-
1
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJ, Staden R, Young IG (1981) Sequence and organization of the human mitochondrial genome. Nature 290, 457-465.
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
de Bruijn, M.H.4
Coulson, A.R.5
Drouin, J.6
Eperon, I.C.7
Nierlich, D.P.8
Roe, B.A.9
Sanger, F.10
Schreier, P.H.11
Smith, A.J.12
Staden, R.13
Young, I.G.14
-
2
-
-
0032868141
-
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
-
Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N (1999) Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat. Genet. 23, 147.
-
(1999)
Nat. Genet.
, vol.23
, pp. 147
-
-
Andrews, R.M.1
Kubacka, I.2
Chinnery, P.F.3
Lightowlers, R.N.4
Turnbull, D.M.5
Howell, N.6
-
3
-
-
59749092546
-
Exaggerated status of "novel" and "pathogenic" mtDNA sequence variants due to inadequate database searches
-
Bandelt HJ, Salas A, Taylor RW, Yao YG (2008) Exaggerated status of "novel" and "pathogenic" mtDNA sequence variants due to inadequate database searches. Hum. Mutat. 30, 191-196.
-
(2008)
Hum. Mutat.
, vol.30
, pp. 191-196
-
-
Bandelt, H.J.1
Salas, A.2
Taylor, R.W.3
Yao, Y.G.4
-
4
-
-
33646375711
-
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
-
Bender A, Krishnan KJ, Morris CM, Taylor GA, Reeve AK, Perry RH, Jaros E, Hersheson JS, Betts J, Klopstock T, Taylor RW, Turnbull DM (2006) High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease. Nat. Genet. 38, 515-517.
-
(2006)
Nat. Genet.
, vol.38
, pp. 515-517
-
-
Bender, A.1
Krishnan, K.J.2
Morris, C.M.3
Taylor, G.A.4
Reeve, A.K.5
Perry, R.H.6
Jaros, E.7
Hersheson, J.S.8
Betts, J.9
Klopstock, T.10
Taylor, R.W.11
Turnbull, D.M.12
-
5
-
-
0035160315
-
Quantification and sequencing of somatic deleted mtDNA in single cells: Evidence for partially duplicated mtDNA in aged human tissues
-
Bodyak ND, Nekhaeva E, Wei JY, Khrapko K (2001) Quantification and sequencing of somatic deleted mtDNA in single cells: Evidence for partially duplicated mtDNA in aged human tissues. Hum. Mol. Genet. 10, 17-24.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 17-24
-
-
Bodyak, N.D.1
Nekhaeva, E.2
Wei, J.Y.3
Khrapko, K.4
-
6
-
-
0031885843
-
Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscle
-
Brierley EJ, Johnson MA, Lightowlers RN, James OF, Turnbull DM (1998) Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscle. Ann. Neurol. 43, 217-223.
-
(1998)
Ann. Neurol.
, vol.43
, pp. 217-223
-
-
Brierley, E.J.1
Johnson, M.A.2
Lightowlers, R.N.3
James, O.F.4
Turnbull, D.M.5
-
7
-
-
0036258718
-
Ageing muscle: Clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function
-
Fayet G, Jansson M, Sternberg D, Moslemi AR, Blondy P, Lombes A, Fardeau M, Oldfors A (2002) Ageing muscle: Clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function. Neuromuscul. Disord. 12, 484-493.
-
(2002)
Neuromuscul. Disord.
, vol.12
, pp. 484-493
-
-
Fayet, G.1
Jansson, M.2
Sternberg, D.3
Moslemi, A.R.4
Blondy, P.5
Lombes, A.6
Fardeau, M.7
Oldfors, A.8
-
8
-
-
0026754574
-
Reactive oxygen species and the central nervous system
-
Halliwell B (1992) Reactive oxygen species and the central nervous system. J. Neurochem. 59, 1609-1623.
-
(1992)
J. Neurochem.
, vol.59
, pp. 1609-1623
-
-
Halliwell, B.1
-
9
-
-
33644875533
-
mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences
-
Ingman M, Gyllensten U (2006) mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences. Nucleic Acids Res. 34, D749-D751.
-
(2006)
Nucleic Acids Res.
, vol.34
-
-
Ingman, M.1
Gyllensten, U.2
-
10
-
-
33646351299
-
Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons
-
Kraytsberg Y, Kudryavtseva E, McKee AC, Geula C, Kowall NW, Khrapko K (2006) Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons. Nat. Genet. 38, 518-520.
-
(2006)
Nat. Genet.
, vol.38
, pp. 518-520
-
-
Kraytsberg, Y.1
Kudryavtseva, E.2
McKee, A.C.3
Geula, C.4
Kowall, N.W.5
Khrapko, K.6
-
11
-
-
39749124232
-
What causes mitochondrial DNA deletions in human cells?
-
Krishnan KJ, Reeve AK, Samuels DC, Chinnery PF, Blackwood JK, Taylor RW, Wanrooij S, Spelbrink JN, Lightowlers RN, Turnbull DM (2008) What causes mitochondrial DNA deletions in human cells? Nat. Genet. 40, 275-279.
-
(2008)
Nat. Genet.
, vol.40
, pp. 275-279
-
-
Krishnan, K.J.1
Reeve, A.K.2
Samuels, D.C.3
Chinnery, P.F.4
Blackwood, J.K.5
Taylor, R.W.6
Wanrooij, S.7
Spelbrink, J.N.8
Lightowlers, R.N.9
Turnbull, D.M.10
-
12
-
-
22344456832
-
Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging
-
Kujoth GC, Hiona A, Pugh TD, Someya S, Panzer K, Wohlgemuth SE, Hofer T, Seo AY, Sullivan R, Jobling WA, Morrow JD, Van Remmen H, Sedivy JM, Yamasoba T, Tanokura M, Weindruch R, Leeuwenburgh C, Prolla TA (2005) Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging. Science 309, 481-484.
-
(2005)
Science
, vol.309
, pp. 481-484
-
-
Kujoth, G.C.1
Hiona, A.2
Pugh, T.D.3
Someya, S.4
Panzer, K.5
Wohlgemuth, S.E.6
Hofer, T.7
Seo, A.Y.8
Sullivan, R.9
Jobling, W.A.10
Morrow, J.D.11
Van Remmen, H.12
Sedivy, J.M.13
Yamasoba, T.14
Tanokura, M.15
Weindruch, R.16
Leeuwenburgh, C.17
Prolla, T.A.18
-
13
-
-
0032030309
-
Mutations in mitochondrial DNA accumulate differentially in three different human tissues during ageing
-
Liu VW, Zhang C, Nagley P (1998) Mutations in mitochondrial DNA accumulate differentially in three different human tissues during ageing. Nucleic Acids Res. 26, 1268-1275.
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 1268-1275
-
-
Liu, V.W.1
Zhang, C.2
Nagley, P.3
-
14
-
-
0042845125
-
-
MITOMAP Available at: (Accessed: 8 June 2009)
-
MITOMAP (2009) MITOMAP: A Human Mitochondrial Genome Database. Available at: http://www.mitomap.org (Accessed: 8 June 2009).
-
(2009)
MITOMAP: A Human Mitochondrial Genome Database
-
-
-
15
-
-
0037117576
-
Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues
-
Nekhaeva E, Bodyak ND, Kraytsberg Y, McGrath SB, Van Orsouw NJ, Pluzhnikov A, Wei JY, Vijg J, Khrapko K (2002) Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues. Proc. Natl. Acad. Sci. USA., 99, 5521-5526.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 5521-5526
-
-
Nekhaeva, E.1
Bodyak, N.D.2
Kraytsberg, Y.3
McGrath, S.B.4
Van Orsouw, N.J.5
Pluzhnikov, A.6
Wei, J.Y.7
Vijg, J.8
Khrapko, K.9
-
16
-
-
38749102795
-
Nature of mitochondrial DNA deletions in Substantia Nigra neurons
-
Reeve AK, Krishnan KJ, Elson JL, Morris CM, Bender A, Lightowlers RN, Turnbull DM (2008) Nature of mitochondrial DNA deletions in Substantia Nigra neurons. Am. J. Hum. Genet. 82, 228-235.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 228-235
-
-
Reeve, A.K.1
Krishnan, K.J.2
Elson, J.L.3
Morris, C.M.4
Bender, A.5
Lightowlers, R.N.6
Turnbull, D.M.7
-
17
-
-
39049156470
-
Prevalence of mitochondrial DNA disease in adults
-
Schaefer AM, McFarland R, Blakely EL, He L, Whittaker RG, Taylor RW, Chinnery PF, Turnbull DM (2008) Prevalence of mitochondrial DNA disease in adults. Ann. Neurol. 63, 35-39.
-
(2008)
Ann. Neurol.
, vol.63
, pp. 35-39
-
-
Schaefer, A.M.1
McFarland, R.2
Blakely, E.L.3
He, L.4
Whittaker, R.G.5
Taylor, R.W.6
Chinnery, P.F.7
Turnbull, D.M.8
-
18
-
-
17744393686
-
Mitochondrial DNA mutations in human disease
-
Taylor RW, Turnbull DM (2005) Mitochondrial DNA mutations in human disease. Nat. Rev. Gen. 6, 389-402.
-
(2005)
Nat. Rev. Gen.
, vol.6
, pp. 389-402
-
-
Taylor, R.W.1
Turnbull, D.M.2
-
19
-
-
0035432034
-
The determination of complete human mitochondrial DNA sequences in single cells: Implications for the study of somatic mitochondrial DNA point mutations
-
Taylor RW, Taylor GA, Durham SE, Turnbull DM (2001) The determination of complete human mitochondrial DNA sequences in single cells: Implications for the study of somatic mitochondrial DNA point mutations. Nucleic Acids Res. 29, E74.
-
(2001)
Nucleic Acids Res.
, vol.29
-
-
Taylor, R.W.1
Taylor, G.A.2
Durham, S.E.3
Turnbull, D.M.4
-
20
-
-
0347600946
-
Mitochondrial mutations in human colonic crypt stem cells
-
Taylor RW, Barron MJ, Borthwick GM, Gospel A, Chinnery PF, Samuels DC, Taylor GA, Plusa SM, Meddham SJ, Greaves LC, Kirkwood BL, Turnbull DM (2003) Mitochondrial mutations in human colonic crypt stem cells. J. Clin. Invest. 112, 1351-1360.
-
(2003)
J. Clin. Invest.
, vol.112
, pp. 1351-1360
-
-
Taylor, R.W.1
Barron, M.J.2
Borthwick, G.M.3
Gospel, A.4
Chinnery, P.F.5
Samuels, D.C.6
Taylor, G.A.7
Plusa, S.M.8
Meddham, S.J.9
Greaves, L.C.10
Kirkwood, B.L.11
Turnbull, D.M.12
-
21
-
-
2642580016
-
Premature ageing in mice expressing defective mitochondrial DNA polymerase
-
Trifunovic A, Wredenberg A, Falkenberg M, Spelbrink JN, Rovio AT, Bruder CE, Bohlooly YM, Gidlof S, Oldfors A, Wibom R, Tornell J, Jacobs HT, Larsson NG (2004) Premature ageing in mice expressing defective mitochondrial DNA polymerase. Nature 429, 417-423.
-
(2004)
Nature
, vol.429
, pp. 417-423
-
-
Trifunovic, A.1
Wredenberg, A.2
Falkenberg, M.3
Spelbrink, J.N.4
Rovio, A.T.5
Bruder, C.E.6
Bohlooly, Y.M.7
Gidlof, S.8
Oldfors, A.9
Wibom, R.10
Tornell, J.11
Jacobs, H.T.12
Larsson, N.G.13
-
22
-
-
41349087783
-
DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice
-
Vermulst M, Wanagat J, Kujoth GC, Bielas JH, Rabinovitch PS, Prolla TA, Loeb LA (2008) DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice. Nat. Genet. 40, 392-394.
-
(2008)
Nat. Genet.
, vol.40
, pp. 392-394
-
-
Vermulst, M.1
Wanagat, J.2
Kujoth, G.C.3
Bielas, J.H.4
Rabinovitch, P.S.5
Prolla, T.A.6
Loeb, L.A.7
-
23
-
-
0342762078
-
Insensitivity of cultured rat cortical neurons to mitochondrial DNA synthesis inhibitors: Evidence for a slow turnover of mitochondrial DNA
-
Wang GJ, Nutter LM, Thayer SA (1997) Insensitivity of cultured rat cortical neurons to mitochondrial DNA synthesis inhibitors: Evidence for a slow turnover of mitochondrial DNA. Biochem. Pharmacol. 54, 181-187.
-
(1997)
Biochem. Pharmacol.
, vol.54
, pp. 181-187
-
-
Wang, G.J.1
Nutter, L.M.2
Thayer, S.A.3
|