메뉴 건너뛰기




Volumn 6, Issue 2, 1994, Pages 152-156

Instability of short tandem repeats (microsatellites) in human cancers

Author keywords

[No Author keywords available]

Indexed keywords

DNA MINISATELLITE;

EID: 0028362315     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0294-152     Document Type: Article
Times cited : (414)

References (23)
  • 2
    • 0026767610 scopus 로고
    • Dynamic mutations: A new class of mutations causing human disease
    • Richards, R. I. & Sutherland, G. R. Dynamic mutations: A new class of mutations causing human disease. Cell 70, 709-712 (1992).
    • (1992) Cell , vol.70 , pp. 709-712
    • Richards, R.I.1    Sutherland, G.R.2
  • 3
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes
    • The Huntington’s Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. Cell 72, 971-983 (1993).
    • (1993) Cell , vol.72 , pp. 971-983
  • 4
    • 0028240475 scopus 로고
    • Triplet repeats strike again
    • Miwa, S. Triplet repeats strike again. Nature Genet. 6, 3-4 (1994).
    • (1994) Nature Genet , vol.6 , pp. 3-4
    • Miwa, S.1
  • 5
    • 0026601924 scopus 로고
    • Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
    • Harley, H. G. et al. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature 355, 545-546 (1992).
    • (1992) Nature , vol.355 , pp. 545-546
    • Harley, H.G.1
  • 6
    • 0026603841 scopus 로고
    • Myotonic dystrophy mutation: An unstable repeat in the 3' untranslated region of the gene
    • Mahadevan, M. et al. Myotonic dystrophy mutation: an unstable repeat in the 3' untranslated region of the gene. Science 255, 1253-1255 (1992).
    • (1992) Science , vol.255 , pp. 1253-1255
    • Mahadevan, M.1
  • 7
    • 0027416537 scopus 로고
    • Linkage disequilibrium between the fragile X mutations and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes
    • Oudet, C. et al. Linkage disequilibrium between the fragile X mutations and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes. Am. J. hum. Genet. 52, 297-304 (1993).
    • (1993) Am. J. hum. Genet , vol.52 , pp. 297-304
    • Oudet, C.1
  • 8
    • 0026935782 scopus 로고
    • A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome
    • Wooster, R. et al. A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome. Nature Genet. 2, 132-134 (1992).
    • (1992) Nature Genet , vol.2 , pp. 132-134
    • Wooster, R.1
  • 9
    • 0027158031 scopus 로고
    • Clues to the pathogenesis of familial colorectal cancer
    • Aaltonen, L. A. et al. Clues to the pathogenesis of familial colorectal cancer. Science 280, 812-816 (1993).
    • (1993) Science , vol.280 , pp. 812-816
    • Aaltonen, L.A.1
  • 10
    • 0027314411 scopus 로고
    • Microsateilite instability in cancer of the proximal colon
    • Thibodeau, S. N., Bren, G. & Schaid, D. Microsateilite instability in cancer of the proximal colon. Science 260, 816-819 (1993).
    • (1993) Science , vol.260 , pp. 816-819
    • Thibodeau, S.N.1    Bren, G.2    Schaid, D.3
  • 11
    • 0027285475 scopus 로고
    • Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesls
    • Ionov, Y. et al. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesls. Nature 363, 558-561 (1993).
    • (1993) Nature , vol.363 , pp. 558-561
    • Ionov, Y.1
  • 12
    • 0027263363 scopus 로고
    • Genetic mapping of a locus predisposing to human colorectal cancer
    • Peltomaki, P. et al. Genetic mapping of a locus predisposing to human colorectal cancer. Science 260, 810-812 (1993).
    • (1993) Science , vol.260 , pp. 810-812
    • Peltomaki, P.1
  • 13
    • 0026893558 scopus 로고
    • A further teranucleotide repeat polymorphism in the vWF gene
    • Kimpton, C., Walton, A. & Gill, P. A further teranucleotide repeat polymorphism in the vWF gene. Hum. molec. Genet. 1, 287 (1992).
    • (1992) Hum. molec. Genet , vol.1 , pp. 287
    • Kimpton, C.1    Walton, A.2    Gill, P.3
  • 14
    • 0025164249 scopus 로고
    • Tetranucleotide repeat polymorphism in the vWF gene
    • van Amstel, H. K. & Reitsma, P. H. Tetranucleotide repeat polymorphism in the vWF gene. Nucl. Acids Res. 18, 4957 (1990).
    • (1990) Nucl. Acids Res , vol.18 , pp. 4957
    • van Amstel, H.K.1    Reitsma, P.H.2
  • 15
    • 0027462891 scopus 로고
    • A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: Implications for mechanisms of mutation at short tandem repeat loci
    • Mahtani, M. M. & Willard, H. F. A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci. Hum. molec. Genet. 2, 431-437 (1993).
    • (1993) Hum. molec. Genet , vol.2 , pp. 431-437
    • Mahtani, M.M.1    Willard, H.F.2
  • 16
    • 0026446099 scopus 로고
    • A second generation linkage map of the human genome
    • Weissenbach, J. et al. A second generation linkage map of the human genome. Nature 359, 794-800 (1992).
    • (1992) Nature , vol.359 , pp. 794-800
    • Weissenbach, J.1
  • 17
    • 0026652095 scopus 로고
    • Isolation and characterisation of (AC)n microsateilite genetic markers from human chromosome 16
    • Thompson, A. D. et al. Isolation and characterisation of (AC)n microsateilite genetic markers from human chromosome 16. Genomics 13, 402-408 (1992).
    • (1992) Genomics , vol.13 , pp. 402-408
    • Thompson, A.D.1
  • 18
    • 0027251874 scopus 로고
    • Origin of the expansion mutation in myotonic dystrophy
    • Imbert, G., Kretz, C., Johnson, K. & Mandel, J. L. Origin of the expansion mutation in myotonic dystrophy. Nature Genet. 4, 72-76 (1993).
    • (1993) Nature Genet , vol.4 , pp. 72-76
    • Imbert, G.1    Kretz, C.2    Johnson, K.3    Mandel, J.L.4
  • 19
    • 0026080951 scopus 로고
    • Frequent somatic imbalance of markerallelesforcnromosome 1 in human primary breast carcinoma
    • Devilee, P. et al. Frequent somatic imbalance of markerallelesforcnromosome 1 in human primary breast carcinoma. Cancer Res. 51, 1020-1025 (1991).
    • (1991) Cancer Res , vol.51 , pp. 1020-1025
    • Devilee, P.1
  • 20
    • 0025259643 scopus 로고
    • The locus of the polymorphic epithelial mucin (PEM) tumour antigen on chromosome 1 q21 shows a high fequency of alteration in primary human breast tumours
    • Gendler, S. J. et al. The locus of the polymorphic epithelial mucin (PEM) tumour antigen on chromosome 1 q21 shows a high fequency of alteration in primary human breast tumours. Int. J. Cancer 45, 431-435 (1990).
    • (1990) Int. J. Cancer , vol.45 , pp. 431-435
    • Gendler, S.J.1
  • 21
    • 0025157834 scopus 로고
    • Informativeness of human (dC-dA)n-(dC-dT)n polymorphisms
    • Weber, J. L. Informativeness of human (dC-dA)n-(dC-dT)n polymorphisms. Genomics 7, 524-530 (1990).
    • (1990) Genomics , vol.7 , pp. 524-530
    • Weber, J.L.1
  • 22
    • 0027532034 scopus 로고
    • Short direct repeats flanking deletions, and duplicating insertions in p53 gene in human cancers
    • Jego, N., Thomas, G. & Hamelin, R. Short direct repeats flanking deletions, and duplicating insertions in p53 gene in human cancers. Oncogene 8, 209-213 (1993).
    • (1993) Oncogene , vol.8 , pp. 209-213
    • Jego, N.1    Thomas, G.2    Hamelin, R.3
  • 23
    • 0027401792 scopus 로고
    • Mutational analysis of patients with adenomatous polyposis: Identical inactivating mutations in unrelated individuals
    • Groden, J. et al. Mutational analysis of patients with adenomatous polyposis: identical inactivating mutations in unrelated individuals. Am. J. hum. Genet. 52, 263-272 (1993).
    • (1993) Am. J. hum. Genet , vol.52 , pp. 263-272
    • Groden, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.