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Items: 1 to 20 of 48

1.

MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome.

Wan M, Zhao K, Lee SS, Francke U.

Hum Mol Genet. 2001 May 1;10(10):1085-92.

PMID:
11331619
2.

Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.

Hoffbuhr KC, Moses LM, Jerdonek MA, Naidu S, Hoffman EP.

Ment Retard Dev Disabil Res Rev. 2002;8(2):99-105. Review.

PMID:
12112735
3.

Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations.

Amir RE, Zoghbi HY.

Am J Med Genet. 2000 Summer;97(2):147-52. Review.

PMID:
11180222
4.

Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.

Van den Veyver IB, Zoghbi HY.

Brain Dev. 2001 Dec;23 Suppl 1:S147-51. Review.

PMID:
11738862
5.
6.

Rett syndrome: a surprising result of mutation in MECP2.

Dragich J, Houwink-Manville I, Schanen C.

Hum Mol Genet. 2000 Oct;9(16):2365-75. Review.

PMID:
11005791
8.

Methyl-CpG-binding protein 2 mutations in Rett syndrome.

Van den Veyver IB, Zoghbi HY.

Curr Opin Genet Dev. 2000 Jun;10(3):275-9. Review.

PMID:
10826991
9.

MeCP2 in neurons: closing in on the causes of Rett syndrome.

Caballero IM, Hendrich B.

Hum Mol Genet. 2005 Apr 15;14 Spec No 1:R19-26. Review. Erratum in: Hum Mol Genet. 2005 Jul 15;14(14):2089.

PMID:
15809268
10.

Mutations and polymorphisms in the human methyl CpG-binding protein MECP2.

Miltenberger-Miltenyi G, Laccone F.

Hum Mutat. 2003 Aug;22(2):107-15. Review.

PMID:
12872250
11.

MeCP2 and other methyl-CpG binding proteins.

Jørgensen HF, Bird A.

Ment Retard Dev Disabil Res Rev. 2002;8(2):87-93. Review.

PMID:
12112733
12.

The role of X-chromosome inactivation in the manifestation of Rett syndrome.

Takagi N.

Brain Dev. 2001 Dec;23 Suppl 1:S182-5. Review.

PMID:
11738869
13.

Rett syndrome: from the gene to the disease.

Matijevic T, Knezevic J, Slavica M, Pavelic J.

Eur Neurol. 2009;61(1):3-10. doi: 10.1159/000165342. Epub 2008 Oct 24. Review.

PMID:
18948693
14.

Rett syndrome: of girls and mice--lessons for regression in autism.

Glaze DG.

Ment Retard Dev Disabil Res Rev. 2004;10(2):154-8. Review.

PMID:
15362175
15.

Genetic basis of Rett syndrome.

Van den Veyver IB, Zoghbi HY.

Ment Retard Dev Disabil Res Rev. 2002;8(2):82-6. Review.

PMID:
12112732
16.

The MECP2 gene mutation screening in Rett syndrome patients from Croatia.

Matijević T, Knezević J, Barisić I, Resić B, Culić V, Pavelić J.

Ann N Y Acad Sci. 2006 Dec;1091:225-32. Review.

PMID:
17341617
17.

Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2).

Moog U, Smeets EE, van Roozendaal KE, Schoenmakers S, Herbergs J, Schoonbrood-Lenssen AM, Schrander-Stumpel CT.

Eur J Paediatr Neurol. 2003;7(1):5-12. Review.

PMID:
12615169
18.

Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations.

Shahbazian MD, Zoghbi HY.

Curr Opin Neurol. 2001 Apr;14(2):171-6. Review.

PMID:
11262731
19.

Rett syndrome: the complex nature of a monogenic disease.

Renieri A, Meloni I, Longo I, Ariani F, Mari F, Pescucci C, Cambi F.

J Mol Med (Berl). 2003 Jun;81(6):346-54. Epub 2003 May 16. Review.

PMID:
12750821
20.

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