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Neuronal dystonin isoform 2 is a mediator of endoplasmic reticulum structure and function

Dystonin/Bpag1 is a cytoskeletal linker protein whose loss of function in dystonia musculorum (dt) mice results in hereditary sensory neuropathy. Although loss of expression of neuronal dystonin isoforms (dystonin-a1/dystonin-a2) is sufficient to cause dt pathogenesis, the diverging function of each...

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Detalhes bibliográficos
Main Authors: Ryan, Scott D., Ferrier, Andrew, Sato, Tadasu, O'Meara, Ryan W., De Repentigny, Yves, Jiang, Susan X., Hou, Sheng T., Kothary, Rashmi
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society for Cell Biology 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3279385/
https://ncbi.nlm.nih.gov/pubmed/22190742
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E11-06-0573
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