The Nesprin Family Member ANC-1 Regulates Synapse Formation and Axon Termination by Functioning in a Pathway with RPM-1 and β-Catenin

Mutations in Nesprin-1 and 2 (also called Syne-1 and 2) are associated with numerous diseases including autism, cerebellar ataxia, cancer, and Emery-Dreifuss muscular dystrophy. Nesprin-1 and 2 have conserved orthologs in flies and worms called MSP-300 and abnormal nuclear Anchorage 1 (ANC-1), respe...

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Detaylı Bibliyografya
Asıl Yazarlar: Tulgren, Erik D., Turgeon, Shane M., Opperman, Karla J., Grill, Brock
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2014
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4091705/
https://ncbi.nlm.nih.gov/pubmed/25010424
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1004481
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