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Cardiolipin promotes electron transport between ubiquinone and complex I to rescue PINK1 deficiency
PINK1 is mutated in Parkinson’s disease (PD), and mutations cause mitochondrial defects that include inefficient electron transport between complex I and ubiquinone. Neurodegeneration is also connected to changes in lipid homeostasis, but how these are related to PINK1-induced mitochondrial dysfunct...
Autores principales: | Vos, Melissa, Geens, Ann, Böhm, Claudia, Deaulmerie, Liesbeth, Swerts, Jef, Rossi, Matteo, Craessaerts, Katleen, Leites, Elvira P., Seibler, Philip, Rakovic, Aleksandar, Lohnau, Thora, De Strooper, Bart, Fendt, Sarah-Maria, Morais, Vanessa A., Klein, Christine, Verstreken, Patrik |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346965/ https://www.ncbi.nlm.nih.gov/pubmed/28137779 http://dx.doi.org/10.1083/jcb.201511044 |
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