Kodavati M, Wang H, Guo W, Mitra J, Hegde P, Provasek V
Nat Commun. 2024; 15(1):2156.
PMID: 38461154
PMC: 10925063.
DOI: 10.1038/s41467-024-45978-6.
Iakovou E, Kourti M
Front Aging Neurosci. 2022; 14:827900.
PMID: 35769600
PMC: 9234325.
DOI: 10.3389/fnagi.2022.827900.
Napoli E, McLennan Y, Schneider A, Tassone F, Hagerman R, Giulivi C
Front Mol Biosci. 2020; 7:578640.
PMID: 33195422
PMC: 7642626.
DOI: 10.3389/fmolb.2020.578640.
Ziada A, Lu M, Ignas-Menzies J, Paintsil E, Li M, Ogbuagu O
Aging Cell. 2019; 18(6):e13018.
PMID: 31407474
PMC: 6826146.
DOI: 10.1111/acel.13018.
Srivastava S
Genes (Basel). 2017; 8(12).
PMID: 29257072
PMC: 5748716.
DOI: 10.3390/genes8120398.
Mitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderly.
Tranah G, Lam E, Katzman S, Nalls M, Zhao Y, Evans D
Biochim Biophys Acta. 2012; 1817(9):1691-700.
PMID: 22659402
PMC: 3389152.
DOI: 10.1016/j.bbabio.2012.05.012.
A novel mitochondrial tRNA(Val) T1658C mutation identified in a CPEO family.
Yan N, Cai S, Guo B, Mou Y, Zhu J, Chen J
Mol Vis. 2010; 16:1736-42.
PMID: 20806033
PMC: 2927373.
Mitochondrial-nuclear epistasis: implications for human aging and longevity.
Tranah G
Ageing Res Rev. 2010; 10(2):238-52.
PMID: 20601194
PMC: 2995012.
DOI: 10.1016/j.arr.2010.06.003.
Mitochondrial function as a determinant of life span.
Lanza I, Nair K
Pflugers Arch. 2009; 459(2):277-89.
PMID: 19756719
PMC: 2801852.
DOI: 10.1007/s00424-009-0724-5.
Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNA(Val) causing MNGIE-like gastrointestinal dysmotility and cachexia.
Horvath R, Bender A, Abicht A, Holinski-Feder E, Czermin B, Trips T
J Neurol. 2009; 256(5):810-5.
PMID: 19252805
DOI: 10.1007/s00415-009-5023-8.
Human disease-associated mitochondrial mutations fixed in nonhuman primates.
de Magalhaes J
J Mol Evol. 2005; 61(4):491-7.
PMID: 16132471
DOI: 10.1007/s00239-004-0258-6.
The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method.
Murdock D, Christacos N, Wallace D
Nucleic Acids Res. 2000; 28(21):4350-5.
PMID: 11058135
PMC: 113143.
DOI: 10.1093/nar/28.21.4350.
Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells.
Trounce I, Schmiedel J, Yen H, Hosseini S, Brown M, Olson J
Nucleic Acids Res. 2000; 28(10):2164-70.
PMID: 10773087
PMC: 105374.
DOI: 10.1093/nar/28.10.2164.
Mutations in mitochondrial DNA accumulate differentially in three different human tissues during ageing.
Liu V, Zhang C, Nagley P
Nucleic Acids Res. 1998; 26(5):1268-75.
PMID: 9469836
PMC: 147381.
DOI: 10.1093/nar/26.5.1268.
Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes.
Blok R, Gook D, Thorburn D, Dahl H
Am J Hum Genet. 1997; 60(6):1495-501.
PMID: 9199572
PMC: 1716104.
DOI: 10.1086/515453.
Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging.
Pallotti F, Chen X, Bonilla E, Schon E
Am J Hum Genet. 1996; 59(3):591-602.
PMID: 8751860
PMC: 1914925.
Free-radical-induced mutation vs redox regulation: costs and benefits of genes in organelles.
Allen J, Raven J
J Mol Evol. 1996; 42(5):482-92.
PMID: 8662000
DOI: 10.1007/BF02352278.
Oxidative damage and mitochondrial decay in aging.
Shigenaga M, Hagen T, Ames B
Proc Natl Acad Sci U S A. 1994; 91(23):10771-8.
PMID: 7971961
PMC: 45108.
DOI: 10.1073/pnas.91.23.10771.
Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle.
Melov S, Shoffner J, Kaufman A, Wallace D
Nucleic Acids Res. 1995; 23(20):4122-6.
PMID: 7479075
PMC: 307353.
DOI: 10.1093/nar/23.20.4122.