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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 13, 2015
Dysregulation of glutamine transporter SNAT1 in Rett syndrome microglia: a mechanism for mitochondrial dysfunction and neurotoxicityLee-Way Jin, Makoto Horiuchi, Heike Wulff, et al.
Human Molecular Genetics|February 21, 2002
Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cellsAlice Wong, Lucia Cavelier, Heather E Collins-Schramm, et al.
Brain : a Journal of Neurology|February 25, 2005
Isolation of transcriptomal changes attributable to LHON mutations and the cybridization processSteven R Danielson, Valerio Carelli, Guolin Tan, et al.
Mitochondrion|October 27, 2019
Cetylpyridinium chloride is a potent AMP-activated kinase (AMPK) inducer and has therapeutic potential in cancerSonia A Allen, Sandipan Datta, Jose Sandoval, et al.
Human Molecular Genetics|February 6, 2015
Mitochondrial complex I deficiency leads to inflammation and retinal ganglion cell death in the Ndufs4 mouseAlfred K Yu, Lanying Song, Karl D Murray, et al.
The Journal of Biological Chemistry|November 7, 2009
Decreased superoxide production in macrophages of long-lived p66Shc knock-out miceAlexey A Tomilov, Vincent Bicocca, Robert A Schoenfeld, et al.
Human Molecular Genetics|August 13, 2014
Dyclonine rescues frataxin deficiency in animal models and buccal cells of patients with Friedreich's ataxiaSunil Sahdeo, Brian D Scott, Marissa Z McMackin, et al.
Metabolism: Clinical and Experimental|June 12, 2012
Shc proteins influence the activities of enzymes involved in fatty acid oxidation and ketogenesisKevork Hagopian, Alexey A Tomilov, Natalia Tomilova, et al.
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