The genetics and pathology of oxidative phosphorylation

By J. Smeitink, L. Heuvel, S. Dimauro. Nature reviews genetics, 2001

731 citations recorded by the source corpus.

Subfields: Clinical Biochemistry, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/eeb57cadb2c9bb21d8e243983d50fe3814de20b8

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In Molecular Biology

1. M. Juhaszova
2. D. Zorov
3. Steven J. Sollott
4. Michael R Hamblin

Citations in the corpus

• Mitochondrial dysfunction as a cause of optic neuropathies. (2004, background): “Diseases caused by its dysfunction may be due to nDNA defects and thus follow the Mendelian genetic rules; or they may be due to mutations that occur in the mtDNA, which express their pathogenic potential according to the peculiar rules of mitochondrial genetics (Wallace, 1999; Smeitink et al., 2001”
• Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release. (2014, background): “It has been noticed that at least 40% of all mitochondrial disorders are associated with mutations in subunits of complex I (402).”