-
1
-
-
0031574362
-
Reduced steady-state levels of mitochondrial RNA and increased mitochondrial DNA amount in human brain with aging
-
Barrientos A, Casademont J, Cardellach F, Estivill X, Urbano-Marquez A, N unes V (1997) Reduced steady-state levels of mitochondrial RNA and increased mitochondrial DNA amount in human brain with aging. Mol Brain Res 52:284-289
-
(1997)
Mol Brain Res
, vol.52
, pp. 284-289
-
-
Barrientos, A.1
Casademont, J.2
Cardellach, F.3
Estivill, X.4
Urbano-Marquez, A.5
N Unes, V.6
-
2
-
-
0034704125
-
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation
-
Brown MD, Trounce IA, Jun AS, Allen JC, Wallace DC (2000) Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation. J Biol Chem 275:39831-39836
-
(2000)
J Biol Chem
, vol.275
, pp. 39831-39836
-
-
Brown, M.D.1
Trounce, I.A.2
Jun, A.S.3
Allen, J.C.4
Wallace, D.C.5
-
3
-
-
0029969778
-
A case-control study of Leber's hereditary optic neuropathy
-
Chalmers RM, Harding AE (1996) A case-control study of Leber's hereditary optic neuropathy. Brain 119:1481-1486
-
(1996)
Brain
, vol.119
, pp. 1481-1486
-
-
Chalmers, R.M.1
Harding, A.E.2
-
4
-
-
0000869712
-
Primary LHON mutations: Trying to separate "fruyt" from "chaf."
-
Howell N (1994) Primary LHON mutations: trying to separate "fruyt" from "chaf." Clin Neurosci 2:130-137
-
(1994)
Clin Neurosci
, vol.2
, pp. 130-137
-
-
Howell, N.1
-
5
-
-
0025944560
-
Leber hereditary optic neuropathy: Identification of the same mitochondrial ND1 mutation in six pedigrees
-
Howell N, Bindoff LA, McCullough DA, Kubacka I, Poulton J, Mackey D, Taylor L, Turnbull DM (1991) Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees. Am J Hum Genet 49:939-950
-
(1991)
Am J Hum Genet
, vol.49
, pp. 939-950
-
-
Howell, N.1
Bindoff, L.A.2
McCullough, D.A.3
Kubacka, I.4
Poulton, J.5
Mackey, D.6
Taylor, L.7
Turnbull, D.M.8
-
6
-
-
0025910614
-
A new mtDNA mutation associated with Leber hereditary optic neuropathy
-
Huoponen K, Vilkki J, Aula P, Nikoskelainen EK (1991) A new mtDNA mutation associated with Leber hereditary optic neuropathy. Am J Hum Genet 48:1147-1153
-
(1991)
Am J Hum Genet
, vol.48
, pp. 1147-1153
-
-
Huoponen, K.1
Vilkki, J.2
Aula, P.3
Nikoskelainen, E.K.4
-
7
-
-
0026757115
-
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy
-
Johns DR, Neufeld MJ, Park RD (1992) An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy. Biochem Biophys Res Commun 187:1551-1557
-
(1992)
Biochem Biophys Res Commun
, vol.187
, pp. 1551-1557
-
-
Johns, D.R.1
Neufeld, M.J.2
Park, R.D.3
-
8
-
-
0027502505
-
Leber's hereditary optic neuropathy clinical manifestations of the 14484 mutation
-
Johns DR, Heher KL, Miller NR, Smith KH (1993) Leber's hereditary optic neuropathy clinical manifestations of the 14484 mutation. Arch Ophthalmol 111:495-498
-
(1993)
Arch Ophthalmol
, vol.111
, pp. 495-498
-
-
Johns, D.R.1
Heher, K.L.2
Miller, N.R.3
Smith, K.H.4
-
9
-
-
0032429396
-
Aging- And smoking-associated alteration in the relative content of mitochondrial DNA in human lung
-
Lee HC, Lu CY, Fahn HJ, Wei YH (1998) Aging- and smoking-associated alteration in the relative content of mitochondrial DNA in human lung. FEBS Lett 441:292-296
-
(1998)
FEBS Lett
, vol.441
, pp. 292-296
-
-
Lee, H.C.1
Lu, C.Y.2
Fahn, H.J.3
Wei, Y.H.4
-
10
-
-
0031965731
-
Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy
-
Mashima Y, Yamada K, Wakakura M, Kigasawa K, Kudoh J, Shimizu N, Oguchi Y (1998) Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy. Curr Eye Res 17:403-408
-
(1998)
Curr Eye Res
, vol.17
, pp. 403-408
-
-
Mashima, Y.1
Yamada, K.2
Wakakura, M.3
Kigasawa, K.4
Kudoh, J.5
Shimizu, N.6
Oguchi, Y.7
-
11
-
-
0025881563
-
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation
-
Newman NJ, Lott MT, Wallace DC (1991) The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. Am J Ophthalmol 111:750-762
-
(1991)
Am J Ophthalmol
, vol.111
, pp. 750-762
-
-
Newman, N.J.1
Lott, M.T.2
Wallace, D.C.3
-
12
-
-
0041971164
-
Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia
-
Nishioka T, Tasaki M, Soemantri A, Dyat M, Susanto JC, Tamam M, Sudarmanto B, Ishida T (2003) Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia. J Hum Genet 48:385-389
-
(2003)
J Hum Genet
, vol.48
, pp. 385-389
-
-
Nishioka, T.1
Tasaki, M.2
Soemantri, A.3
Dyat, M.4
Susanto, J.C.5
Tamam, M.6
Sudarmanto, B.7
Ishida, T.8
-
13
-
-
0028221662
-
Leber's hereditary optic neuropathy: Correlations between mitochondrial genotype and visual outcome
-
Oostra RJ, Bolhuis PA, Wijburg FA, Zorn-Ende G, Bleeker-Wagemakers EM (1994) Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome. J Med Genet 31:280-286
-
(1994)
J Med Genet
, vol.31
, pp. 280-286
-
-
Oostra, R.J.1
Bolhuis, P.A.2
Wijburg, F.A.3
Zorn-Ende, G.4
Bleeker-Wagemakers, E.M.5
-
14
-
-
0028949749
-
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
-
Riordan-Eva P, Sanders MD, Govan GG, Sweeney MG, Da Costa J, Harding AE (1995) The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain 118:319-337
-
(1995)
Brain
, vol.118
, pp. 319-337
-
-
Riordan-Eva, P.1
Sanders, M.D.2
Govan, G.G.3
Sweeney, M.G.4
Da Costa, J.5
Harding, A.E.6
-
15
-
-
0023762872
-
Mitochondrial DNA molecules and virtual number of mitochondria per cell in mammalian cells
-
Robin ED, Wong R (1988) Mitochondrial DNA molecules and virtual number of mitochondria per cell in mammalian cells. J Cell Physiol 136:507-513
-
(1988)
J Cell Physiol
, vol.136
, pp. 507-513
-
-
Robin, E.D.1
Wong, R.2
-
16
-
-
0028349620
-
Platelet mitochondrial function in Leber's hereditary optic neuropathy
-
Smith PR, Cooper JM, Govan GG, Harding AE, Schapira AHV (1994) Platelet mitochondrial function in Leber's hereditary optic neuropathy. J Neurol Sci 122:80-83
-
(1994)
J Neurol Sci
, vol.122
, pp. 80-83
-
-
Smith, P.R.1
Cooper, J.M.2
Govan, G.G.3
Harding, A.E.4
Schapira, A.H.V.5
-
17
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AMS, Elsas LJ II, Nikoskelainen EK (1988) Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 242:1427-1430
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Ams, L.6
Elsas II, L.J.7
Nikoskelainen, E.K.8
-
18
-
-
0028306912
-
Purification of genomic DNA from human whole blood by isopropanol-fractionation with concentrated NaI and SDS
-
Wang L, Hirayasu K, Ishizawa M, Kobayashi Y (1994) Purification of genomic DNA from human whole blood by isopropanol-fractionation with concentrated NaI and SDS. Nucleic Acids Res 22:1774-1775
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 1774-1775
-
-
Wang, L.1
Hirayasu, K.2
Ishizawa, M.3
Kobayashi, Y.4
-
19
-
-
0037084559
-
Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells
-
Wong A, Cavelier L, Collins-Schramm HE, Seldin MF, McGrogan M, Savontaus ML, Cortopassi GA (2002) Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells. Hum Mol Genet 11:431-438
-
(2002)
Hum Mol Genet
, vol.11
, pp. 431-438
-
-
Wong, A.1
Cavelier, L.2
Collins-Schramm, H.E.3
Seldin, M.F.4
McGrogan, M.5
Savontaus, M.L.6
Cortopassi, G.A.7
-
20
-
-
0036724369
-
Increase of mitochondrial DNA in blood cells of patients with Leber's hereditary optic neuropathy with 11778 mutation
-
Yen MY, Chen CS, Wang AG, Wei YH (2002) Increase of mitochondrial DNA in blood cells of patients with Leber's hereditary optic neuropathy with 11778 mutation. Br J Ophthalmol 86:1027-1030
-
(2002)
Br J Ophthalmol
, vol.86
, pp. 1027-1030
-
-
Yen, M.Y.1
Chen, C.S.2
Wang, A.G.3
Wei, Y.H.4
|