Sex differences in Mecp2-mutant Rett syndrome model mice and the impact of cellular mosaicism in phenotype development-Reference-Cited by-同舟云学术

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Sex differences in Mecp2-mutant Rett syndrome model mice and the impact of cellular mosaicism in phenotype development

Published:2020-02 Issue: Volume:1729 Page:146644
ISSN:0006-8993
Container-title:Brain Research
language:en
Short-container-title:Brain Research

Author:

Ribeiro Mayara C.,MacDonald Jessica L.

Funder

National Institutes of Health

International Rett Syndrome Foundation

Publisher

Elsevier BV

Subject

Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience

Reference120 articles.

1. Effect of sarizotan, a 5-HT1a and D2-like receptor agonist, on respiration in three mouse models of rett syndrome;Abdala;Am. J. Respir. Cell Mol. Biol.,2014

2. Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes;Allemang-Grand;Mol. Autism,2017

3. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes;Amir;Ann. Neurol.,2000

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

5. Cell-genotype specific effects of Mecp2 mutation on spontaneous and nicotinic acetylcholine receptor-evoked currents in medial prefrontal cortical pyramidal neurons in female Rett model mice;Asgarihafshejani;Neuroscience,2019

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