Digitale Bibliotheek
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                             116 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Abnormalities of chromosomes 12p13 and 15q26-QTER in congenital fibrosarcoma Knezevich, S.R.
1997
98 2 p. 153-
1 p.
artikel
2 Abnormal number of centrosomes and development of aneuploidy and nuclear pleomorphism in breast tumor cells Gusev, Y.
1997
98 2 p. 153-
1 p.
artikel
3 Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: Clinicopathological features Dal Cin, P.
1997
98 2 p. 157-
1 p.
artikel
4 A(870)E mutation of the androgen receptor gene in a patient with complete androgen insensitivity syndrome and sertoli cell tumor Knoke, I
1997
98 2 p. 139-141
3 p.
artikel
5 A fast technique for analysis of formalin-fixed, paraffin embedded tissues by fluorescence in situ hybridization with alpha satellite probes Barril, N.
1997
98 2 p. 167-
1 p.
artikel
6 A midi-satellite sequence at 1P36 frequently deleted in human tumors is amplified during normal differentiation Ambros, P.F.
1997
98 2 p. 147-
1 p.
artikel
7 A mouse model for ataxia-telangiectasia: genetic mechanisms of tumorigenesis Barlow, C.
1997
98 2 p. 146-
1 p.
artikel
8 Amplification of HMGIC in an endometrial polyp Dal Cin, P.
1997
98 2 p. 158-
1 p.
artikel
9 Analysis by CGH of the tumor cell lines of the NCI anticancer drug discovery screen du Manoir, S.
1997
98 2 p. 158-
1 p.
artikel
10 Analysis of p16 (CDKN2/MTS-1/INK4A) gene mutations in malignant and nonmalignant endobronchial tissue obtained by fiberoptic bronchoscopy Senner, G.D.
1997
98 2 p. 166-
1 p.
artikel
11 Analysis of uterine serous carcinoma by comparative genomic hybridization Tashiro, H.
1997
98 2 p. 163-
1 p.
artikel
12 An amplified gene encodes the translation initiation factor elF-4gamma which induces an immune response in a patient with squamous cell lung carcinoma Meese, E.
1997
98 2 p. 161-
1 p.
artikel
13 Aneusomy detection by fluorescence in situ hybridization (FISH) using bladder washings: correlation with cytology, cytogenetics and clinical features predicts recurrence and defines test limitations Slovak, M.L.
1997
98 2 p. 150-
1 p.
artikel
14 Announcement 1997
98 2 p. 173-
1 p.
artikel
15 Announcement 1997
98 2 p. 174-
1 p.
artikel
16 Announcement 1997
98 2 p. 172-
1 p.
artikel
17 Application of Abati's method for retention of morphology and subsequent identification of tumor cells in fresh tissue specimens after fish analysis Harris, C.
1997
98 2 p. 159-
1 p.
artikel
18 A simple procedure to rehybridization on nuclei analysed previously by fish Carvalho-Salles, A.B.
1997
98 2 p. 167-
1 p.
artikel
19 Assaying disease-specific gene expression by CDNA micro-arrays Bittner, M.L.
1997
98 2 p. 150-
1 p.
artikel
20 Assessment of numerical chromosome abnormalities in thyroid neoplasia by fluorescence in situ hybridization Block, A.W.
1997
98 2 p. 156-
1 p.
artikel
21 A study of the genetic progression of human cutaneous malignant melanoma by comparative genomic hybridization Wiltshire, R.N.
1997
98 2 p. 170-
1 p.
artikel
22 CGH analysis of pancreatic adenocarcinoma cell lines Griffin, C.A.
1997
98 2 p. 159-
1 p.
artikel
23 CGH patterns in head and neck squamous cell carcinomas Bockmühl, U.
1997
98 2 p. 156-
1 p.
artikel
24 Characterization of a new human neuroblastoma cell line Kao, Y.S.
1997
98 2 p. 171-
1 p.
artikel
25 Characterization of the 17p amplicon in human sarcomas — microsatellite marker analysis Wolf, M.
1997
98 2 p. 169-
1 p.
artikel
26 Chromosomal abnormalities in low grade chondrosarcoma and a review of the literature Swarts, Sarah J.
1997
98 2 p. 126-130
5 p.
artikel
27 Chromosomal anomalies in a case of proliferative myositis McComb, Erin N.
1997
98 2 p. 142-144
3 p.
artikel
28 Chromosome 3 abnormalities in lung tumors detected by fluorescence in situ hybridization Rabenhorst, S.H.
1997
98 2 p. 164-
1 p.
artikel
29 Chromosome analysis and comparison of the benign cystic and malignant squamous components of an ovarian teratoma Noumoff, J.S.
1997
98 2 p. 159-
1 p.
artikel
30 Chromosome instability in 75 untreated ovarian cancer patients Parza, N.Z.
1997
98 2 p. 171-
1 p.
artikel
31 Chromosome 17 involvement in neuroblastoma: An overview Van Roy, N.
1997
98 2 p. 168-
1 p.
artikel
32 Chromosome microdissection identifies amplified and overexpressed cDNAs in human ovarian carcinoma Cargile, C.B.
1997
98 2 p. 170-
1 p.
artikel
33 Clinical cytogenetic correlations in solid tumors Taetle, R.
1997
98 2 p. 151-
1 p.
artikel
34 Clinical utility of her-2/NEU amplification as a prognostic indicator in patients with breast cancer Cross, S.A.
1997
98 2 p. 157-
1 p.
artikel
35 Cloning of a novel transcription factor like gene amplified in human low and high grade glioma Fischer, U.
1997
98 2 p. 152-
1 p.
artikel
36 Cloning of genes involved in cancer progression by a combination of functional and positional cloning Barrett, J.C.
1997
98 2 p. 154-
1 p.
artikel
37 Comparative genomic hybridization analysis of meningiomas Khan, J.
1997
98 2 p. 171-
1 p.
artikel
38 Comparative genomic hybridization and representational difference analysis as tools to identify and molecularly clone tumor-specific chromosomal anomalies Simons, A.
1997
98 2 p. 171-
1 p.
artikel
39 Comparative genomic hybridization to arrayed DNA targets (CGHa) for high resolution analysis of DNA sequence copy number changes Pinkel, D.
1997
98 2 p. 150-
1 p.
artikel
40 Comparison of cytogenetic and flow cytometric results of renal cell carcinoma (RCC) performed in the southwest oncology group (SWOG) Dobin, S.M.
1997
98 2 p. 151-
1 p.
artikel
41 Comparison of fluorescence in-situ hybridization (fish) and bladder tumor antigen test (BTA®) in bladder cancer: A pilot study McConnell, T.S.
1997
98 2 p. 161-
1 p.
artikel
42 Complex karyotypes consistently found in most adenocarcinomas of the pancreas Morsberger, L.A.
1997
98 2 p. 162-
1 p.
artikel
43 Correlations between cytogenetic findings and histology based on 382 benign thyroid hyerplasias and adenomas Belge, G.
1997
98 2 p. 156-
1 p.
artikel
44 Cytogenetic analysis of a glioblastoma in a patient with turcot syndrome Roherty, S.E.
1997
98 2 p. 165-
1 p.
artikel
45 Cytogenetic analysis of epithelial pancreatic neoplasms Long, P.
1997
98 2 p. 161-
1 p.
artikel
46 Cytogenetic and fluorescence in situ hybridization analyses of a microcystic adnexal carcinoma with del(6)(q23q25) Wohlfahrt, Caspar
1997
98 2 p. 106-110
5 p.
artikel
47 Cytogenetic evidence of polyclonality in epithelial tumors Mitelman, Felix
1997
98 2 p. 150-
1 p.
artikel
48 Cytogenetic study of pituitary adenomas Bettio, Daniela
1997
98 2 p. 131-136
6 p.
artikel
49 Deletion map of chromosome 16q in ductal carcinoma in situ of the breast: refining a putative tumor suppressor gene region Chen, T.
1997
98 2 p. 154-
1 p.
artikel
50 Detection of amplified genes in human cancer by comparative genomic hybridization Kallioniemi, A.
1997
98 2 p. 148-
1 p.
artikel
51 Detection of chromosome deletions in direct tumor preparations using fluorescence in situ hybridization Rao, K.P.
1997
98 2 p. 164-
1 p.
artikel
52 Detection of heterozygous mutations in brca1 using high density oligonucleotide arrays and two-color fluorescence analysis Hacia, J.G.
1997
98 2 p. 155-
1 p.
artikel
53 Detection of p16 gene deletions in gliomas: Fish vs. quantitative PCR Perry, A.
1997
98 2 p. 163-
1 p.
artikel
54 Development of aneuploidy and nuclear pleomorphism in thyroid follicular cells of TGCT transgenic mice Gusev, Y.
1997
98 2 p. 159-
1 p.
artikel
55 Different breast tumors with involvement of different HMG genes in the same patient Dal Cin, P.
1997
98 2 p. 157-
1 p.
artikel
56 Discrimination between multicentric and multifocal breast carcinoma by cytogenetic investigation of macroscopically distinct ipsilateral lesions Teixeira, M.R.
1997
98 2 p. 152-
1 p.
artikel
57 DNA gains and losses in gastrointestinal tract stromal tumors, leiomyomas, and leiomyosarcomas using comparative genomic hybridization El-Rifai, W.
1997
98 2 p. 158-
1 p.
artikel
58 DNA sequence copy number changes in lipomatous tumors Jadwiga, S.
1997
98 2 p. 148-
1 p.
artikel
59 Dual-color fluorescence in situ hybridization for detecting the t(x;18)(p11.2;q11.2) associated with synovial sarcoma in inter-phase and metaphase nuclei Li, S.
1997
98 2 p. 167-
1 p.
artikel
60 E1a transformed normal human prostate epithelial cells contain a 16q deletion Chin, R.K.
1997
98 2 p. 157-
1 p.
artikel
61 Estrogenic effects of nonylphenol on PS2, MUC1 and ER expressions in human breast cancer cells MCF-7 Ren, L.
1997
98 2 p. 165-
1 p.
artikel
62 Evidence for gene amplification in pancreatic adenocarcinoma using fish and characterization of marker chromosomes by chromosome microdissection Hawkins, A.L.
1997
98 2 p. 160-
1 p.
artikel
63 Fish analysis of the CDKN2/p16 gene in oral squamous cell carcinoma (OSCC) Shuster, M.
1997
98 2 p. 166-
1 p.
artikel
64 Fish and CGH studies of gene rearrangement and amplification in drug resistance Knutsen, T.
1997
98 2 p. 160-
1 p.
artikel
65 Fish characterization of chromosomes 8 and 17, HER2/neu, c-MYC and P53 in endometrial cancers Young, S.R.
1997
98 2 p. 169-
1 p.
artikel
66 Fish mapping of 8q12 translocation breakpoints in pleomorphic adenomas of the salivary glands Röijer, E.
1997
98 2 p. 167-
1 p.
artikel
67 Frequent DNA copy number changes in mantle cell lymphoma: Gain of 3q and loss of 11q22 Monni, O.
1997
98 2 p. 162-
1 p.
artikel
68 Gains and losses of genomic material in fibroadenenoma, carcinoma in situ and atypical hyperplasia of the breast analyzed by comparative genomic hybridization Lu, Y.-J.
1997
98 2 p. 166-
1 p.
artikel
69 Genetic analysis of early childhood and ovarian germ cell tumors by comparative genomic hybridization (CGH) Perlman, E.J.
1997
98 2 p. 162-
1 p.
artikel
70 Genetic basis of a histogenetic model of tumorigenesis of epithelial renal tumors Decker, H.J.
1997
98 2 p. 154-
1 p.
artikel
71 Genetic imbalances in primary breat tumors and proliferative breast diseases Varella-Garcia, M.
1997
98 2 p. 168-
1 p.
artikel
72 Genetic progression in astrocytoma Mohapatra, G.
1997
98 2 p. 148-
1 p.
artikel
73 Genomic analyses of three regions of increased copy number discovered using CGH Gray, J.
1997
98 2 p. 148-
1 p.
artikel
74 Hairy cell leukemia variant with t(2;8)(p12;q24) abnormality Wong, K.F.
1997
98 2 p. 102-105
4 p.
artikel
75 Hidden paracentric inversions of chromosome arm 12q affecting the HMGIC gene Wanschura, S.
1997
98 2 p. 168-
1 p.
artikel
76 High percentage of chromosome lq gain in hepato-cellular carcinomas as detected by comparative genomic hybridization Wong, N.
1997
98 2 p. 169-
1 p.
artikel
77 HMGI-C and HMGI(Y) expression in uterine leiomyomata: dysregulation of architectural factors in a benign neoplasm Morton, C.C.
1997
98 2 p. 151-
1 p.
artikel
78 Identification of a major susceptibility locus for human prostate cancer Trent, J.M.
1997
98 2 p. 146-
1 p.
artikel
79 Identification of a ring chromosome in a myxoid MFH with chromosome microdissection and fish Meloni, A.M.
1997
98 2 p. 162-
1 p.
artikel
80 Identification of two distinct regions on 1p36 involved in merkel cell carcinoma Van Gele, M.
1997
98 2 p. 153-
1 p.
artikel
81 Improving the precision of CGH analysis Piper, J.
1997
98 2 p. 149-
1 p.
artikel
82 Incidence of cancer in Italian ataxia telangiectasia families Chessa, L.
1997
98 2 p. 156-
1 p.
artikel
83 Increasing metastatic potential is associated with induced chromosome 14 translocations in a previously nonmetastatic murine melanoma cell line Nemeth, Margit A
1997
98 2 p. 119-125
7 p.
artikel
84 Involvement of the HMGIY gene in mesenchymal tumors with 6p21 aberrations Kazmierczak, B.
1997
98 2 p. 151-
1 p.
artikel
85 Karyotyping of a new EBV-associated nasopharyngeal carcinoma cell line Bik-Yu Hui, A.
1997
98 2 p. 160-
1 p.
artikel
86 Leptomeningeal metastasis from a paraspinal rhabdomyosarcoma with a der(13)t(1;13)(q23;q32) in a 14-month-old boy Kline, Ronald M
1997
98 2 p. 97-101
5 p.
artikel
87 Low frequency of TEL/AML1 in adult acute lymphoblastic leukemia Kwong, Y.L.
1997
98 2 p. 137-138
2 p.
artikel
88 Mathematical tools for spectral karyotyping (SKY) analysis Garini, Y.
1997
98 2 p. 170-
1 p.
artikel
89 Mesothelioma and lung carcinomas Björkqvist, A.-M.
1997
98 2 p. 149-
1 p.
artikel
90 Microdissecting the molecular stages of cancer progression, invasion and metastasis Emmert Buck, M.
1997
98 2 p. 154-
1 p.
artikel
91 Molecular cloning of chromosome 8q12 aberrations in pleomorphic adenomas of the salivary glands Kas, K.
1997
98 2 p. 160-
1 p.
artikel
92 Molecular cytogenetic analyses of 7Q31 in prostate cancer Jenkins, R.
1997
98 2 p. 152-
1 p.
artikel
93 Molecular cytogenetic analysis of early primary melanoma Dennis, T.R.
1997
98 2 p. 158-
1 p.
artikel
94 Monosomy 22 in a mixed germ cell-sex cord-stromal tumor of the ovary Speleman, F.
1997
98 2 p. 168-
1 p.
artikel
95 Multicolor fish studies of HER2/neu and chromosome 17 using archived paraffin embedded ovarian cancer samples Young, S.R.
1997
98 2 p. 170-
1 p.
artikel
96 Multicolor visual analysis of replication initiation using extended DNA mapping Windle, B.
1997
98 2 p. 147-
1 p.
artikel
97 Multifaceted assessment of genetic alterations in oralcancer Gollin, S.M.
1997
98 2 p. 152-
1 p.
artikel
98 Multiple genetic abnormalities including evidence of chromosome 11q13 rearrangement detected in pituitary adenomas by comparative genomic hybridization Metzger, A.K.
1997
98 2 p. 161-
1 p.
artikel
99 New approaches for analyzing tumor cell genomes: M-FISH and LM-RCA Speicher, M.R.
1997
98 2 p. 146-
1 p.
artikel
100 1p36 Rearrangements may be important in non-Hodgkin's lymphoma Pfeifer, A.L.
1997
98 2 p. 164-
1 p.
artikel
101 Presence of isochromosome 7q in Wilms' tumor as the sole change Pool, T.L.
1997
98 2 p. 164-
1 p.
artikel
102 Recurring chromosome breakpoints at 6q13–21 in histologically benign, but locally aggressive cartilaginous lesions Sawyer, J.R.
1997
98 2 p. 166-
1 p.
artikel
103 Search for genes involved in breast cancer predisposition, progression and metastasis based on CGH findings Kallioniemi, O.P.
1997
98 2 p. 149-
1 p.
artikel
104 Seventh international workshop on chromosomes in solid tumors Trent, Jeffrey M.
1997
98 2 p. 145-
1 p.
artikel
105 Sex-related differences and lack of i(12p) found in cytogenetic characterization of 82 pediatric germ cell tumors Bussey, K.J.
1997
98 2 p. 155-
1 p.
artikel
106 Spectral karyotyping Schröck, Evelin
1997
98 2 p. 146-
1 p.
artikel
107 Stage specific chromosomal aberrations in solid tumor progression Ried, T.
1997
98 2 p. 149-
1 p.
artikel
108 Studies of the three-dimensional architecture of human chromosome territories Cremer, T.
1997
98 2 p. 147-
1 p.
artikel
109 Telomeric association in women with breast and uterine cervix cancer Paz-y-Miño, César
1997
98 2 p. 115-118
4 p.
artikel
110 The human of ECT2 (Epithelial Cell Transforming Gene 2) mapping on chromosome 3q26.1–3q26.2 IS amplified in ovarian cancer cells Yang, J.-M.
1997
98 2 p. 169-
1 p.
artikel
111 The pancreas cancer genome project Kern, S.E.
1997
98 2 p. 155-
1 p.
artikel
112 Transcript mapping in a 46kb sequenced region at the core of 12q13.3 amplification in human cancers Meltzer, P.S.
1997
98 2 p. 147-
1 p.
artikel
113 Two different Philadelphia chromosomes in a cell line from an AML-M0 patient González García, Juan Ramón
1997
98 2 p. 111-114
4 p.
artikel
114 Unusual karyotypes in two synovial sarcomas Roland, B.
1997
98 2 p. 165-
1 p.
artikel
115 Use of a chromosome specific probe (10q22) to detect a tumor suppressor locus, in familial juvenile polyposis Jacoby, R.
1997
98 2 p. 153-
1 p.
artikel
116 Whole arm translocations in solid tumors and hematologic malignancy — formation and clinical significance Richkind, K.E.
1997
98 2 p. 165-
1 p.
artikel
                             116 gevonden resultaten
 
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