Molecular and Synaptic Bases of CDKL5 Disorder-Reference-Cited by-同舟云学术

Molecular and Synaptic Bases of CDKL5 Disorder

Published:2018-10-19 Issue:1 Volume:79 Page:8-19
ISSN:1932-8451
Container-title:Developmental Neurobiology
language:en
Short-container-title:Develop Neurobiol

Author:

Zhu Yong-Chuan¹^ORCID,Xiong Zhi-Qi¹

Affiliation:

1. Institute of Neuroscience and State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences; Chinese Academy of Sciences; Shanghai China

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Developmental Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/dneu.22639/fullpdf

Reference78 articles.

1. Mapping pathological phenotypes in a mouse model of CDKL5 disorder;Amendola;PLoS One,2014

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

3. The role of the striatum in social behavior;Báez-Mendoza;Frontiers in Neuroscience,2013

4. Recurrent mutations in the CDKL5 gene: genotype-phenotype relationships;Bahi-Buisson;American Journal of Medical Genetics Part A,2012

5. Developments in neuronal cell culture;Banker;Nature,1988

Cited by 61 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. CDKL5 regulates p62-mediated selective autophagy and confers protection against neurotropic viruses;Journal of Clinical Investigation;2024-01-02

2. Rett and Rett-related disorders: Common mechanisms for shared symptoms?;Experimental Biology and Medicine;2023-12-06

3. Long‐term treatment with ganaxolone for seizures associated with cyclin‐dependent kinase‐like 5 deficiency disorder: Two‐year open‐label extension follow‐up;Epilepsia;2023-11-29

4. Clinical and functional study of two de novo variations of CDKL5 gene;neurogenetics;2023-08-16

5. Discovery and characterization of a specific inhibitor of serine-threonine kinase cyclin-dependent kinase-like 5 (CDKL5) demonstrates role in hippocampal CA1 physiology;eLife;2023-07-25