Reduction of TMEM97 increases NPC1 protein levels and restores cholesterol trafficking in Niemann-pick type C1 disease cells

Niemann-Pick type C disease (NP-C) is a progressive lysosomal lipid storage disease caused by mutations in the NPC1 and NPC2 genes. NPC1 is essential for transporting cholesterol and other lipids out of lysosomes, but little is known about the mechanisms that control its cellular abundance and local...

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Detalles Bibliográficos
Autores principales: Ebrahimi-Fakhari, Darius, Wahlster, Lara, Bartz, Fabian, Werenbeck-Ueding, Jennifer, Praggastis, Maria, Zhang, Jessie, Joggerst-Thomalla, Brigitte, Theiss, Susanne, Grimm, Dirk, Ory, Daniel S., Runz, Heiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179952/
https://www.ncbi.nlm.nih.gov/pubmed/27378690
http://dx.doi.org/10.1093/hmg/ddw204

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179952/
https://www.ncbi.nlm.nih.gov/pubmed/27378690
http://dx.doi.org/10.1093/hmg/ddw204

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