Reversal of a mitochondrial DNA defect in human skeletal muscle

This publication has 13 references indexed in Scilit:

• Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids
  Nature 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 therapy
  Human Molecular Genetics, 1996
• Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy
  Human 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 Primates
  Ophthalmology, 1992
• Diseases of the Mitochondrial DNA
  Annual Review of Biochemistry, 1992
• Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by Complementation
  Science, 1989
• Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome
  Biochemical and Biophysical Research Communications, 1989
• On auxotrophy for pyrimidines of respiration‐deficient chick embryo cells
  European Journal of Biochemistry, 1984
• Sequence and organization of the human mitochondrial genome
  Nature, 1981