Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle von Melov, S., Shoffner, J. M., Kaufman, A., Wallace, D. C.

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Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain von Mecocci, Patrizia, MacGarvey, Usha, Kaufman, Allan E., Koontz, Deborah, Shoffner, John M., Wallace, Douglas C., Beal, M. Flint

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Maternal inheritance and the evaluation of oxidative phosphorylation diseases von Shoffner, John M

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Tau Pathology in a Family with Dementia and a P301L Mutation in Tau von Mirra, Suzanne S, Murrell, Jill R, Gearing, Marla, Spillantini, Maria G, Goedert, Michel, Crowther, R Anthony, Levey, Allan I, Jones, Randi, Green, Joanne, Shoffner, John M, Wainer, Bruce H, Schmidt, Marie L, Trojanowski, John Q, Ghetti, Bernardino

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Mitochondrial DNA Variants Observed in Alzheimer Disease and Parkinson Disease Patients von Shoffner, John M., Brown, Michael D., Torroni, Antonio, Lott, Marie T., Cabell, Margaret F., Mirra, Suzanne S., Beal, M.Flint, Yang, Chi-Chuan, Gearing, Marla, Salvo, Rino, Watts, Ray L., Juncos, Jorge L., Hansen, Lawrence A., Crain, Barbara J., Fayad, Michel, Reckord, Calvin L., Wallace, Douglas C.

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Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients von HORTON, T. M, GRAHAM, B. H, CORRAL-DEBRINSKI, M, SHOFFNER, J. M, KAUFMAN, A. E, BEAL, M. F, WALLACE, D. C

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Mitochondrial oxidative phosphorylation defects in parkinson's disease von Shoffner, John M., Watts, Ray L., Juncos, Jorge L., Torroni, Antonio, Wallace, Douglas C.

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Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation von Shoffner, John M., Brown, Michael D., Stugard, Carol, June, Albert S., Pollock, Stephen, Haas, Richard H., Kaufman, Allan, Koontz, Deborah, Kim, Yoon, Graham, Jennifer R., Smith, Edwin, Dixon, John, Wallace, Douglas C.

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Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age von Corral-Debrinski, Marisol, Horton, Terzah, Lott, Marie T, Shoffner, John M, Flint Beal, M, Wallace, Douglas C

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Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease von Corral-Debrinski, M., Shoffner, J.M., Lott, M.T., Wallace, D.C.

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Oxidative phosphorylation defect associated with primary adrenal insufficiency von North, Kathryn, Korson, Mark S., Krawiecki, Nicolas, Shoffner, John M., Holm, Ingrid A.

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An Introduction: Oxidative Phosphorylation Diseases von Shoffner, John M.

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Insulin resistance associated with maternally inherited diabetes and deafness von Gebhart, Suzanne S.P., Shoffner, John M., Koontz, Deborah, Kaufman, Allan, Wallace, Douglas

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Mitochondrial DNA mutations in human degenerative diseases and aging von Wallace, Douglas C., Shoffner, John M., Trounce, Ian, Brown, Michael D., Ballinger, Scott W., Corral-Debrinski, Marisol, Horton, Terzah, Jun, Albert S., Lott, Marie T.

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Oxidative phosphorylation defects and Alzheimer's disease von Shoffner, J M

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Genetic Mapping of Human Heart-Skeletal Muscle Adenine Nucleotide Translocator and Its Relationship to the Facioscapulohumeral Muscular Dystrophy Locus von Haraguchi, Y., Chung, A.B., Torroni, A., Stepien, G., Shoffner, J.M., Wasmuth, J.J., Costigan, D.A., Polak, M., Altherr, M.R., Winokur, S.T., Wallace, D.C.

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Diseases resulting from mitochondrial DNA point mutations von Wallace, D. C., Lott, M. T., Shoffner, J. M., Brown, M. D.

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Mitochondrial oxidative phosphorylation defects in Parkinson's disease von Wallace, D. C., Shoffner, J. M., Watts, R. L., Juncos, J. L., Torroni, Antonio

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Molecular Analysis of Oxidative Phosphorylation Diseases for Detection of Mitochondrial DNA Mutations von Shoffner, John M.

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Mitochondrial defects in basal ganglia diseases von Shoffner, John M.

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