Human Diseases with Defects in Oxidative Phosphorylation

This publication has 34 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 myopathy
  Human Molecular Genetics, 1994
• Mitochondrial cytopathies
  Current Opinion in Neurobiology, 1993
• Lacticacidemia
  Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1993
• The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains
  Quarterly Reviews of Biophysics, 1992
• Subunit IV of human cytochrome c oxidase, polymorphism and a putative isoform
  Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1992
• Identification of the subunits of F1F0-ATPase from bovine heart mitochondria
  Biochemistry, 1991
• Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies
  Biochimica et Biophysica Acta (BBA) - Bioenergetics, 1990
• Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
  New England Journal of Medicine, 1989
• Sequence and organization of the human mitochondrial genome
  Nature, 1981
• Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
  Proceedings of the National Academy of Sciences, 1979