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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:J Cell Biol
Päätekijät: Kumar, Nikit, Leonzino, Marianna, Hancock-Cerutti, William, Horenkamp, Florian A., Li, PeiQi, Lees, Joshua A., Wheeler, Heather, Reinisch, Karin M., De Camilli, Pietro
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Rockefeller University Press 2018
Aiheet:
Research Articles
Linkit: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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