
S6 |
p. 55- 1 p. |
artikel |
74 |
405 Aurora kinases A and B are required for KRAS-induced lung cell oncogenicity
|
Santos, E.O. Ozorio dos |
|
2014 |
50 |
S6 |
p. 129-130 2 p. |
artikel |
75 |
Author Index
|
|
|
2014 |
50 |
S6 |
p. 205-228 24 p. |
artikel |
76 |
266 Auxiliar treatment by targeting the extracellular matrix to improve drug delivery and therapeutic response
|
Henke, E. |
|
2014 |
50 |
S6 |
p. 89- 1 p. |
artikel |
77 |
124 A WT1-derived peptide protects against metastatic melanoma in a syngeneic model by in vivo immunomodulatory effects on dendritic cells
|
Massaoka, M.H. |
|
2014 |
50 |
S6 |
p. 43-44 2 p. |
artikel |
78 |
156 Behaviour of platinum(IV) complexes with prodrug function in different models of hypoxia
|
Brynzak, E. |
|
2014 |
50 |
S6 |
p. 53- 1 p. |
artikel |
79 |
106 Beta-3 integrin inhibition reduces inflammatory cytokine release but not anti-cancer activity of oncolytic adenovirus in ovarian cancer
|
Browne, A.K. |
|
2014 |
50 |
S6 |
p. 38- 1 p. |
artikel |
80 |
315 Biological characterization of TAS3681, a new type of androgen receptor antagonist with androgen receptor downregulating activity
|
Minamiguchi, K. |
|
2014 |
50 |
S6 |
p. 103- 1 p. |
artikel |
81 |
569 Biological consequences of selective inhibition of the first BET bromodomain
|
Seitzberg, J.G. |
|
2014 |
50 |
S6 |
p. 184- 1 p. |
artikel |
82 |
465 Biomarker analysis in Phase 1b study of anti-cancer stem cell antibody Tarextumab (TAR) in combination with nab-paclitaxel and gemcitabine (Nab-P+Gem) demonstrates pharmacodynamic (PD) modulation of the Notch pathway in patients (pts) with untreated metastatic pancreatic cancer (mPC)
|
Kapoun, A. |
|
2014 |
50 |
S6 |
p. 152- 1 p. |
artikel |
83 |
331 Biomarker discovery and validation for assessing the response to cMet inhibition and functional inactivation
|
Jung, S. |
|
2014 |
50 |
S6 |
p. 107- 1 p. |
artikel |
84 |
434 Bipolar androgen therapy for men with castration sensitive and castration resistant prostate cancer: Reversing resistance and maintaining sensitivity to androgen ablative therapies
|
Denmeade, S.R. |
|
2014 |
50 |
S6 |
p. 143- 1 p. |
artikel |
85 |
338 BM-1252 (APG-1252): a potent dual specific Bcl-2/Bcl-xL inhibitor that achieves complete tumor regression with minimal platelet toxicity
|
Bai, L. |
|
2014 |
50 |
S6 |
p. 109-110 2 p. |
artikel |
86 |
242 BMN 673 as single agent and in combination with temozolomide or PI3K pathway inhibitors in small cell lung cancer and gastric cancer models
|
Feng, Y. |
|
2014 |
50 |
S6 |
p. 81- 1 p. |
artikel |
87 |
169 BRAF mutation testing in cell-free DNA from plasma of patients with advanced cancers using a novel, rapid, automated molecular diagnostics prototype platform (Idylla™)
|
Janku, F. |
|
2014 |
50 |
S6 |
p. 56-57 2 p. |
artikel |
88 |
35 BRCA1 expression exploratory analysis in patients of the phase III trial of trabectedin vs. doxorubicin-based chemotherapy as first-line therapy in translocation-related sarcomas
|
Aracil, M. |
|
2014 |
50 |
S6 |
p. 17- 1 p. |
artikel |
89 |
46 Broad-spectrum preclinical combination activity of eribulin combined with various anticancer agents in human breast cancer, lung cancer, ovarian cancer, and melanoma xenograft models
|
Asano, M. |
|
2014 |
50 |
S6 |
p. 20- 1 p. |
artikel |
90 |
119 3-Bromopyruvate as an inducer of immunogenic cell death in colon cancer cells
|
Jung, K.H. |
|
2014 |
50 |
S6 |
p. 42- 1 p. |
artikel |
91 |
347 Can a link between the EGFR and cMET pathway in non-small cell lung cancer explain resistance against targeted therapies and open new therapeutic opportunities?
|
van der Steen, N. |
|
2014 |
50 |
S6 |
p. 112- 1 p. |
artikel |
92 |
68 Can the P53 status predict the outcome of Polo-like kinase 1 inhibition in non-small cell lung cancer cell lines?
|
Van den Bossche, J. |
|
2014 |
50 |
S6 |
p. 27- 1 p. |
artikel |
93 |
555 CB-5083, a first in class inhibitor of the AAA-ATPase p97/VCP, induces irresolvable ER stress that results in antitumor activity in solid and hematological tumor models
|
Yakes, F. |
|
2014 |
50 |
S6 |
p. 180- 1 p. |
artikel |
94 |
422 CBL0137, a novel NFkB suppressor and p53 activator, is highly effective in pre-clinical models of neuroblastoma
|
Haber, M. |
|
2014 |
50 |
S6 |
p. 135- 1 p. |
artikel |
95 |
306 CC-115 inhibits DNA damage and repair pathways in vitro
|
Tsuji, T. |
|
2014 |
50 |
S6 |
p. 100- 1 p. |
artikel |
96 |
168 CDCP1 as a new marker of aggressiveness in triple-negative breast cancers
|
Campiglio, M. |
|
2014 |
50 |
S6 |
p. 56- 1 p. |
artikel |
97 |
498 CDK4/6 inhibitor (LY2835219) exhibits potent anti-tumor activity in human lung cancer cell lines with intact retinoblastoma
|
Goldman, J.W. |
|
2014 |
50 |
S6 |
p. 162- 1 p. |
artikel |
98 |
43 CDKN1A-mediated responsiveness of MLL-AF4-positive acute lymphoblastic leukemia to Aurora kinase-A inhibitors
|
Hung, L. |
|
2014 |
50 |
S6 |
p. 19-20 2 p. |
artikel |
99 |
108 CD70 (TNFSF7), a receptor involved in acute immune modulation of viral infection, is frequently overexpressed in solid and hematological malignancies
|
Jacobs, J. |
|
2014 |
50 |
S6 |
p. 39- 1 p. |
artikel |
100 |
587 Cellular pharmacokinetics and molecular pharmacodynamics studies of the BRD-BET inhibitor OTX015 in sensitive and resistant leukemic cell lines
|
Odore, E. |
|
2014 |
50 |
S6 |
p. 189- 1 p. |
artikel |
101 |
397 Characterization of molecular targets of therapy in Non-Small Cell Lung Cancer (NSCLC) utilizing a liquid biopsy
|
Greene, S. |
|
2014 |
50 |
S6 |
p. 127- 1 p. |
artikel |
102 |
129 Characterization of PD-L1 expression in circulating tumor cells (CTCs) of non-small cell lung cancer (NSCLC) patients
|
Krupa, R. |
|
2014 |
50 |
S6 |
p. 45- 1 p. |
artikel |
103 |
577 Characterization of the cellular mechanism of action of the first in class investigational inhibitor of the Ubiquitin Activating Enzyme, MLN7243
|
Milhollen, M. |
|
2014 |
50 |
S6 |
p. 186- 1 p. |
artikel |
104 |
402 Characterization of the oncogenic properties of mutant isocitrate dehydrogenase 1 (IDH1R132H) in human primary cells
|
Barradas, M. |
|
2014 |
50 |
S6 |
p. 128-129 2 p. |
artikel |
105 |
28 Characterization of the type of cell death induced by novel tambjamine analogs in lung cancer
|
Martín, A. Rodilla |
|
2014 |
50 |
S6 |
p. 15- 1 p. |
artikel |
106 |
245 Chk1 is a potential novel therapeutic target that regulates cell survival and potentiates chemotherapy in osteosarcoma (OS) models
|
Strauss, S.J. |
|
2014 |
50 |
S6 |
p. 82- 1 p. |
artikel |
107 |
107 CIGB-247: Anti-VEGF therapeutic vaccine in patients with advanced solid tumors
|
Hernández-Bernal, F. |
|
2014 |
50 |
S6 |
p. 38- 1 p. |
artikel |
108 |
428 Clinical acquired resistance to combined RAF/EGFR or RAF/MEK inhibition in BRAF mutant colorectal cancer (CRC) patients through MAPK pathway alterations
|
Corcoran, R. |
|
2014 |
50 |
S6 |
p. 141- 1 p. |
artikel |
109 |
41 Clinical activity of BIND-014 (docetaxel nanoparticles for injectable suspension) as second-line therapy in patients (pts) with Stage III/IV non-small cell lung cancer
|
Natale, R. |
|
2014 |
50 |
S6 |
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231 Clinical pharmacodynamic assay development for the first in class investigational ubiquitin activating enzyme (UAE) inhibitor MLN7243
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Bahamón, B. |
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2014 |
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111 |
324 Clinical pharmacokinetics (PK), translational PK/pharmacodynamics (PD), and exposure–adverse events (AEs) relationship of MLN2480, an oral investigational pan-RAF kinase inhibitor
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Zhou, X. |
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2014 |
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p. 105-106 2 p. |
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112 |
462 Clinical sequencing of cancer in real-time by digital sequencing of cell-free DNA for tailoring targeted therapy in refractory cancer patients
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Talasaz, A. |
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2014 |
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p. 151- 1 p. |
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113 |
66 Clinical validity of new genetic biomarkers of irinotecan neutropenia: An independent replication study
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Innocenti, F. |
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2014 |
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p. 26-27 2 p. |
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114 |
468 Clinicopathologic implication of c-MYC gene copy number gain and overexpression in colorectal cancer
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Lee, K. |
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2014 |
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p. 153- 1 p. |
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115 |
CME Accreditation
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2014 |
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395 cMet: Proof-of-concept clinical trial with volitinib in patients with advanced papillary renal cell cancer (PRCC)
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Choueiri, T.K. |
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2014 |
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p. 126-127 2 p. |
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117 |
458 Combinational genome and proteome survey of therapeutic targets of hepatocellular carcinoma
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Yamada, T. |
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2014 |
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p. 150- 1 p. |
artikel |
118 |
327 Combination of MDM2 antagonists with RAS pathway inhibitors in colorectal cancer
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Higgins, B. |
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2014 |
50 |
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p. 106- 1 p. |
artikel |
119 |
174 Combination of molecular and drug response data in patient-derived xenografts to assist patient stratification
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Cairo, S. |
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2014 |
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p. 58- 1 p. |
artikel |
120 |
387 Combination of the ERK inhibitor GDC-0994 with the MEK inhibitor cobimetinib significantly enhances anti-tumor activity in KRAS and BRAF mutant tumor models
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Merchant, M. |
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2014 |
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p. 124- 1 p. |
artikel |
121 |
99 Combination screening of investigational oncology agents
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Holbeck, S. |
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2014 |
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p. 36- 1 p. |
artikel |
122 |
208 Combined treatment of a DNA-PKcs inhibitor (NU7441) and ionizing radiation causes a differential mode of cell death in a panel of NSCLC cell lines and exhibits robust radiosensitisation
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Saha, D. |
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2014 |
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p. 68- 1 p. |
artikel |
123 |
295 Combining forces: Study of the cytotoxic effect of the MDM2 inhibitor Nutlin-3 in combination with CDDP in non-small cell lung cancer cell lines
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Deben, C. |
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2014 |
50 |
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p. 97- 1 p. |
artikel |
124 |
33 Combining the long-acting topoisomerase 1-inhibitor etirinotecan pegol with the PARP inhibitor rucaparib to provide anti-tumor synergy without increased toxicity
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Hoch, U. |
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2014 |
50 |
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p. 16-17 2 p. |
artikel |
125 |
511 ComboPredictor: identification of synergy biomarkers and enrichment within tumor sample populations
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Tomilo, M. |
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2014 |
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p. 166- 1 p. |
artikel |
126 |
102 Comparison of platinum/taxane and anthracycline-based therapies in ovarian PDX models: Correlating stage of biopsy collection and engrafting with in vivo drug sensitivity
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Meade, J. |
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2014 |
50 |
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p. 37- 1 p. |
artikel |
127 |
250 Comprehensive genomic profiling of pancreatic acinar cell carcinomas identifies recurrent RAF fusions and frequent inactivation of DNA repair genes
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Chmielecki, J. |
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2014 |
50 |
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p. 84- 1 p. |
artikel |
128 |
415 Comprehensive next generation sequencing of solid tumors from 669 adolescents and young adults reveals a distinct spectrum of targetable genomic alterations
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Morosini, D. |
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2014 |
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p. 132-133 2 p. |
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129 |
Conference Committees
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2014 |
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p. xi- 1 p. |
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130 |
263 Controlled release of cisplatin using hyaluronic oligosaccharides-coated gold nanoparticles as an efficient delivery system applied to the treatment of pancreatic tumors
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Parkkola, H. |
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2014 |
50 |
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p. 87-88 2 p. |
artikel |
131 |
127 Correlation of clinical activity of pembrolizumab (MK-3475) with immunohistochemical staining for programmed death-1 ligand (PD-L1) in ≥50% of tumor cells in a prospective non-small cell lung cancer (NSCLC) validation population
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Garon, E.G. |
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2014 |
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p. 44-45 2 p. |
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132 |
359 Correlation of tumour-associated macrophage, but not tumour-infiltrating lymphocyte, levels with progression-free survival in patients with metastatic renal cell carcinoma treated with axitinib
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Williams, J.A. |
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2014 |
50 |
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p. 116- 1 p. |
artikel |
133 |
451 Correlative and updated clinical endpoint analysis of a multicenter phase II trial of selumetinib (AZD6244) plus erlotinib in chemotherapy-refractory advanced pancreatic adenocarcinoma (PDAC)
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Ko, A.H. |
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2014 |
50 |
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p. 148- 1 p. |
artikel |
134 |
87 Critical difference in development of acquired resistance to MDM2 inhibitor SAR405838 in vitro and in vivo
|
Hoffman-Luca, G. |
|
2014 |
50 |
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p. 32-33 2 p. |
artikel |
135 |
125 Critical issues in the clinical development of oncolytic viruses – A regulatory perspective
|
Schuessler-Lenz, M. |
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2014 |
50 |
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p. 44- 1 p. |
artikel |
136 |
449 Cytokine induces MIR-424 expression and modulates SOCS2/STAT5 signaling pathway in oral cancer
|
Shiah, S.G. |
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2014 |
50 |
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p. 147- 1 p. |
artikel |
137 |
363 Cytosolic p21 is a pharmacodynamic marker of CHEK1 and IKK inhibition in ovarian cancer cells
|
Kim, M. |
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2014 |
50 |
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p. 117- 1 p. |
artikel |
138 |
67 Cytotoxic response as a result of the cross-talk between UGT mediated metabolism and modulation of UGT activity by C-1311 and C-1305 acridinone antitumor agents in selected solid tumor cell lines
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Mazerska, Z. |
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2014 |
50 |
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p. 27- 1 p. |
artikel |
139 |
271 Data integration and graph analysis for cancer genomics and drug discovery
|
Bernard, B. |
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2014 |
50 |
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p. 90- 1 p. |
artikel |
140 |
444 Debio 1143 in combination with carboplatin and paclitaxel in patients with non-small cell lung cancer (NSCLC), triple-negative breast cancer (TNBC) and platinum-refractory epithelial ovarian cancer (EOC). Preliminary results of a Phase I dose-escalation study
|
Le Tourneau, C. |
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2014 |
50 |
S6 |
p. 146- 1 p. |
artikel |
141 |
120 Density of CD 8 +ve T cells & CD 56 +ve NK cells in follicular adenoma & papillary carcinoma of thyroid in Pakistani population
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Varda, J. |
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2014 |
50 |
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p. 42- 1 p. |
artikel |
142 |
430 Design and structure–activity relationships of highly potent and bioavailable imidazolinone FASN KR domain inhibitors
|
Bignan, G. |
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2014 |
50 |
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p. 141-142 2 p. |
artikel |
143 |
509 Detecting gene amplification in circulating tumor cells of patients with gastric cancer for clinical trial
|
Mishima, Y. |
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2014 |
50 |
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p. 166- 1 p. |
artikel |
144 |
533 Detection of recurrent novel fusion transcripts from whole transcriptome sequencing of 120 primary breast cancer
|
Kim, J. |
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2014 |
50 |
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p. 173- 1 p. |
artikel |
145 |
80 Determination of an oxidative stress gene signature in inflammatory breast cancer patient tumors and development of a novel redox modulatory strategy in overcoming chemotherapy resistance and mediating anti-tumor efficacy
|
Devi, G.R. |
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2014 |
50 |
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p. 31- 1 p. |
artikel |
146 |
491 Development and characteristics of resistance to the HER family tyrosine kinase inhibitor AZD8931
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Brunton, V.G. |
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2014 |
50 |
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p. 160- 1 p. |
artikel |
147 |
489 Development and clinical validation of a quantitative mass spectrometric assay for PD-L1 protein in FFPE NSCLC samples
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An, E. |
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2014 |
50 |
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p. 159- 1 p. |
artikel |
148 |
538 Development of a novel anti-tumor antibody targeting CXADR
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Kawada, M. |
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2014 |
50 |
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p. 175- 1 p. |
artikel |
149 |
313 Development of a one-step isolation platform for exosomal RNA and circulating cell-free DNA from cancer plasma samples
|
Enderle, D. |
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2014 |
50 |
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p. 102- 1 p. |
artikel |
150 |
488 Development of a publicly accessible knowledgebase to facilitate decision support for clinical cancer genomics reporting
|
Shaw, K. |
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2014 |
50 |
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p. 159- 1 p. |
artikel |
151 |
548 Development of a small molecule activator of protein phosphatase 2A for the treatment of prostate cancer
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McClinch, K. |
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2014 |
50 |
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p. 178- 1 p. |
artikel |
152 |
232 Development of a targeted NGS assay system for patient enrollment to the NCI-MATCH study
|
Williams, M. |
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2014 |
50 |
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p. 78- 1 p. |
artikel |
153 |
559 Development of a unique biologic for treating cysteine-dependent malignancies
|
Stone, E. |
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2014 |
50 |
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p. 181- 1 p. |
artikel |
154 |
429 Development of extracellular signal-regulated kinase 5 (ERK5) inhibitors for anti-cancer therapy
|
Myers, S. |
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2014 |
50 |
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p. 141- 1 p. |
artikel |
155 |
257 Development of peptide-mediated drug delivery systems for colon cancer targeted imaging and therapy
|
Wu, H.C. |
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2014 |
50 |
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p. 86- 1 p. |
artikel |
156 |
51 Development of rational combination therapy strategies to optimize treatment for GPNMB expressing Her2+ and triple negative breast cancer
|
Rose, A. |
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2014 |
50 |
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p. 22- 1 p. |
artikel |
157 |
486 Development of small molecule activators of protein phosphatase 2A for the treatment of lung cancer
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Sangodkar, J. |
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2014 |
50 |
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p. 158-159 2 p. |
artikel |
158 |
244 Development of xenoimplants from germline BRCA1/2 mutant breast cancer (BC) for the identification of predictive biomarkers, mechanisms of resistance against poly(ADP-ribose) polymerase (PARP) inhibitors and evaluation of novel therapies
|
Cruz, C. |
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2014 |
50 |
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p. 82- 1 p. |
artikel |
159 |
369 Diagnosis and molecular targeting for individualized treatment of patients with pre-neoplastic lesions and locally advanced cervical cancer
|
Moreno-Acosta, P.M.A. |
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2014 |
50 |
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p. 119- 1 p. |
artikel |
160 |
516 Different genetic profiles of resistant and sensitive patients with EGFR wild type NSCLC undergoing tyrosine kinase inhibitor (TKI) treatment
|
Ulivi, P.U. |
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2014 |
50 |
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p. 168- 1 p. |
artikel |
161 |
57 Differential antitumor activity of trabectedin, lurbinectedin, Zalypsis and PM00128 against a panel of human cells deficient in transcription and NER factors
|
Moneo, V. |
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2014 |
50 |
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p. 24- 1 p. |
artikel |
162 |
190 Differential chemosensitivity between CETCs and tumour spheroids in cancer patients with solid tumors
|
Zimon, D. |
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2014 |
50 |
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p. 62- 1 p. |
artikel |
163 |
73 Differential pathway resiliency in response to MAPK inhibition in BRAF-mutant cancer
|
Sos, M. |
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2014 |
50 |
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p. 28-29 2 p. |
artikel |
164 |
341 Dinaciclib alters cell cycle dynamics and induces cell death in Soft Tissue Sarcomas
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Margalef, N. Mulet |
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2014 |
50 |
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p. 110- 1 p. |
artikel |
165 |
270 Discovery, development and optimization of low molecular weight EPH–ephrin protein–protein inhibitors
|
Tognolini, M. |
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2014 |
50 |
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p. 90- 1 p. |
artikel |
166 |
552 Discovery of an unexpected vulnerability of cancer stem-like cells via a functional dissection of EMT biology
|
Feng, Y. |
|
2014 |
50 |
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p. 179- 1 p. |
artikel |
167 |
279 Discovery of multiple kinases inhibitors, DBPR114, as the novel anti-cancer agent
|
Hsieh, H.P. |
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2014 |
50 |
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p. 92-93 2 p. |
artikel |
168 |
59 Discovery of novel inhibitor of FOXO nuclear–cytoplasmic shuttling from natural products of marine origin
|
Correa, F.J. Castillo |
|
2014 |
50 |
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p. 24- 1 p. |
artikel |
169 |
356 Discovery of novel pyrido[2,3-b]pyrazine as fibroblast growth factor receptor (FGFR-1, 2, 3 & 4) kinase inhibitors with nanomolar affinity
|
Angibaud, P. |
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2014 |
50 |
S6 |
p. 115- 1 p. |
artikel |
170 |
370 Discovery of the genes that underpin the transition to malignant phenotype of breast tissues in a highly consanguineous region
|
Gupta, I. |
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2014 |
50 |
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p. 119- 1 p. |
artikel |
171 |
495 Divergent androgen regulation of UPR pathways drives prostate cancer
|
Arnoldussen, Y.J. |
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2014 |
50 |
S6 |
p. 161- 1 p. |
artikel |
172 |
229 DNA methyltransferase 1 expression in human solid tumors and lymphomas by immunohistochemistry
|
Yang, S.X. |
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2014 |
50 |
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p. 77- 1 p. |
artikel |
173 |
221 Docosahexaenoic acid along with modulation of actin binding proteins reduces cancer cell migration
|
Ali, M. |
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2014 |
50 |
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p. 75- 1 p. |
artikel |
174 |
472 Do we hit the target? Phospho-reactome measurements determine efficacy of targeted therapies
|
van't Veer, L. |
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2014 |
50 |
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p. 154- 1 p. |
artikel |
175 |
162 Drug–drug interaction predictions for MLN2480, an investigational pan-RAF inhibitor, based on nonclinical data
|
Balani, S.K. |
|
2014 |
50 |
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p. 54-55 2 p. |
artikel |
176 |
411 Druggability of p16 deleted pediatric leukemia: The novel cell line POETIC3 identifies potential agents and drug combinations for mechanism based targeted therapeutics
|
Reimer, J. |
|
2014 |
50 |
S6 |
p. 131- 1 p. |
artikel |
177 |
154 Drug response database with PDX tumor models in biomarker-driven multi-drug multi-arm clinical trial settings
|
Jiang, J. |
|
2014 |
50 |
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p. 52- 1 p. |
artikel |
178 |
554 Dual EZH2 and EHMT2 histone methyltransferase inhibition increases biological efficacy in breast cancer cells
|
Brown, R. |
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2014 |
50 |
S6 |
p. 179-180 2 p. |
artikel |
179 |
332 Dual PI3K delta/gamma inhibition by RP6530 accentuates bortezomib activity in multiple myeloma cell lines
|
Viswanadha, S. |
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2014 |
50 |
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p. 108- 1 p. |
artikel |
180 |
45 Early preclinical study of BO-2094 for treatment of human colon cancer, in combination with 5-fluorouracil
|
Su, T.L. |
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2014 |
50 |
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p. 20- 1 p. |
artikel |
181 |
91 4E-BP1 expression levels determine sensitivity of triple negative breast cancer cells to mTOR inhibitors
|
Jastrzebski, K. |
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2014 |
50 |
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p. 34- 1 p. |
artikel |
182 |
487 EC-70124, a multi-kinase inhibitor, blocks NF-kB and STAT3 dependent signaling in prostate cancer stem cells
|
Civenni, G. |
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2014 |
50 |
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p. 159- 1 p. |
artikel |
183 |
Editorial Board
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2014 |
50 |
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p. ii- 1 p. |
artikel |
184 |
37 Effect of a microtubule-targeting drug on cell–cell contacts in bladder epithelial tumour cells
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Antón-Aparicio, L.M. |
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2014 |
50 |
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p. 17-18 2 p. |
artikel |
185 |
165 Effect of zoledronic acid on the post-translational modification of activated leukocyte cell adhesion molecule (ALCAM) in cancer cells
|
Toth, R. |
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2014 |
50 |
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p. 55- 1 p. |
artikel |
186 |
179 Effects of human breast cancer cells secreted factors on macrophage differentiation
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de Sousa, S. Coimbra |
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2014 |
50 |
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p. 59- 1 p. |
artikel |
187 |
226 Efficacy of cancer preventing drugs administered by intermittent dosing regimens
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Steele, V.E. |
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2014 |
50 |
S6 |
p. 76- 1 p. |
artikel |
188 |
381 Efficacy of specific FGFR inhibitors against gatekeeper resistance mutations and shared mechanism of cell death in FGFR2-dependent endometrial cancer cell lines
|
Packer, L. |
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2014 |
50 |
S6 |
p. 122- 1 p. |
artikel |
189 |
452 eIF2alpha phosphorylation determines the adaptation of tuberous sclerosis complex mutant cells to stress and their response to anti-tumor therapies
|
Koromilas, A. |
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2014 |
50 |
S6 |
p. 148- 1 p. |
artikel |
190 |
94 Elucidating mechanisms of resistance to FGFR inhibitors in endometrial cancer
|
Packer, L. |
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2014 |
50 |
S6 |
p. 35- 1 p. |
artikel |
191 |
579 Eph/ephrin-B interactions modulate a BAFF-R/TACI dependent survival of chronic lymphocytic leukemia (CLL) cells mediated in vitro by bone marrow stromal cells
|
Alonso-Colmenar, L.M. |
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2014 |
50 |
S6 |
p. 187- 1 p. |
artikel |
192 |
134 Epigenetic immunomodulation by SGI-110 combined with immune checkpoint blockade for new therapeutic strategies
|
Covre, A. |
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2014 |
50 |
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p. 47- 1 p. |
artikel |
193 |
241 Epigenetic loss-of-function BRCA1 mediates tumor cure by single dose radiotherapy
|
Campagne, C. |
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2014 |
50 |
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p. 81- 1 p. |
artikel |
194 |
18 Establishment and characterization of a Merkel Cell carcinoma PDX panel: Screening for potentially useful therapies
|
Wick, M.J. |
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2014 |
50 |
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p. 12- 1 p. |
artikel |
195 |
178 Establishment of patient-derived xenografts (PDX) models for small cell lung (SCL) as a pre-clinical platform for drug development
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Broudy, T. |
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2014 |
50 |
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p. 59- 1 p. |
artikel |
196 |
146 Establishment of patient-derived xenografts (PDX) models for triple negative breast cancer (TNBC) as a pre-clinical platform for drug development
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Thatte, J. |
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2014 |
50 |
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p. 50- 1 p. |
artikel |
197 |
222 Estimating predictive values of short-term morphologic assays of cancer chemoprevention for efficacy in animal tumor assays
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Dunn, B. |
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2014 |
50 |
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p. 75- 1 p. |
artikel |
198 |
417 Evaluating the activity of the p53-MDM2 inhibitor NDD0005 in Ewing sarcoma
|
Pecqueur, J. |
|
2014 |
50 |
S6 |
p. 133- 1 p. |
artikel |
199 |
532 Evaluation of a BRCAness signature as a predictive biomarker of response to veliparib/carboplatin plus standard neoadjuvant therapy in high-risk breast cancer: results from the I-SPY 2 trial
|
Glas, A. |
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2014 |
50 |
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p. 173- 1 p. |
artikel |
200 |
425 Evaluation of drug reactions to anti-neoplastic agents in Phase I clinical trials
|
Bupathi, M. |
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2014 |
50 |
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p. 136- 1 p. |
artikel |
201 |
96 Evaluation of hormone therapies in a panel of breast PDX models: Relevance of ER status on sensitivity to letrozole and tamoxifen
|
Wick, M.J. |
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2014 |
50 |
S6 |
p. 35- 1 p. |
artikel |
202 |
522 Evaluation of the efficacy of melatonin in breast cancer metastasis mediated by ROCK-1
|
Borin, T. |
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2014 |
50 |
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p. 169-170 2 p. |
artikel |
203 |
580 Evaluation of the pan-BET-bromodomain inhibitor OTX015 as a single agent and in combination with everolimus (RAD001) in triple-negative breast cancer models
|
Vázquez, R. |
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2014 |
50 |
S6 |
p. 187- 1 p. |
artikel |
204 |
290 Exosome analysis in cancer patients: From the preclinical towards the clinical application: Trial design
|
Mertens, I. |
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2014 |
50 |
S6 |
p. 96- 1 p. |
artikel |
205 |
448 Exposure to EGFR inhibitors influences release of extracellular vesicles by tumor cells
|
van der Meel, R. |
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2014 |
50 |
S6 |
p. 147- 1 p. |
artikel |
206 |
534 Expression of c-MET in invasive meningioma
|
Yun, S. |
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2014 |
50 |
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p. 174- 1 p. |
artikel |
207 |
192 Extensive characterization of patient derived colon cancer xenografts for preclinical biomarker identification
|
Vuaroqueaux, V. |
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2014 |
50 |
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p. 62-63 2 p. |
artikel |
208 |
259 Factors that limit delivery of Cdk4/6 inhibitor palbociclib to GBM
|
Parrish, K. |
|
2014 |
50 |
S6 |
p. 86- 1 p. |
artikel |
209 |
302 FAK inhibitor VS-6063 (defactinib) targets mesothelioma cancer stem cells which are enriched by standard of care chemotherapy
|
Pachter, J. |
|
2014 |
50 |
S6 |
p. 99- 1 p. |
artikel |
210 |
473 FDG PET/CT as imaging biomarker in the era of molecular targeting therapies: sequential FDG PET/CT demonstrated biological response and acquisition of resistance to tyrosine kinase inhibitor therapy for renal cell carcinoma
|
Nakaigawa, N. |
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2014 |
50 |
S6 |
p. 154- 1 p. |
artikel |
211 |
1 Feasibility of large-scale genomic testing to facilitate enrollment on genomically-matched clinical trials
|
Meric-Bernstam, F. |
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2014 |
50 |
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p. 3- 1 p. |
artikel |
212 |
476 FGFR2 targeting with allosteric inhibitor RPT835
|
Tsimafeyeu, I. |
|
2014 |
50 |
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p. 155- 1 p. |
artikel |
213 |
364 First-in-human phase 1 study of MLN2480, an investigational oral pan-RAF kinase inhibitor, in patients (pts) with relapsed or refractory solid tumors, including BRAF/NRAS-mutant melanoma
|
Middleton, M. |
|
2014 |
50 |
S6 |
p. 117- 1 p. |
artikel |
214 |
320 First-in-human study with ARQ 092, a novel pan AKT-inhibitor, in subjects with advanced solid tumors or recurrent malignant lymphoma
|
Saleh, M. |
|
2014 |
50 |
S6 |
p. 104- 1 p. |
artikel |
215 |
504 Frequent loss-of-function mutations in MLK4 suppresses signaling in the JNK-cJUN-p21/p15 pathway to promote growth of colon cancer cells
|
Marusiak, A. |
|
2014 |
50 |
S6 |
p. 164- 1 p. |
artikel |
216 |
109 Functional activity, but not PD-1 expression level, differentiates primary CLL from healthy PD1+ T cells using SCNP
|
Liang, S. |
|
2014 |
50 |
S6 |
p. 39- 1 p. |
artikel |
217 |
175 Functional analysis of [methyl-3H]choline uptake in glioblastoma cells: Influence of anti-cancer and central nervous system drugs
|
Inazu, M. |
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2014 |
50 |
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p. 58- 1 p. |
artikel |
218 |
396 Gastrointestinal stromal tumor associated with neurofibromatosis type I
|
Takahashi, T. |
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2014 |
50 |
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p. 127- 1 p. |
artikel |
219 |
139 GBR1302: a BEAT® bispecific antibody for the treatment of HER2 positive cancers
|
Croset, A. |
|
2014 |
50 |
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p. 48- 1 p. |
artikel |
220 |
General Information
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2014 |
50 |
S6 |
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artikel |
221 |
15 Genetic and molecular validation of uterine sarcoma patient-derived xenograft models
|
Cuppens, T. |
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2014 |
50 |
S6 |
p. 11- 1 p. |
artikel |
222 |
198 Genetic and pharmacological inhibition of PIM-1 reduces tumor development in a K-Ras-driven mouse model of non-small cell lung cancer
|
Aguirre, E. |
|
2014 |
50 |
S6 |
p. 64- 1 p. |
artikel |
223 |
297 Genetic and pharmacologic inhibition of EPHA2 promotes apoptosis in NSCLC
|
Chen, J. |
|
2014 |
50 |
S6 |
p. 98- 1 p. |
artikel |
224 |
88 Genome-wide drug sensitivity screens in haploid mouse embryonic stem cells
|
Pettitt, S.J. |
|
2014 |
50 |
S6 |
p. 33- 1 p. |
artikel |
225 |
218 Genomic analysis identifies novel drivers and targetable pathways in inflammatory breast cancer patient samples
|
Moran, D.M. |
|
2014 |
50 |
S6 |
p. 74- 1 p. |
artikel |
226 |
303 Genomic and epigenomic analysis identify potential therapeutic targets in luminal B breast cancer molecular subtype
|
Klouche, L. Addou |
|
2014 |
50 |
S6 |
p. 99- 1 p. |
artikel |
227 |
167 Genomic characterisation of 1003 cancer cell-lines
|
Bignall, G. |
|
2014 |
50 |
S6 |
p. 56- 1 p. |
artikel |
228 |
433 Genomic predictors of therapeutic sensitivity to TAS-119, a selective inhibitor of Aurora-A kinase
|
Sootome, H. |
|
2014 |
50 |
S6 |
p. 142-143 2 p. |
artikel |
229 |
319 Genomic profiling of uterine leiomyosarcomas reveal frequent alterations in Akt/mammalian target of rapamycin (mTOR) pathway genes and other actionable genomic abnormalities linked to targeted therapies
|
Elvin, J.A. |
|
2014 |
50 |
S6 |
p. 104- 1 p. |
artikel |
230 |
414 Genomic profiling using a clinical next generation sequencing (NGS) assay reveals genomic alterations to guide targeted therapy in advanced neuroblastoma patients
|
Ali, S. |
|
2014 |
50 |
S6 |
p. 132- 1 p. |
artikel |
231 |
485 Glutathione S-transferases M1–5 reduce the aggressive behaviour in breast cancer by modulating the PI3K/AKT pathway
|
Bergamaschi, A. |
|
2014 |
50 |
S6 |
p. 158- 1 p. |
artikel |
232 |
566 GNS396 and analogues are potent new small molecules to target and kill chemotherapy-resistant subpopulation cells in acute myeloid leukemia
|
Bassissi, F. |
|
2014 |
50 |
S6 |
p. 183- 1 p. |
artikel |
233 |
427 Hematotoxicity potential of new drug candidates measured in hematopoietic progenitors in bone marrow samples
|
Ballesteros, J. |
|
2014 |
50 |
S6 |
p. 136-137 2 p. |
artikel |
234 |
228 Her2–3 heterodimer is a new and better than HER2 IHC score for clinical outcome prognosis
|
Weitsman, G. |
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2014 |
50 |
S6 |
p. 77- 1 p. |
artikel |
235 |
230 High correlation between clinical responses to first line AML patients treated with cytarabine and idarubicin and their pharmacological profiles in patient samples measured by ExviTech
|
Ballesteros, J. |
|
2014 |
50 |
S6 |
p. 77-78 2 p. |
artikel |
236 |
204 High-throughput functional screening identifies the flavoreductase POR as a principal determinant of sensitivity to the hypoxia-targeting prodrug SN30000
|
Hunter, F.W. |
|
2014 |
50 |
S6 |
p. 66- 1 p. |
artikel |
237 |
214 Homologous recombination deficiency (HRD) score and niraparib efficacy in high grade ovarian cancer
|
Haluska, P. |
|
2014 |
50 |
S6 |
p. 72-73 2 p. |
artikel |
238 |
191 Homotypic and heterotypic cell signaling transduction using a dielectrophoresis microfluidic device
|
Gabriel, M. Tellez |
|
2014 |
50 |
S6 |
p. 62- 1 p. |
artikel |
239 |
260 Hsp90 Inhibitor Drug Conjugates (HDC): Payloads and possibilities
|
Chimmanamada, D. |
|
2014 |
50 |
S6 |
p. 87- 1 p. |
artikel |
240 |
563 Hsp90 pharmacoproteomics: Harnessing pleiotropy for therapeutic synergy
|
Goldstein, R. |
|
2014 |
50 |
S6 |
p. 182- 1 p. |
artikel |
241 |
514 Hypoxia inducible factor (HIF)-1a expression levels and p53 mutations are prognostic factors for survival in breast cancer patients treated with neoadjuvant chemotherapy
|
Molina-Vila, M. |
|
2014 |
50 |
S6 |
p. 167- 1 p. |
artikel |
242 |
351 hz515H7, a humanized antibody exerts its antitumor activity via antagonism of the CXCR4/SDF-1 axis, and through effector functions
|
Klinguer-Hamour, C. |
|
2014 |
50 |
S6 |
p. 113- 1 p. |
artikel |
243 |
325 Identification and characterization of an irreversible inhibitor of CDK2
|
Martin, M. |
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2014 |
50 |
S6 |
p. 106- 1 p. |
artikel |
244 |
517 Identification and characterization of selective MELK kinase inhibitors
|
Carpinelli, P. |
|
2014 |
50 |
S6 |
p. 168- 1 p. |
artikel |
245 |
379 Identification and rational in silico-based targeting of a novel mediator of metastatic breast cancer
|
Clarkson, R. |
|
2014 |
50 |
S6 |
p. 122- 1 p. |
artikel |
246 |
160 Identification of fusion genes through kinome-centered RNA sequencing in different types of solid tumors
|
Mittempergher, L. |
|
2014 |
50 |
S6 |
p. 54- 1 p. |
artikel |
247 |
581 Identification of genomic and chromatin features that predict transcriptional response to BET bromodomain inhibition
|
Mertz, J. |
|
2014 |
50 |
S6 |
p. 187-188 2 p. |
artikel |
248 |
104 Identification of inhibitors of tryptophan metabolizing enzymes for cancer immunotherapy by high-throughput screening
|
Zaman, G. |
|
2014 |
50 |
S6 |
p. 37-38 2 p. |
artikel |
249 |
594 Identification of novel EZH2 inhibitor scaffolds
|
Espanel, X. |
|
2014 |
50 |
S6 |
p. 191- 1 p. |
artikel |
250 |
480 Identification of novel small molecules as selective PAK4 allosteric modulators (PAMs) by stable isotope labeling of amino acids in cells (SILAC)
|
Senapedis, W. |
|
2014 |
50 |
S6 |
p. 156- 1 p. |
artikel |
251 |
206 Identification of novel targets for radiosensitisation of non-small cell lung cancer by secretome analysis
|
Sharma, A. |
|
2014 |
50 |
S6 |
p. 67- 1 p. |
artikel |
252 |
111 Identification of peptides which could block PD-1 checkpoint for NSCLC immunotherapy
|
Zhu, Y. |
|
2014 |
50 |
S6 |
p. 39- 1 p. |
artikel |
253 |
383 Identification of potent and selective tankyrase 1/2 inhibitors with activity in a subset of APC mutant colorectal cancer
|
Guichard, S.M. |
|
2014 |
50 |
S6 |
p. 123- 1 p. |
artikel |
254 |
95 Identification of synthetic lethality compounds from natural products for cancers
|
Ng, K.W. |
|
2014 |
50 |
S6 |
p. 35- 1 p. |
artikel |
255 |
180 Identifying and monitoring somatic mutations in cell free DNA of patients with metastatic melanoma
|
Wisell, J. |
|
2014 |
50 |
S6 |
p. 59-60 2 p. |
artikel |
256 |
466 IGF2 drives IGF oncogenic signaling in HCC and emerges as a potential target for therapies
|
Quetglas, I.M. |
|
2014 |
50 |
S6 |
p. 152- 1 p. |
artikel |
257 |
311 IGF-1R inhibition induced activation of Yes/SFK acts as a by-pass resistance pathway in rhabdomyosarcoma
|
Wan, X. |
|
2014 |
50 |
S6 |
p. 101- 1 p. |
artikel |
258 |
317 IKKβ inhibition suppresses sphere formation and self-renewal of lung cancer initiating cells
|
Carneiro-Lobo, T. |
|
2014 |
50 |
S6 |
p. 103- 1 p. |
artikel |
259 |
142 IL-17 as a novel molecular target for prostate cancer prevention
|
de Angulo, A. |
|
2014 |
50 |
S6 |
p. 49- 1 p. |
artikel |
260 |
110 IL-6/STAT3/Fra-1 signaling axis promotes colorectal cancer aggressiveness through epithelial–mesenchymal transition
|
Shao, J. |
|
2014 |
50 |
S6 |
p. 39- 1 p. |
artikel |
261 |
8 Imaging growth and anti-cancer activity in orthotopic patient derived tumors
|
Baugher, M. |
|
2014 |
50 |
S6 |
p. 9- 1 p. |
artikel |
262 |
6 Imaging in cancer immunology: Phenotyping of multiple immune cell subsets in-situ in FFPE tissue sections
|
Mansfield, J.R. |
|
2014 |
50 |
S6 |
p. 8-9 2 p. |
artikel |
263 |
126 IMCgp100: A novel bi-specific biologic for the treatment of malignant melanoma
|
Shingler, W. |
|
2014 |
50 |
S6 |
p. 44- 1 p. |
artikel |
264 |
137 Immune checkpoint blockade enhances measles virotherapy
|
Engeland, C.E. |
|
2014 |
50 |
S6 |
p. 48- 1 p. |
artikel |
265 |
501 Immunological STAT3 knockdown associated with anti-tumor activity in pre-clinical models translates to clinical samples, suggesting immune modulation contributes to the clinical activity of AZD9150, a therapeutic STAT3 ASO
|
McCoon, P. |
|
2014 |
50 |
S6 |
p. 163-164 2 p. |
artikel |
266 |
151 Impact of EGFR amplification pattern on the expression of miRNA-200c in primary glioblastoma multiforme
|
Hidalgo, L. Muñoz |
|
2014 |
50 |
S6 |
p. 51-52 2 p. |
artikel |
267 |
237 Impact of phase 1 expansion cohorts on probability of success in phase 2 and time-to-drug-approval: analysis of 385 new drugs in oncology
|
Bugano, D. |
|
2014 |
50 |
S6 |
p. 79-80 2 p. |
artikel |
268 |
262 Improved cytotoxic activity of Nor-β-lapachone-loaded PLGA microcapsules in PC3M prostate cancer cell line
|
Pessoa, C. |
|
2014 |
50 |
S6 |
p. 87- 1 p. |
artikel |
269 |
595 Improving specificity of epigenetic therapy through combined targeting of DNA and histone methylation
|
Sato, T. |
|
2014 |
50 |
S6 |
p. 192- 1 p. |
artikel |
270 |
74 Increased EDN1 expression mediates acquired resistance to the combination therapy of PI3K and MEK inhibitors for colorectal cancer
|
Bhattacharya, B. |
|
2014 |
50 |
S6 |
p. 29- 1 p. |
artikel |
271 |
367 Induction of apoptosis and inhibition of angiogenesis by novel fusion protein – AD-O54.9 as a new preclinical strategy in cancer treatment
|
Rozga, P. |
|
2014 |
50 |
S6 |
p. 118- 1 p. |
artikel |
272 |
380 Induction of apoptosis with a novel dual cIAP1/XIAP antagonist in models of melanoma
|
Ward, G. |
|
2014 |
50 |
S6 |
p. 122- 1 p. |
artikel |
273 |
86 Influence of EGFR exon 19 mutation subtypes on survival outcomes in advanced stage Asian non-small cell lung cancer patients receiving TKI therapy
|
Chowbay, B. |
|
2014 |
50 |
S6 |
p. 32- 1 p. |
artikel |
274 |
464 Influence of warm and cold ischemia on molecular patterns in clinical biospecimen
|
Unger, F.T. |
|
2014 |
50 |
S6 |
p. 151-152 2 p. |
artikel |
275 |
510 Inhibition of STAT3 enhances the radiosensitising effect of temozolomide in malignant glioma cells in vitro and in vivo
|
Kim, I. |
|
2014 |
50 |
S6 |
p. 166- 1 p. |
artikel |
276 |
293 Inhibition of the cell cycle regulated Cdc7 kinase pathway is an efficacious therapeutic approach for hematologic malignancies and solid tumors
|
Santos, R. |
|
2014 |
50 |
S6 |
p. 96-97 2 p. |
artikel |
277 |
310 Inhibition of Trk-driven tumors by the pan-Trk inhibitor RXDX-101
|
Anderson, D. |
|
2014 |
50 |
S6 |
p. 101- 1 p. |
artikel |
278 |
346 Inhibition of Wnt pathway by novel thiazole-based Traf2- and Nck-interacting kinase (TNIK) inhibitor
|
Uno, Y. |
|
2014 |
50 |
S6 |
p. 112- 1 p. |
artikel |
279 |
199 Inhibitor of differentiation 1 (Id1) expression in lung cancer cells and liver microenvironment is required for liver metastasis (LM) development from non-small cell lung cancer (NSCLC) by regulating EMT-related and proliferation-related proteins
|
Castanon, E. |
|
2014 |
50 |
S6 |
p. 65- 1 p. |
artikel |
280 |
390 Inhibitors of EZH2 act synergistically with type 1 interferon to induce a potent interferon-stimulated gene response, triggering apoptosis in diffuse large B-cell lymphoma
|
Bradley, B. |
|
2014 |
50 |
S6 |
p. 125- 1 p. |
artikel |
281 |
345 Interaction of plitidepsin with eEF1A in living tumor cells
|
García, C. |
|
2014 |
50 |
S6 |
p. 111-112 2 p. |
artikel |
282 |
42 Interaction of SJG-136 with cognate sequences of oncogenic transcription factors
|
Mantaj, J. |
|
2014 |
50 |
S6 |
p. 19- 1 p. |
artikel |
283 |
163 Interrogation of pharmacogenes in cancer patients using targeted DNA sequencing
|
Innocenti, F. |
|
2014 |
50 |
S6 |
p. 55- 1 p. |
artikel |
284 |
578 Invadopodia are required for cancer cell extravasation and are a therapeutic target for metastasis
|
Leong, H.S. |
|
2014 |
50 |
S6 |
p. 187- 1 p. |
artikel |
285 |
531 In vitro and in vivo anti-tumor activity of ARQ 092, a potent and selective pan-AKT inhibitor
|
Yu, Y. |
|
2014 |
50 |
S6 |
p. 172-173 2 p. |
artikel |
286 |
481 In vitro and vivo evaluation of the pan FGFR inhibitor ARQ 087 and selective pan AKT inhibitor ARQ 092 in endometrial cancer: potential for combination therapy
|
Meade, J. |
|
2014 |
50 |
S6 |
p. 156-157 2 p. |
artikel |
287 |
203 Ionizing radiation induced phosphatidylserine externalization on endothelial cell surface – a potential target for vascular targeting
|
Zhao, Z. |
|
2014 |
50 |
S6 |
p. 66- 1 p. |
artikel |
288 |
483 Irreversible covalent pan-FGFR inhibitors are highly efficacious against FGFR-dependent cancers
|
Phan, V.T. |
|
2014 |
50 |
S6 |
p. 157- 1 p. |
artikel |
289 |
527 Is CRAF required for the maintenance of KRAS mutant non-small cell lung cancer?
|
Russell, P. |
|
2014 |
50 |
S6 |
p. 171- 1 p. |
artikel |
290 |
477 Jab1/Csn5: a new player driving the resistance to HER2-targeted therapies for breast cancer
|
Claret, F. |
|
2014 |
50 |
S6 |
p. 155- 1 p. |
artikel |
291 |
328 Jagged1 expression and its relevance in metastatic progression of breast cancers
|
Bednarz-Knoll, N. |
|
2014 |
50 |
S6 |
p. 106-107 2 p. |
artikel |
292 |
235 Kinetic analysis of dynamic 11C thymidine PET imaging studies: Compartmental and nonparametric approaches
|
Murphy, S. |
|
2014 |
50 |
S6 |
p. 79- 1 p. |
artikel |
293 |
234 Kinetic analysis of dynamic 11C-verapamil PET study: Compartmental v adaptive mixture models comparison
|
Hernandez, F. |
|
2014 |
50 |
S6 |
p. 79- 1 p. |
artikel |
294 |
358 Knockdown of beta-catenin with dicer-substrate siRNAs down-regulates Wnt/beta-catenin pathway signaling
|
Pursell, N. |
|
2014 |
50 |
S6 |
p. 115-116 2 p. |
artikel |
295 |
8LBA Activity of the PARP inhibitor olaparib in ATM-deficient gastric cancer: from preclinical models to the clinic
|
Hodgson, D. |
|
2014 |
50 |
S6 |
p. 198- 1 p. |
artikel |
296 |
9LBA Antitumor activity of ASP8273, an irreversible mutant selective EGFR-TKI, in NSCLC patients with tumors harboring EGFR activating mutations and T790M resistance mutation
|
Murakami, H. |
|
2014 |
50 |
S6 |
p. 198- 1 p. |
artikel |
297 |
4LBA A phase 1 study of first-in-class microRNA-34 mimic, MRX34, in patients with hepatocellular carcinoma or advanced cancer with liver metastasis
|
Beg, M. |
|
2014 |
50 |
S6 |
p. 196- 1 p. |
artikel |
298 |
1LBA Clinical safety and activity in a phase I trial of AG-120, a first in class, selective, potent inhibitor of the IDH1-mutant protein, in patients with IDH1 mutant positive advanced hematologic malignancies
|
Pollyea, D.A. |
|
2014 |
50 |
S6 |
p. 195- 1 p. |
artikel |
299 |
3LBA Initial report of a first-in-human study of the first-in-class fatty acid synthase (FASN) inhibitor, TVB-2640
|
Infante, J. |
|
2014 |
50 |
S6 |
p. 195-196 2 p. |
artikel |
300 |
10LBA Interim phase 2 results of study CO-1686-008: A phase 1/2 study of the irreversible, mutant selective, EGFR inhibitor rociletinib (CO-1686) in patients with advanced non small cell lung cancer
|
Soria, J. |
|
2014 |
50 |
S6 |
p. 199- 1 p. |
artikel |
301 |
7LBA Phase 1 dose-expansion study of AMG 900, a pan-Aurora kinase inhibitor, in adult patients with advanced taxane-resistant solid tumors
|
Markman, B. |
|
2014 |
50 |
S6 |
p. 197-198 2 p. |
artikel |
302 |
6LBA Phase 1 first-in-human study of the enhancer of zeste-homolog 2 (EZH2) histone methyl transferase inhibitor E7438 as a single agent in patients with advanced solid tumors or B cell lymphoma
|
Ribrag, V. |
|
2014 |
50 |
S6 |
p. 197- 1 p. |
artikel |
303 |
11LBA Phase I study of the selective BRAFV600 inhibitor encorafenib (LGX818) combined with cetuximab and with or without the α-specific PI3K inhibitor alpelisib (BYL719) in patients with advanced BRAF mutant colorectal cancer
|
Tabernero, J. |
|
2014 |
50 |
S6 |
p. 199- 1 p. |
artikel |
304 |
5LBA Results of a first-in-man phase I trial assessing OTX015, an orally available BET-bromodomain (BRD) inhibitor, in advanced hematologic malignancies
|
Stathis, A. |
|
2014 |
50 |
S6 |
p. 196- 1 p. |
artikel |
305 |
2LBA The identification of potent and selective inhibitors of oncogenes in medullary thyroid carcinoma and lung adenocarcinoma disease models
|
Fritzl, S. |
|
2014 |
50 |
S6 |
p. 195- 1 p. |
artikel |
306 |
261 Lesion characterization with ferumoxytol MRI in patients with advanced solid tumors and correlation with treatment response to MM-398, nanoliposomal irinotecan (nal-IRI)
|
Ramanathan, R.K. |
|
2014 |
50 |
S6 |
p. 87- 1 p. |
artikel |
307 |
Letter of Welcome
|
Soria, Jean-Charles |
|
2014 |
50 |
S6 |
p. vii- 1 p. |
artikel |
308 |
161 Leveraging a novel DNA barcoding platform for integrated profiling and pharmacodynamic readouts
|
Castro, C. |
|
2014 |
50 |
S6 |
p. 54- 1 p. |
artikel |
309 |
75 Loss of PTEN leads to acquired resistance to the PI3Ka inhibitor BYL719: a case of convergent evolution under selective therapeutic pressure
|
Castel, P. |
|
2014 |
50 |
S6 |
p. 29- 1 p. |
artikel |
310 |
55 Low, frequent doses of PM060184 induce remarkable in vivo antitumor activity
|
Aviles, P. |
|
2014 |
50 |
S6 |
p. 23- 1 p. |
artikel |
311 |
391 LOXO-101, a pan TRK inhibitor, for the treatment of TRK-driven cancers
|
Winski, S. |
|
2014 |
50 |
S6 |
p. 125- 1 p. |
artikel |
312 |
494 LPA6 promotes growth and tumorigenicity of hepatocellular carcinoma via activation of PIM-3 proto-oncogene kinase
|
Lopane, C. |
|
2014 |
50 |
S6 |
p. 161- 1 p. |
artikel |
313 |
47 Lurbinectedin (PM01183) specifically targets RNA Pol II for degradation via the proteasome pathway in a transcription and TC-NER dependent fashion
|
Santamaria, G. |
|
2014 |
50 |
S6 |
p. 20-21 2 p. |
artikel |
314 |
562 Lysophosphatidic acid-induced breast cancer metastasis depends on LPA1/ZEB1/miR-21-activation pathway
|
Sahay, D. |
|
2014 |
50 |
S6 |
p. 182- 1 p. |
artikel |
315 |
118 Major synergy between Coxsackievirus A21 (CAVATAK™) and radiotherapy or chemotherapy in bladder cancer
|
Simpson, G.R. |
|
2014 |
50 |
S6 |
p. 41-42 2 p. |
artikel |
316 |
574 M-COPA, a Golgi disruptor, inhibits cell surface expression of MET protein and exhibits antitumor activity against MET-addicted cancers
|
Ohashi, Y. |
|
2014 |
50 |
S6 |
p. 185-186 2 p. |
artikel |
317 |
5 Mechanism based targeted therapy for hereditary leiomyomatosis and renal cell cancer (HLRCC) and sporadic papillary renal cell carcinoma: interim results from a phase 2 study of bevacizumab and erlotinib
|
Srinivasan, R. |
|
2014 |
50 |
S6 |
p. 8- 1 p. |
artikel |
318 |
591 Mechanistic analysis of reversible FASN inhibition in preclinical tumor models identifies highly susceptible tumor types and enriches biomarker discovery for clinical applications
|
Heuer, T.S. |
|
2014 |
50 |
S6 |
p. 190-191 2 p. |
artikel |
319 |
445 MEK inhibition enhances gemcitabine efficacy by increasing MDM2-mediated ubiquitination and degradation of RRM1
|
Vena, F. |
|
2014 |
50 |
S6 |
p. 146- 1 p. |
artikel |
320 |
543 MEK1/2 specific inhibitor, SMK-17 selectively induces apoptosis in β-catenin mutated tumors
|
Kiga, M. |
|
2014 |
50 |
S6 |
p. 176- 1 p. |
artikel |
321 |
282 Membrane anchorage of Stat3 via artificial protein lipidation
|
Avadisian, M. |
|
2014 |
50 |
S6 |
p. 93- 1 p. |
artikel |
322 |
375 MER as a novel therapeutic target in colorectal cancer
|
Wong, K. |
|
2014 |
50 |
S6 |
p. 120-121 2 p. |
artikel |
323 |
298 Met degradation by SAIT301, a Met monoclonal antibody, reduces the invasion and migration of nasopharyngeal cancer cells via inhibition of EGR-1 expression
|
Kim, C. |
|
2014 |
50 |
S6 |
p. 98- 1 p. |
artikel |
324 |
44 Metformin and its impact on gastric cancer patients survival after gastrectomy
|
Lee, C.K. |
|
2014 |
50 |
S6 |
p. 20- 1 p. |
artikel |
325 |
205 Metformin to modulate AMP-kinase and enhance chemotherapy and radiotherapy in non-small cell lung cancer
|
Troncone, M.J. |
|
2014 |
50 |
S6 |
p. 67- 1 p. |
artikel |
326 |
54 MGMT methylation assessed by methyl-BEAMing technique is a prognostic and predictive biomarker in glioblastoma and metastatic colorectal cancer patients
|
Barault, L. |
|
2014 |
50 |
S6 |
p. 23- 1 p. |
artikel |
327 |
502 MI130004, an antibody–drug conjugate including a novel payload of marine origin: Evidences of in vivo activity
|
Aviles, P.M. |
|
2014 |
50 |
S6 |
p. 164- 1 p. |
artikel |
328 |
256 Minicell packaged targeted delivery of shRNA to cancer cells
|
Jivrajani, M. |
|
2014 |
50 |
S6 |
p. 85-86 2 p. |
artikel |
329 |
20 miR-25 is a key regulator of prostate cancer invasiveness by modulation of the cross-talk between Notch and TGF-β signaling
|
Zoni, E. |
|
2014 |
50 |
S6 |
p. 12-13 2 p. |
artikel |
330 |
545 MiRNAs related to KRAS mutational status in resectable non-small cell lung cancer
|
Gallach, S. |
|
2014 |
50 |
S6 |
p. 177- 1 p. |
artikel |
331 |
76 Mixed lineage kinases activate MEK independently of RAF to mediate resistance to RAF inhibitors
|
Marusiak, A.A. |
|
2014 |
50 |
S6 |
p. 29-30 2 p. |
artikel |
332 |
14 Mixeno mouse models for in vivo evaluation of anti-human cancer immunotherapeutics
|
Zhang, J. |
|
2014 |
50 |
S6 |
p. 11- 1 p. |
artikel |
333 |
438 MM-131: A bispecific antibody that inhibits c-Met signaling through avid binding to the EpCAM tumor antigen
|
Harms, B.D. |
|
2014 |
50 |
S6 |
p. 144- 1 p. |
artikel |
334 |
570 Modulation of chromatin-related processes in DNA damage response as a potential strategy to treat acute myeloid leukemia
|
Chomej, K. |
|
2014 |
50 |
S6 |
p. 184- 1 p. |
artikel |
335 |
172 Modulation of estrogen-dependent transcription by cohesin in MCF7 human breast adenocarcinoma cells
|
Dasgupta, T. |
|
2014 |
50 |
S6 |
p. 57- 1 p. |
artikel |
336 |
243 Modulation of PI3K/mTOR pathway following PARP inhibition in small cell lung cancer
|
Cardnell, R.J. |
|
2014 |
50 |
S6 |
p. 81-82 2 p. |
artikel |
337 |
275 Modulation of PIP2 levels through small molecule inhibition of PIP5K
|
Andrews, D. |
|
2014 |
50 |
S6 |
p. 91- 1 p. |
artikel |
338 |
254 Molecular analysis in breast cancer: correlation with Immunohistochemical classification and pathologic complete response (pCR) to neoadjuvant chemotherapy (NAC)
|
Baulies, S. |
|
2014 |
50 |
S6 |
p. 85- 1 p. |
artikel |
339 |
189 Molecular and pharmacological characterization of primary mesothelioma tumor cell lines orthotopically xenografted in nude mice
|
Pisano, C. |
|
2014 |
50 |
S6 |
p. 62- 1 p. |
artikel |
340 |
460 Molecular biomarkers of inflammatory signature in melanoma
|
Ekmekcioglu, S. |
|
2014 |
50 |
S6 |
p. 150- 1 p. |
artikel |
341 |
421 Molecular profiling for factors predicting sensitivity or resistance to therapy in relapsed child cancer
|
Saletta, F. |
|
2014 |
50 |
S6 |
p. 135- 1 p. |
artikel |
342 |
184 Molecular profiling of heterogeneous tumor cells
|
Chenchik, A. |
|
2014 |
50 |
S6 |
p. 60- 1 p. |
artikel |
343 |
225 Molecular targets of interest to the NCI PREVENT cancer preclinical drug development program
|
Shoemaker, R.H. |
|
2014 |
50 |
S6 |
p. 76- 1 p. |
artikel |
344 |
436 Monitoring activity of RXDX-101 in Phase 1/2 patients using a pharmacodynamic assay for TrkA activation
|
Murphy, D. |
|
2014 |
50 |
S6 |
p. 143-144 2 p. |
artikel |
345 |
454 Monitoring therapy response and resistance mutations in circulating RNA and DNA of plasma from patients with malignant melanoma
|
Enderle, D. |
|
2014 |
50 |
S6 |
p. 149- 1 p. |
artikel |
346 |
7 Mouse clinical trial – A new preclinical study concept using patient-derived xenografts
|
Vuaroqueaux, V. |
|
2014 |
50 |
S6 |
p. 9- 1 p. |
artikel |
347 |
153 Moving beyond in vitro models and addressing the challenges of pooled RNAi screens in mouse xenografts
|
Tedesco, D. |
|
2014 |
50 |
S6 |
p. 52- 1 p. |
artikel |
348 |
10 mTOR inhibition with everolimus – a novel treatment option for head and neck cancer identified in a translational research study using patient-derived xenografts
|
Klinghammer, K. |
|
2014 |
50 |
S6 |
p. 10- 1 p. |
artikel |
349 |
357 Multi-color flow cytometry immunophenotyping for detection of CSC in NSCLC
|
Martinez-Romero, A. |
|
2014 |
50 |
S6 |
p. 115- 1 p. |
artikel |
350 |
227 Multiplexed ICE COLD-PCR: A mutation detection methodology for achieving sensitivities of <0.01% using either Sanger or NGS
|
Wu, G. |
|
2014 |
50 |
S6 |
p. 76-77 2 p. |
artikel |
351 |
339 NAMPT inhibition as strategy to impair tumor growth
|
Cerezo, A. |
|
2014 |
50 |
S6 |
p. 110- 1 p. |
artikel |
352 |
361 Nanoformulations of the PARP inhibitors olaparib and BMN 673 for cancer nanotherapy
|
Sridhar, S. |
|
2014 |
50 |
S6 |
p. 116- 1 p. |
artikel |
353 |
588 Neddylation as a therapeutic target in refractory pediatric malignancies: Evaluation of the activating enzyme inhibitor MLN4924
|
Ruan, Y. |
|
2014 |
50 |
S6 |
p. 189-190 2 p. |
artikel |
354 |
159 Neoadjuvant chemotherapy in breast cancer patients induces expression of miR-34a and miR-122
|
Freres, P. |
|
2014 |
50 |
S6 |
p. 53-54 2 p. |
artikel |
355 |
374 Neuregulin 1 (NRG1) expression is a predictive biomarker for response to AV-203, an ERBB3 inhibitory antibody, in human tumor models
|
Meetze, K. |
|
2014 |
50 |
S6 |
p. 120- 1 p. |
artikel |
356 |
196 Neuropilin 2 (NRP2) modifies CXCL12/CXCR4 signaling and promotes lymph node metastases in colon cancer
|
Schneider, H. |
|
2014 |
50 |
S6 |
p. 64- 1 p. |
artikel |
357 |
413 Next-generation sequencing identifies the mechanism of tumourigenesis caused by loss of SMARCB1 in malignant rhabdoid tumours
|
Finetti, M.A. |
|
2014 |
50 |
S6 |
p. 132- 1 p. |
artikel |
358 |
12 Next generation sequencing (NGS) guided therapy prediction for the treatment of glioblastoma multiforme (GBM)
|
Sarkaria, J. |
|
2014 |
50 |
S6 |
p. 10-11 2 p. |
artikel |
359 |
64 Nifuroxazide halogenic derivatives induce ROS-mediated apoptosis and display antitumor activity against metastatic melanoma
|
de Farias, C. Fernandez |
|
2014 |
50 |
S6 |
p. 26- 1 p. |
artikel |
360 |
239 Niraparib, a selective PARP 1/2 inhibitor, is efficacious in pre-clinical models of small-cell lung cancer
|
Wang, Y. |
|
2014 |
50 |
S6 |
p. 80-81 2 p. |
artikel |
361 |
31 N-Myc amplification sensitizes tumor cells to inhibition by Danusertib, an Aurora kinase inhibitor
|
Carpinelli, P. |
|
2014 |
50 |
S6 |
p. 16- 1 p. |
artikel |
362 |
589 N-myc downstream regulated gene 1 (NDRG1) as a novel anti-angiogenic and therapeutic target for VEGF/VEGF receptor signaling by vascular endothelial cells
|
Watari, K. |
|
2014 |
50 |
S6 |
p. 190- 1 p. |
artikel |
363 |
561 Nonclinical characterization of the first in class investigational ubiquitin activating enzyme inhibitor MLN7243 in cellular and in vivo models of cancer in support of a phase I study
|
Milhollen, M. |
|
2014 |
50 |
S6 |
p. 181-182 2 p. |
artikel |
364 |
424 Nonclinical safety assessment of a humanized anti-OX40 agonist antibody, MOXR0916
|
Prell, R. |
|
2014 |
50 |
S6 |
p. 136- 1 p. |
artikel |
365 |
385 Noninvasive monitoring of acquired EGFR-T790M mutation and discovery of its heterogeneity in patients with advanced NSCLC treated with EGFR-TKI
|
Ye, X. |
|
2014 |
50 |
S6 |
p. 123-124 2 p. |
artikel |
366 |
443 Notch3-targeted antibody drug conjugates have superior preclinical efficacy to Notch signaling inhibitors
|
Geles, K.G. |
|
2014 |
50 |
S6 |
p. 145- 1 p. |
artikel |
367 |
267 Novel adjuvant therapy with leptin peptide receptor antagonist-2 conjugated to nanoparticles (IONP-LPrA2) to minimize chemoresistance in triple negative breast cancer
|
Harmon, T. |
|
2014 |
50 |
S6 |
p. 89- 1 p. |
artikel |
368 |
322 Novel alternative splice variants as potential biomarkers and therapeutic targets in aggressive prostate cancer in men of African descent
|
Patierno, S. |
|
2014 |
50 |
S6 |
p. 105- 1 p. |
artikel |
369 |
212 Novel anti-tumor activity of targeted LSD1 inhibition by GSK2879552
|
Mohammad, H. |
|
2014 |
50 |
S6 |
p. 72- 1 p. |
artikel |
370 |
22 Novel combination therapy, TAS-102 combined with the anti-EGFR antibody or the anti-VEGF antibody showed therapeutic benefit toward colorectal cancer xenografts
|
Ishida, K. |
|
2014 |
50 |
S6 |
p. 13- 1 p. |
artikel |
371 |
274 Novel cysteine derivatives for the next generation anticancer agents acting on KSP
|
Ogo, N. |
|
2014 |
50 |
S6 |
p. 91- 1 p. |
artikel |
372 |
281 Novel hybrid drug design strategy to circumvent erlotinib resistance and to optimize its pharmacokinetic properties for treating lung cancer
|
Poon, D.C.S. |
|
2014 |
50 |
S6 |
p. 93- 1 p. |
artikel |
373 |
576 Novel inhibitors of peritoneal seeding
|
Shen, Y. |
|
2014 |
50 |
S6 |
p. 186- 1 p. |
artikel |
374 |
571 Novel potent inhibitors of the Histone Demethylase KDM1A: Synthesis, pharmacological evaluation and in vivo activity
|
Varasi, M. |
|
2014 |
50 |
S6 |
p. 185- 1 p. |
artikel |
375 |
447 Novel, quantitative in vivo shRNA screening approach identifies new molecular targets to block cancer metastasis
|
Willetts, L. |
|
2014 |
50 |
S6 |
p. 147- 1 p. |
artikel |
376 |
71 Novel regulation of estrogen receptor transcription by the PI3K pathway
|
Toska, E. |
|
2014 |
50 |
S6 |
p. 28- 1 p. |
artikel |
377 |
116 Novel targets for antibody–drug conjugate therapy
|
Grandi, A.G. |
|
2014 |
50 |
S6 |
p. 41- 1 p. |
artikel |
378 |
318 Novel therapeutic targets for ARID1A mutant ovarian clear cell carcinoma (OCCC)
|
Miller, R.E. |
|
2014 |
50 |
S6 |
p. 103-104 2 p. |
artikel |
379 |
170 Novel, ultra-deep next-generation sequencing for BRAF mutation testing using small amount of cell-free DNA from plasma of patients with advanced cancers
|
Janku, F. |
|
2014 |
50 |
S6 |
p. 57- 1 p. |
artikel |
380 |
26 NPD926, a small molecule inducer of reactive oxygen species, kills cancer cells via glutathione depletion
|
Kawamura, T. |
|
2014 |
50 |
S6 |
p. 14- 1 p. |
artikel |
381 |
368 NP137, the first humanized monoclonal antibody directed against netrin-1, exhibits antitumor activity by inducing dependence receptors-mediated cell death
|
Delcros, J.G. |
|
2014 |
50 |
S6 |
p. 118-119 2 p. |
artikel |
382 |
72 Nrf2 as a molecular target in overwhelming chemoresistance in breast cancer therapy
|
Samadi, N. |
|
2014 |
50 |
S6 |
p. 28- 1 p. |
artikel |
383 |
550 Nupharidine inhibits NF-kB activity, induces apoptosis and has synergistic cytotoxic activity with cisplatin and etoposide
|
Gopas, J. |
|
2014 |
50 |
S6 |
p. 178-179 2 p. |
artikel |
384 |
432 ODM-203, a novel, selective and balanced FGFR and VEGFR inhibitor with strong anti-tumor activity in FGFR- and VEGFR-dependent cancer models
|
Holmström, T. |
|
2014 |
50 |
S6 |
p. 142- 1 p. |
artikel |
385 |
350 Oncogenic Ras mutants differentially utilize PLC-dependent calcium flux and PKC activation for MAPK signaling
|
Pitt, C. |
|
2014 |
50 |
S6 |
p. 113- 1 p. |
artikel |
386 |
314 Optimal sequencing schedules for combining BRAF inhibition with BCL-2 inhibition
|
Schalck, A. |
|
2014 |
50 |
S6 |
p. 102- 1 p. |
artikel |
387 |
400 Optimization of novel pyrido[2,3-b]pyrazine based small molecule fibroblast growth factor receptor 1, 2, 3 & 4 (FGFR) inhibitors into a potential clinical candidate
|
Angibaud, P. |
|
2014 |
50 |
S6 |
p. 128- 1 p. |
artikel |
388 |
572 Oral panobinostat in patients with advanced tumors and impaired renal function: Relationship between pharmacokinetics and key safety parameters
|
Porro, M. |
|
2014 |
50 |
S6 |
p. 185- 1 p. |
artikel |
389 |
567 OTX015, a BET-bromodomain (BET-BRD) inhibitor, potentiates the in vitro effects of chemotherapy drugs and targeted agents in human leukemic cell lines
|
Astorgues-Xerri, L. |
|
2014 |
50 |
S6 |
p. 183- 1 p. |
artikel |
390 |
564 OTX015, a novel BET-BRD inhibitor is active in non-small-cell lung cancer cell (NSCLC) lines harboring different oncogenic mutations
|
Riveiro, M. |
|
2014 |
50 |
S6 |
p. 182- 1 p. |
artikel |
391 |
469 OTX015, a novel BET-bromodomain (BET-BRD) inhibitor, is a promising anticancer agent for human glioblastoma
|
Ouafik, L. |
|
2014 |
50 |
S6 |
p. 153- 1 p. |
artikel |
392 |
220 Overcoming drug-resistance in multiple myeloma by XPO1 inhibitor combination therapy
|
Turner, J. |
|
2014 |
50 |
S6 |
p. 74-75 2 p. |
artikel |
393 |
258 Pancreatic cancer cells expressing the OATP1B3 transporter show promising sensitivity to the highly cytotoxic microcystin-LR molecule
|
Kounnis, V. |
|
2014 |
50 |
S6 |
p. 86- 1 p. |
artikel |
394 |
194 Pancreatic ductal organoids as a new platform for drug discovery
|
Ponz-Sarvise, M. |
|
2014 |
50 |
S6 |
p. 63- 1 p. |
artikel |
395 |
246 PARP inhibitors trap PARP1 onto damaged DNA via catalytic inhibition and not by an allosteric mechanism
|
Hopkins, T. |
|
2014 |
50 |
S6 |
p. 82-83 2 p. |
artikel |
396 |
354 PCR-based assay for BRAFV600 mutation analysis in ctDNA: clinical results from plasma and serum samples
|
Gonzalez-Cao, M. |
|
2014 |
50 |
S6 |
p. 114- 1 p. |
artikel |
397 |
410 Pediatric Preclinical Testing Program (PPTP) Evaluation of the p53-MDM2 Antagonist MK-8242
|
Smith, M. |
|
2014 |
50 |
S6 |
p. 131- 1 p. |
artikel |
398 |
21 Pharmacogenomics of mithramycin in thoracic malignancies
|
Figg, W. |
|
2014 |
50 |
S6 |
p. 13- 1 p. |
artikel |
399 |
478 Pharmacological disruption of the Astrocytic Elevated Gene-1 (AEG1) in anticancer intervention: PB0412_3 (PB03) as a first-in-class AEG1 interacting agent
|
Jimeno, J. |
|
2014 |
50 |
S6 |
p. 156- 1 p. |
artikel |
400 |
499 Phase 2a study of copanlisib, a novel phosphatidylinositol-3-kinase (PI3K) inhibitor, in patients with relapsed/refractory, indolent or aggressive lymphoma
|
Dreyling, M. |
|
2014 |
50 |
S6 |
p. 162-163 2 p. |
artikel |
401 |
551 Phase 1B study of CC-486 (oral azacitidine) in tumors associated with a viral etiology
|
von Hoff, D.D. |
|
2014 |
50 |
S6 |
p. 179- 1 p. |
artikel |
402 |
253 Phase 1 correlative study of ARQ761, a β-lapachone analogue that promotes NQ01-mediated programmed cancer cell necrosis
|
Gerber, D. |
|
2014 |
50 |
S6 |
p. 84-85 2 p. |
artikel |
403 |
382 Phase Ib study of oral dual-PI3K/mTOR inhibitor GDC-0980 in combination with capecitabine and mFOLFOX6 + bevacizumab in patients with advanced solid tumors and colorectal cancer
|
Rosen, L. |
|
2014 |
50 |
S6 |
p. 122-123 2 p. |
artikel |
404 |
34 Phase I, dose-escalation study of the investigational drug D07001-F4, an oral formulation of gemcitabine HCl, in patients (pts) with advanced solid tumors or lymphoma
|
Lin, C. |
|
2014 |
50 |
S6 |
p. 17- 1 p. |
artikel |
405 |
65 Phase II drug metabolism UGT1A enzyme affects cellular response of colon cancer cells to antitumor triazoloacridinone C-1305 treatment
|
Augustin, E. |
|
2014 |
50 |
S6 |
p. 26- 1 p. |
artikel |
406 |
141 Phase I study of ipilimumab with stereotactic radiosurgery for melanoma patients with brain metastases
|
Shi, W. |
|
2014 |
50 |
S6 |
p. 49- 1 p. |
artikel |
407 |
23 Phase I study of lurbinectedin (PM01183) administered on days (D) 1 & 8 every 3 weeks (q3wk) in patients (pts) with solid tumors
|
Ratain, M.J. |
|
2014 |
50 |
S6 |
p. 13-14 2 p. |
artikel |
408 |
586 Phase I study of pan-histone deacetylase inhibitor abexinostat in combination with cisplatin in patients with advanced solid tumors
|
Campone, M. |
|
2014 |
50 |
S6 |
p. 189- 1 p. |
artikel |
409 |
216 Phase I study of panobinostat and fractionated stereotactic re-irradiation therapy (FSRT) for recurrent high grade gliomas
|
Shi, W. |
|
2014 |
50 |
S6 |
p. 73- 1 p. |
artikel |
410 |
219 Phase I trial evaluating the antiviral agent Cidofovir in combination with chemoradiation in cervical cancer patients: A novel approach to treat HPV related malignancies?
|
Deutsch, E. |
|
2014 |
50 |
S6 |
p. 74- 1 p. |
artikel |
411 |
506 Phase (Ph) 1/2a study of TSR-011, a potent inhibitor of ALK and TRK, in advanced solid tumors including crizotinib-resistant ALK positive non-small cell lung cancer
|
Sachdev, J. |
|
2014 |
50 |
S6 |
p. 165- 1 p. |
artikel |
412 |
440 Phenotypic alteration in a highly metastatic variant of the MDA-MB-231 cell line: role of Annexin A1
|
Tu, Y. |
|
2014 |
50 |
S6 |
p. 144-145 2 p. |
artikel |
413 |
362 Phenotypic plasticity in epithelial progenitors and mesenchymal carcinoma is regulated by Axl signaling
|
Engelsen, A. |
|
2014 |
50 |
S6 |
p. 117- 1 p. |
artikel |
414 |
39 Phytochemical indole-3-carbinol synergizes strongly with fludarabine and induces p53-dependent and -independent cell death in chronic lymphocytic leukemia cells irrespective of their IGHV mutation state and treatment resistances
|
Perez-Chacon, G. |
|
2014 |
50 |
S6 |
p. 18- 1 p. |
artikel |
415 |
386 PI3K and MEK inhibitor combination toxicities and relative dose intensity: Vall d'Hebron experience
|
Azaro, A. |
|
2014 |
50 |
S6 |
p. 124- 1 p. |
artikel |
416 |
101 PIK3CA mutation-targeting compounds analyses using NCI60 cell line panel
|
Bando, H. |
|
2014 |
50 |
S6 |
p. 36-37 2 p. |
artikel |
417 |
304 PI3′-Kinase inhibition forestalls the development of drug resistance in BRAFV600E/PTENNull melanoma
|
Deuker, M. |
|
2014 |
50 |
S6 |
p. 100- 1 p. |
artikel |
418 |
439 PI3K/mTOR inhibitor VS-5584 targets cancer stem cells and prevents tumor regrowth after chemotherapy in preclinical models of small cell lung cancer
|
Kolev, V. |
|
2014 |
50 |
S6 |
p. 144- 1 p. |
artikel |
419 |
437 PIM kinase inhibitor AZD1208 sensitises SCLC to BH3 mimetic AZD4320
|
Sloane, R. |
|
2014 |
50 |
S6 |
p. 144- 1 p. |
artikel |
420 |
365 Pim-1 kinase: Validated as a therapeutic cancer target for MYC-driven tumours
|
Renner, O. |
|
2014 |
50 |
S6 |
p. 118- 1 p. |
artikel |
421 |
58 Pipecolidepsin A, Stellatolide A and Irvalec: New cyclodepsipeptides of marine origin with antitumor activity
|
Molina-Guijarro, J.M. |
|
2014 |
50 |
S6 |
p. 24- 1 p. |
artikel |
422 |
150 Pirin downregulates E-cadherin gene expression and contributes to EMT
|
Komai, K. |
|
2014 |
50 |
S6 |
p. 51- 1 p. |
artikel |
423 |
453 Plasma metabolomic signature of novel signal transduction inhibitors from preclinical identification to clinical validation
|
Ang, J.E. |
|
2014 |
50 |
S6 |
p. 148-149 2 p. |
artikel |
424 |
52 Platinum(IV) derivatives of oxaliplatin: Cellular effects and in vivo potency
|
Göschl, S. |
|
2014 |
50 |
S6 |
p. 22- 1 p. |
artikel |
425 |
377 Plucked hair as a platform for monitoring pharmacodynamic and mechanistic consequences of clinical exposure to the Wnt/beta-catenin inhibitor PRI-724
|
Miele, G. |
|
2014 |
50 |
S6 |
p. 121- 1 p. |
artikel |
426 |
284 Poly(ADP-ribose) glycohydrolase (PARG) inhibitors increase nuclear poly(ADP-ribose) after methylating DNA damage
|
Jordan, A. |
|
2014 |
50 |
S6 |
p. 94- 1 p. |
artikel |
427 |
418 Population pharmacokinetics of intravenous bolus 5-fluorouracil in a phase I trial for children and young adults with recurrent ependymoma
|
Turner, D.C. |
|
2014 |
50 |
S6 |
p. 133-134 2 p. |
artikel |
428 |
321 Potent and selective inhibition of EZH2 by AU-2121 leads to significant tumor growth inhibition in mutant EZH2 dependent non-Hodgkin lymphoma
|
Ahmed, S. |
|
2014 |
50 |
S6 |
p. 104-105 2 p. |
artikel |
429 |
490 Potent and selective inhibitors of the KRAS-signaling nanocluster protein, CNKSR1, block oncogenic KRAS signaling and mut-KRAS cell growth
|
Kirkpatrick, L. |
|
2014 |
50 |
S6 |
p. 160- 1 p. |
artikel |
430 |
286 Potent and selective non-sulfamate-containing small molecule inhibitors of the ubiquitin activating enzyme
|
Paiva, S. |
|
2014 |
50 |
S6 |
p. 95- 1 p. |
artikel |
431 |
474 Potentiation of oxaliplatin in colon cancer by JNK inhibition
|
Vasilevskaya, I. |
|
2014 |
50 |
S6 |
p. 154-155 2 p. |
artikel |
432 |
316 Potent, partial agonists at ERalpha as selective estrogen mimics for treatment of tamoxifen-resistant breast cancer
|
Thatcher, G. |
|
2014 |
50 |
S6 |
p. 103- 1 p. |
artikel |
433 |
450 Precise gene editing of mutant NRAS using CRISPR to determine sensitivity to trametinib
|
Hose, C. |
|
2014 |
50 |
S6 |
p. 147-148 2 p. |
artikel |
434 |
113 Preclinical activity and pharmacodynamic biomarkers of W014A, a PD-1 decoy peptide blocking both PD-1 immune checkpoint ligands, PD-L1 and PD-L2
|
Bailly, C. |
|
2014 |
50 |
S6 |
p. 40- 1 p. |
artikel |
435 |
138 Preclinical activity and safety of MGD006, a CD123xCD3 Bispecific DART® molecule for the treatment of hematological malignancies
|
Moore, P. |
|
2014 |
50 |
S6 |
p. 48- 1 p. |
artikel |
436 |
547 Preclinical activity of Debio 1347, an oral selective FGFR1, 2, 3 inhibitor, in models harboring FGFR alterations
|
Chessex, A. Vaslin |
|
2014 |
50 |
S6 |
p. 177-178 2 p. |
artikel |
437 |
340 Preclinical activity of the VEGFR, FGFR and PDGFR inhibitor lucitanib in FGFR2 aberrant endometrial and gastric cancer models
|
Guffanti, F. |
|
2014 |
50 |
S6 |
p. 110- 1 p. |
artikel |
438 |
166 Pre-clinical and clinical activity of Anti-DLL4 (demcizumab) in combination with gemcitabine plus nab-paclitaxel in pancreatic cancer
|
Hidalgo, M. |
|
2014 |
50 |
S6 |
p. 55-56 2 p. |
artikel |
439 |
209 Pre-clinical and translational pharmacology, pharmacokinetics and pharmacodynamics for a humanized anti-OX40 antibody MOXR0916, a T-cell agonist in the treatment of solid tumors
|
Sukumaran, S. |
|
2014 |
50 |
S6 |
p. 71- 1 p. |
artikel |
440 |
223 Preclinical assessment of nintedanib for chemoprevention in hepatocellular carcinoma
|
Tovar, V. |
|
2014 |
50 |
S6 |
p. 75- 1 p. |
artikel |
441 |
459 Preclinical characterization of CC-115, a novel inhibitor of DNA-PK and mTOR kinase currently under clinical investigation
|
Mortensen, D.S. |
|
2014 |
50 |
S6 |
p. 150- 1 p. |
artikel |
442 |
152 Preclinical characterization of MM-151, an oligoclonal antibody therapeutic that targets EGFR by three distinct mechanisms of action
|
King, A. |
|
2014 |
50 |
S6 |
p. 52- 1 p. |
artikel |
443 |
330 Preclinical development of BIS-1602, first in class growth hormone releasing hormone antagonist
|
Maxuitenko, Y.Y. |
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2014 |
50 |
S6 |
p. 107- 1 p. |
artikel |
444 |
249 Preclinical efficacy of the PARP inhibitor rucaparib (CO-338/AG014699/PF-01367338) in pancreatic cancer models with homologous recombination deficiencies (HRD)
|
Robillard, L. |
|
2014 |
50 |
S6 |
p. 83- 1 p. |
artikel |
445 |
497 Preclinical evaluation of dimeric IAP proteins inhibitor APG-1387, in triple negative breast cancer both in vitro and in vivo
|
Wang, G. |
|
2014 |
50 |
S6 |
p. 162- 1 p. |
artikel |
446 |
565 Preclinical evaluation of OTX015, a novel BET-BRD inhibitor, on small cell lung cancer (SCLC) cell lines
|
Ijaz, N. |
|
2014 |
50 |
S6 |
p. 183- 1 p. |
artikel |
447 |
255 Pre-clinical in vivo characterization of MLN7243, an investigational ubiquitin activating enzyme inhibitor, in solid tumor models
|
Traore, T. |
|
2014 |
50 |
S6 |
p. 85- 1 p. |
artikel |
448 |
493 Preclinical pharmacokinetic (PK)/pharmacodynamic (PD)/Efficacy modeling for MLN2480, an investigational pan-RAF kinase inhibitor, in A375 and SKMEL-2 human melanoma xenografts
|
Patel, M. |
|
2014 |
50 |
S6 |
p. 161- 1 p. |
artikel |
449 |
300 Preclinical pharmacologic characterization of GSK2849330, a monoclonal AccretaMab® antibody with optimized ADCC and CDC activity directed against HER3
|
Clarke, N. |
|
2014 |
50 |
S6 |
p. 98-99 2 p. |
artikel |
450 |
457 Preclinical pharmacology of AZD5312, a generation 2.5 antisense oligonucletotide targeting the androgen receptor with differentiated activity from enzalutamide
|
Davies, B.R. |
|
2014 |
50 |
S6 |
p. 150- 1 p. |
artikel |
451 |
130 Preclinical results of ProCervix, a first in class, first in indication therapeutic vaccine targeting HPV16/18 infected women
|
Esquerre, M. |
|
2014 |
50 |
S6 |
p. 45- 1 p. |
artikel |
452 |
544 Preclinical studies of a dual Bcl-2/Bcl-xL inhibitor APG-1252 with strong anti-tumor efficacy and significantly reduced platelet toxicity
|
Wang, H. |
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2014 |
50 |
S6 |
p. 176-177 2 p. |
artikel |
453 |
Presenting Authors List
|
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2014 |
50 |
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p. 201-204 4 p. |
artikel |
454 |
265 Pretargeted nanoparticles to deliver both chemotherapeutics and radiation for the treatment of lymphoma
|
Fang, C. |
|
2014 |
50 |
S6 |
p. 88- 1 p. |
artikel |
455 |
496 Prevalence of MET amplification, MET expression, and MET-related genomic alterations in non-small cell lung cancer (NSCLC)
|
Ang, A.L. |
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2014 |
50 |
S6 |
p. 161-162 2 p. |
artikel |
456 |
289 Progress in drugging CYP1A1, 1B1 and CYP2W1 overexpressed in cancer
|
Pors, K. |
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2014 |
50 |
S6 |
p. 95- 1 p. |
artikel |
457 |
353 Protein expression for receptor activator of NFkB (RANK) and its ligand (RANKL) in non-small cell lung cancer (NSCLC)
|
D'Arcangelo, M. |
|
2014 |
50 |
S6 |
p. 114- 1 p. |
artikel |
458 |
553 PRPF6, a tri-snRNP spliceosome protein, regulates the alternative splicing of a distinct oncogenic ZAK variant and promotes colon tumor growth
|
Firestein, R. |
|
2014 |
50 |
S6 |
p. 179- 1 p. |
artikel |
459 |
463 PTPN11 is a central node in intrinsic and acquired resistance to targeted cancer drugs
|
Prahallad, A. |
|
2014 |
50 |
S6 |
p. 151- 1 p. |
artikel |
460 |
492 Quantification of exportin-1 (XPO1) occupancy by selective inhibitors of nuclear export (SINE)
|
Crochiere, M. |
|
2014 |
50 |
S6 |
p. 160- 1 p. |
artikel |
461 |
149 Quantitative mutational assessment of circulating tumor DNA using massively parallel deep sequencing in plasma and urine from advanced colorectal cancer patients
|
Poole, J.C. |
|
2014 |
50 |
S6 |
p. 51- 1 p. |
artikel |
462 |
79 Quantitative proteomics as a tool to identify resistance mechanisms in erlotinib-resistant subclones of the non-small cell lung cancer cell line HCC827
|
Jacobsen, K. |
|
2014 |
50 |
S6 |
p. 30- 1 p. |
artikel |
463 |
56 Radiosensitizing effect of sodium metaarsenite in a metastatic brain tumor model
|
Kang, W.Y. |
|
2014 |
50 |
S6 |
p. 23-24 2 p. |
artikel |
464 |
63 Radium-223 dichloride – Efficacy and mode-of-action in a mouse model of prostate cancer bone metastasis
|
Suominen, M.I. |
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2014 |
50 |
S6 |
p. 25-26 2 p. |
artikel |
465 |
188 RANBP2 knock-down is synthetic lethal with BRAF V600E in colon cancer
|
Vecchione, L. |
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2014 |
50 |
S6 |
p. 61-62 2 p. |
artikel |
466 |
173 Ras-mediated activation of mitogen-activated protein kinase pathway unleashes basement membrane damaging activity of serine protease hepsin
|
Tervonen, T. |
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2014 |
50 |
S6 |
p. 57-58 2 p. |
artikel |
467 |
148 RAS synthetic lethal interactions from yeast to human cells
|
van Wageningen, S. |
|
2014 |
50 |
S6 |
p. 51- 1 p. |
artikel |
468 |
582 Rational for targeting chromatin-modifying genes in clear-cell renal cell carcinomas
|
Malouf, G. |
|
2014 |
50 |
S6 |
p. 188- 1 p. |
artikel |
469 |
431 Real-time pharmacokinetic (PK) results from an ongoing randomized, parallel-dose phase 1 study of onapristone in patients (pts) with progesterone receptor (PR)-expressing cancers
|
Lokiec, F. |
|
2014 |
50 |
S6 |
p. 142- 1 p. |
artikel |
470 |
384 REDX04988, a novel dual B-RAF/C-RAF inhibitor and a potential therapeutic for BRAF-mutant colorectal cancer
|
Rainard, J. |
|
2014 |
50 |
S6 |
p. 123- 1 p. |
artikel |
471 |
143 Regional bias of intratumoral genetic heterogeneity of nucleotide repeats in colon cancers with microsatellite instability
|
An, C. |
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2014 |
50 |
S6 |
p. 49-50 2 p. |
artikel |
472 |
82 Regorafenib resistance in colorectal carcinoma is associated with enhanced expression of type II interleukin 1 receptor and reversed by MEK/ERK inhibitor
|
Mar, A.C. |
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2014 |
50 |
S6 |
p. 31- 1 p. |
artikel |
473 |
140 Relationship between programmed death ligand 1 (PD-L1) expression and clinical outcome in patients (pts) with melanoma (MEL) treated with pembrolizumab (pembro; MK-3475)
|
Daud, A. |
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2014 |
50 |
S6 |
p. 48-49 2 p. |
artikel |
474 |
32 Replication stress is a determinant of synergy between gemcitabine and Chk1 inhibition
|
Koh, S.B. |
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2014 |
50 |
S6 |
p. 16- 1 p. |
artikel |
475 |
482 Repurposing the antihelminthic mebendazole as a hedgehog inhibitor
|
Larsen, A.R. |
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2014 |
50 |
S6 |
p. 157- 1 p. |
artikel |
476 |
176 Resolvin D2 has mitogenic activity in estrogen receptor positive breast cancer cell lines via activation of estrogen receptor
|
Al-Zaubai, N. |
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2014 |
50 |
S6 |
p. 58-59 2 p. |
artikel |
477 |
217 Results of a phase I, open-label, multicentre study to assess the safety, tolerability, pharmacokinetics and preliminary anti-tumour activity of AZD9150 in patients with advanced/metastatic hepatocellular carcinoma
|
Kang, Y.K. |
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2014 |
50 |
S6 |
p. 73-74 2 p. |
artikel |
478 |
416 Results of phase I study of bolus 5-fluorouracil in children and young adults with recurrent ependymoma
|
Wright, K.D. |
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2014 |
50 |
S6 |
p. 133- 1 p. |
artikel |
479 |
238 Reversal of primary and acquired PARP-inhibitor resistance in BRCA-mutated triple-negative breast cancers by inhibition of transcriptional cyclin-dependent kinases (CDKs)
|
Johnson, S. |
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2014 |
50 |
S6 |
p. 80- 1 p. |
artikel |
480 |
539 Reversing the epithelial to mesenchymal transition with N-myc downstream regulated gene-1 and novel iron chelators in pancreatic cancer
|
Fouani, L. |
|
2014 |
50 |
S6 |
p. 175- 1 p. |
artikel |
481 |
399 Rho-GTPase, RAC1 and Cdc42 mediates Wnt–beta-catenin signals for metastasis associated phenotypes in TNBC: A proof of concept study
|
Dey, N. |
|
2014 |
50 |
S6 |
p. 128- 1 p. |
artikel |
482 |
335 RICTOR amplification as a novel molecular target for the treatment of lung cancer
|
Cheng, H. |
|
2014 |
50 |
S6 |
p. 108-109 2 p. |
artikel |
483 |
558 RNA G-quadruplexes cause eIF4A-dependent oncogene translation in cancer
|
Wendel, H. |
|
2014 |
50 |
S6 |
p. 181- 1 p. |
artikel |
484 |
423 RNA helicase A is essential for 1p36 gene KIF1Bβ tumor suppression in neuroblastomas
|
Chen, Z.X. |
|
2014 |
50 |
S6 |
p. 135- 1 p. |
artikel |
485 |
309 RNA sequencing and in silico analysis identifies an unannotated antisense long non-coding RNA involved in cancer progression
|
Inoue, S. |
|
2014 |
50 |
S6 |
p. 101- 1 p. |
artikel |
486 |
92 Role of ERK nuclear translocation in cisplatin-sensitive and -resistant ovarian cancer cells
|
Dilruba, S. |
|
2014 |
50 |
S6 |
p. 34- 1 p. |
artikel |
487 |
455 Role of MDM2 as therapeutic target in gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs)
|
Briest, F. |
|
2014 |
50 |
S6 |
p. 149- 1 p. |
artikel |
488 |
2 Safety and early evidence of activity of a first-in-human phase I study of the novel cancer stem cell (CSC) targeting antibody OMP-52M51 (anti-Notch1) administered intravenously to patients with certain advanced solid tumors
|
Patnaik, A. |
|
2014 |
50 |
S6 |
p. 7- 1 p. |
artikel |
489 |
292 Salmonella typhimurium A1-R decoys quiescent cancer cells to cycle rendering them chemosensitive
|
Yano, S. |
|
2014 |
50 |
S6 |
p. 96- 1 p. |
artikel |
490 |
343 Salmonella typhimurium A1-R effectively targets experimental breast cancer brain metastasis
|
Zhang, Y. |
|
2014 |
50 |
S6 |
p. 111- 1 p. |
artikel |
491 |
Scientific Programme – Details
|
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|
2014 |
50 |
S6 |
p. xx-lxxi nvt p. |
artikel |
492 |
Scientific Programme – Overview
|
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|
2014 |
50 |
S6 |
p. xviii-xix nvt p. |
artikel |
493 |
471 Screening of Champions predictive TumorGraft platform guides the clinical development of the selective dual BRAF-EGFR inhibitor CEP-32496
|
Ruggeri, B. |
|
2014 |
50 |
S6 |
p. 154- 1 p. |
artikel |
494 |
344 Search for new blood biomarkers for response to antiangiogenic therapy in non-small cell lung cancer patients
|
Rodríguez-Garzotto, A. |
|
2014 |
50 |
S6 |
p. 111- 1 p. |
artikel |
495 |
247 Selective inhibitors of nuclear export (SINE) block the expression of DNA damage repair proteins and sensitize cancer cells to DNA damage therapeutic agents
|
Kashyap, T. |
|
2014 |
50 |
S6 |
p. 83- 1 p. |
artikel |
496 |
371 Selective targeting of head and neck cancer cells by perturbing reactive oxygen species homeostasis
|
Kwon, M. |
|
2014 |
50 |
S6 |
p. 119- 1 p. |
artikel |
497 |
40 Selectivity and mechanism of action studies for Polo Box-targeted, non-ATP based inhibitors of PLK1
|
Baxter, M. |
|
2014 |
50 |
S6 |
p. 18-19 2 p. |
artikel |
498 |
305 Selinexor, a novel selective inhibitor of nuclear export, potentiates the antitumor activity of gemcitabine against pancreatic cancer by nuclear retention of p27
|
Amit, M. |
|
2014 |
50 |
S6 |
p. 100- 1 p. |
artikel |
499 |
337 Sensitisation of HPV+ HNSCC to cytotoxic treatments by targeting the G2/M checkpoint with AZ-1775 to improve survival
|
Osman, A. |
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2014 |
50 |
S6 |
p. 109- 1 p. |
artikel |
500 |
157 Sensitive and specific detection of 1p/19q codeletion in gliomas by next generation sequencing
|
Dubbink, E. |
|
2014 |
50 |
S6 |
p. 53- 1 p. |
artikel |
501 |
394 Sensitivity of acute myeloid leukemia cells to a urokinase-activated anthrax lethal toxin (PrAgU2/lf) is dependent on uPAR expression and phospho-MEK1/2 levels
|
Bekdash, A. |
|
2014 |
50 |
S6 |
p. 126- 1 p. |
artikel |
502 |
81 Sensitization of triple-negative breast cancer to PI3K inhibition by cotargeting IGF1R
|
de Lint, K. |
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2014 |
50 |
S6 |
p. 31- 1 p. |
artikel |
503 |
278 Sentinel lymph nodes mapping of macrophage targeted mannosyl human serum albumin-indocyanine detected by combined color and near infrared fluorescence imaging system in esophagus
|
Quan, Y. |
|
2014 |
50 |
S6 |
p. 92- 1 p. |
artikel |
504 |
426 Serum levels of CCL22 and CCL25 might predict skin rash induction the commonest adverse event by bendamustine in the treatment of malignant lymphoma
|
Terni, Y. |
|
2014 |
50 |
S6 |
p. 136- 1 p. |
artikel |
505 |
575 SF3B1 mutations are associated with alternative splicing in ER-positive breast cancer
|
Maguire, S. |
|
2014 |
50 |
S6 |
p. 186- 1 p. |
artikel |
506 |
456 SF3B1 mutations induce disease relevant aberrant mRNA splicing in cancer and confer sensitivity to spliceosome inhibition
|
Buonamici, S. |
|
2014 |
50 |
S6 |
p. 149- 1 p. |
artikel |
507 |
536 Shifts in microRNA expression pattern can facilitate the cancer cell stemness
|
Halytskiy, V. |
|
2014 |
50 |
S6 |
p. 174- 1 p. |
artikel |
508 |
333 Short antisense oligonucleotides antagonize Lin28 and enable pre-let-7 processing and suppression of cell growth in human hepatocarcinoma cells
|
Roos, M. |
|
2014 |
50 |
S6 |
p. 108- 1 p. |
artikel |
509 |
273 Significance of serine-167 and cysteine-129 residues in the active site of the immune-suppressive enzyme indoleamine 2,3-dioxygenase 1 (IDO1) for the binding of novel inhibitors
|
Tomek, P. |
|
2014 |
50 |
S6 |
p. 91- 1 p. |
artikel |
510 |
49 siRNA targeting of mitochondrial thymidine kinase 2 (TK2) sensitizes cancer cells to gemcitabine and increases mitochondrial toxicity
|
Di Cresce, C. |
|
2014 |
50 |
S6 |
p. 21- 1 p. |
artikel |
511 |
393 Small modification of ceritinib enhances the activity against ALK
|
Park, C.H. |
|
2014 |
50 |
S6 |
p. 126- 1 p. |
artikel |
512 |
100 Small molecules selectively targeting breast cancer cells
|
Sakoff, J. |
|
2014 |
50 |
S6 |
p. 36- 1 p. |
artikel |
513 |
155 SNIPER(TACC3) degrades TACC3 protein via the ubiquitin–proteasome pathway and induces apoptosis in cancer cells expressing a large amount of TACC3
|
Ohoka, N. |
|
2014 |
50 |
S6 |
p. 52-53 2 p. |
artikel |
514 |
Societies' Profiles
|
|
|
2014 |
50 |
S6 |
p. ix-x nvt p. |
artikel |
515 |
60 Sodium metaarsenite cytotoxic activity is associated with telomere length and many types of arsenic transporters in non-small cell lung cancer
|
Park, Y.M. |
|
2014 |
50 |
S6 |
p. 24-25 2 p. |
artikel |
516 |
512 Somatically mutated ABL1 represents an actionable and essential lung cancer survival gene
|
Testoni, E. |
|
2014 |
50 |
S6 |
p. 167- 1 p. |
artikel |
517 |
183 Spatio-temporal characterization of tumor growth and invasion
|
Jimenez, A.M. |
|
2014 |
50 |
S6 |
p. 60- 1 p. |
artikel |
518 |
372 Specific inhibition of hTERT expression by targeting common promoter mutations which cause quadruplex DNA instability
|
Miller, D. |
|
2014 |
50 |
S6 |
p. 120- 1 p. |
artikel |
519 |
84 Src family kinase activation is a compensatory survival mechanism for acquired resistance to EGFR-TKIs in lung cancer cells
|
Ono, M. |
|
2014 |
50 |
S6 |
p. 32- 1 p. |
artikel |
520 |
197 Statistical aspects of kinetic analysis of gliomas with FDG-PET
|
Hawe, D. |
|
2014 |
50 |
S6 |
p. 64- 1 p. |
artikel |
521 |
593 Strategies to overcome resistance to BET bromodomain inhibitor in KRAS/LKB1 mutant NSCLC
|
Soucheray, M. |
|
2014 |
50 |
S6 |
p. 191- 1 p. |
artikel |
522 |
307 Stromal delivery of long Pentraxin-3 impairs FGF/FGFR-dependent tumor growth and metastasis
|
Giacomini, A. |
|
2014 |
50 |
S6 |
p. 100-101 2 p. |
artikel |
523 |
407 Structural basis for inhibition of ligand-dependent and -independent ErbB3 activation by KTN3379
|
Alvarado, D. |
|
2014 |
50 |
S6 |
p. 130- 1 p. |
artikel |
524 |
17 Studies on glycoprotein expression differences between MCF-7 and MCF-7-Z
|
Ner-Kluza, J. |
|
2014 |
50 |
S6 |
p. 12- 1 p. |
artikel |
525 |
Subject Index
|
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|
2014 |
50 |
S6 |
p. 229-239 11 p. |
artikel |
526 |
573 Suppression of c-Myc oncogene and hematological tumor growth by a novel benzazepine BET inhibitor
|
Gelato, K.A. |
|
2014 |
50 |
S6 |
p. 185- 1 p. |
artikel |
527 |
36 Suppression of metastasis and improvement of drug distribution by eribulin mesylate
|
Ozawa, Y. |
|
2014 |
50 |
S6 |
p. 17- 1 p. |
artikel |
528 |
224 Synergic tumor growth suppression with carbohydrate-restriction diet and natural AMP-dependent protein kinase activators
|
Choi, M. |
|
2014 |
50 |
S6 |
p. 76- 1 p. |
artikel |
529 |
349 Synergistic drug combinations that target beta-catenin-driven and MYC-driven cancers
|
Uitdehaag, J.C.M. |
|
2014 |
50 |
S6 |
p. 113- 1 p. |
artikel |
530 |
98 Synergistic inhibition of HER2 positive breast cancer by triptolide and lapatinib
|
Chalugun, P. |
|
2014 |
50 |
S6 |
p. 36- 1 p. |
artikel |
531 |
513 Synergistic inhibition of ovarian and endometrial cancer cell lines using combined treatment of ARQ 092 and ARQ 087 in vitro and in vivo
|
Yu, Y. |
|
2014 |
50 |
S6 |
p. 167- 1 p. |
artikel |
532 |
19 Syngeneic models for developing cancer therapeutics targeting immune system
|
Zhang, L. |
|
2014 |
50 |
S6 |
p. 12- 1 p. |
artikel |
533 |
288 Synthetic isomalyngamide A analogs that inhibit breast cancer migration
|
Li, W. |
|
2014 |
50 |
S6 |
p. 95- 1 p. |
artikel |
534 |
294 Synthetic lethal screen identifies Aurora A as a selective target in HPV driven cervical cancer
|
Gabrielli, B. |
|
2014 |
50 |
S6 |
p. 97- 1 p. |
artikel |
535 |
187 Targeted genomic profiling of penile squamous cell carcinoma using the Oncomine cancer research panel
|
McDaniel, A.S. |
|
2014 |
50 |
S6 |
p. 61- 1 p. |
artikel |
536 |
419 Targeted inhibition of casein kinase II (CK2) produces a strong therapeutic effect in pediatric leukemia
|
Dovat, S. |
|
2014 |
50 |
S6 |
p. 134- 1 p. |
artikel |
537 |
366 Targeting colorectal and pancreatic cancer stem cells with the LGR5 monoclonal antibody BNC101
|
Chu, P. |
|
2014 |
50 |
S6 |
p. 118- 1 p. |
artikel |
538 |
524 Targeting MET for a differentiation therapy of rhabdomyosarcoma
|
Skrzypek, K. |
|
2014 |
50 |
S6 |
p. 170- 1 p. |
artikel |
539 |
404 Targeting PI3K somatic mutations reduces invasion and EMT in squamous cell carcinoma of the lung
|
Cavazzoni, A. |
|
2014 |
50 |
S6 |
p. 129- 1 p. |
artikel |
540 |
123 Targeting tryptophan metabolism in human lung cancer
|
Deshane, J. |
|
2014 |
50 |
S6 |
p. 43- 1 p. |
artikel |
541 |
442 Targeting urokinase plasminogen activator for radioimmunotherapy using an antagonistic internalizing human antibody
|
LeBeau, A. |
|
2014 |
50 |
S6 |
p. 145- 1 p. |
artikel |
542 |
401 TAS-121, a highly potent and mutant-specific EGFR inhibitor, overcomes T790M-acquired resistance with promising antitumor activity through specific inhibition of mutant EGFR signaling
|
Kato, M. |
|
2014 |
50 |
S6 |
p. 128- 1 p. |
artikel |
543 |
592 TAS-116, a highly selective inhibitor of heat shock protein 90a/β, inhibits tumor growth in biliary tract cancer mouse models
|
Ohkubo, S. |
|
2014 |
50 |
S6 |
p. 191- 1 p. |
artikel |
544 |
515 TAS-115, a potent MET/VEGFR-targeted kinase inhibitor, is a new therapeutic approach for the treatment of bone metastasis of lung cancer
|
Gomori, A. |
|
2014 |
50 |
S6 |
p. 167-168 2 p. |
artikel |
545 |
398 TAS-119 a selective inhibitor of Aurora A kinase, potentiates taxane therapy in breast and lung cancer models
|
Nakatsuru, Y. |
|
2014 |
50 |
S6 |
p. 127-128 2 p. |
artikel |
546 |
29 TAS-114 is a novel dUTPase/DPD inhibitor, its DPD inhibition reduces capecitabine dosage but does not diminish therapeutic window in human tumor xenografts
|
Yano, W. |
|
2014 |
50 |
S6 |
p. 15- 1 p. |
artikel |
547 |
27 TAS-102 treatment results in high trifluridine incorporation into DNA with pyrimidine metabolic pathway markedly up-regulated in cancer
|
Oguchi, K. |
|
2014 |
50 |
S6 |
p. 15- 1 p. |
artikel |
548 |
128 T cell-mediated cancer immunotherapy through OX40 agonism
|
Huseni, M. |
|
2014 |
50 |
S6 |
p. 45- 1 p. |
artikel |
549 |
541 The abnormal bone remodeling associated with prostate cancer bone metastasis is attenuated by TAS-115, the dual inhibitor for HGF/VEGF signaling
|
Fujita, H. |
|
2014 |
50 |
S6 |
p. 176- 1 p. |
artikel |
550 |
505 The anti-ErbB3 antibody, EV20, counteracts vemurafenib resistance in BRAF-mutated colorectal cancer stem cells
|
Sala, G. |
|
2014 |
50 |
S6 |
p. 164-165 2 p. |
artikel |
551 |
568 The BET bromodomain inhibitor OTX015 shows synergy with several anticancer agents in preclinical models of mantle cell lymphoma (MCL) and multiple myeloma (MM)
|
Bernasconi, E. |
|
2014 |
50 |
S6 |
p. 184- 1 p. |
artikel |
552 |
529 The Cancer Research UK Stratified Medicine Programme: From national screening to national trial
|
Mirabile, I. |
|
2014 |
50 |
S6 |
p. 172- 1 p. |
artikel |
553 |
446 The cancer stem cell inhibitors VS-6063 (defactinib) and VS-5584 exhibit synergistic anticancer activity in preclinical models of mesothelioma
|
Xu, Q. |
|
2014 |
50 |
S6 |
p. 146-147 2 p. |
artikel |
554 |
240 The combination of Chk-1 and ATR inhibitor synergistically kills cancer cells
|
Sanjiv, K. |
|
2014 |
50 |
S6 |
p. 81- 1 p. |
artikel |
555 |
584 The correlation between EMT and cancer stemness in lung adenocarcinoma affects on its prognosis
|
Sowa, T. |
|
2014 |
50 |
S6 |
p. 188- 1 p. |
artikel |
556 |
158 The development of a series of orthotopic solid tumour models of prostate, lung and ovarian cancer using optical and X ray imaging
|
Batey, M. |
|
2014 |
50 |
S6 |
p. 53- 1 p. |
artikel |
557 |
323 The development of short form of mimic microRNA for lung cancer therapy
|
Ohno, S. |
|
2014 |
50 |
S6 |
p. 105- 1 p. |
artikel |
558 |
283 The development of the first selective inhibitors of the UBA5 enzyme to probe for E1 activity in diseased cells
|
da Silva, S.R. |
|
2014 |
50 |
S6 |
p. 94- 1 p. |
artikel |
559 |
479 The discovery and development of potent and specific anti-SialylTn antibodies for the treatment of solid tumors
|
Meetze, K. |
|
2014 |
50 |
S6 |
p. 156- 1 p. |
artikel |
560 |
287 The discovery and optimization of small molecule antagonists of the WDR5–MLL interaction
|
Al-Awar, R. |
|
2014 |
50 |
S6 |
p. 95- 1 p. |
artikel |
561 |
277 The discovery and pre-clinical development of the first clinical stage EZH2-inhibitor, EPZ-6438 (E7438)
|
Kuntz, K. |
|
2014 |
50 |
S6 |
p. 92- 1 p. |
artikel |
562 |
252 The DNA damage response gene Schlafen 11 (SLFN11) is a transcriptional target of ETS transcription factors in Ewing's sarcoma and other cancers
|
Pommier, Y. |
|
2014 |
50 |
S6 |
p. 84- 1 p. |
artikel |
563 |
50 The effect of esomeprazole, a proton pump inhibitor, on the pharmacokinetics of the investigational Aurora A kinase inhibitor alisertib (MLN8237) in patients with advanced solid tumors or lymphomas
|
Zhou, X. |
|
2014 |
50 |
S6 |
p. 21-22 2 p. |
artikel |
564 |
336 The effect of food on the pharmacokinetics of the investigational Aurora A kinase (AAK) inhibitor, alisertib (MLN8237), in patients (pts) with advanced solid tumors or lymphomas
|
Zhou, X. |
|
2014 |
50 |
S6 |
p. 109- 1 p. |
artikel |
565 |
207 The enhancement of radiotherapy efficacy with docetaxel-titanate nanotubes as a new nanohybrid for localized high risk prostate cancer
|
Mirjolet, C. |
|
2014 |
50 |
S6 |
p. 67- 1 p. |
artikel |
566 |
30 The fungal-derived cyclohexadepsipeptide Destruxin E exerts multifaceted anticancer and antiangiogenic activities
|
Dornetshuber-Fleiss, R. |
|
2014 |
50 |
S6 |
p. 16- 1 p. |
artikel |
567 |
518 The HSP90 inhibitor, AT13387, overcomes resistance to crizotinib and second generation ALK inhibitors
|
Courtin, A. |
|
2014 |
50 |
S6 |
p. 168- 1 p. |
artikel |
568 |
193 The identification of new therapies for ependymoma subgroups
|
Boulos, N. |
|
2014 |
50 |
S6 |
p. 63- 1 p. |
artikel |
569 |
38 The indolyl-chalcone CDD-026 induces cancer cell death through targeting of STMN1 and mitotic catastrophe
|
Wegiel, B. |
|
2014 |
50 |
S6 |
p. 18- 1 p. |
artikel |
570 |
200 The influence of different cMET and EGFR backgrounds on the cytotoxicity of cMET and EGFR small molecule inhibitors in vitro
|
van der Steen, N. |
|
2014 |
50 |
S6 |
p. 65- 1 p. |
artikel |
571 |
585 The investigational HSP90 inhibitor ganetespib displays robust single agent activity in gastric cancer models both as monotherapy and in combination with standard of care therapeutics
|
He, S. |
|
2014 |
50 |
S6 |
p. 188-189 2 p. |
artikel |
572 |
269 The NCI-60 as an effective tool for scaffold hopping: A phenotypic systems-based approach to the design of novel chemotherapeutics
|
Wishka, D.G. |
|
2014 |
50 |
S6 |
p. 89-90 2 p. |
artikel |
573 |
202 The novel microtubule-destabilizing drug BAL101553 (prodrug of BAL27862) sensitizes a treatment refractory tumor model to ionizing radiation
|
Broggini-Tenzer, A. |
|
2014 |
50 |
S6 |
p. 65-66 2 p. |
artikel |
574 |
583 The 8p11 amplicon in luminal breast cancers harbors multiple interacting epigenome modifying oncogenes: implications for epigenome-targeted therapy
|
Ethier, S. |
|
2014 |
50 |
S6 |
p. 188- 1 p. |
artikel |
575 |
412 The Pediatric Preclinical Testing Program (PPTP): Analysis of the first 10 years in vivo testing
|
Houghton, P. |
|
2014 |
50 |
S6 |
p. 131-132 2 p. |
artikel |
576 |
546 The PI3Kbeta/delta inhibitor AZD8186 combines with the dual mTORC1/2 inhibitor AZD2014 to give comprehensive PI3K pathway inhibition and drive tumour regression in vivo
|
Simon, B. |
|
2014 |
50 |
S6 |
p. 177- 1 p. |
artikel |
577 |
312 The prognostic role of mesothelin expression and its association with KRAS mutation in advanced lung adenocarcinoma
|
Thomas, A. |
|
2014 |
50 |
S6 |
p. 102- 1 p. |
artikel |
578 |
441 The role of méthylation in metastasis of oral squamous cell carcinoma: understanding the OSCC methylome
|
Clausen, M. |
|
2014 |
50 |
S6 |
p. 145- 1 p. |
artikel |
579 |
475 The synergistic anti-proliferative effect of combining the FGFR inhibitor, ARQ 087 with the AKT inhibitor, ARQ 092 in human cancer cell lines and PDX models
|
Marchlik, E. |
|
2014 |
50 |
S6 |
p. 155- 1 p. |
artikel |
580 |
103 The use of next generation sequencing (NGS) in the management of metastatic breast cancer (MBC): Defining a model for genomic-driven therapies
|
Austin, L. |
|
2014 |
50 |
S6 |
p. 37- 1 p. |
artikel |
581 |
186 The use of Quantitative Textural Analysis imaging biomarkers to predict response to temsirolimus treatment in advanced HCC subjects
|
Korn, R. |
|
2014 |
50 |
S6 |
p. 61- 1 p. |
artikel |
582 |
89 Tie-2 regulates the stemness of prostate cancer cells
|
Tang, K. |
|
2014 |
50 |
S6 |
p. 33- 1 p. |
artikel |
583 |
521 Tisular expression of the EGFR and N-Glycolyl GM3 Ganglioside as recognized by ior egf/r3 and 14F7 Mabs in triple negative breast cancer
|
Perez, A. Calvo |
|
2014 |
50 |
S6 |
p. 169- 1 p. |
artikel |
584 |
542 Tivantinib in combination with gemcitabine shows strong antitumor activity on mesothelioma cell lines and cytoskeletal effects via inhibition of actin
|
Simonelli, M. |
|
2014 |
50 |
S6 |
p. 176- 1 p. |
artikel |
585 |
114 Toll-like receptor 5 agonist entolimod as a potential anticancer immunotherapeutic agent
|
Burdelya, L. |
|
2014 |
50 |
S6 |
p. 40- 1 p. |
artikel |
586 |
48 Trabectedin and lurbinectedin are effective against leukemic cells derived from patients affected by chronic and juvenile myelomonocytic leukemia
|
Romano, M. |
|
2014 |
50 |
S6 |
p. 21- 1 p. |
artikel |
587 |
470 Transcriptional regulation of cancer stem cells marker CD133 by p53
|
Park, E.K. |
|
2014 |
50 |
S6 |
p. 153-154 2 p. |
artikel |
588 |
409 Transcription factor activating protein 2 beta (TFAP2B) mediates neuronal differentiation in neuroblastoma
|
Ikram, F. |
|
2014 |
50 |
S6 |
p. 130-131 2 p. |
artikel |
589 |
201 Transcriptome analysis of CD133-positive stem cells and prognostic value of survivin in colorectal cancer
|
Kim, S. |
|
2014 |
50 |
S6 |
p. 65- 1 p. |
artikel |
590 |
182 TRAP1 represents a key mediator of stemness and glycolytic metabolism in colorectal cancer cells
|
Lettini, G. |
|
2014 |
50 |
S6 |
p. 60- 1 p. |
artikel |
591 |
Travel Grants
|
|
|
2014 |
50 |
S6 |
p. xvii- 1 p. |
artikel |
592 |
484 Treatment of advanced solid tumors with golvatinib (E7050) in combination with lenvatinib (E7080)
|
Kwak, E.L. |
|
2014 |
50 |
S6 |
p. 158- 1 p. |
artikel |
593 |
185 Treatment of patient-derived NSCLC xenograft preclinical models using image-guided small animal irradiation
|
Papadopoulou, N. |
|
2014 |
50 |
S6 |
p. 60-61 2 p. |
artikel |
594 |
500 Triple blockade with LEE011, everolimus, and exemestane in women with ER+/HER2− advanced/metastatic breast cancer: results from a Phase Ib clinical trial
|
Bardia, A. |
|
2014 |
50 |
S6 |
p. 163- 1 p. |
artikel |
595 |
90 Tumor infiltrating leukocyte subpopulations as a biomarker of response and resistance to targeted therapy in patients with BRAF mutation-positive metastatic melanoma
|
Kelley, M.C. |
|
2014 |
50 |
S6 |
p. 33-34 2 p. |
artikel |
596 |
136 Tumor-infiltrating lymphocytes (TILs) following intratumoral administration of ONCOS-102 are associated with prolonged overall survival in last line solid tumor patients
|
Pesonen, S. |
|
2014 |
50 |
S6 |
p. 47- 1 p. |
artikel |
597 |
360 Tumor suppressive microRNA-192 as a prognostic factor for recurrence of surgically resected non-small cell lung cancer
|
Hong, J.H. |
|
2014 |
50 |
S6 |
p. 116- 1 p. |
artikel |
598 |
77 Tumor suppressive roles of miR-221 and miR-222 in lung cancer
|
Sato, M. |
|
2014 |
50 |
S6 |
p. 30- 1 p. |
artikel |
599 |
535 Tumor targeting and tissue distribution of solitomab (AMG 110; anti-EpCAM BiTE®) in human EpCAM-positive tumor bearing mice
|
Warnders, F.J. |
|
2014 |
50 |
S6 |
p. 174- 1 p. |
artikel |
600 |
376 Tumor-targeting Salmonella typhimurium A1-R enhances gemcitabine–bevacizumab efficacy on a patient-derived orthotopic xenograft (PDOX) pancreatic cancer nude mouse model
|
Hiroshima, Y. |
|
2014 |
50 |
S6 |
p. 121- 1 p. |
artikel |
601 |
467 Two in one – Delivery of apoptotic signal into cancer cells by new class of TRAIL derived, fusion protein
|
Pawlak, S.D. |
|
2014 |
50 |
S6 |
p. 152-153 2 p. |
artikel |
602 |
348 Two NSCLC-PDXs with different EGFR exon 20-insertions respond differently to different TKIs
|
Li, H. |
|
2014 |
50 |
S6 |
p. 112- 1 p. |
artikel |
603 |
299 Tyk2-src dependence of kidney cancer
|
Krishnan, B. |
|
2014 |
50 |
S6 |
p. 98- 1 p. |
artikel |
604 |
352 UNC2025, a novel small molecule MerTK and Flt3 tyrosine kinase inhibitor, has therapeutic activity and promotes sensitivity to chemotherapy in animal models of acute leukemia
|
Graham, D. |
|
2014 |
50 |
S6 |
p. 114- 1 p. |
artikel |
605 |
503 UNC2025: A small molecule inhibitor of merTK with efficacy in mouse melanoma models
|
Earp, S. |
|
2014 |
50 |
S6 |
p. 164- 1 p. |
artikel |
606 |
215 Updated clinical and preliminary correlative results of ARIEL2, a Phase 2 study to identify ovarian cancer patients likely to respond to rucaparib
|
Swisher, E. |
|
2014 |
50 |
S6 |
p. 73- 1 p. |
artikel |
607 |
248 Use of ATR inhibitor in combination with topoisomerase I inhibitor kills cancer cells by disabling DNA replication initiation and fork elongation
|
Jossé, R. |
|
2014 |
50 |
S6 |
p. 83- 1 p. |
artikel |
608 |
392 Using modelling & simulation to integrate mouse PK–PD-efficacy with preliminary human PK data to inform the Phase II doses and schedule for the experimental c-Met inhibitor AZD6094 (Volitinib)
|
Jones, R. |
|
2014 |
50 |
S6 |
p. 125-126 2 p. |
artikel |
609 |
301 Using PK/PD/efficacy modeling to predict potential of AZD9291 to target brain metastases from advanced NSCLC with EGFR sensitizing mutations (EGFRm+)
|
Yates, J. |
|
2014 |
50 |
S6 |
p. 99- 1 p. |
artikel |
610 |
97 Utilization of low passage adenoid cystic carcinoma PDX models to identify novel combination therapies
|
Wick, M.J. |
|
2014 |
50 |
S6 |
p. 35-36 2 p. |
artikel |
611 |
177 Validation of 3D primary organoid cultures of colorectal carcinoma as discovery and validation platform for personalized cancer therapy
|
Halonen, P. |
|
2014 |
50 |
S6 |
p. 59- 1 p. |
artikel |
612 |
520 Validation of Nanostring for FGFR1 gene expression analysis in squamous non-small cell lung cancer (sqNSCLC) tissue
|
Rooney, C. |
|
2014 |
50 |
S6 |
p. 169- 1 p. |
artikel |
613 |
264 Vasculogenic mimicry in small cell lung cancer
|
Trapani, F. |
|
2014 |
50 |
S6 |
p. 88- 1 p. |
artikel |
614 |
540 Vemurafenib alters glucose utilization in BRAF-driven human melanoma cells
|
Miniotis, M. Falck |
|
2014 |
50 |
S6 |
p. 175-176 2 p. |
artikel |
615 |
13 Whole exome sequence analysis of canine transitional cell carcinoma of the bladder
|
Duval, D.L. |
|
2014 |
50 |
S6 |
p. 11- 1 p. |
artikel |
616 |
236 Whole genomic assay on endoscopic ultrasound-guided fine needle aspiration samples of unresectable pancreatic cancer
|
Ha, J.M. |
|
2014 |
50 |
S6 |
p. 79- 1 p. |
artikel |
617 |
85 Wnt secretion is required to maintain Wnt activity in colon cancer
|
Voloshanenko, O. |
|
2014 |
50 |
S6 |
p. 32- 1 p. |
artikel |
618 |
560 ZEN3365 is a novel BET bromodomain inhibitor for the treatment of hematologic malignancies and solid tumors
|
McLure, K.G. |
|
2014 |
50 |
S6 |
p. 181- 1 p. |
artikel |
619 |
131 Zfra activates novel Hyal2+ CD3– CD19– memory spleen cells to block cancer growth, stemness, and metastasis in vivo
|
Chang, N. |
|
2014 |
50 |
S6 |
p. 46- 1 p. |
artikel |