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Trends in Molecular Medicine|December 6, 2001
Animal models for respiratory chain diseaseN G Larsson, P RustinProceedings of the National Academy of Sciences of the United States of America|March 22, 2001
Increased in vivo apoptosis in cells lacking mitochondrial DNA gene expressionJ Wang, J P Silva, C M Gustafsson, et al.Proceedings of the National Academy of Sciences of the United States of America|March 29, 2000
Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathyH Li, J Wang, H Wilhelmsson, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2001
Late-onset corticohippocampal neurodepletion attributable to catastrophic failure of oxidative phosphorylation in MILON miceL Sörensen, M Ekstrand, J P Silva, et al.Nature Genetics|March 21, 1998
Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in miceN G Larsson, J Wang, H Wilhelmsson, et al.Journal of Inherited Metabolic Disease|August 2, 2003
Mitochondrial oxidative phosphorylation: pitfalls and tips in measuring and interpreting enzyme activitiesD Chretien, P RustinPlant Physiology|August 1, 1986
Malate Metabolism in Leaf Mitochondria from the Crassulacean Acid Metabolism Plant Kalanchoë blossfeldiana PoellnP Rustin, C LanceThe Biochemical Journal|February 15, 1991
Succinate-driven reverse electron transport in the respiratory chain of plant mitochondria. The effects of rotenone and adenylates in relation to malate and oxaloacetate metabolismP Rustin, C LanceArchives of Biochemistry and Biophysics|May 15, 1986
The control of malate dehydrogenase activity by adenine nucleotides in purified potato tuber (Solanum tuberosum L.) mitochondriaP Rustin, M ValatAmerican Journal of Medical Genetics|October 2, 2001
Clinical spectrum and diagnosis of mitochondrial disordersA Munnich, P RustinPageof 18