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Ephrin-B1 regulates axon guidance by reverse signaling through a PDZ-dependent mechanism
Mutations in the ephrin-B1 gene result in craniofrontonasal syndrome (CFNS) in humans, a congenital disorder that includes a wide range of craniofacial, skeletal, and neurological malformations. In addition to the ability of ephrin-B1 to forward signal through its cognate EphB tyrosine kinase recept...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2009
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2704468/ https://ncbi.nlm.nih.gov/pubmed/19515977 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gad.1807209 |
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