VPS13A and VPS13C are lipid transport proteins differentially localized at ER contact sites

Mutations in the human VPS13 genes are responsible for neurodevelopmental and neurodegenerative disorders including chorea acanthocytosis (VPS13A) and Parkinson’s disease (VPS13C). The mechanisms of these diseases are unknown. Genetic studies in yeast hinted that Vps13 may have a role in lipid excha...

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Publicado en:J Cell Biol
Main Authors: Kumar, Nikit, Leonzino, Marianna, Hancock-Cerutti, William, Horenkamp, Florian A., Li, PeiQi, Lees, Joshua A., Wheeler, Heather, Reinisch, Karin M., De Camilli, Pietro
Formato: Artigo
Idioma:Inglês
Publicado: Rockefeller University Press 2018
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Research Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6168267/
https://ncbi.nlm.nih.gov/pubmed/30093493
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201807019
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