Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins
<p>Abstract</p> <p>Background</p> <p>In mammals, there is evidence suggesting that methyl-CpG binding proteins may play a significant role in histone modification through their association with modification complexes that can deacetylate and/or methylate nucleosomes in...
Main Authors: | Canfield Theresa K, Luo Ping, Varadarajan Kartik R, Gartler Stanley M, Traynor Jeff, Francke Uta, Hansen R Scott |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2004-09-01
|
Series: | BMC Biology |
Online Access: | http://www.biomedcentral.com/1741-7007/2/21 |
Similar Items
-
Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations
by: Lazzeroni Laura, et al.
Published: (2002-11-01) -
Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease
by: Shervin Pejhan, et al.
Published: (2021-01-01) -
A Novel Methyl-CpG Binding Protein 2 (MeCP2) Variant in an Indian Girl with Rett Syndrome
by: Pratiksha Chheda, et al.
Published: (2021-04-01) -
Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets
by: Kwan Helen C, et al.
Published: (2007-06-01) -
Abnormal X : autosome ratio, but normal X chromosome inactivation in human triploid cultures
by: Norwood Thomas H, et al.
Published: (2006-07-01)