Complex I deficiency in Parkinson's disease frontal cortex von Parker, W. Davis, Parks, Janice K, Swerdlow, Russell H

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Aberrant mitochondrial RNA in the role of aging and aging associated diseases von Chen, Yucai, Parker, W. Davis, Chen, Hongyi, Yang, Kunfang

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Mitochondrial ND5 mutations in idiopathic Parkinson’s disease von Parker, W. Davis, Parks, Janice K.

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Parkinson's disease transgenic mitochondrial cybrids generate Lewy inclusion bodies von Trimmer, Patricia A., Borland, M. Kathleen, Keeney, Paula M., Bennett, James P., Parker, W. Davis

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Origin and functional consequences of the complex I defect in Parkinson's disease von Swerdlow, Russell H., Parks, Janice K., Miller, Scott W., Davis, Robert E., Tuttle, Jeremy B., Trimmer, Patricia A., Sheehan, Jason P., Bennett Jr, James P., Parker Jr, W. Davis

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Mitochondrial abnormalities in cybrid cell models of sporadic Alzheimer's disease worsen with passage in culture von Trimmer, Patricia A., Keeney, Paula M., Borland, M.Kate, Simon, Frederic A., Almeida, Jatanna, Swerdlow, Russell H., Parks, Janice P., Parker, W.Davis, Bennett, James P.

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Effects of memantine on mitochondrial function von McAllister, Jenna, Ghosh, Sangeeta, Berry, Diana, Park, Melissa, Sadeghi, Sina, Wang, Kai Xuan, Parker, W. Davis, Swerdlow, Russell H.

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High frequency of mitochondrial complex I mutations in Parkinson’s disease and aging von Smigrodzki, Rafal, Parks, Janice, Parker, W.Davis

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Genetic algorithm for analysis of mutations in Parkinson's disease von Smigrodzki, Rafal, Goertzel, Ben, Pennachin, Cassio, Coelho, Lucio, Prosdocimi, Francisco, Parker, W. Davis

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Neuroleptic medications inhibit complex I of the electron transport chain von Burkhardt, Carolyn, Kelly, James P., Lim, Young-Hwa, Filley, Christopher M., Parker Jr, W. Davis

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Neurotoxic Aβ peptides increase oxidative stress in vivo through NMDA‐receptor and nitric‐oxide‐synthase mechanisms, and inhibit complex IV activity and induce a mitochondrial perm... von Parks, Janice K., Smith, Trisha S., Trimmer, Patricia A., Bennett, James P., Parker, W. Davis

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Mutations in Mitochondrial Cytochrome c Oxidase Genes Segregate with Late-Onset Alzheimer Disease von Davis, Robert E., Miller, Scott, Herrnstadt, Corinna, Ghosh, Soumitra S., Fahy, Eoin, Shinobu, Leslie A., Galasko, Douglas, Thal, Leon J., Beal, M. Flint, Howell, Neil, Parker, W. Davis

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Reduction of MPP+-induced hydroxyl radical formation and nigrostriatal MPTP toxicity by inhibiting nitric oxide synthase von Smith, Trisha Spencer, Swerdlow, Russell H, Parker, W Davis, Bennett, James P

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Alzheimer's disease cybrids replicate β-amyloid abnormalities through cell death pathways von Khan, Shaharyar M., Cassarino, David S., Abramova, Nicole N., Keeney, Paula M., Borland, M. Kate, Trimmer, Patricia A., Krebs, Clara T., Bennett, Jason C., Parks, Janice K., Swerdlow, Russell H., Parker Jr, W. Davis, Bennett Jr, James P.

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Mitochondrial Dysfunction in Idiopathic Parkinson Disease von Parker, W. Davis, Swerdlow, Russell H.

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Cytochrome C Oxidase in Alzheimer's Disease Brain: Purification and Characterization von Parker, W Davis, Parks, Janice K

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Use of Cytoplasmic Hybrid Cell Lines for Elucidating the Role of Mitochondrial Dysfunction in Alzheimer's Disease and Parkinson's Disease von GHOSH, SOUMITRA S., SWERDLOW, RUSSELL H., MILLER, SCOTT W., SHEEMAN, BRINA, PARKER Jr, W. DAVIS, DAVIS, ROBERT E.

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Abnormal Mitochondrial Morphology in Sporadic Parkinson's and Alzheimer's Disease Cybrid Cell Lines von Trimmer, Patricia A., Swerdlow, Russell H., Parks, Janice K., Keeney, Paula, Bennett, James P., Miller, Scott W., Davis, Robert E., Parker, W.Davis

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Maternal inheritance in Parkinson's disease von Wooten, G. Frederick, Currie, Lillian J., Bennett, James P., Harrison, Madaline B., Trugman, Joel M., Parker Jr, W. Davis

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Mitochondrial abnormalities in non-alcoholic steatohepatitis von Caldwell, Stephen H, Swerdlow, Russell H, Khan, Elaine M, Iezzoni, Julia C, Hespenheide, Elizabeth E, Parks, Janice K, Parker, W.Davis

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