Reversal of a mitochondrial DNA defect in human skeletal muscle
- 1 July 1997
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 16 (3), 222-224
- https://doi.org/10.1038/ng0797-222
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acidsNature Genetics, 1997
- A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapyHuman Molecular Genetics, 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
- MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.Proceedings of the National Academy of Sciences, 1992
- Extraocular Muscle Regeneration in PrimatesOphthalmology, 1992
- Diseases of the Mitochondrial DNAAnnual Review of Biochemistry, 1992
- Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by ComplementationScience, 1989
- Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndromeBiochemical and Biophysical Research Communications, 1989
- On auxotrophy for pyrimidines of respiration‐deficient chick embryo cellsEuropean Journal of Biochemistry, 1984
- Sequence and organization of the human mitochondrial genomeNature, 1981