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 |