ELUCIDATION OF THE BIOCHEMICAL DEFECTS IN HUMAN DISEASES ASSOCIATED WITH MISSENSE POINT MUTATIONS OF MITOCHONDRIAL DNA: A BASIS OF THERAPEUTICAL STRATEGIES

Scientific Publications

• 1999 MOLECULAR & GENERAL GENETICS

  The Drosophila melanogaster gene for the NADH : ubiquinone oxidoreductase acyl carrier protein: developmental expression analysis and evidence for alternatively spliced forms

• 1997 NEUROLOGY

  Leber's hereditary optic neuropathy: Biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype

• 1997 MOLECULAR ASPECTS OF MEDICINE

  Changes in mitochondrial complex I activity and coenzyme Q binding site in Leber's hereditary optic neuropathy (LHON)

• 1996 BIOCHEMICAL JOURNAL

  The specificity of mitochondrial complex I for ubiquinones

• 1996 ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS

  The interaction of Q analogs, particularly hydroxydecyl benzoquinone (idebenone), with the respiratory complexes of heart mitochondria