-
1
-
-
0035109346
-
Mitochondrial genome instability in human cancers
-
Bianchi NO, Bianchi MS, Richard SM. Mitochondrial genome instability in human cancers. Mutat Res. 2001;488:9-23.
-
(2001)
Mutat Res
, vol.488
, pp. 9-23
-
-
Bianchi, N.O.1
Bianchi, M.S.2
Richard, S.M.3
-
2
-
-
0032868141
-
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
-
Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Tumbull DM, Howell N. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA [letter]. Nat Genet. 1999;23:147.
-
(1999)
Nat Genet
, vol.23
, pp. 147
-
-
Andrews, R.M.1
Kubacka, I.2
Chinnery, P.F.3
Lightowlers, R.N.4
Tumbull, D.M.5
Howell, N.6
-
3
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson S, Bankier AT, Barrell BG, et al. Sequence and organization of the human mitochondrial genome. Nature. 1981;290:457-465.
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
-
5
-
-
0036316413
-
Age-dependent decline of DNA repair activity for oxidative lesions in rat brain mitochondria
-
Chen D, Cao G, Hastings T, et al. Age-dependent decline of DNA repair activity for oxidative lesions in rat brain mitochondria. J Neurochem. 2002;81:1273-1284.
-
(2002)
J Neurochem
, vol.81
, pp. 1273-1284
-
-
Chen, D.1
Cao, G.2
Hastings, T.3
-
6
-
-
0037029132
-
Mitochondrial DNA repair of oxidative damage in mammalian cells
-
Bohr VA, Stevnsner T, Souza-Pinto NO. Mitochondrial DNA repair of oxidative damage in mammalian cells. Gene. 2002;286:127-134.
-
(2002)
Gene
, vol.286
, pp. 127-134
-
-
Bohr, V.A.1
Stevnsner, T.2
Souza-Pinto, N.O.3
-
7
-
-
0034972303
-
High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection
-
Coller HA, Khrapko K, Bodyak ND, Nekhaeva E, Herrero-Jimenez P, Thilly WG. High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection. Nat Genet. 2001;28:147-150.
-
(2001)
Nat Genet
, vol.28
, pp. 147-150
-
-
Coller, H.A.1
Khrapko, K.2
Bodyak, N.D.3
Nekhaeva, E.4
Herrero-Jimenez, P.5
Thilly, W.G.6
-
8
-
-
0033761979
-
Mitochondrial DNA mutations in the pathogenesis of human disease
-
Chinnery PF, Turnbull DM. Mitochondrial DNA mutations in the pathogenesis of human disease. Mol Med Today. 2000;6:425-432.
-
(2000)
Mol Med Today
, vol.6
, pp. 425-432
-
-
Chinnery, P.F.1
Turnbull, D.M.2
-
9
-
-
0033525773
-
Mitochondrial diseases in man and mouse
-
Wallace DC. Mitochondrial diseases in man and mouse. Science. 1999;283:1482-1488.
-
(1999)
Science
, vol.283
, pp. 1482-1488
-
-
Wallace, D.C.1
-
10
-
-
0029147133
-
Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome
-
Rotig A, Bourgeron T, Chretien D, Rustin P, Munnich A. Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome. Hum Mol Genet. 1995;4:1327-1330.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1327-1330
-
-
Rotig, A.1
Bourgeron, T.2
Chretien, D.3
Rustin, P.4
Munnich, A.5
-
11
-
-
0034142678
-
From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes
-
Gattermann N. From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes. Leuk Res. 2000;24:141-151.
-
(2000)
Leuk Res
, vol.24
, pp. 141-151
-
-
Gattermann, N.1
-
12
-
-
0038281403
-
Mitochondrial DNA mutations in patients with myelodysplastic syndromes
-
Shin MG, Kajigaya S, Levin BC, Young NS. Mitochondrial DNA mutations in patients with myelodysplastic syndromes. Blood. 2003;101:3118-3125.
-
(2003)
Blood
, vol.101
, pp. 3118-3125
-
-
Shin, M.G.1
Kajigaya, S.2
Levin, B.C.3
Young, N.S.4
-
13
-
-
0037180245
-
Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: Is there a common mechanism?
-
Chinnery PF, Samuels DC, Elson J, Turnbull DM. Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism? Lancet. 2002;360:1323-1325.
-
(2002)
Lancet
, vol.360
, pp. 1323-1325
-
-
Chinnery, P.F.1
Samuels, D.C.2
Elson, J.3
Turnbull, D.M.4
-
14
-
-
0033804530
-
Hypervariable sites in the mtDNA control region are mutational hotspots
-
Stoneking M. Hypervariable sites in the mtDNA control region are mutational hotspots. Am J Hum Genet. 2000;67:1029-1032.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1029-1032
-
-
Stoneking, M.1
-
15
-
-
0036211695
-
MitoAnalyzer, a computer program and interactive web site to determine the effects of single nucleotide polymorphisms (SNPs) and mutations in human mitochondrial DNA
-
Lee MS, Levin BC. MitoAnalyzer, a computer program and interactive web site to determine the effects of single nucleotide polymorphisms (SNPs) and mutations in human mitochondrial DNA. Mitochondrion. 2002;1:321-326.
-
(2002)
Mitochondrion
, vol.1
, pp. 321-326
-
-
Lee, M.S.1
Levin, B.C.2
-
16
-
-
0037418174
-
Control region mtDNA variants: Longevity, climatic adaptation, and a forensic conundrum
-
Coskun PE, Ruiz-Pesini E, Wallace DC. Control region mtDNA variants: longevity, climatic adaptation, and a forensic conundrum. Proc Natl Acad Sci U S A. 2003;100:2174-2176.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 2174-2176
-
-
Coskun, P.E.1
Ruiz-Pesini, E.2
Wallace, D.C.3
-
17
-
-
15644370476
-
A common mitochondrial DNA variant is associated with insulin resistance in adult life
-
Poulton J, Brown MS, Cooper A, Marchington DR, Phillips DI. A common mitochondrial DNA variant is associated with insulin resistance in adult life. Diabetologia. 1998;41:54-58.
-
(1998)
Diabetologia
, vol.41
, pp. 54-58
-
-
Poulton, J.1
Brown, M.S.2
Cooper, A.3
Marchington, D.R.4
Phillips, D.I.5
-
18
-
-
0035476227
-
Identification of a mononucleotide repeat as a major target for mitochondrial DNA alterations in human tumors
-
Sanchez-Cespedes M, Parrella P, Nomoto S, et al. Identification of a mononucleotide repeat as a major target for mitochondrial DNA alterations in human tumors. Cancer Res. 2001;61:7015-7019.
-
(2001)
Cancer Res
, vol.61
, pp. 7015-7019
-
-
Sanchez-Cespedes, M.1
Parrella, P.2
Nomoto, S.3
-
19
-
-
0034434583
-
Mitochondrial DNA disorders
-
Naviaux RK. Mitochondrial DNA disorders. Eur J Pediatr. 2000;159(suppl 3):S219-S226.
-
(2000)
Eur J Pediatr
, vol.159
, Issue.SUPPL. 3
-
-
Naviaux, R.K.1
-
20
-
-
0036062340
-
Mitochondrial oxygen consumption and ineffective haematopoiesis in patients with myelodysplastic syndromes
-
Bowen D, Peddie C. Mitochondrial oxygen consumption and ineffective haematopoiesis in patients with myelodysplastic syndromes. Br J Haematol. 2002;118:345-346.
-
(2002)
Br J Haematol
, vol.118
, pp. 345-346
-
-
Bowen, D.1
Peddie, C.2
-
21
-
-
0037417898
-
Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes
-
Zhang J, Asin-Cayuela J, Fish J, et al. Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes. Proc Natl Acad Sci U S A. 2003;100:1116-1121.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 1116-1121
-
-
Zhang, J.1
Asin-Cayuela, J.2
Fish, J.3
-
22
-
-
0033151863
-
Cell-by-cell scanning of whole mitochondrial genomes in aged human heart reveals a significant fraction of myocytes with clonally expanded deletions
-
Khrapko K, Bodyak N, Thilly WG, et al. Cell-by-cell scanning of whole mitochondrial genomes in aged human heart reveals a significant fraction of myocytes with clonally expanded deletions. Nucleic Acids Res. 1999;27:2434-2441.
-
(1999)
Nucleic Acids Res
, vol.27
, pp. 2434-2441
-
-
Khrapko, K.1
Bodyak, N.2
Thilly, W.G.3
-
23
-
-
0031439483
-
Variable levels of a heteroplasmic point mutation in individual hair roots
-
Bendall KE, Macaulay VA, Sykes BC. Variable levels of a heteroplasmic point mutation in individual hair roots. Am J Hum Genet. 1997;61:1303-1308.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1303-1308
-
-
Bendall, K.E.1
Macaulay, V.A.2
Sykes, B.C.3
-
24
-
-
0030788198
-
A family exhibiting heteroplasmy in the human mitochondrial DNA control region reveals both somatic mosaicism and pronounced segregation of mitotypes
-
Wilson MR, Polanskey D, Replogle J, DiZinno JA, Budowle B. A family exhibiting heteroplasmy in the human mitochondrial DNA control region reveals both somatic mosaicism and pronounced segregation of mitotypes. Hum Genet. 1997;100:167-171.
-
(1997)
Hum Genet
, vol.100
, pp. 167-171
-
-
Wilson, M.R.1
Polanskey, D.2
Replogle, J.3
DiZinno, J.A.4
Budowle, B.5
-
25
-
-
0031736203
-
Somatic mutations of the mitochondrial genome in human colorectal tumours
-
Polyak K, Li Y, Zhu H, et al. Somatic mutations of the mitochondrial genome in human colorectal tumours. Nat Genet. 1998;20:291-293.
-
(1998)
Nat Genet
, vol.20
, pp. 291-293
-
-
Polyak, K.1
Li, Y.2
Zhu, H.3
-
26
-
-
0025944643
-
Replacement of bovine mitochondrial DNA by a sequence variant within one generation
-
Koehler CM, Lindberg GL, Brown DR, et al. Replacement of bovine mitochondrial DNA by a sequence variant within one generation. Genetics. 1991;129:247-255.
-
(1991)
Genetics
, vol.129
, pp. 247-255
-
-
Koehler, C.M.1
Lindberg, G.L.2
Brown, D.R.3
-
27
-
-
0030898192
-
A high observed substitution rate in the human mitochondrial DNA control region
-
Parsons TJ, Muniec DS, Sullivan K, et al. A high observed substitution rate in the human mitochondrial DNA control region. Nat Genet. 1997;15:363-368.
-
(1997)
Nat Genet
, vol.15
, pp. 363-368
-
-
Parsons, T.J.1
Muniec, D.S.2
Sullivan, K.3
-
28
-
-
0037633511
-
Inter- and intragenerational transmission of a human mitochondrial DNA heteroplasmy among 13 maternally-related individuals and differences between and within tissues in two family members
-
Sekiguchi K, Kasai K, Levin BC. Inter- and intragenerational transmission of a human mitochondrial DNA heteroplasmy among 13 maternally-related individuals and differences between and within tissues in two family members. Mitochondrion. 2003;2:401-414.
-
(2003)
Mitochondrion
, vol.2
, pp. 401-414
-
-
Sekiguchi, K.1
Kasai, K.2
Levin, B.C.3
-
29
-
-
0035097502
-
Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age
-
Elson JL, Samuels DC, Turnbull DM, Chinnery PF. Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age. Am J Hum Genet. 2001;68:802-806.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 802-806
-
-
Elson, J.L.1
Samuels, D.C.2
Turnbull, D.M.3
Chinnery, P.F.4
-
30
-
-
0036242399
-
Frequent intracellular clonal expansions of somatic mtDNA mutations: Significance and mechanisms
-
Coller HA, Bodyak ND, Khrapko K. Frequent intracellular clonal expansions of somatic mtDNA mutations: significance and mechanisms. Ann N Y Acad Sci. 2002;959:434-447.
-
(2002)
Ann N Y Acad Sci
, vol.959
, pp. 434-447
-
-
Coller, H.A.1
Bodyak, N.D.2
Khrapko, K.3
-
31
-
-
0037117576
-
Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues
-
Nekhaeva E, Bodyak ND, Kraytsberg Y, et al. Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues. Proc Natl Acad Sci U S A. 2002;99:5521-5526.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 5521-5526
-
-
Nekhaeva, E.1
Bodyak, N.D.2
Kraytsberg, Y.3
-
32
-
-
0036221005
-
Evidence for the de novo regeneration of the pattern of the length heteroplasmy associated with the T16189C variant in the control (D-loop) region of mitochondrial DNA
-
Malik S, Sudoyo H, Pramoonjago P, Sukarna T, Darwis D, Marzuki S. Evidence for the de novo regeneration of the pattern of the length heteroplasmy associated with the T16189C variant in the control (D-loop) region of mitochondrial DNA. J Hum Genet. 2002;47:122-130.
-
(2002)
J Hum Genet
, vol.47
, pp. 122-130
-
-
Malik, S.1
Sudoyo, H.2
Pramoonjago, P.3
Sukarna, T.4
Darwis, D.5
Marzuki, S.6
-
33
-
-
0033135836
-
Mitochondrial 16189 variant, thinness at birth, and type-2 diabetes
-
ALSPAC study team. Avon Longitudinal Study of Pregnancy and Childhood
-
Casteels K, Ong K, Phillips D, Bendall H, Pembrey M. Mitochondrial 16189 variant, thinness at birth, and type-2 diabetes. ALSPAC study team. Avon Longitudinal Study of Pregnancy and Childhood. Lancet. 1999;353:1499-1500.
-
(1999)
Lancet
, vol.353
, pp. 1499-1500
-
-
Casteels, K.1
Ong, K.2
Phillips, D.3
Bendall, H.4
Pembrey, M.5
-
34
-
-
0035925906
-
A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations
-
Khogali SS, Mayosi BM, Beattie JM, McKenna WJ, Watkins H, Poulton J. A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations. Lancet. 2001;357:1265-1267.
-
(2001)
Lancet
, vol.357
, pp. 1265-1267
-
-
Khogali, S.S.1
Mayosi, B.M.2
Beattie, J.M.3
McKenna, W.J.4
Watkins, H.5
Poulton, J.6
|