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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Bibliografski detalji
Glavni autori: Wang, Xuelin, Zhang, Wei, Cheever, Thomas, Schwarz, Valentin, Opperman, Karla, Hutter, Harald, Koepp, Deanna, Chen, Lihsia
Format: Artigo
Jezik:Inglês
Izdano: The Rockefeller University Press 2008
Teme:
Research Articles
Online pristup: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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