-
1
-
-
13444302610
-
Mitochondrial dysfunction plays a key role in progressive axonal loss ill Multiple Sclerosis
-
Andrews HE, Nichols PP, Bates D, Turnbull DM (2005) Mitochondrial dysfunction plays a key role in progressive axonal loss ill Multiple Sclerosis. Med Hypotheses 64: 669-677.
-
(2005)
Med Hypotheses
, vol.64
, pp. 669-677
-
-
Andrews, H.E.1
Nichols, P.P.2
Bates, D.3
Turnbull, D.M.4
-
2
-
-
33644817756
-
Mitochondrial dysfunction as a cause of axonal degeneration in multiple sclerosis patients
-
Dutta R, McDonough J, Yin X, Peterson J, Chang A, et al. (2006) Mitochondrial dysfunction as a cause of axonal degeneration in multiple sclerosis patients. Ann Neurol 59: 478-489.
-
(2006)
Ann Neurol
, vol.59
, pp. 478-489
-
-
Dutta, R.1
McDonough, J.2
Yin, X.3
Peterson, J.4
Chang, A.5
-
3
-
-
2542541258
-
Parent-of-origin effect in multiple sclerosis: Observations in half-siblings
-
Ebers GC, Sadovnick AD, Dyment DA, Yee IM, Willer CJ, et al. (2004) Parent-of-origin effect in multiple sclerosis: observations in half-siblings. Lancet 363: 1773-1774.
-
(2004)
Lancet
, vol.363
, pp. 1773-1774
-
-
Ebers, G.C.1
Sadovnick, A.D.2
Dyment, D.A.3
Yee, I.M.4
Willer, C.J.5
-
4
-
-
0026782507
-
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
-
Harding AE, Sweeney MG, Miller DH, Mumford CJ, Kellar-Wood H, et al. (1992) Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Brain 115 (Pt 4): 979-989.
-
(1992)
Brain
, vol.115
, Issue.PART 4
, pp. 979-989
-
-
Harding, A.E.1
Sweeney, M.G.2
Miller, D.H.3
Mumford, C.J.4
Kellar-Wood, H.5
-
5
-
-
0028147810
-
Biochemical alterations in multiple sclerosis lesions and normal-appearing white matter detected by in vivo 31P and 1H spectroscopic imaging
-
Husted CA, Goodin DS, Hugg JW, Maudsley AA, Tsuruda JS, et al. (1994) Biochemical alterations in multiple sclerosis lesions and normal-appearing white matter detected by in vivo 31P and 1H spectroscopic imaging. Ann Neurol 36: 157-165.
-
(1994)
Ann Neurol
, vol.36
, pp. 157-165
-
-
Husted, C.A.1
Goodin, D.S.2
Hugg, J.W.3
Maudsley, A.A.4
Tsuruda, J.S.5
-
6
-
-
0031766122
-
Oxidative damage to DNA in plaques of MS brains
-
Vladimirova O, O'Connor J, Cahill A, Alder H, Butunoi C, et al. (1998) Oxidative damage to DNA in plaques of MS brains. Mult Scler 4: 413-418.
-
(1998)
Mult Scler
, vol.4
, pp. 413-418
-
-
Vladimirova, O.1
O'Connor, J.2
Cahill, A.3
Alder, H.4
Butunoi, C.5
-
7
-
-
0034662806
-
Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis
-
Lu F, Selak M, O'Connor J, Croul S, Lorenzana C, et al. (2000) Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis. J Neurol Sci 177: 95-103.
-
(2000)
J Neurol Sci
, vol.177
, pp. 95-103
-
-
Lu, F.1
Selak, M.2
O'Connor, J.3
Croul, S.4
Lorenzana, C.5
-
8
-
-
33846025116
-
Mitochondrial protein nitration primes neurodegeneration in experimental autoimmune encephalomyelitis
-
Qi X, Lewin AS, Sun L, Hauswirth WW, Guy J (2006) Mitochondrial protein nitration primes neurodegeneration in experimental autoimmune encephalomyelitis. J Biol Chem 281: 31950-31962.
-
(2006)
J Biol Chem
, vol.281
, pp. 31950-31962
-
-
Qi, X.1
Lewin, A.S.2
Sun, L.3
Hauswirth, W.W.4
Guy, J.5
-
9
-
-
0029279163
-
Mitochondrial DNA mutations in multiple sclerosis
-
Kalman B, Lublin FD, Alder H (1995) Mitochondrial DNA mutations in multiple sclerosis. Mult Scler 1: 32-36.
-
(1995)
Mult Scler
, vol.1
, pp. 32-36
-
-
Kalman, B.1
Lublin, F.D.2
Alder, H.3
-
11
-
-
0029014947
-
Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis
-
Chalmers RM, Robertson N, Kellar-Wood H, Compston DA, Harding AE (1995) Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis. J Neurol 242: 332-334.
-
(1995)
J Neurol
, vol.242
, pp. 332-334
-
-
Chalmers, R.M.1
Robertson, N.2
Kellar-Wood, H.3
Compston, D.A.4
Harding, A.E.5
-
12
-
-
0030247011
-
Characterization of the mitochondrial DNA in patients with multiple sclerosis
-
Kalman B, Lublin FD, Alder H (1996) Characterization of the mitochondrial DNA in patients with multiple sclerosis. J Neurol Sci 140: 75-84.
-
(1996)
J Neurol Sci
, vol.140
, pp. 75-84
-
-
Kalman, B.1
Lublin, F.D.2
Alder, H.3
-
13
-
-
0032412074
-
Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes
-
Wilichowski E, Ohlenbusch A, Hanefeld F (1998) Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes. Neuropediatrics 29: 307-312.
-
(1998)
Neuropediatrics
, vol.29
, pp. 307-312
-
-
Wilichowski, E.1
Ohlenbusch, A.2
Hanefeld, F.3
-
14
-
-
0028337837
-
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
-
Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE (1994) Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Ann Neurol 36: 109-112.
-
(1994)
Ann Neurol
, vol.36
, pp. 109-112
-
-
Kellar-Wood, H.1
Robertson, N.2
Govan, G.G.3
Compston, D.A.4
Harding, A.E.5
-
15
-
-
0029153643
-
No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan
-
Nishimura M, Obayashi H, Ohta M, Uchiyama T, Hao Q, et al. (1995) No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan. Neurology 45: 1333-1334.
-
(1995)
Neurology
, vol.45
, pp. 1333-1334
-
-
Nishimura, M.1
Obayashi, H.2
Ohta, M.3
Uchiyama, T.4
Hao, Q.5
-
16
-
-
0030640474
-
Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis
-
Kalman B, Rodriguez-Valdez JL, Bosch U, Lublin FD (1997) Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis. Mult Scler 2: 279-282.
-
(1997)
Mult Scler
, vol.2
, pp. 279-282
-
-
Kalman, B.1
Rodriguez-Valdez, J.L.2
Bosch, U.3
Lublin, F.D.4
-
17
-
-
0032897253
-
Large scale screening of die mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians
-
Kalman B, Li S, Chatterjee D, O'Connor J, Voehl MR, et al. (1999) Large scale screening of die mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians. Acta Neurol Scand 99: 16-25.
-
(1999)
Acta Neurol Scand
, vol.99
, pp. 16-25
-
-
Kalman, B.1
Li, S.2
Chatterjee, D.3
O'Connor, J.4
Voehl, M.R.5
-
18
-
-
4444369952
-
Mitochondrial haplogroups in Basque multiple sclerosis patients
-
Otaegui D, Saenz A, Martinez-Zabaleta M, Villoslada P, Fernandez-Manchola I, et al. (2004) Mitochondrial haplogroups in Basque multiple sclerosis patients. Mult Scler 10: 532-535.
-
(2004)
Mult Scler
, vol.10
, pp. 532-535
-
-
Otaegui, D.1
Saenz, A.2
Martinez-Zabaleta, M.3
Villoslada, P.4
Fernandez-Manchola, I.5
-
19
-
-
33846170890
-
Mitochonchrial DNA variants in Bulgarian patients affected by multiple sclerosis
-
Mihailova SM, Ivanova MI, Quin LM, Naumova EJ (2007) Mitochonchrial DNA variants in Bulgarian patients affected by multiple sclerosis. Eur J Neurol 14: 44-47.
-
(2007)
Eur J Neurol
, vol.14
, pp. 44-47
-
-
Mihailova, S.M.1
Ivanova, M.I.2
Quin, L.M.3
Naumova, E.J.4
-
20
-
-
10644221868
-
Genetic variants of Complex I in multiple sclerosis
-
Vyshkina T, Banisor I, Shugart YY, Leist TP, Kalman B (2005) Genetic variants of Complex I in multiple sclerosis. J Neurol Sci 228: 55-64.
-
(2005)
J Neurol Sci
, vol.228
, pp. 55-64
-
-
Vyshkina, T.1
Banisor, I.2
Shugart, Y.Y.3
Leist, T.P.4
Kalman, B.5
-
21
-
-
28044433209
-
-
Houshmand M, Sanati MH, Babrzadeh F, Ardalan A,Teimori M, et al. (2005) Population screening for association of mitochondrial haplogroups BM,J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients. Mult Scler 11: 728-730.
-
Houshmand M, Sanati MH, Babrzadeh F, Ardalan A,Teimori M, et al. (2005) Population screening for association of mitochondrial haplogroups BM,J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients. Mult Scler 11: 728-730.
-
-
-
-
22
-
-
0029759665
-
Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement
-
Mayr-Wohlfart U, Paulus C, Henneberg A, Rodel G (1996) Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement. Acta Neurol Scand 94: 167-171.
-
(1996)
Acta Neurol Scand
, vol.94
, pp. 167-171
-
-
Mayr-Wohlfart, U.1
Paulus, C.2
Henneberg, A.3
Rodel, G.4
-
23
-
-
0020686503
-
New diagnostic criteria for multiple sclerosis: Guidelines for research protocols
-
Poser CM, Paty DW, Scheinberg L, McDonald WI, Davis FA, et al. (1983) New diagnostic criteria for multiple sclerosis: guidelines for research protocols. Ann Neurol 13: 227-231.
-
(1983)
Ann Neurol
, vol.13
, pp. 227-231
-
-
Poser, C.M.1
Paty, D.W.2
Scheinberg, L.3
McDonald, W.I.4
Davis, F.A.5
-
24
-
-
0035432034
-
The determination or 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 or complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations. Nucleic Acids Res 29: E74-74.
-
(2001)
Nucleic Acids Res
, vol.29
-
-
Taylor, R.W.1
Taylor, G.A.2
Durham, S.E.3
Turnbull, D.M.4
-
25
-
-
0032868141
-
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
-
Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, et al. (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
-
26
-
-
0030468182
-
Classification of European mtDNAs from an analysis or three European populations
-
Torroni A, Huoponen K, Francalacci P, Petrozzi M, Morelli L, et al. (1996) Classification of European mtDNAs from an analysis or three European populations. Genetics 144: 1835-1850.
-
(1996)
Genetics
, vol.144
, pp. 1835-1850
-
-
Torroni, A.1
Huoponen, K.2
Francalacci, P.3
Petrozzi, M.4
Morelli, L.5
-
27
-
-
0033940855
-
Geographic patterns of mtDNA diversity in Europe
-
Simoni L, Calafell F, Pettener D, Bertranpetit J, Barbujani G (2000) Geographic patterns of mtDNA diversity in Europe. Am J Hum Genet 66: 262-278.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 262-278
-
-
Simoni, L.1
Calafell, F.2
Pettener, D.3
Bertranpetit, J.4
Barbujani, G.5
-
28
-
-
0033764821
-
Tracing European founder lineages in the Near Eastern mtDNA pool
-
Richards M, Macaulay V, Hickey E, Vega E, Sykes B, et al. (2000) Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet 67: 1251-1276.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1251-1276
-
-
Richards, M.1
Macaulay, V.2
Hickey, E.3
Vega, E.4
Sykes, B.5
-
29
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
Dudbridge F (2003) Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 25: 115-121.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 115-121
-
-
Dudbridge, F.1
-
30
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE (1998) PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 63: 259-266.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
31
-
-
24044550689
-
PEDSTATS: Descriptive statistics, graphics and quality assessment for gene mapping data
-
Wigginton JE, Abecasis GR (2005) PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data. Bioinformatics 21: 3415-3447.
-
(2005)
Bioinformatics
, vol.21
, pp. 3415-3447
-
-
Wigginton, J.E.1
Abecasis, G.R.2
-
32
-
-
33645474357
-
The power to detect disease associations with mitochondrial DNA haplogroups
-
Samuels DC, Carothers AD, Horton R, Chinnery PF (2006) The power to detect disease associations with mitochondrial DNA haplogroups. Am J Hum Genet 78: 713-720.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 713-720
-
-
Samuels, D.C.1
Carothers, A.D.2
Horton, R.3
Chinnery, P.F.4
-
33
-
-
0030056515
-
Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase
-
Pitkanen S, Robinson BH (1996) Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase. J Clin Invest 98: 345-351.
-
(1996)
J Clin Invest
, vol.98
, pp. 345-351
-
-
Pitkanen, S.1
Robinson, B.H.2
-
34
-
-
1642382090
-
Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency
-
Ugalde C, Janssen RJ, van den Heuvel LP, Smeitink JA, Nijtmans LG (2004) Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency. Hum Mol Genet 13: 659-667.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 659-667
-
-
Ugalde, C.1
Janssen, R.J.2
van den Heuvel, L.P.3
Smeitink, J.A.4
Nijtmans, L.G.5
-
35
-
-
34248140693
-
Novel role for mitochondria: Protein kinase Ctheta-dependent oxidative signaling organelles in activation-induced T-cell death
-
Kaminski M, Kiessling M, Suss D, Krammer PH, Gulow K (2007) Novel role for mitochondria: protein kinase Ctheta-dependent oxidative signaling organelles in activation-induced T-cell death. Mol Cell Biol 27: 3625-3639.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 3625-3639
-
-
Kaminski, M.1
Kiessling, M.2
Suss, D.3
Krammer, P.H.4
Gulow, K.5
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