Mitochondrial fusion and function in Charcot–Marie–Tooth type 2A patient fibroblasts with mitofusin 2 mutations
- 26 January 2008
- journal article
- Published by Elsevier in Experimental Neurology
- Vol. 211 (1) , 115-127
- https://doi.org/10.1016/j.expneurol.2008.01.010
Abstract
No abstract availableKeywords
This publication has 52 references indexed in Scilit:
- Inherited Mitochondrial Diseases of DNA ReplicationAnnual Review of Medicine, 2008
- A Conserved Role for Phosphatidylinositol 3-Kinase but Not Akt Signaling in Mitochondrial Adaptations that Accompany Physiological Cardiac HypertrophyCell Metabolism, 2007
- Mitochondrial Dynamics in DiseaseNew England Journal of Medicine, 2007
- Human Misato regulates mitochondrial distribution and morphologyExperimental Cell Research, 2007
- Complementation between mouse Mfn1 and Mfn2 protects mitochondrial fusion defects caused by CMT2A disease mutationsThe Journal of cell biology, 2007
- Disruption of Fusion Results in Mitochondrial Heterogeneity and DysfunctionJournal of Biological Chemistry, 2005
- Mitochondrial GTPase mitofusin 2 mutation in Charcot?Marie?Tooth neuropathy type 2AHuman Genetics, 2004
- Marked aging‐related decline in efficiency of oxidative phosphorylation in human skin fibroblastsThe FASEB Journal, 2003
- Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophyNature Genetics, 2000
- Coamplification of Nuclear Pseudogenes and Assessment of Heteroplasmy of Mitochondrial DNA MutationsBiochemical and Biophysical Research Communications, 1998