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Volumn 114, Issue 5, 2004, Pages 439-447

A study of the distributional characteristics of FMR1 transcript levels in 238 individuals

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSINE; DNA; GLYCINE; RNA; FMR1 PROTEIN, HUMAN; FRAGILE X MENTAL RETARDATION PROTEIN; MESSENGER RNA; NERVE PROTEIN; PRIMER DNA; RNA BINDING PROTEIN;

EID: 2542507386     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-004-1086-x     Document Type: Article
Times cited : (112)

References (21)
  • 1
    • 0027377580 scopus 로고
    • FMR1 protein: Conserved RNP family domains and selective RNA binding
    • Ashley CTJ, Wilkinson KD, Reines D, Warren ST (1993) FMR1 protein: conserved RNP family domains and selective RNA binding. Science 262:563-566
    • (1993) Science , vol.262 , pp. 563-566
    • Ashley, C.T.J.1    Wilkinson, K.D.2    Reines, D.3    Warren, S.T.4
  • 3
    • 0027375451 scopus 로고
    • Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test
    • Brown WT, Houck GE, Jeziorowska A, Levinson FN, Ding X, Dobkin C, Zhong J, et al (1993) Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test. JAMA 270:1569-1575
    • (1993) JAMA , vol.270 , pp. 1569-1575
    • Brown, W.T.1    Houck, G.E.2    Jeziorowska, A.3    Levinson, F.N.4    Ding, X.5    Dobkin, C.6    Zhong, J.7
  • 5
    • 0035746538 scopus 로고    scopus 로고
    • FMR1 and the fragile X syndrome: Human genome epidemiology review
    • Crawford DC, Acuna JM, Sherman SL (2001) FMR1 and the fragile X syndrome: human genome epidemiology review. Gen Med 3:359-371
    • (2001) Gen. Med. , vol.3 , pp. 359-371
    • Crawford, D.C.1    Acuna, J.M.2    Sherman, S.L.3
  • 8
    • 0035503902 scopus 로고    scopus 로고
    • Triplet repeats, RNA secondary structure and toxic gain-of-function models for pathogenesis
    • Galvao R, Mendes-Soares L, Camara J, Jaco I, Carmo-Fonseca M (2001) Triplet repeats, RNA secondary structure and toxic gain-of-function models for pathogenesis. Brain Res Bull 56:191-201
    • (2001) Brain Res. Bull. , vol.56 , pp. 191-201
    • Galvao, R.1    Mendes-Soares, L.2    Camara, J.3    Jaco, I.4    Carmo-Fonseca, M.5
  • 10
    • 0036591683 scopus 로고    scopus 로고
    • The fragile X premutation: Into the phenotypic fold
    • Hagerman RJ, Hagerman PJ (2002) The fragile X premutation: into the phenotypic fold. Curr Opin Genet Dev 12:278-283
    • (2002) Curr. Opin. Genet. Dev. , vol.12 , pp. 278-283
    • Hagerman, R.J.1    Hagerman, P.J.2
  • 12
    • 0041880131 scopus 로고    scopus 로고
    • RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila
    • Jin P, Zamescu DC, Zhang F, Pearson CE, Lucchesi JC, Moses K, Warren ST (2003) RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila. Neuron 39:739-747
    • (2003) Neuron , vol.39 , pp. 739-747
    • Jin, P.1    Zamescu, D.C.2    Zhang, F.3    Pearson, C.E.4    Lucchesi, J.C.5    Moses, K.6    Warren, S.T.7
  • 13
    • 0035394437 scopus 로고    scopus 로고
    • Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers
    • Kenneson A, Zhang F, Hagerdorn CH, Warren ST (2001) Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers. Hum Mol Genet 10:1449-1454
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 1449-1454
    • Kenneson, A.1    Zhang, F.2    Hagerdorn, C.H.3    Warren, S.T.4
  • 14
    • 0029955568 scopus 로고    scopus 로고
    • Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population
    • Meadows K, Pettay D, Newman J, Hersey J, Ashley AE, Sherman SL (1996) Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population. Am J Med Genet 64:425-433
    • (1996) Am. J. Med. Genet. , vol.64 , pp. 425-433
    • Meadows, K.1    Pettay, D.2    Newman, J.3    Hersey, J.4    Ashley, A.E.5    Sherman, S.L.6
  • 16
    • 0034522229 scopus 로고    scopus 로고
    • Premature ovarian failure in the fragile X syndrome
    • Sherman SL (2000) Premature ovarian failure in the fragile X syndrome. Am J Med Genet 97:189-194
    • (2000) Am. J. Med. Genet. , vol.97 , pp. 189-194
    • Sherman, S.L.1
  • 20
    • 1842318283 scopus 로고
    • Characterization and expression of a cDNA encoding the human androgen receptor
    • Tilley WD, Marcelli M, McPhaul MJ (1989) Characterization and expression of a cDNA encoding the human androgen receptor. Proc Natl Acad Sci USA 86:327-331
    • (1989) Proc. Natl. Acad. Sci. USA , vol.86 , pp. 327-331
    • Tilley, W.D.1    Marcelli, M.2    McPhaul, M.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.