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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Detalhes bibliográficos
Main Authors: Wang, Xuelin, Zhang, Wei, Cheever, Thomas, Schwarz, Valentin, Opperman, Karla, Hutter, Harald, Koepp, Deanna, Chen, Lihsia
Formato: Artigo
Idioma:Inglês
Publicado em: The Rockefeller University Press 2008
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Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2213605/
https://ncbi.nlm.nih.gov/pubmed/18195110
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.200704178
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