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Volumn 10, Issue 2, 2000, Pages

Human genetics: Methylation moves into medicine

Author keywords

[No Author keywords available]

Indexed keywords

MAMMALIA;

EID: 0033952930     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0960-9822(00)00286-4     Document Type: Article
Times cited : (18)

References (17)
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    • Li E, Bestor TH, Jaenisch R: Targeted mutation of the DNA methyltransferase gene results in embryonic lethality. Cell 1992, 69:915-926.
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    • Li, E.1    Bestor, T.H.2    Jaenisch, R.3
  • 2
    • 0023848337 scopus 로고
    • Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: The ICF syndrome
    • Maraschio P, Zuffardi O, Dalla Fior T, Tiepolo L: Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome. J Med Genet 1988, 25:173-180.
    • (1988) J Med Genet , vol.25 , pp. 173-180
    • Maraschio, P.1    Zuffardi, O.2    Dalla Fior, T.3    Tiepolo, L.4
  • 5
    • 0033153303 scopus 로고    scopus 로고
    • The human DNA methyltransferases (DNMTs) 1, 3a and 3b: Coordinate mRNA expression in normal tissues and overexpression in tumors
    • Robertson KD, Uzvolgyi E, Liang G, Talmadge C, Sumegi J, Gonzales FA, Jones PA: The human DNA methyltransferases (DNMTs) 1, 3a and 3b: coordinate mRNA expression in normal tissues and overexpression in tumors. Nucleic Acids Res 1999, 27:2291-2298.
    • (1999) Nucleic Acids Res , vol.27 , pp. 2291-2298
    • Robertson, K.D.1    Uzvolgyi, E.2    Liang, G.3    Talmadge, C.4    Sumegi, J.5    Gonzales, F.A.6    Jones, P.A.7
  • 7
    • 0033615717 scopus 로고    scopus 로고
    • DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
    • Okano M, Bell DW, Haber DA, Li E: DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell 1999, 99:247-257.
    • (1999) Cell , vol.99 , pp. 247-257
    • Okano, M.1    Bell, D.W.2    Haber, D.A.3    Li, E.4
  • 9
    • 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: Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 1999, 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
  • 11
    • 0020507697 scopus 로고
    • A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
    • Hagberg B, Aicardi J, Dias K, Ramos O: A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Ann Neurol 1983, 14:471-479.
    • (1983) Ann Neurol , vol.14 , pp. 471-479
    • Hagberg, B.1    Aicardi, J.2    Dias, K.3    Ramos, O.4
  • 13
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    • Genetic aspects of Rett syndrome
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    • (1988) J Child Neurol , vol.3 , Issue.SUPPL.
    • Zoghbi, H.1
  • 14
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    • Workshop on autonomic function in Rett syndrome
    • Engerstrom IW, Kerr A: Workshop on autonomic function in Rett syndrome. Brain Dev 1988, 20:323-326.
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    • Engerstrom, I.W.1    Kerr, A.2
  • 15
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    • MeCP2 is a transcriptional represser with abundant binding sites in genomic chromatin
    • Nan X, Campoy F, Bird A: MeCP2 is a transcriptional represser with abundant binding sites in genomic chromatin. Cell 1997, 88:471-481.
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    • Nan, X.1    Campoy, F.2    Bird, A.3
  • 16
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    • The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse
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    • Tate, P.1    Skarnes, W.2    Bird, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.