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Science 5 March 1999:
Vol. 283. no. 5407, pp. 1482 - 1488
DOI: 10.1126/science.283.5407.1482

Review

Mitochondrial Diseases in Man and Mouse

Douglas C. Wallace

Over the past 10 years, mitochondrial defects have been implicated in a wide variety of degenerative diseases, aging, and cancer. Studies on patients with these diseases have revealed much about the complexities of mitochondrial genetics, which involves an interplay between mutations in the mitochondrial and nuclear genomes. However, the pathophysiology of mitochondrial diseases has remained perplexing. The essential role of mitochondrial oxidative phosphorylation in cellular energy production, the generation of reactive oxygen species, and the initiation of apoptosis has suggested a number of novel mechanisms for mitochondrial pathology. The importance and interrelationship of these functions are now being studied in mouse models of mitochondrial disease.

The author is at the Center for Molecular Medicine, Emory University, 1462 Clifton Road, Suite 420, Atlanta, GA 30322, USA. E-mail: dwallace{at}gmm.gen.emory.edu


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   Abstract »    Full Text »    PDF »
Brain and brawn: Parallels in oxidative strength.
P. I. Moreira, K. Honda, X. Zhu, A. Nunomura, G. Casadesus, M. A. Smith, and G. Perry (2006)
Neurology 66, S97-S101
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Mitochondrial DNA Content Increase in Response to Cigarette Smoking.
B. G. Masayesva, E. Mambo, R. J. Taylor, O. G. Goloubeva, S. Zhou, Y. Cohen, K. Minhas, W. Koch, J. Sciubba, A. J. Alberg, et al. (2006)
Cancer Epidemiol. Biomarkers Prev. 15, 19-24
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