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Journal of Neurochemistry|November 2, 2007
Therapeutic effects of coenzyme Q10 (CoQ10) and reduced CoQ10 in the MPTP model of ParkinsonismCarine Cleren, Lichuan Yang, Beverly Lorenzo, 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.
Neurobiology of Disease|October 12, 2004
A novel systemically active caspase inhibitor attenuates the toxicities of MPTP, malonate, and 3NP in vivoLichuan Yang, Shuei Sugama, Ronald P Mischak, et al.
Biochemical and Biophysical Research Communications|February 1, 2002
Sequence analysis of the entire mitochondrial genome in Parkinson's diseaseCristofol Vives-Bauza, Antoni L Andreu, Giovanni Manfredi, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 18, 1994
Foot-and-mouth disease virus particles contain replicase protein 3DJ F Newman, P G Piatti, B M Gorman, et al.
Journal of Neurochemistry|June 6, 2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic miceAlpaslan Dedeoglu, James K Kubilus, Lichuan Yang, 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.
Neuro-Degenerative Diseases|July 16, 2011
Truncated peroxisome proliferator-activated receptor-γ coactivator 1α splice variant is severely altered in Huntington's diseaseAshu Johri, Anatoly A Starkov, Abhishek Chandra, et al.
Journal of Neurochemistry|May 19, 2004
3-Nitropropionic acid-induced neurotoxicity--assessed by ultra high resolution positron emission tomography with comparison to magnetic resonance spectroscopyAnna-Liisa Brownell, Y Iris Chen, Meixiang Yu, et al.
Experimental Neurology|March 17, 2007
Matrix metalloproteinase-9 regulates TNF-alpha and FasL expression in neuronal, glial cells and its absence extends life in a transgenic mouse model of amyotrophic lateral sclerosisMahmoud Kiaei, Khatuna Kipiani, Noel Y Calingasan, et al.
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