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The Journal of Clinical Investigation|February 17, 2000
RXRalpha overexpression in cardiomyocytes causes dilated cardiomyopathy but fails to rescue myocardial hypoplasia in RXRalpha-null fetusesV Subbarayan, M Mark, N Messadeq, et al.Biochimica Et Biophysica Acta|August 22, 1997
Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in humanP Rustin, T Bourgeron, B Parfait, et al.Human Genetics|April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndromeB Parfait, D Chretien, A Rötig, et al.Acta Chirurgica Belgica|July 1, 1975
[Preliminary results of immuno-surgical treatment of primary melanoma (author's transl)]R Vanwicjk, P Rustin, S Malek-Mansour, et al.Neuromuscular Disorders : NMD|September 1, 1993
Expression of respiratory chain deficiencies in human cultured cellsT Bourgeron, D Chretien, P Amati, et al.Mechanisms of Ageing and Development|May 10, 2000
For debate: defective mitochondria, free radicals, cell death, aging-reality or myth-ochondria?P Rustin, J C von Kleist-Retzow, Z Vajo, et al.The American Journal of Physiology|July 1, 1994
Mitochondrial biogenesis and development of respiratory chain enzymes in kidney cells: role of glucocorticoidsF Djouadi, J Bastin, T Gilbert, et al.Journal of the Neurological Sciences|July 1, 1992
Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibresA Oldfors, N G Larsson, E Holme, et al.American Journal of Human Genetics|March 1, 1993
Multiple symmetric lipomas with high levels of mtDNA with the tRNA(Lys) A-->G(8344) mutation as the only manifestation of disease in a carrier of myoclonus epilepsy and ragged-red fibers (MERRF) syndromeE Holme, N G Larsson, A Oldfors, et al.Muscle & Nerve. Supplement|January 1, 1995
OXPHOS defects and mitochondrial DNA mutations in cardiomyopathyM Zeviani, C Mariotti, C Antozzi, et al.Pageof 18