A Personalized Model of COQ2 Nephropathy Rescued by the Wild-Type COQ2 Allele or Dietary Coenzyme Q(10) Supplementation

Clinical studies have identified patients with nephrotic syndrome caused by mutations in genes involved in the biosynthesis of coenzyme Q(10) (CoQ(10)), a lipid component of the mitochondrial electron transport chain and an important antioxidant. However, the cellular mechanisms through which these...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Am Soc Nephrol
Autors principals: Zhu, Jun-yi, Fu, Yulong, Richman, Adam, Zhao, Zhanzheng, Ray, Patricio E., Han, Zhe
Format: Artigo
Idioma:Inglês
Publicat: American Society of Nephrology 2017
Matèries:
Basic Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5576924/
https://ncbi.nlm.nih.gov/pubmed/28428331
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2016060626
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars