Specific Mutations in Methyl-CpG-Binding Protein 2 Confer Different Severity in Rett Syndrome

Neurology - United States
doi 10.1212/01.wnl.0000291011.54508.aa
Full Text
Abstract

Available in full text

Categories
Neurology
Date
Authors
Publisher

Ovid Technologies (Wolters Kluwer Health)

Related search

Methyl CpG Binding Protein 2 (MECP2; RTT)

Science-Business eXchange
2012English

Epigenome: What We Learned From Rett Syndrome, a Neurological Disease Caused by Mutation of a Methyl-CpG Binding Protein

Clinical Neurology
Neurology
2013English

DNA Binding Restricts the Intrinsic Conformational Flexibility of Methyl CpG Binding Protein 2 (MeCP2)

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2011English

The Methyl-CpG-Binding Protein MeCP2 and Neurological Disease

Biochemical Society Transactions
Biochemistry
2008English

Impaired Memory CD8 T Cell Development in the Absence of Methyl-CpG-Binding Domain Protein 2

Journal of Immunology
AllergyImmunology
2006English

In Sickness and in Health: The Role of Methyl-CpG Binding Protein 2 in the Central Nervous System

European Journal of Neuroscience
Neuroscience
2011English

Single Sevoflurane Exposure Increases Methyl-CpG Island Binding Protein 2 Phosphorylation in the Hippocampus of Developing Mice

Molecular Medicine Reports
OncologyGeneticsMolecular BiologyBiochemistryCancer ResearchMolecular Medicine
2014English

Mechanism of Transcriptional Regulation by Methyl-CpG Binding Protein MBD1

Molecular and Cellular Biology
Cell BiologyMolecular Biology
2000English

Mutations in Ribosomal Protein L10e Confer Resistance to the Fungal-Specific Eukaryotic Elongation Factor 2 Inhibitor Sordarin

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
1999English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy