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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...
Autores principales: | Jeong, Sung-Jin, Luo, Rong, Singer, Kathleen, Giera, Stefanie, Kreidberg, Jordan, Kiyozumi, Daiji, Shimono, Chisei, Sekiguchi, Kiyotoshi, Piao, Xianhua |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
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 |
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