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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...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Public Library of Science
2013
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3706371/ https://ncbi.nlm.nih.gov/pubmed/23874761 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0068781 |
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