Works matching IS 10452257 AND DT 1997 AND VI 20 AND IP 1
Results: 15
Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 16, doi. 10.1002/(SICI)1098-2264(199709)20:1<16::AID-GCC3>3.0.CO;2-C
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The effect of different TP53 mutations on the chromosomal stability of a human colonic adenoma derived cell line with endogenous wild type TP53 activity, before and after DNA damage.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 44, doi. 10.1002/(SICI)1098-2264(199709)20:1<44::AID-GCC7>3.0.CO;2-9
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Hamartoma of the breast with involvement of 6p21 and rearrangement of HMGIY.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 90, doi. 10.1002/(SICI)1098-2264(199709)20:1<90::AID-GCC13>3.0.CO;2-J
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FHIT gene and the FRA3B region are not involved in the genetics of renal cell carcinomas.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 9, doi. 10.1002/(SICI)1098-2264(199709)20:1<9::AID-GCC2>3.0.CO;2-Z
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17q12-21 amplicon, a novel recurrent genetic change in intestinal type of gastric carcinoma: A comparative genomic hybridization study.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 38, doi. 10.1002/(SICI)1098-2264(199709)20:1<38::AID-GCC6>3.0.CO;2-A
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Codeletion of the JUN proto-oncogene and the CDKN2A tumor-suppressor gene in HRAS-transformed rat embryo fibroblast cell lines.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 82, doi. 10.1002/(SICI)1098-2264(199709)20:1<82::AID-GCC12>3.0.CO;2-H
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Immunoglobulin/ Myc recombinations in Murine Peyer's patch follicles.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 1, doi. 10.1002/(SICI)1098-2264(199709)20:1<1::AID-GCC1>3.0.CO;2-Z
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Molecular cytogenetic analysis of a nontumorigenic human breast epithelial cell line that eventually turns tumorigenic: Validation of an analytical approach combining karyotyping, comparative genomic hybridization, chromosome painting, and single-locus fluorescence in situ hybridization
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 30, doi. 10.1002/(SICI)1098-2264(199709)20:1<30::AID-GCC5>3.0.CO;2-A
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Novel MLL-CBP fusion transcript in therapy-related chronic myelomonocytic leukemia with a t(11;16) (q23;p13) chromosome translocation.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 60, doi. 10.1002/(SICI)1098-2264(199709)20:1<60::AID-GCC9>3.0.CO;2-7
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Cytogenetic, fluorescence in situ hybridisation, and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphocytic leukaemia.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 73, doi. 10.1002/(SICI)1098-2264(199709)20:1<73::AID-GCC11>3.0.CO;2-G
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Analysis of the fragile histidine triad gene in primary gastric carcinomas and gastric carcinoma cell lines.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 98, doi. 10.1002/(SICI)1098-2264(199709)20:1<98::AID-GCC15>3.0.CO;2-B
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Absence of TP53 alterations in pheochromocytomas and medullary thyroid carcinomas.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 24, doi. 10.1002/(SICI)1098-2264(199709)20:1<24::AID-GCC4>3.0.CO;2-B
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Analysis of the BRCA1 and BRCA2 genes in sporadic meningiomas.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 53, doi. 10.1002/(SICI)1098-2264(199709)20:1<53::AID-GCC8>3.0.CO;2-8
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BCL3 rearrangements and t(14;19) in chronic lymphocytic leukemia and other B-cell malignancies: A molecular and cytogenetic study.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 64, doi. 10.1002/(SICI)1098-2264(199709)20:1<64::AID-GCC10>3.0.CO;2-F
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Loss of heterozygosity of chromosome 13 in Merkel cell carcinoma.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 93, doi. 10.1002/(SICI)1098-2264(199709)20:1<93::AID-GCC14>3.0.CO;2-G
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