Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome-Reference-Cited by-同舟云学术

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Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome

Published:2019-08-14 Issue: Volume:13 Page:
ISSN:1662-5102
Container-title:Frontiers in Cellular Neuroscience
language:
Short-container-title:Front. Cell. Neurosci.

Author:

Keidar Liraz,Gerlitz Gabi,Kshirsagar Aditya,Tsoory Michael,Olender Tsviya,Wang Xing,Yang Ying,Chen Yu-Sheng,Yang Yun-Gui,Voineagu Irina,Reiner Orly

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience

Reference110 articles.

1. NUDF, a fungal homolog of the human LIS1 protein, functions as a dimer in vivo.;Ahn;J. Biol. Chem.,2001

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

3. HTSeq–a Python framework to work with high-throughput sequencing data.;Anders;Bioinformatics,2015

4. An ensemble of regulatory elements controls Runx3 spatiotemporal expression in subsets of dorsal root ganglia proprioceptive neurons.;Appel;Genes Dev.,2016

5. Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA.;Ballestar;Biochemistry.,2000

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