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Molecular Neurodegeneration|April 28, 2011
A mutation in the dynein heavy chain gene compensates for energy deficit of mutant SOD1 mice and increases potentially neuroprotective IGF-1Anissa Fergani, Judith Eschbach, Hugues Oudart, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 23, 2003
Up-regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosisLuc Dupuis, Franck di Scala, Frédérique Rene, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|July 24, 2009
Dietary palmitate and linoleate oxidations, oxidative stress, and DNA damage differ according to season in mouse lemurs exposed to a chronic food deprivationSylvain Giroud, Martine Perret, Caroline Gilbert, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 8, 2012
The nuclear receptor REV-ERBα is required for the daily balance of carbohydrate and lipid metabolismJulien Delezie, Stéphanie Dumont, Hugues Dardente, et al.
Journal of Lipid Research|April 18, 2007
Increased peripheral lipid clearance in an animal model of amyotrophic lateral sclerosisAnissa Fergani, Hugues Oudart, Jose-Luis Gonzalez De Aguilar, et al.
Plos One|May 1, 2009
Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neuronsLuc Dupuis, Jose-Luis Gonzalez de Aguilar, Andoni Echaniz-Laguna, et al.
Biochimica Et Biophysica Acta|October 5, 2010
Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissuesJudith Eschbach, Anissa Fergani, Hugues Oudart, et al.
Cell Metabolism|April 5, 2011
PARP-1 inhibition increases mitochondrial metabolism through SIRT1 activationPéter Bai, Carles Cantó, Hugues Oudart, et al.
Cell Metabolism|April 5, 2011
PARP-2 regulates SIRT1 expression and whole-body energy expenditurePéter Bai, Carles Canto, Attila Brunyánszki, et al.
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