MITOCHONDRIAL-DNA MUTATIONS ASSOCIATED WITH AGE

Linnane A.W., Marzuki S., Ozawa T., Tanaka M., Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases, Lancet, 1, pp. 642-645, (1989)

Ozawa T., Yoneda M., Tanaka M., Ohno K., Sato W., Suzuki H., Nishikimi M., Yamamoto M., Nonaka I., Horai S., Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy, Biochem. Biophys. Res. Commun., 154, pp. 1240-1247, (1988)

Trounce I., Byrne E., Marzuki S., Decline in skeletal muscle mitochondrial respiratory chain function: Possible factor in ageing, Lancet, 2, pp. 637-639, (1989)

Grivell L.A., Mitochondrial DNA: Small, beautiful and essential, Nature, 341, pp. 569-571, (1989)

Sato W., Tanaka M., Ohno K., Yamamoto T., Takada G., Ozawa T., Multiple populations of deleted mitochondrial DNA detected by a novel gene amplification method, Biochem. Biophys. Res. Commun., 162, pp. 664-672, (1989)

Ino H., Tanaka M., Ohno K., Hattori K., Ikebe S., Ozawa T., Ichiki T., Kobayashi M., Wada Y., Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyophathy, Lancet, 337, pp. 234-235, (1991)

Wallace D.C., Singh G., Lott M.T., Hodge J.A., Schurr T.G., Lezza A., Eisas L.J., Nikoskelainen E.K., Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy, Science, 242, pp. 1427-1430, (1988)

Wallace D.C., Zheng X., Lott M.T., Shoffner J.M., Hodge J.A., Kelley R.I., Epstein C.M., Hopkins L.C., Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease, Cell, 66, pp. 601-610, (1988)

Yoneda M., Tsuji S., Yamauchi T., Inuzuka T., Miyatake T., Horai S., Ozawa T., Mitochondrial DNA mutation in family with Leber’s hereditary optic neuropathy, Lancet, 1, pp. 1076-1077, (1989)

Yoneda M., Tanno S., Horai S., Ozawa T., Miyatake T., Tsuji S., A common mitochondrial DNA mutation in the t-RNA^Lys of patients with myoclonus epilepsy associated with ragged-red fibers, Biochem. Int., 27, pp. 789-796, (1990)

Linnane A.W., Marzuki S., Ozawa T., Tanaka M., Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases, Lancet, 1, pp. 642-645, (1989)

Ozawa T., Yoneda M., Tanaka M., Ohno K., Sato W., Suzuki H., Nishikimi M., Yamamoto M., Nonaka I., Horai S., Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy, Biochem. Biophys. Res. Commun., 154, pp. 1240-1247, (1988)

Trounce I., Byrne E., Marzuki S., Decline in skeletal muscle mitochondrial respiratory chain function: Possible factor in ageing, Lancet, 2, pp. 637-639, (1989)

Grivell L.A., Mitochondrial DNA: Small, beautiful and essential, Nature, 341, pp. 569-571, (1989)

Sato W., Tanaka M., Ohno K., Yamamoto T., Takada G., Ozawa T., Multiple populations of deleted mitochondrial DNA detected by a novel gene amplification method, Biochem. Biophys. Res. Commun., 162, pp. 664-672, (1989)

Ino H., Tanaka M., Ohno K., Hattori K., Ikebe S., Ozawa T., Ichiki T., Kobayashi M., Wada Y., Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyophathy, Lancet, 337, pp. 234-235, (1991)

Wallace D.C., Singh G., Lott M.T., Hodge J.A., Schurr T.G., Lezza A., Eisas L.J., Nikoskelainen E.K., Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy, Science, 242, pp. 1427-1430, (1988)

Wallace D.C., Zheng X., Lott M.T., Shoffner J.M., Hodge J.A., Kelley R.I., Epstein C.M., Hopkins L.C., Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease, Cell, 66, pp. 601-610, (1988)

Yoneda M., Tsuji S., Yamauchi T., Inuzuka T., Miyatake T., Horai S., Ozawa T., Mitochondrial DNA mutation in family with Leber’s hereditary optic neuropathy, Lancet, 1, pp. 1076-1077, (1989)

Yoneda M., Tanno S., Horai S., Ozawa T., Miyatake T., Tsuji S., A common mitochondrial DNA mutation in the t-RNA^Lys of patients with myoclonus epilepsy associated with ragged-red fibers, Biochem. Int., 27, pp. 789-796, (1990)