-
1
-
-
0030447980
-
Misconceptions about mitochondria and mammalian fertilization: Implications for theories on human evolution
-
Ankel-Simons F, Cummins JM (1996) Misconceptions about mitochondria and mammalian fertilization: implications for theories on human evolution. Proc Natl Acad Sci USA 93: 13859-13863
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 13859-13863
-
-
Ankel-Simons, F.1
Cummins, J.M.2
-
2
-
-
0029003333
-
Complementation and segregation behavior of disease causing mitochondrial DNA mutations in cellular model systems
-
Attardi G, Yoneda M, Chomyn A (1995) Complementation and segregation behavior of disease causing mitochondrial DNA mutations in cellular model systems. Biochim Biophys Acta 1271:241-248
-
(1995)
Biochim Biophys Acta
, vol.1271
, pp. 241-248
-
-
Attardi, G.1
Yoneda, M.2
Chomyn, A.3
-
3
-
-
0028049837
-
Relaxed and stringent genomes: Why cytoplasmic genes don't obey Mendel's laws
-
Birky CW Jr (1994) Relaxed and stringent genomes: why cytoplasmic genes don't obey Mendel's laws. J Hered 85: 355-365
-
(1994)
J Hered
, vol.85
, pp. 355-365
-
-
Birky C.W., Jr.1
-
4
-
-
0026621445
-
Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)
-
Boulet L, Karpati G, Shoubridge EA (1992) Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF). Am J Hum Genet 51:1187-1200
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1187-1200
-
-
Boulet, L.1
Karpati, G.2
Shoubridge, E.A.3
-
5
-
-
0031885843
-
Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscle
-
Brierley EJ, Johnson MA, Lightowlers RN, James OFW, 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.W.4
Turnbull, D.M.5
-
6
-
-
0030670573
-
The clinical features, investigation and management of patients with mitochondrial DNA defects
-
Chinnery PF, Turnbull DM (1997) The clinical features, investigation and management of patients with mitochondrial DNA defects. J Neurol Neurosurg Psychiatry 63:559-563
-
(1997)
J Neurol Neurosurg Psychiatry
, vol.63
, pp. 559-563
-
-
Chinnery, P.F.1
Turnbull, D.M.2
-
7
-
-
0029842846
-
Mitochondrial DNA gets the drift
-
Clayton DA (1996) Mitochondrial DNA gets the drift. Nat Genet 14:123-125
-
(1996)
Nat Genet
, vol.14
, pp. 123-125
-
-
Clayton, D.A.1
-
8
-
-
0015935220
-
5-Bromodeoxyuridine labeling of monomeric and catenated circular mitochondrial DNA in HeLa cells
-
Flory PJ, Vinograd J (1973) 5-Bromodeoxyuridine labeling of monomeric and catenated circular mitochondrial DNA in HeLa cells. J Mol Biol 74:81-94
-
(1973)
J Mol Biol
, vol.74
, pp. 81-94
-
-
Flory, P.J.1
Vinograd, J.2
-
9
-
-
0014690248
-
Apparent turnover of mitochondrial deoxyribonucleic acid and mitochondrial phospholipids in the tissues of the rat
-
Gross NJ, Getz GS, Rabinowitz M (1969) Apparent turnover of mitochondrial deoxyribonucleic acid and mitochondrial phospholipids in the tissues of the rat. J Biol Chem 244: 1552-1562
-
(1969)
J Biol Chem
, vol.244
, pp. 1552-1562
-
-
Gross, N.J.1
Getz, G.S.2
Rabinowitz, M.3
-
10
-
-
0025836655
-
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
-
Hayashi J, Ohta S, Kikuchi A, Takemitsu M, Goto Y, Nonaka I (1991) Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction. Proc Natl Acad Sci USA 88: 10614-10618
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 10614-10618
-
-
Hayashi, J.1
Ohta, S.2
Kikuchi, A.3
Takemitsu, M.4
Goto, Y.5
Nonaka, I.6
-
11
-
-
0030755073
-
mtDNA recombination: What do in vitro data mean?
-
Howell N (1997) mtDNA recombination: what do in vitro data mean? Am J Hum Genet 61:19-22
-
(1997)
Am J Hum Genet
, vol.61
, pp. 19-22
-
-
Howell, N.1
-
12
-
-
0029638664
-
Mitochondrial DNA and disease
-
Johns D (1995) Mitochondrial DNA and disease. New Engl J Med 333:638-644
-
(1995)
New Engl J Med
, vol.333
, pp. 638-644
-
-
Johns, D.1
-
14
-
-
0029812866
-
Mitochondrial DNA and RNA processing in MELAS
-
Kaufmann P, Koga Y, Shanske S, Hirano M, DiMauro S, King MP, Schon EA (1996) Mitochondrial DNA and RNA processing in MELAS. Ann Neurol 40:172-180
-
(1996)
Ann Neurol
, vol.40
, pp. 172-180
-
-
Kaufmann, P.1
Koga, Y.2
Shanske, S.3
Hirano, M.4
DiMauro, S.5
King, M.P.6
Schon, E.A.7
-
15
-
-
0029587469
-
Molecular genetic aspects of human mitochondrial disorders
-
Larsson NG, Clayton DA (1995) Molecular genetic aspects of human mitochondrial disorders. Annu Rev Genet 29: 151-178
-
(1995)
Annu Rev Genet
, vol.29
, pp. 151-178
-
-
Larsson, N.G.1
Clayton, D.A.2
-
16
-
-
0025345775
-
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome
-
Larsson NG, Holme E, Kristiansson B, Oldfors A, Tulinius M (1990) Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome. Pediatr Res 28: 131-136
-
(1990)
Pediatr Res
, vol.28
, pp. 131-136
-
-
Larsson, N.G.1
Holme, E.2
Kristiansson, B.3
Oldfors, A.4
Tulinius, M.5
-
17
-
-
0031930319
-
Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice
-
Larsson NG, Wang J, Wilhelmsson H, Oldfors A, Rustin P, Lewandoski M, Barsh GS, et al (1998) Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice. Nat Genet 18:231-236
-
(1998)
Nat Genet
, vol.18
, pp. 231-236
-
-
Larsson, N.G.1
Wang, J.2
Wilhelmsson, H.3
Oldfors, A.4
Rustin, P.5
Lewandoski, M.6
Barsh, G.S.7
-
18
-
-
0030664064
-
Mammalian mitochondrial genetics: Heredity, heteroplasmy and disease
-
Lightowlers RN, Chinnery PF, Turnbull DM, Howell N (1997) Mammalian mitochondrial genetics: heredity, heteroplasmy and disease. Trends Genet 13:450-455
-
(1997)
Trends Genet
, vol.13
, pp. 450-455
-
-
Lightowlers, R.N.1
Chinnery, P.F.2
Turnbull, D.M.3
Howell, N.4
-
19
-
-
0024398752
-
Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient fibers of a patient with Kearns-Sayre syndrome
-
Mita S, Schmidt B, Schon EA, DiMauro S, Bonilla E (1989) Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient fibers of a patient with Kearns-Sayre syndrome. Proc Natl Acad Sci USA 86:9509-9513
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 9509-9513
-
-
Mita, S.1
Schmidt, B.2
Schon, E.A.3
Dimauro, S.4
Bonilla, E.5
-
20
-
-
0026907560
-
Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions
-
Moraes CT, Ricci E, Petruzzella V, Shanske S, DiMauro S, Schon EA, Bonilla E (1992) Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions. Nat Genet 1:359-367
-
(1992)
Nat Genet
, vol.1
, pp. 359-367
-
-
Moraes, C.T.1
Ricci, E.2
Petruzzella, V.3
Shanske, S.4
DiMauro, S.5
Schon, E.A.6
Bonilla, E.7
-
21
-
-
0027280499
-
Noninvasive diagnosis of the MELAS syndrome from blood DNA
-
Poulton J, Morten K (1993) Noninvasive diagnosis of the MELAS syndrome from blood DNA. Ann Neurol 34:116
-
(1993)
Ann Neurol
, vol.34
, pp. 116
-
-
Poulton, J.1
Morten, K.2
-
23
-
-
0030577222
-
Maternal inheritance and the evaluation of oxidative phosphorylation diseases
-
Shoffner JM (1996) Maternal inheritance and the evaluation of oxidative phosphorylation diseases. Lancet 348: 1283-1288
-
(1996)
Lancet
, vol.348
, pp. 1283-1288
-
-
Shoffner, J.M.1
-
24
-
-
0028229152
-
Mitochondrial DNA diseases: Histological and cellular studies
-
Shoubridge EA (1994) Mitochondrial DNA diseases: histological and cellular studies. J Bioenerg Biomembr 26: 301-310
-
(1994)
J Bioenerg Biomembr
, vol.26
, pp. 301-310
-
-
Shoubridge, E.A.1
-
25
-
-
0025276996
-
Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease
-
Shoubridge EA, Karpati G, Hastings KE (1990) Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease. Cell 62:43-49
-
(1990)
Cell
, vol.62
, pp. 43-49
-
-
Shoubridge, E.A.1
Karpati, G.2
Hastings, K.E.3
-
26
-
-
0028330313
-
Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
-
Tokunaga M, Mita S, Murakami T, Kumamoto T, Uchino M, Nonaka I, Ando M (1994) Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Ann Neurol 35:413-419
-
(1994)
Ann Neurol
, vol.35
, pp. 413-419
-
-
Tokunaga, M.1
Mita, S.2
Murakami, T.3
Kumamoto, T.4
Uchino, M.5
Nonaka, I.6
Ando, M.7
-
27
-
-
0031908201
-
An essential guide to mtDNA maintenance
-
Turnbull DM, Lightowlers RN (1998) An essential guide to mtDNA maintenance. Nat Genet 18:199-200
-
(1998)
Nat Genet
, vol.18
, pp. 199-200
-
-
Turnbull, D.M.1
Lightowlers, R.N.2
-
28
-
-
0026624980
-
Diseases of the mitochondrial DNA
-
Wallace DC (1992) Diseases of the mitochondrial DNA. Annu Rev Biochem 61:1175-1212
-
(1992)
Annu Rev Biochem
, vol.61
, pp. 1175-1212
-
-
Wallace, D.C.1
-
29
-
-
0029045299
-
Mitochondrial DNA variation in human evolution, degenerative disease, and aging
-
-(1995) Mitochondrial DNA variation in human evolution, degenerative disease, and aging. Am J Hum Genet 57:201-223
-
(1995)
Am J Hum Genet
, vol.57
, pp. 201-223
-
-
-
30
-
-
0029071513
-
Mitochondrial DNA mutations in human degenerative diseases and aging
-
Wallace DC, Shoffner JM, Trounce I, Brown MD, Ballinger SW, Corral-Debrinski M, Horton T, et al (1995) Mitochondrial DNA mutations in human degenerative diseases and aging. Biochim Biophys Acta 1271:141-151
-
(1995)
Biochim Biophys Acta
, vol.1271
, pp. 141-151
-
-
Wallace, D.C.1
Shoffner, J.M.2
Trounce, I.3
Brown, M.D.4
Ballinger, S.W.5
Corral-Debrinski, M.6
Horton, T.7
-
31
-
-
0031020420
-
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
-
Weber K, Wilson JN, Taylor L, Brierley E, Johnson MA, Turnbull DM, Bindoff LA (1997) A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle. Am J Hum Genet 60:373-380
-
(1997)
Am J Hum Genet
, vol.60
, pp. 373-380
-
-
Weber, K.1
Wilson, J.N.2
Taylor, L.3
Brierley, E.4
Johnson, M.A.5
Turnbull, D.M.6
Bindoff, L.A.7
-
32
-
-
0028607374
-
Quantitation of mitochondrial DNA in human lymphoblasts by a competitive polymerase chain reaction method: Application to the study of inhibitors of mitochondrial DNA content
-
Zhang H, Cooney DA, Sreenath A, Zhan Q, Agbaria R, Stowe EE, Fornace AJ, et al (1994) Quantitation of mitochondrial DNA in human lymphoblasts by a competitive polymerase chain reaction method: application to the study of inhibitors of mitochondrial DNA content. Mol Pharmacol 46: 1063-1069
-
(1994)
Mol Pharmacol
, vol.46
, pp. 1063-1069
-
-
Zhang, H.1
Cooney, D.A.2
Sreenath, A.3
Zhan, Q.4
Agbaria, R.5
Stowe, E.E.6
Fornace, A.J.7
|