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Misfolding, altered membrane distributions, and the unfolded protein response contribute to pathogenicity differences in Na,K-ATPase ATP1A3 mutations

Missense mutations in ATP1A3, the α3 isoform of Na,K-ATPase, cause neurological phenotypes that differ greatly in symptoms and severity. A mechanistic basis for differences is lacking, but reduction of activity alone cannot explain them. Isogenic cell lines with endogenous α1 and inducible exogenous...

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Detalhes bibliográficos
Publicado no:J Biol Chem
Main Authors: Arystarkhova, Elena, Ozelius, Laurie J., Brashear, Allison, Sweadner, Kathleen J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7949067/
https://ncbi.nlm.nih.gov/pubmed/33144327
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA120.015271
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