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Disease-associated mutations in human BICD2 hyperactivate motility of dynein–dynactin

Bicaudal D2 (BICD2) joins dynein with dynactin into a ternary complex (termed DDB) capable of processive movement. Point mutations in the BICD2 gene have been identified in patients with a dominant form of spinal muscular atrophy, but how these mutations cause disease is unknown. To investigate this...

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Bibliografski detalji
Izdano u:J Cell Biol
Glavni autori: Huynh, Walter, Vale, Ronald D.
Format: Artigo
Jezik:Inglês
Izdano: The Rockefeller University Press 2017
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5626548/
https://ncbi.nlm.nih.gov/pubmed/28883039
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201703201
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