The Molecular Basis of MeCP2 Function in the Brain-Reference-Cited by-同舟云学术

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The Molecular Basis of MeCP2 Function in the Brain

Published:2020-03 Issue:6 Volume:432 Page:1602-1623
ISSN:0022-2836
Container-title:Journal of Molecular Biology
language:en
Short-container-title:Journal of Molecular Biology

Author:

Tillotson Rebekah,Bird Adrian

Funder

Wellcome Trust Centre

Wellcome Investigator Award

Rett Syndrome Research Trust Consortium

European Research Council

Publisher

Elsevier BV

Subject

Molecular Biology,Structural Biology

Reference196 articles.

1. Disease model discovery from 3,328 gene knockouts by the international mouse phenotyping Consortium;Meehan;Nat. Genet.,2017

2. Large-scale discovery of novel genetic causes of developmental disorders;Nature,2015

3. Rett syndrome: revised diagnostic criteria and nomenclature, Ann;Neul;Neurol. Now.,2010

4. Early progressive encephalopathy in boys and MECP2 mutations;Kankirawatana;Neurology,2006

5. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

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1. Mitochondrial dysfunction and increased reactive oxygen species production in MECP2 mutant astrocytes and their impact on neurons;Scientific Reports;2024-09-04

2. Progress towards understanding risk factor mechanisms in the development of autism spectrum disorders;BIOCHEM SOC T;2024

3. Differential dynamics specify MeCP2 function at nucleosomes and methylated DNA;Nature Structural & Molecular Biology;2024-08-20

4. A multi-model approach defines function altering MECP2 missense variants identified in individuals with autism spectrum disorder;2024-08-13

5. Altered activity of mPFC pyramidal neurons and parvalbumin-expressing interneurons during social interactions in aMecp2mouse model for Rett syndrome;2024-08-06

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