The C. elegans L1CAM homologue LAD-2 functions as a coreceptor in MAB-20/Sema2–mediated axon guidance

The L1 cell adhesion molecule (L1CAM) participates in neuronal development. Mutations in the human L1 gene can cause the neurological disorder CRASH (corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraplegia, and hydrocephalus). This study presents genetic data that shows that L1-...

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Detalles Bibliográficos
Autores principales: Wang, Xuelin, Zhang, Wei, Cheever, Thomas, Schwarz, Valentin, Opperman, Karla, Hutter, Harald, Koepp, Deanna, Chen, Lihsia
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2008
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213605/
https://www.ncbi.nlm.nih.gov/pubmed/18195110
http://dx.doi.org/10.1083/jcb.200704178

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213605/
https://www.ncbi.nlm.nih.gov/pubmed/18195110
http://dx.doi.org/10.1083/jcb.200704178

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