The Pathophysiology of Mitochondrial Biogenesis: Towards Four Decades of Mitochondrial DNA Research
- 30 November 2000
- journal article
- review article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 71 (3) , 481-495
- https://doi.org/10.1006/mgme.2000.3083
Abstract
No abstract availableKeywords
This publication has 100 references indexed in Scilit:
- Overexpression of the catalytic subunit of DNA polymerase γ results in depletion of mitochondrial DNA in Drosophila melanogasterMolecular Genetics and Genomics, 2000
- A Drosophila model of Parkinson's diseaseNature, 2000
- Vertebrate Mitochondrial DNA—A Circle of SurprisesExperimental Cell Research, 2000
- Mitochondrial disordersMolecular Human Reproduction, 1997
- Neurological presentations of mitochondrial diseasesJournal of Inherited Metabolic Disease, 1996
- Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathyHuman Molecular Genetics, 1994
- Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletionNature Genetics, 1992
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Fibrous structures within the matrix of developing chick embryo mitochondriaExperimental Cell Research, 1962