메뉴 건너뛰기




Volumn 1, Issue 6, 1998, Pages 773-781

FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis

Author keywords

[No Author keywords available]

Indexed keywords

SATELLITE DNA;

EID: 0032059864     PISSN: 10972765     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1097-2765(00)80077-5     Document Type: Article
Times cited : (81)

References (42)
  • 1
    • 0027209516 scopus 로고
    • Allelic diversity at minisatellite MS205 (D16S309): Evidence for polarised variability
    • Armour, J.A.L., Harris, P.C., and Jeffreys, A.J. (1993). Allelic diversity at minisatellite MS205 (D16S309): evidence for polarised variability. Hum. Mol. Genet. 2, 1137-1145.
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 1137-1145
    • Armour, J.A.L.1    Harris, P.C.2    Jeffreys, A.J.3
  • 2
    • 0027281010 scopus 로고
    • Characterisation of the COL2A1 VNTR polymorphism
    • Berg, E.S., and Olaisen, B. (1993). Characterisation of the COL2A1 VNTR polymorphism. Genomics 16, 350-354.
    • (1993) Genomics , vol.16 , pp. 350-354
    • Berg, E.S.1    Olaisen, B.2
  • 3
    • 0028238234 scopus 로고
    • Complex recombination events at the hypermutable minisatellite CEB1 (D2S90)
    • Buard, J., and Vergnaud, G. (1994). Complex recombination events at the hypermutable minisatellite CEB1 (D2S90). EMBO J. 13, 3202-3210.
    • (1994) EMBO J. , vol.13 , pp. 3202-3210
    • Buard, J.1    Vergnaud, G.2
  • 4
    • 0030911978 scopus 로고    scopus 로고
    • Big, bad minisatellites
    • Buard, J., and Jeffreys, A. (1997). Big, bad minisatellites. Nat. Genet. 15, 327-328.
    • (1997) Nat. Genet. , vol.15 , pp. 327-328
    • Buard, J.1    Jeffreys, A.2
  • 7
    • 0029053371 scopus 로고
    • Trinucleotide repeats that expand in human disease form hairpin structures in vitro
    • Gacy, M.A., Goellner, G., Juranic, N., Macura, S., and McMurray, C.T. (1995). Trinucleotide repeats that expand in human disease form hairpin structures in vitro. Cell 81, 533-540.
    • (1995) Cell , vol.81 , pp. 533-540
    • Gacy, M.A.1    Goellner, G.2    Juranic, N.3    Macura, S.4    McMurray, C.T.5
  • 12
    • 85030037341 scopus 로고    scopus 로고
    • Construction of a genetic and physical map spanning the bromodeoxyuridine-inducible fragile site on human chromosome 10q25.2
    • abstract #1764
    • Hewett, D.R., Handt, O., Mulley, J.C., Eyre, H., Mao, J., Le Paslier, D., Sutherland, G.R., and Richards, R.I. (1996). Construction of a genetic and physical map spanning the bromodeoxyuridine-inducible fragile site on human chromosome 10q25.2. Am. J. Hum. Genet. 59, A304 (abstract #1764).
    • (1996) Am. J. Hum. Genet. , vol.59
    • Hewett, D.R.1    Handt, O.2    Mulley, J.C.3    Eyre, H.4    Mao, J.5    Le Paslier, D.6    Sutherland, G.R.7    Richards, R.I.8
  • 13
    • 0027251874 scopus 로고
    • Origin of the expansion mutation in myotonic dystrophy
    • Imbert, G., Kretz, C., Johnson, K., and Mandel, J.-L. (1993). Origin of the expansion mutation in myotonic dystrophy. Nat. Genet. 4, 72-76.
    • (1993) Nat. Genet. , vol.4 , pp. 72-76
    • Imbert, G.1    Kretz, C.2    Johnson, K.3    Mandel, J.-L.4
  • 19
    • 0028360849 scopus 로고
    • Cryptic and polar variation of the Fragile X repeat could result in predisposing normal alleles
    • Kunst, C.B., and Warren, S.T. (1994). Cryptic and polar variation of the Fragile X repeat could result in predisposing normal alleles. Cell 77, 853-861.
    • (1994) Cell , vol.77 , pp. 853-861
    • Kunst, C.B.1    Warren, S.T.2
  • 21
    • 0031228399 scopus 로고    scopus 로고
    • What is expanded in progressive myoclonus epilepsy?
    • Lalioti, M.D., Scott, H.S., and Antonarakis, S. (1997b). What is expanded in progressive myoclonus epilepsy? Nat. Genet. 17, 17-18.
    • (1997) Nat. Genet. , vol.17 , pp. 17-18
    • Lalioti, M.D.1    Scott, H.S.2    Antonarakis, S.3
  • 22
    • 0025800526 scopus 로고
    • Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
    • La Spada, A.R., Wilson, E.M., Lubahn, D.B., Harding, A.E., and Fischbeck, K.H. (1991). Androgen receptor gene mutations in X-linked spinal and bulbar muscular 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
  • 24
    • 0030737538 scopus 로고    scopus 로고
    • Trinucleotide repeats associated with human disease
    • Mitas, M. (1997). Trinucleotide repeats associated with human disease. Nucleic Acids Res. 25, 2245-2253.
    • (1997) Nucleic Acids Res. , vol.25 , pp. 2245-2253
    • Mitas, M.1
  • 31
    • 0026767610 scopus 로고
    • Dynamic mutations: A new class of mutations causing human genetic disease
    • Richards, R.I., and Sutherland, G.R. (1992). Dynamic mutations: a new class of mutations causing human genetic disease. Cell 70, 709-712.
    • (1992) Cell , vol.70 , pp. 709-712
    • Richards, R.I.1    Sutherland, G.R.2
  • 32
    • 0030664357 scopus 로고    scopus 로고
    • Dynamic mutations: Possible mechanisms and significance in human disease
    • Richards, R.I., and Sutherland, G.R. (1997). Dynamic mutations: possible mechanisms and significance in human disease. Trends Biochem. Sci. 22, 432-436.
    • (1997) Trends Biochem. Sci. , vol.22 , pp. 432-436
    • Richards, R.I.1    Sutherland, G.R.2
  • 35
    • 0019849991 scopus 로고
    • Heritable fragile sites on human chromosomes. VII. Children homozygous for the BrdU-requiring fra(10)q25 are phenotypically normal
    • Sutherland, G.R. (1981). Heritable fragile sites on human chromosomes. VII. Children homozygous for the BrdU-requiring fra(10)q25 are phenotypically normal. Am. J. Hum. Genet. 33, 946-949.
    • (1981) Am. J. Hum. Genet. , vol.33 , pp. 946-949
    • Sutherland, G.R.1
  • 36
    • 0019983936 scopus 로고
    • Heritable fragile sites on human chromosomes. IX. Population cytogenetics and segregation analysis of BrdU requiring fragile site at 10q25
    • Sutherland, G.R. (1982). Heritable fragile sites on human chromosomes. IX. Population cytogenetics and segregation analysis of BrdU requiring fragile site at 10q25. Am. J. Hum. Genet. 34, 753-756.
    • (1982) Am. J. Hum. Genet. , vol.34 , pp. 753-756
    • Sutherland, G.R.1
  • 37
    • 0029061046 scopus 로고
    • The molecular basis of fragile sites in human chromosomes
    • Sutherland, G.R., and Richards, R.I. (1995). The molecular basis of fragile sites in human chromosomes. Curr. Opin. Genet. Dev. 5, 323-327.
    • (1995) Curr. Opin. Genet. Dev. , vol.5 , pp. 323-327
    • Sutherland, G.R.1    Richards, R.I.2
  • 38
    • 0018940085 scopus 로고
    • Heritable fragile sites on human chromosomes. V. A new class of fragile site requiring BrdU for expression
    • Sutherland, G.R., Baker, E., and Seshadri, R.S. (1980). Heritable fragile sites on human chromosomes. V. A new class of fragile site requiring BrdU for expression. Am. J. Hum. Genet. 32, 542-548.
    • (1980) Am. J. Hum. Genet. , vol.32 , pp. 542-548
    • Sutherland, G.R.1    Baker, E.2    Seshadri, R.S.3
  • 39
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in Fragile X syndrome
    • Verkerk, A.J.M.H., Pieretti, M., Sutcliffe, J.S., Fu, Y.-H., Kuhl, D.P.A., Pizzuti, A., Reiner, O., Richards, S., Victoria, M.F., Zhang, F., et al. (1991). Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in Fragile X syndrome. Cell 65, 905-914.
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.M.H.1    Pieretti, M.2    Sutcliffe, J.S.3    Fu, Y.-H.4    Kuhl, D.P.A.5    Pizzuti, A.6    Reiner, O.7    Richards, S.8    Victoria, M.F.9    Zhang, F.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.