Rett (syndrome de)
Bibliographie
Maladies hérédo-dégénératives, syndrome de Rett, J. Mancini neurologie pédiatrique, Médecine-Sciences Flammarion, page 758-762.
Siriani N, Naidu S, Pereira J, Pillotto RF, Hoffman EP. Rett syndrome confirmation of X-linked dominant inheritance, and localisation of the gene to Xq28. Am J Hum Genet 1998 ; 393 : 1552-8.
2Amir 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. Nature Genet 1999 ; 23 : 185-8.
Jones PL, Veenstra GJC, Wade PA, Vermaak D, Kass SU, et al. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. Nature Genet 1998 ; 19 : 187-91.
Taddei A, Almouzni G. Les acétyl-transférases et désacétylases des histones : des co-régulateurs de la transcription. Méd/Sci 1997 ; 13: p.1205-11.
Coy JF, Sedlacek Z, Bächner D, Delius H, Poustka A. A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3'-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression. Hum Mol Genet 1999 ; 8 : 1253-62 .
Hendrich B, Abbott C, McQueen H, Chambers D, Cross S, Bird A. Genomic structure and genomic mapping of the murine and human mbd1, mbd2, mbd3, mbd4 genes. Mamm Genome 1999 ; 10 : 906-12.
Willard HF, Hendrich BD. Breaking the silence in Rett syndrome. Nature Genet 1999 ; 23 : 127-8. Tate P, Skarnes W, Bird A. The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse. Nature Genet 1996 ; 12 : 205-8.
Siriani N, Naidu S, Pereira J, Pillotto RF, Hoffman EP. Rett syndrome confirmation of X-linked dominant inheritance, and localisation of the gene to Xq28. Am J Hum Genet 1998 ; 393 : 1552-8.
2Amir 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. Nature Genet 1999 ; 23 : 185-8.
Jones PL, Veenstra GJC, Wade PA, Vermaak D, Kass SU, et al. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. Nature Genet 1998 ; 19 : 187-91.
Taddei A, Almouzni G. Les acétyl-transférases et désacétylases des histones : des co-régulateurs de la transcription. Méd/Sci 1997 ; 13: p.1205-11.
Coy JF, Sedlacek Z, Bächner D, Delius H, Poustka A. A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3'-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression. Hum Mol Genet 1999 ; 8 : 1253-62 .
Hendrich B, Abbott C, McQueen H, Chambers D, Cross S, Bird A. Genomic structure and genomic mapping of the murine and human mbd1, mbd2, mbd3, mbd4 genes. Mamm Genome 1999 ; 10 : 906-12.
Willard HF, Hendrich BD. Breaking the silence in Rett syndrome. Nature Genet 1999 ; 23 : 127-8. Tate P, Skarnes W, Bird A. The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse. Nature Genet 1996 ; 12 : 205-8.
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