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Susan E Browne

Showing results (1-10 of 26) with videos related to

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Journal of Neurochemistry|June 19, 2013
When too much ATP is a bad thing: a pivotal role for P2X7 receptors in motor neuron degenerationSusan E Browne
Annals of the New York Academy of Sciences|December 17, 2008
Mitochondria and Huntington's disease pathogenesis: insight from genetic and chemical modelsSusan E Browne
Neurochemical Research|March 25, 2004
The energetics of Huntington's diseaseSusan E Browne, M Flint Beal
Antioxidants & Redox Signaling|October 13, 2006
Oxidative damage in Huntington's disease pathogenesisSusan E Browne, M Flint Beal
International Review of Neurobiology|January 7, 2003
Toxin-induced mitochondrial dysfunctionSusan E Browne, M Flint Beal
Neurobiology of Disease|April 18, 2006
Bioenergetic abnormalities in discrete cerebral motor pathways presage spinal cord pathology in the G93A SOD1 mouse model of ALSSusan E Browne, Lichuan Yang, Jon-Paul DiMauro, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 10, 2004
Mitochondrial alpha-ketoglutarate dehydrogenase complex generates reactive oxygen speciesAnatoly A Starkov, Gary Fiskum, Christos Chinopoulos, et al.
Journal of Neurochemistry|March 19, 2003
Iron porphyrin treatment extends survival in a transgenic animal model of amyotrophic lateral sclerosisAnnie S Wu, Mahmoud Kiaei, Norberto Aguirre, et al.
Neuromolecular Medicine|June 23, 2005
Neuroprotective effects of oral administration of triacetyluridine against MPTP neurotoxicityPeter Klivenyi, Gabrielle Gardian, Noel Y Calingasan, et al.
Free Radical Biology & Medicine|March 17, 2004
Treatment with a catalytic antioxidant corrects the neurobehavioral defect in ataxia-telangiectasia miceSusan E Browne, L Jackson Roberts, Phyllis A Dennery, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Journal of Neurochemistry|June 19, 2013
When too much ATP is a bad thing: a pivotal role for P2X7 receptors in motor neuron degenerationSusan E Browne
Annals of the New York Academy of Sciences|December 17, 2008
Mitochondria and Huntington's disease pathogenesis: insight from genetic and chemical modelsSusan E Browne
Neurochemical Research|March 25, 2004
The energetics of Huntington's diseaseSusan E Browne, M Flint Beal
Antioxidants & Redox Signaling|October 13, 2006
Oxidative damage in Huntington's disease pathogenesisSusan E Browne, M Flint Beal
International Review of Neurobiology|January 7, 2003
Toxin-induced mitochondrial dysfunctionSusan E Browne, M Flint Beal
Neurobiology of Disease|April 18, 2006
Bioenergetic abnormalities in discrete cerebral motor pathways presage spinal cord pathology in the G93A SOD1 mouse model of ALSSusan E Browne, Lichuan Yang, Jon-Paul DiMauro, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 10, 2004
Mitochondrial alpha-ketoglutarate dehydrogenase complex generates reactive oxygen speciesAnatoly A Starkov, Gary Fiskum, Christos Chinopoulos, et al.
Journal of Neurochemistry|March 19, 2003
Iron porphyrin treatment extends survival in a transgenic animal model of amyotrophic lateral sclerosisAnnie S Wu, Mahmoud Kiaei, Norberto Aguirre, et al.
Neuromolecular Medicine|June 23, 2005
Neuroprotective effects of oral administration of triacetyluridine against MPTP neurotoxicityPeter Klivenyi, Gabrielle Gardian, Noel Y Calingasan, et al.
Free Radical Biology & Medicine|March 17, 2004
Treatment with a catalytic antioxidant corrects the neurobehavioral defect in ataxia-telangiectasia miceSusan E Browne, L Jackson Roberts, Phyllis A Dennery, et al.
Pageof 3