Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 329

1.

The neurobiology of Rett syndrome.

Akbarian S.

Neuroscientist. 2003 Feb;9(1):57-63. Review.

PMID:
12580340
[PubMed - indexed for MEDLINE]
2.

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]
3.

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
[PubMed - indexed for MEDLINE]
Free Article
4.

Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain.

Armstrong DD, Deguchi K, Antallfy B.

J Child Neurol. 2003 Oct;18(10):683-7.

PMID:
14649549
[PubMed - indexed for MEDLINE]
5.

The biological functions of the methyl-CpG-binding protein MeCP2 and its implication in Rett syndrome.

Nan X, Bird A.

Brain Dev. 2001 Dec;23 Suppl 1:S32-7. Review.

PMID:
11738839
[PubMed - indexed for MEDLINE]
6.

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]
7.

Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry.

LaSalle JM, Goldstine J, Balmer D, Greco CM.

Hum Mol Genet. 2001 Aug 15;10(17):1729-40.

PMID:
11532982
[PubMed - indexed for MEDLINE]
Free Article
8.

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome.

Horike S, Cai S, Miyano M, Cheng JF, Kohwi-Shigematsu T.

Nat Genet. 2005 Jan;37(1):31-40. Epub 2004 Dec 19.

PMID:
15608638
[PubMed - indexed for MEDLINE]
9.

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.

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

Hum Mol Genet. 2005 Apr 15;14(8):1049-58. Epub 2005 Mar 9.

PMID:
15757975
[PubMed - indexed for MEDLINE]
Free Article
10.

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.

Stancheva I, Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR.

Mol Cell. 2003 Aug;12(2):425-35.

PMID:
14536082
[PubMed - indexed for MEDLINE]
11.

Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex.

Akbarian S, Chen RZ, Gribnau J, Rasmussen TP, Fong H, Jaenisch R, Jones EG.

Neurobiol Dis. 2001 Oct;8(5):784-91.

PMID:
11592848
[PubMed - indexed for MEDLINE]
12.

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
[PubMed - indexed for MEDLINE]
Free Article
13.

Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2.

Chen WG, Chang Q, Lin Y, Meissner A, West AE, Griffith EC, Jaenisch R, Greenberg ME.

Science. 2003 Oct 31;302(5646):885-9.

PMID:
14593183
[PubMed - indexed for MEDLINE]
Free Article
14.

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
[PubMed - indexed for MEDLINE]
15.

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation.

Shahbazian MD, Antalffy B, Armstrong DL, Zoghbi HY.

Hum Mol Genet. 2002 Jan 15;11(2):115-24.

PMID:
11809720
[PubMed - indexed for MEDLINE]
Free Article
16.

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.

Guy J, Hendrich B, Holmes M, Martin JE, Bird A.

Nat Genet. 2001 Mar;27(3):322-6.

PMID:
11242117
[PubMed - indexed for MEDLINE]
17.

Rett syndrome: a prototypical neurodevelopmental disorder.

Neul JL, Zoghbi HY.

Neuroscientist. 2004 Apr;10(2):118-28. Review.

PMID:
15070486
[PubMed - indexed for MEDLINE]
18.

Association by guilt: identification of DLX5 as a target for MeCP2 provides a molecular link between genomic imprinting and Rett syndrome.

Bapat S, Galande S.

Bioessays. 2005 Jul;27(7):676-80. Review.

PMID:
15954098
[PubMed - indexed for MEDLINE]
19.

Importance of Rett syndrome in child neurology.

Dunn HG.

Brain Dev. 2001 Dec;23 Suppl 1:S38-43. Review.

PMID:
11738840
[PubMed - indexed for MEDLINE]
20.

Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA.

Ballestar E, Yusufzai TM, Wolffe AP.

Biochemistry. 2000 Jun 20;39(24):7100-6.

PMID:
10852707
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk