Mitochondrial DNA mutation and the ageing process: bioenergy and pharmacological intervention
Tài liệu tham khảo
Abu-Erreish, 1978, Age-related changes in cytochrome concentration of myocardial mitochondria, Mech. Ageing Dev., 7, 425, 10.1016/0047-6374(78)90083-0
Anderson, 1981, Sequence and organization of the human mitochondrial genome, Nature, 290, 457, 10.1038/290457a0
Attardi, 1988, Biogenesis of mitochondria, Annu. Rev. Cell Biol., 4, 289, 10.1146/annurev.cb.04.110188.001445
Bandy, 1990, Mitochondrial mutations may increase oxidative stress: implications for carcinogenesis and aging?, Free Radical Biol. Med., 8, 523, 10.1016/0891-5849(90)90152-9
Bolhuis, 1990, Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy, Biochem. Biophys. Res. Commun., 170, 994, 10.1016/0006-291X(90)90490-E
Cardellach, 1989, Decline in skeletal muscle mitochondrial respiratory chain function with ageing, Lancet, i, 637
Chase, 1972, Biogenesis of mitochondria during Xenopus laevis development, Dev. Biol., 27, 504, 10.1016/0012-1606(72)90189-3
Conover, 1962, DT diaphorase. II. Relation to respiratory chain of intact mitochondria, Biochim. Biophys. Acta, 58, 189, 10.1016/0006-3002(62)90998-8
Cortopassi, 1990, Detection of a specific mitochondrial DNA deletion in tissues of older humans, Nucleic Acids Res., 18, 6927, 10.1093/nar/18.23.6927
Crane, 1985, Transplasma-membrane redox systems in growth and development, Biochim. Biophys. Acta, 811, 233, 10.1016/0304-4173(85)90013-8
Dawid, 1972, Maternal and cytoplasmic inheritance of mitochondrial DNA in Xenopus, Dev. Biol., 29, 152, 10.1016/0012-1606(72)90052-8
Degoul, 1991, Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies, Nucleic Acids Res., 19, 493, 10.1093/nar/19.3.493
Desjardins, 1985, Ethidium bromide-induced loss of mitochondrial DNA from primary chicken embryo fibroblasts, Mol. Cell. Biol., 5, 1163, 10.1128/MCB.5.5.1163
Eleff, 1984, 31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle, 81, 3529
Finch, 1972, Enzyme activities, gene function and ageing in mammals (review), Exp. Geront., 7, 53, 10.1016/0531-5565(72)90035-6
Harding, 1991, Neurological disease and mitochondrial genes, Trends Neurosci., 14, 132, 10.1016/0166-2236(91)90081-5
Harman, 1983, Free radical theory of aging: Consequences of mitochondrial aging, Age, 6, 86, 10.1007/BF02432509
Harman, 1991, The aging process: Major risk factor for disease and death, 88, 5360
Hattori, 1991, Age-dependent increase in deleted mitochondrial DNA in human heart: Possible contributory factor to presbycardia, Am. Heart J., 121, 1735, 10.1016/0002-8703(91)90020-I
Hauswirth, 1985, Transmission genetics of mammalian mitochondria: A molecular model and experimental evidence, Vol. II, 49
Hayakawa, 1991, Age-associated accumulation of 8-hydroxydeoxyguanosine in mitochondrial DNA of human diaphragm, Biochem. Biophys. Res. Commun., 179, 1023, 10.1016/0006-291X(91)91921-X
Hayflick, 1985, Theories of biological aging, Exp. Geront., 20, 145, 10.1016/0531-5565(85)90032-4
Ikebe, 1990, Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence, Biochem. Biophys. Res. Commun., 170, 1044, 10.1016/0006-291X(90)90497-B
Jinnai, 1990, A case of mitochondrial myopathy, encephalophaty and lactic acidosis due to cytochrome c oxidase deficiency with neurogenic muscular changes, Eur. Neurol., 30, 56, 10.1159/000116641
King, 1989, Human cells lacking mtDNA: Repopulation with exogenous mitochondria by complementation, Science, 246, 500, 10.1126/science.2814477
Koehler, 1991, Replacement of bovine mitochondrial DNA by a sequence variant within one generation, Genetics, 129, 247, 10.1093/genetics/129.1.247
Kuchino, 1987, Misreading of DNA templates containing 8-hydroxydeoxyguanosine at the modified base and at adjacent residues, Nature, 327, 77, 10.1038/327077a0
Linnace, 1992, Mitochondrial disease and the ageing process: From microbe to man, 119
Linnane, 1989, Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases, Lancet, i, 642, 10.1016/S0140-6736(89)92145-4
Linnane, 1990, Mitochondrial gene mutation: The ageing process and degenerative diseases, Biochem. Int., 22, 1067
Linnane, 1992, Mitochondrial mutations and tje ageing process, 137
Masoro, 1991, Biology of ageing: Facts, thoughts, and experimental approaches, Lab. Invest., 65, 500
Masoro, 1982, Action of food restriction in delaying the aging process, 79, 4239
Miquel, 1991, An integrated theory of aging as the result of mitochondria-DNA mutation in differentiated cells, Arch. Gerontol. Geriatr., 12, 99, 10.1016/0167-4943(91)90022-I
Mita, 1990, Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA, Nucleic Acids Res., 18, 561, 10.1093/nar/18.3.561
Müller-Höcker, 1989, Cytochrome-c-oxidase deficient cardiomyocytes in the human heart - An age-related phenomenon: A histochemical ultracytochemical study, Am. J. Pathol., 134, 1167
Müller-Höcker, 1990, Cytochrome c oxidase deficient fibres in the limb muscle and diaphragm of man without muscular disease: An age-related alteration, J. Neurol. Sci., 100, 14, 10.1016/0022-510X(90)90006-9
Nagley, 1992, Mitochondrial DNA mutation associated with aging and degenerative disease, Ann. NY Acad. Sci., 10.1111/j.1749-6632.1992.tb27440.x
Obermaier-Kusser, 1990, Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR, Biochem. Biophys. Res. Commun., 169, 1007, 10.1016/0006-291X(90)91994-4
Ozawa, 1990, Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy, Biochem. Biophys. Res. Commun., 170, 830, 10.1016/0006-291X(90)92166-W
Pikó, 1988, Studies of sequence heterogeneity of mitochondrial DNA from rat and mouse tissues: Evidence for an increased frequency of deletions/additions with aging, Mech. Ageing Dev., 43, 279, 10.1016/0047-6374(88)90037-1
Sadler, 1990
Sato, 1991
Schon, 1989, A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA, Science, 244, 346, 10.1126/science.2711184
Shoffner, 1990, Oxidative phosphorylation diseases: Disorders of two genomes, Adv. Hum. Genet., 19, 267, 10.1007/978-1-4757-9065-8_5
Shoffner, 1989, Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: A slip-replication model and metabolic therapy, 86, 7952
Sun, 1990, Evidence for coenzyme Q function in transplasma membrane electron transport, Biochem. Biophys. Res. Commun., 172, 979, 10.1016/0006-291X(90)91542-Z
Trounce, 1989, Decline in skeletal muscle mitochondrial respiratory chain function: Possible factor in ageing, Lancet, i, 637, 10.1016/S0140-6736(89)92143-0
Vaillant, 1991, Some biochemical properties of human lymphoblastoid Namalwa cells grown anaerobically, Biochem. Int., 23, 571
Yen, 1991, Ageing-associated 5 kb deletion in human liver mitochondrial DNA, Biochem. Biophys. Res. Commun., 178, 124, 10.1016/0006-291X(91)91788-E
Zhang, 1992, Multiple mitochondrial DNA deletions in an elderly human individual, FEBS Lett., 297, 34, 10.1016/0014-5793(92)80321-7