PubMed

Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets.

Jordan C, Li HH, Kwan HC, Francke U.

BMC Med Genet. 2007 Jun 20;8:36.PMID: 17584923 [PubMed - indexed for MEDLINE]Related articlesFree article

Ube3a expression is not altered in Mecp2 mutant mice.

Jordan C, Francke U.

Hum Mol Genet. 2006 Jul 15;15(14):2210-5. Epub 2006 Jun 5.PMID: 16754645 [PubMed - indexed for MEDLINE]Related articlesFree article

FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice.

Deng V, Matagne V, Banine F, Frerking M, Ohliger P, Budden S, Pevsner J, Dissen GA, Sherman LS, Ojeda SR.

Hum Mol Genet. 2007 Mar 15;16(6):640-50. Epub 2007 Feb 19.PMID: 17309881 [PubMed - indexed for MEDLINE]Related articlesFree article

Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients.

Delgado IJ, Kim DS, Thatcher KN, LaSalle JM, Van den Veyver IB.

BMC Med Genet. 2006 Jul 21;7:61.PMID: 16859563 [PubMed - indexed for MEDLINE]Related articlesFree article

Mecp2-null mice provide new neuronal targets for Rett syndrome.

Urdinguio RG, Lopez-Serra L, Lopez-Nieva P, Alaminos M, Diaz-Uriarte R, Fernandez AF, Esteller M.

PLoS One. 2008;3(11):e3669. Epub 2008 Nov 7.PMID: 18989361 [PubMed - indexed for MEDLINE]Related articlesFree article

Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome.

Peddada S, Yasui DH, LaSalle JM.

Hum Mol Genet. 2006 Jun 15;15(12):2003-14. Epub 2006 May 8.PMID: 16682435 [PubMed - indexed for MEDLINE]Related articlesFree article

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.

Chen RZ, Akbarian S, Tudor M, Jaenisch R.

Nat Genet. 2001 Mar;27(3):327-31.PMID: 11242118 [PubMed - indexed for MEDLINE]Related articles

MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

Balmer D, Arredondo J, Samaco RC, LaSalle JM.

Hum Genet. 2002 Jun;110(6):545-52. Epub 2002 Apr 25.PMID: 12107440 [PubMed - indexed for MEDLINE]Related articles

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency.

Schüle B, Li HH, Fisch-Kohl C, Purmann C, Francke U.

Am J Hum Genet. 2007 Sep;81(3):492-506. Epub 2007 Aug 2.PMID: 17701895 [PubMed - indexed for MEDLINE]Related articlesFree article

Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains.

Itoh M, Ide S, Takashima S, Kudo S, Nomura Y, Segawa M, Kubota T, Mori H, Tanaka S, Horie H, Tanabe Y, Goto Y.

J Neuropathol Exp Neurol. 2007 Feb;66(2):117-23.PMID: 17278996 [PubMed - indexed for MEDLINE]Related articles

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 [PubMed - indexed for MEDLINE]Related articlesFree article

MeCP2 dysfunction in Rett syndrome and related disorders.

Moretti P, Zoghbi HY.

Curr Opin Genet Dev. 2006 Jun;16(3):276-81. Epub 2006 May 2. Review.PMID: 16647848 [PubMed - indexed for MEDLINE]Related articles

Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations.

Traynor J, Agarwal P, Lazzeroni L, Francke U.

BMC Med Genet. 2002 Nov 5;3:12. Epub 2002 Nov 5.PMID: 12418965 [PubMed]Related articlesFree article

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

Samaco RC, Hogart A, LaSalle JM.

Hum Mol Genet. 2005 Feb 15;14(4):483-92. Epub 2004 Dec 22.PMID: 15615769 [PubMed - indexed for MEDLINE]Related articlesFree article

MeCP2 deficiency in the brain decreases BDNF levels by REST/CoREST-mediated repression and increases TRKB production.

Abuhatzira L, Makedonski K, Kaufman Y, Razin A, Shemer R.

Epigenetics. 2007 Oct-Dec;2(4):214-22. Epub 2007 Oct 29.PMID: 18075316 [PubMed - indexed for MEDLINE]Related articles

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 [PubMed - indexed for MEDLINE]Related articles

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. 2003 Jun;81(6):346-54. Epub 2003 May 16. Review.PMID: 12750821 [PubMed - indexed for MEDLINE]Related articles

Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus.

Ben-Shachar S, Chahrour M, Thaller C, Shaw CA, Zoghbi HY.

Hum Mol Genet. 2009 Jul 1;18(13):2431-42. Epub 2009 Apr 15.PMID: 19369296 [PubMed - indexed for MEDLINE]Related articlesFree article

Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain.

Tudor M, Akbarian S, Chen RZ, Jaenisch R.

Proc Natl Acad Sci U S A. 2002 Nov 26;99(24):15536-41. Epub 2002 Nov 13.PMID: 12432090 [PubMed - indexed for MEDLINE]Related articlesFree article

MeCP2, a key contributor to neurological disease, activates and represses transcription.

Chahrour M, Jung SY, Shaw C, Zhou X, Wong ST, Qin J, Zoghbi HY.

Science. 2008 May 30;320(5880):1224-9.PMID: 18511691 [PubMed - indexed for MEDLINE]Related articlesFree article