Global Developmental Gene Expression and Pathway Analysis of Normal Brain Development and Mouse Models of Human Neuronal Migration Defects

Heterozygous LIS1 mutations are the most common cause of human lissencephaly, a human neuronal migration defect, and DCX mutations are the most common cause of X-linked lissencephaly. LIS1 is part of a protein complex including NDEL1 and 14-3-3ε that regulates dynein motor function and microtubule d...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Pramparo, Tiziano, Libiger, Ondrej, Jain, Sonia, Li, Hong, Youn, Yong Ha, Hirotsune, Shinji, Schork, Nicholas J., Wynshaw-Boris, Anthony
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2011
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3053345/
https://ncbi.nlm.nih.gov/pubmed/21423666
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1001331
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados