MTO1-Deficient Mouse Model Mirrors the Human Phenotype Showing Complex I Defect and Cardiomyopathy

Author:

Becker Lore,Kling Eva,Schiller Evelyn,Zeh Ramona,Schrewe Anja,Hölter Sabine M.,Mossbrugger Ilona,Calzada-Wack Julia,Strecker Valentina,Wittig Ilka,Dumitru Iulia,Wenz Tina,Bender Andreas,Aichler Michaela,Janik Dirk,Neff Frauke,Walch Axel,Quintanilla-Fend Leticia,Floss Thomas,Bekeredjian Raffi,Gailus-Durner Valérie,Fuchs Helmut,Wurst Wolfgang,Meitinger Thomas,Prokisch Holger,de Angelis Martin Hrabě,Klopstock Thomas

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference41 articles.

1. MitoP2: an integrative tool for the analysis of the mitochondrial proteome;M Elstner;Molecular biotechnology,2008

2. The pathophysiology of mitochondrial disease as modeled in the mouse;DC Wallace;Genes & Development,2009

3. Human NADH:ubiquinone oxidoreductase;J Smeitink;Journal of bioenergetics and biomembranes,2001

4. The genetics and pathology of oxidative phosphorylation;J Smeitink;Nature reviews Genetics,2001

5. Nuclear genes and mitochondrial translation: a new class of genetic disease;HT Jacobs;Trends in genetics: TIG,2005

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