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Molecular Genetics and Metabolism|April 18, 2000
Screening human EST database for identification of candidate genes in respiratory chain deficiencyA Rötig, I Valnot, C Mugnier, et al.Muscle & Nerve. Supplement|January 1, 1995
Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomasN G Larsson, M H Tulinius, E Holme, et al.Human Molecular Genetics|August 1, 1995
Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndromeA Rötig, T Bourgeron, D Chretien, et al.Biochemical and Biophysical Research Communications|November 30, 1990
The measurement of the rotenone-sensitive NADH cytochrome c reductase activity in mitochondria isolated from minute amount of human skeletal muscleD Chretien, T Bourgeron, A Rötig, et al.Biochemical and Biophysical Research Communications|July 15, 1992
Isolation and characterization of mitochondria from human B lymphoblastoid cell linesT Bourgeron, D Chretien, A Rötig, et al.The Journal of Biological Chemistry|September 15, 1993
Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte culturesT Bourgeron, D Chretien, A Rötig, et al.Molecular and Cellular Biochemistry|October 6, 1997
Nicotinamide adenine dinucleotides permeate through mitochondrial membranes in human Epstein-Barr virus-transformed lymphocytesP Rustin, D Chretien, B Parfait, et al.Pediatric Research|August 1, 1990
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndromeN G Larsson, E Holme, B Kristiansson, et al.Annals of Neurology|November 1, 1991
Leber's hereditary optic neuropathy and complex I deficiency in muscleN G Larsson, O Andersen, E Holme, et al.Plant Physiology|December 1, 1988
Kinetic studies of the form of substrate bound by phosphoenolpyruvate carboxylaseR T Wedding, P Rustin, C R Meyer, et al.Pageof 18