GPR56 Functions Together with α3β1 Integrin in Regulating Cerebral Cortical Development

Loss of function mutations in GPR56, which encodes a G protein-coupled receptor, cause a specific human brain malformation called bilateral frontoparietal polymicrogyria (BFPP). Studies from BFPP postmortem brain tissue and Gpr56 knockout mice have previously showed that GPR56 deletion leads to brea...

Descripción completa

Detalles Bibliográficos
Autores principales: Jeong, Sung-Jin, Luo, Rong, Singer, Kathleen, Giera, Stefanie, Kreidberg, Jordan, Kiyozumi, Daiji, Shimono, Chisei, Sekiguchi, Kiyotoshi, Piao, Xianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706371/
https://www.ncbi.nlm.nih.gov/pubmed/23874761
http://dx.doi.org/10.1371/journal.pone.0068781

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706371/
https://www.ncbi.nlm.nih.gov/pubmed/23874761
http://dx.doi.org/10.1371/journal.pone.0068781

Ejemplares similares