[44]Detection and analysis of mitochondrial DNA and RNA in muscle by in situ hybridization and single-fiber PCR
- 1 January 1996
- book chapter
- Published by Elsevier
- Vol. 264, 522-540
- https://doi.org/10.1016/s0076-6879(96)64046-4
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- 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
- Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?Journal of Clinical Investigation, 1993
- A mitochondrial tRNA anticodon swap associated with a muscle diseaseNature Genetics, 1993
- Molecular analysis of the muscle pathology associated with mitochondrial DNA deletionsNature Genetics, 1992
- Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibresJournal of the Neurological Sciences, 1992
- Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.Molecular and Cellular Biology, 1992
- Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1991
- Analysis of DNA sequence variation in single cellsMethods, 1991
- Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial diseaseCell, 1990
- NONDROPLET ULTRASTRUCTURAL DEMONSTRATION OF CYTOCHROME OXIDASE ACTIVITY WITH A POLYMERIZING OSMIOPHILIC REAGENT, DIAMINOBENZIDINE (DAB)The Journal of cell biology, 1968