메뉴 건너뛰기




Volumn 60, Issue 5, 1996, Pages 391-400

Dynamic mutation loci: Allele distributions in different populations

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; DNA FLANKING REGION; DNA STRUCTURE; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; HUMAN; PRIORITY JOURNAL;

EID: 10544236904     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1469-1809.1996.tb00437.x     Document Type: Article
Times cited : (24)

References (44)
  • 4
    • 0026681851 scopus 로고
    • A genetic marker at the glucokinase gene locus for Type 2 (non-insulin-dependent) diabetes mellitus in Mauritian Creoles
    • CHIU, K. C., PROVINCE, M. A., DOWSE, G. K., ZIMMET, P. Z., WAGNER, G., SERJEANTSON, S. & PERMUTT, M. A. (1992). A genetic marker at the glucokinase gene locus for Type 2 (non-insulin-dependent) diabetes mellitus in Mauritian Creoles Diabetologica 35, 632-638.
    • (1992) Diabetologica , vol.35 , pp. 632-638
    • Chiu, K.C.1    Province, M.A.2    Dowse, G.K.3    Zimmet, P.Z.4    Wagner, G.5    Serjeantson, S.6    Permutt, M.A.7
  • 5
    • 0027495515 scopus 로고
    • Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I
    • CHUNG, M-Y., RANUM, L. P. W., DUVICK, L. A., SERVADIO, A., ZOGHBI, H. Y. & ORR, H. T. (1993). Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I. Nature Genetics, 5, 254-258.
    • (1993) Nature Genetics , vol.5 , pp. 254-258
    • Chung, M.-Y.1    Ranum, L.P.W.2    Duvick, L.A.3    Servadio, A.4    Zoghbi, H.Y.5    Orr, H.T.6
  • 6
    • 0029916569 scopus 로고    scopus 로고
    • Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome
    • EICHLER, E. E., MACPHERSON, J. N., MURRAY, A., JACOBS, P. A., CHAKRAVARTI, A. & NELSON, D. L. (1996). Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome. Human Molecular Genetics 5, 319-330.
    • (1996) Human Molecular Genetics , vol.5 , pp. 319-330
    • Eichler, E.E.1    Macpherson, J.N.2    Murray, A.3    Jacobs, P.A.4    Chakravarti, A.5    Nelson, D.L.6
  • 7
    • 0029042130 scopus 로고
    • Identification of mismatch repair genes and their role in the development of cancer
    • FISCHEL, R. & KOLODNER, R. D. (1995). Identification of mismatch repair genes and their role in the development of cancer. Current Opinion in Genetics and Development 5, 382-395
    • (1995) Current Opinion in Genetics and Development , vol.5 , pp. 382-395
    • Fischel, R.1    Kolodner, R.D.2
  • 8
    • 0030052440 scopus 로고    scopus 로고
    • Ethnicity and myotonic dystrophy: A possible explanation for its absence in sub-Saharan Africa
    • GOLDMAN, A., RAMSAY, M. & JENKINS, T. (1996). Ethnicity and myotonic dystrophy: a possible explanation for its absence in sub-Saharan Africa. Annals of Human Genetics 60, 57-65.
    • (1996) Annals of Human Genetics , vol.60 , pp. 57-65
    • Goldman, A.1    Ramsay, M.2    Jenkins, T.3
  • 11
    • 0028133504 scopus 로고
    • Precursor arrays for triplet repeat expansion at the fragile X locus
    • HIRST, M., GREWAL, P. K. & DAVIES, K. E. (1994). Precursor arrays for triplet repeat expansion at the fragile X locus. Human Molecular Genetics 3, 1553-1560.
    • (1994) Human Molecular Genetics , vol.3 , pp. 1553-1560
    • Hirst, M.1    Grewal, P.K.2    Davies, K.E.3
  • 12
    • 0027251874 scopus 로고
    • Origin of the expansion mutation in myotonic dystrophy
    • IMBERT, G., KRETZ, C., JOHNSON, K. & MANDEL, J.-L. (1993) Origin of the expansion mutation in myotonic dystrophy. Nature Genetics 4, 72-76.
    • (1993) Nature Genetics , vol.4 , pp. 72-76
    • Imbert, G.1    Kretz, C.2    Johnson, K.3    Mandel, J.-L.4
  • 13
    • 0028291079 scopus 로고
    • The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27
    • IMBERT, G., TROTTIER, Y., BECKMANN, J. & MANDEL, J.-L. (1994) The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27. Genomics 21, 667-668.
    • (1994) Genomics , vol.21 , pp. 667-668
    • Imbert, G.1    Trottier, Y.2    Beckmann, J.3    Mandel, J.-L.4
  • 17
    • 0023777572 scopus 로고
    • HLA-DR and -DQ DNA genotyping in seven populations of Asia-Oceania and Australia
    • KOHONEN-CORISH, M. R. J., DUNKLEY, H. & SERJEANTSON, S. W. (1988). HLA-DR and -DQ DNA genotyping in seven populations of Asia-Oceania and Australia. Tissue Antigens 32, 32-40.
    • (1988) Tissue Antigens , vol.32 , pp. 32-40
    • Kohonen-Corish, M.R.J.1    Dunkley, H.2    Serjeantson, S.W.3
  • 19
    • 0025800526 scopus 로고
    • Androgen receptor gene mutations in X-linked spinal and muscular bulbar atrophy
    • LA SPADA, A. R., WILSON, E. M., LUBAHN, D. B., HARDING, A. E. & FISCHBECK, K. H. (1991). Androgen receptor gene mutations in X-linked spinal and muscular bulbar atrophy. Nature 352, 77-79.
    • (1991) Nature , vol.352 , pp. 77-79
    • La Spada, A.R.1    Wilson, E.M.2    Lubahn, D.B.3    Harding, A.E.4    Fischbeck, K.H.5
  • 28
    • 0026767610 scopus 로고
    • Dynamic Mutations: A new class of mutations causing human disease
    • RICHARDS, R. I. & SUTHERLAND, G. R. (1992). Dynamic Mutations: A new class of mutations causing human disease. Cell 70, 709-712.
    • (1992) Cell , vol.70 , pp. 709-712
    • Richards, R.I.1    Sutherland, G.R.2
  • 32
    • 0029091770 scopus 로고
    • Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genes
    • RUBINSZTEIN, D. C., LEGGO, J., COETZEE, G. A., IRVINE, R. A., BUCKLEY, M. & FERGUSON-SMITH, M. A. (1995b). Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genes. Human Molecular Genetics 4, 1585-1590.
    • (1995) Human Molecular Genetics , vol.4 , pp. 1585-1590
    • Rubinsztein, D.C.1    Leggo, J.2    Coetzee, G.A.3    Irvine, R.A.4    Buckley, M.5    Ferguson-Smith, M.A.6
  • 33
    • 0029014180 scopus 로고
    • Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals
    • SERVADIO, A , KOSHY, B., ARMSTRONG, D., ANTALFFY, B., ORR, H. T. & ZOGHBI, H. Y. (1995). Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals. Nature Genetics 10, 94-98.
    • (1995) Nature Genetics , vol.10 , pp. 94-98
    • Servadio, A.1    Koshy, B.2    Armstrong, D.3    Antalffy, B.4    Orr, H.T.5    Zoghbi, H.Y.6
  • 35
    • 0023605559 scopus 로고
    • HLA-DR and -DQ poly-morphisms: New linkage relationships established by RFLP genomic typing in Polynesians and Melanesians
    • SERJEANTSON, S. W. WHITE, B. S., JAZWINSKA, E. C., YENCHITSOMANUS, P. T., MICHLESON, K. N. P. & TRENT, R. J. (1987). HLA-DR and -DQ poly-morphisms: new linkage relationships established by RFLP genomic typing in Polynesians and Melanesians. Human Immunology 20, 145-154.
    • (1987) Human Immunology , vol.20 , pp. 145-154
    • Serjeantson, S.W.1    White, B.S.2    Jazwinska, E.C.3    Yenchitsomanus, P.T.4    Michleson, K.N.P.5    Trent, R.J.6
  • 39
    • 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 (1993). A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's Disease chromosomes. Cell 72, 971-983.
    • (1993) Cell , vol.72 , pp. 971-983
  • 40
    • 0023909533 scopus 로고
    • Globin genes are useful markers to identify genetic similarities between Fijians and Pacific islanders from Polynesia and Melanesia
    • TRENT, R. J., BUCHANAN, J. G., WEBB, A., GOUNDAR, R. P. S., SERUVATU, L. M. & MICKELSON, K. N. P (1988). Globin genes are useful markers to identify genetic similarities between Fijians and Pacific islanders from Polynesia and Melanesia. American Journal of Human Genetics 48, 601-607.
    • (1988) American Journal of Human Genetics , vol.48 , pp. 601-607
    • Trent, R.J.1    Buchanan, J.G.2    Webb, A.3    Goundar, R.P.S.4    Seruvatu, L.M.5    Mickelson, K.N.P.6
  • 41
    • 0025157834 scopus 로고
    • Informativeness of human (dC-dA)n (dG-dT)n polymorphisms
    • WEBER, J. L. (1990). Informativeness of human (dC-dA)n (dG-dT)n polymorphisms. Genomics 7, 524-530.
    • (1990) Genomics , vol.7 , pp. 524-530
    • Weber, J.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.