Altered cofactor regulation with disease-associated p97/VCP mutations

Dominant mutations in p97/VCP (valosin-containing protein) cause a rare multisystem degenerative disease with varied phenotypes that include inclusion body myopathy, Paget’s disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis. p97 disease mutants have altered N-domain conform...

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Опубликовано в: :Proc Natl Acad Sci U S A
Главные авторы: Zhang, Xiaoyi, Gui, Lin, Zhang, Xiaoyan, Bulfer, Stacie L., Sanghez, Valentina, Wong, Daniel E., Lee, YouJin, Lehmann, Lynn, Lee, James Siho, Shih, Pei-Yin, Lin, Henry J., Iacovino, Michelina, Weihl, Conrad C., Arkin, Michelle R., Wang, Yanzhuang, Chou, Tsui-Fen
Формат: Artigo
Язык:Inglês
Опубликовано: National Academy of Sciences 2015
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PNAS Plus
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4394316/
https://ncbi.nlm.nih.gov/pubmed/25775548
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1418820112
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