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

LIS1 is the main causative gene for lissencephaly, while MeCP2 is the main causative gene for Rett syndrome, both of which are neurodevelopmental diseases. Here we report nuclear functions for LIS1 and identify previously unrecognized physical and genetic interactions between the products of these t...

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Detalhes bibliográficos
Publicado no:Front Cell Neurosci
Main Authors: Keidar, Liraz, Gerlitz, Gabi, Kshirsagar, Aditya, Tsoory, Michael, Olender, Tsviya, Wang, Xing, Yang, Ying, Chen, Yu-Sheng, Yang, Yun-Gui, Voineagu, Irina, Reiner, Orly
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019
Assuntos:
Neuroscience
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6703185/
https://ncbi.nlm.nih.gov/pubmed/31474834
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2019.00370
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