Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: A new approach to the study of mitochondrial myopathies
Open Access
- 30 September 1991
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 105 (1), 88-92
- https://doi.org/10.1016/0022-510x(91)90123-o
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial diseaseCell, 1990
- Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: Neuropathology, biochemistry, and molecular geneticsAnnals of Neurology, 1989
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA diseaseCell, 1988
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Application of nile blue and nile red, two fluorescent probes, for detection of lipid droplets in human skeletal muscle.Journal of Histochemistry & Cytochemistry, 1987
- Mitochondrial myopathiesJournal of Inherited Metabolic Disease, 1987
- Invited review: Neural control of phenotypic expression in mammalian muscle fibersMuscle & Nerve, 1985
- Mitochondrial myopathiesAnnals of Neurology, 1985
- Sequence and organization of the human mitochondrial genomeNature, 1981