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Journal of the American Academy of Child and Adolescent Psychiatry
Volumn 39, Issue 5, 2000, Pages 671-674
Genetics of childhood disorders: XIV. A gene for Rett syndrome: News flash
Author keywords

[No Author keywords available]
Indexed keywords

CHILDHOOD DISEASE; CHROMATIN STRUCTURE; CHROMOSOMAL LOCALIZATION; DNA METHYLATION; GENE CONTROL; GENE EXPRESSION; GENE ISOLATION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; PATHOGENESIS; PRIORITY JOURNAL; RETT SYNDROME; SHORT SURVEY; X CHROMOSOME;
EID: 12944254590     PISSN: 08908567     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004583-200005000-00023     Document Type: Article
Times cited : (5)
References (5)
  • 1
    • 0032830639 scopus 로고    scopus 로고
    • Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    • Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY (1999), Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23:185-188
    • (1999) Nat Genet , vol.23 , pp. 185-188
    • Amir, R.E.1    Van Den Veyver, I.B.2    Wan, M.3    Tran, C.Q.4    Francke, U.5    Zoghbi, H.Y.6
  • 2
    • 0028940587 scopus 로고
    • Gene number, noise reduction and biological complexity
    • Bird AP (1995), Gene number, noise reduction and biological complexity. Trends Genet 11:94-100
    • (1995) Trends Genet , vol.11 , pp. 94-100
    • Bird, A.P.1
  • 3
    • 0030710153 scopus 로고    scopus 로고
    • How does DNA methylation repress transcription?
    • Kass SU, Pruss D, Wolffe AP (1997), How does DNA methylation repress transcription? Trends Genet 13:444-449
    • (1997) Trends Genet , vol.13 , pp. 444-449
    • Kass, S.U.1    Pruss, D.2    Wolffe, A.P.3
  • 4
    • 0342437491 scopus 로고    scopus 로고
    • MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
    • Nan X, Campoy J, Bird A (1997), MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin. Cell 88:471-481
    • (1997) Cell , vol.88 , pp. 471-481
    • Nan, X.1    Campoy, J.2    Bird, A.3
  • 5
    • 0031784505 scopus 로고    scopus 로고
    • Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28
    • Webb T, Clarke A, Hanefeld F, Pereira JL, Rosenbloom L, Woods CG (1998), Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28. J Med Genet 35:997-1003
    • (1998) J Med Genet , vol.35 , pp. 997-1003
    • Webb, T.1    Clarke, A.2    Hanefeld, F.3    Pereira, J.L.4    Rosenbloom, L.5    Woods, C.G.6

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.