-
1
-
-
0019423856
-
Sequence organisation of the human mitochondrial genome
-
Anderson, S., Bankier, A.T., Barrell, B.G., de Bruijn, M.H.L., Coulson, A.R., Drouin, J., Eperon, I.C., Nierlich, D.P., Roe, B.A., Sanger, F., Schreier, P.H., Smith, A.J.H., Staden, R., and Young, I.G. (1981). Sequence organisation 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.L.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.H.12
Staden, R.13
Young, I.G.14
-
2
-
-
0031036896
-
Apoptosis and autophagy in nigral neurons of patients with Parkinson's disease
-
Anglade, P., Vyas, S., Javoy Agid, F., Herrero, M.T., Michel, P.P., Marquez, J., Mouatt Prigent, A., Ruberg, M., Hirsch, E.C., and Agid, Y. (1997). Apoptosis and autophagy in nigral neurons of patients with Parkinson's disease. Histol. Histopathol. 12, 25-31.
-
(1997)
Histol. Histopathol.
, vol.12
, pp. 25-31
-
-
Anglade, P.1
Vyas, S.2
Javoy Agid, F.3
Herrero, M.T.4
Michel, P.P.5
Marquez, J.6
Mouatt Prigent, A.7
Ruberg, M.8
Hirsch, E.C.9
Agid, Y.10
-
3
-
-
0031930771
-
Glial pathology but absence of apoptotic nigral neurons in long-standing Parkinson's disease
-
Banati, R.B., Daniel, S.E., and Blunt, S.B. (1998). Glial pathology but absence of apoptotic nigral neurons in long-standing Parkinson's disease. Mov. Disord. 13, 221-227.
-
(1998)
Mov. Disord.
, vol.13
, pp. 221-227
-
-
Banati, R.B.1
Daniel, S.E.2
Blunt, S.B.3
-
4
-
-
0027750939
-
Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes
-
Benecke, R., Strümper, P., and Weiss, H. (1993). Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes. Brain 116, 1451-1463.
-
(1993)
Brain
, vol.116
, pp. 1451-1463
-
-
Benecke, R.1
Strümper, P.2
Weiss, H.3
-
5
-
-
0025831821
-
Respiratory chain abnormalities in skeletal muscle from patients with Parkinson's disease
-
Bindoff, L.A., Birch Machin, M.A., Cartlidge, N.E., Parker, W.D., Jr., and Turnbull, D.M. (1991). Respiratory chain abnormalities in skeletal muscle from patients with Parkinson's disease. J. Neurol. Sci. 104, 203-208.
-
(1991)
J. Neurol. Sci.
, vol.104
, pp. 203-208
-
-
Bindoff, L.A.1
Birch Machin, M.A.2
Cartlidge, N.E.3
Parker W.D., Jr.4
Turnbull, D.M.5
-
6
-
-
0030066069
-
Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patients
-
Brown, M.D., Shoffner, J.M., Kim, Y.L., Jum, A.S., Graham, B.H., Cabell, M.F., Gurley, D.S., and Wallace, D.C. (1996). Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patients. Am. J. Med. Genet. 61, 283-289.
-
(1996)
Am. J. Med. Genet.
, vol.61
, pp. 283-289
-
-
Brown, M.D.1
Shoffner, J.M.2
Kim, Y.L.3
Jum, A.S.4
Graham, B.H.5
Cabell, M.F.6
Gurley, D.S.7
Wallace, D.C.8
-
7
-
-
0029040355
-
In situ evidence for DNA fragmentation in Huntington's disease striatum and Alzheimer's disease temporal lobes
-
Dragunow, M., Faull, R.L.M., Lawlor, P., Beilharz, E.J., Singleton, K., Walker, E.B., and Mee, E. (1995). In situ evidence for DNA fragmentation in Huntington's disease striatum and Alzheimer's disease temporal lobes. Neuroreport 6, 1053-1057.
-
(1995)
Neuroreport
, vol.6
, pp. 1053-1057
-
-
Dragunow, M.1
Faull, R.L.M.2
Lawlor, P.3
Beilharz, E.J.4
Singleton, K.5
Walker, E.B.6
Mee, E.7
-
8
-
-
0026758793
-
Localization of the human 75-kDal Fe-S protein of NADH-coenzyme Q reductase gene (NDUPS1) to 2q33→q34
-
Duncan, A.M.V., Chow, W., Robinson, B.H. (1992). Localization of the human 75-kDal Fe-S protein of NADH-coenzyme Q reductase gene (NDUPS1) to 2q33→q34. Cytogenet. Cell. Genet. 60, 212-213.
-
(1992)
Cytogenet. Cell. Genet.
, vol.60
, pp. 212-213
-
-
Duncan, A.M.V.1
Chow, W.2
Robinson, B.H.3
-
9
-
-
0030811838
-
Association of the mitochondrial tRNA-(A4336G) mutation with Alzheimer's and Parkinson's diseases
-
Egensperger, R., Kösel, S., Schnopp, N.M., Mehraein, P., and Graeber, M.B. (1997). Association of the mitochondrial tRNA-(A4336G) mutation with Alzheimer's and Parkinson's diseases. Neuropathol. Appl. Neurobiol. 23, 315-321.
-
(1997)
Neuropathol. Appl. Neurobiol.
, vol.23
, pp. 315-321
-
-
Egensperger, R.1
Kösel, S.2
Schnopp, N.M.3
Mehraein, P.4
Graeber, M.B.5
-
10
-
-
0032819663
-
Nigral neurons are likely to die of a mechanism other than classical apoptosis in Parkinson's disease
-
in press
-
Graeber, M.B., Grasbon-Frodl, E., Abell-Aleff, P., and Kösel, S. (1999). Nigral neurons are likely to die of a mechanism other than classical apoptosis in Parkinson's disease. In: Parkinsonism and Related Disorders, in press.
-
(1999)
Parkinsonism and Related Disorders
-
-
Graeber, M.B.1
Grasbon-Frodl, E.2
Abell-Aleff, P.3
Kösel, S.4
-
11
-
-
0032937713
-
Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease
-
Grasbon-Frodl, E.M., Kösel, S., Sprinzl, M., von Eitzen, U., Mehraein, P., and Graeber, M.B. (1999). Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease. Neurogenetics 2, 121-127.
-
(1999)
Neurogenetics
, vol.2
, pp. 121-127
-
-
Grasbon-Frodl, E.M.1
Kösel, S.2
Sprinzl, M.3
Von Eitzen, U.4
Mehraein, P.5
Graeber, M.B.6
-
12
-
-
0031859395
-
Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease
-
Gu, M., Cooper, J.M., Taanman, J.W., and Schapira, A.H.V. (1998). Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease. Ann. Neurol. 44, 177-186.
-
(1998)
Ann. Neurol.
, vol.44
, pp. 177-186
-
-
Gu, M.1
Cooper, J.M.2
Taanman, J.W.3
Schapira, A.H.V.4
-
13
-
-
0027435899
-
Iron induced oxidative stress and mitochondrial dysfunction: Relevance to Parkinson's disease
-
Hartley, A., Cooper, J.M., and Schapira, A.H.V. (1993). Iron induced oxidative stress and mitochondrial dysfunction: relevance to Parkinson's disease. Brain Res. 627, 349-353.
-
(1993)
Brain Res.
, vol.627
, pp. 349-353
-
-
Hartley, A.1
Cooper, J.M.2
Schapira, A.H.V.3
-
14
-
-
0032054295
-
Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease
-
Hattori, N., Yoshino, H., Tanaka, M., Suzuki, H., and Mizuno, Y. (1998). Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease. Genomics 49, 52-58.
-
(1998)
Genomics
, vol.49
, pp. 52-58
-
-
Hattori, N.1
Yoshino, H.2
Tanaka, M.3
Suzuki, H.4
Mizuno, Y.5
-
15
-
-
0030698810
-
The apoptosis-necrosis paradox. Apoptogenetic proteases activated after mitochondrial permeability transition determine the mode of cell death
-
Hirsch, T., Marchetti, P., Susin, S.A., Dallaporta, B., Zamzami, N., Marzo, I., Geuskens, M., and Kroemer, G. (1997). The apoptosis-necrosis paradox. Apoptogenetic proteases activated after mitochondrial permeability transition determine the mode of cell death. Oncogene 15, 1573-1581.
-
(1997)
Oncogene
, vol.15
, pp. 1573-1581
-
-
Hirsch, T.1
Marchetti, P.2
Susin, S.A.3
Dallaporta, B.4
Zamzami, N.5
Marzo, I.6
Geuskens, M.7
Kroemer, G.8
-
16
-
-
0028854722
-
Point mutations of mitochondrial genome in Parkinson's disease
-
Ikebe, S., Tanaka, M., and Ozawa, T. (1995). Point mutations of mitochondrial genome in Parkinson's disease. Mol. Brain Res. 28, 281-295.
-
(1995)
Mol. Brain Res.
, vol.28
, pp. 281-295
-
-
Ikebe, S.1
Tanaka, M.2
Ozawa, T.3
-
17
-
-
0028316759
-
Unaltered aconitase activity, but decreased complex I activity in Substantia nigra pars compacta of patients with Parkinson's disease
-
Janetzky, B., Hauck, S., Youdim, M.B.H., Riederer, P., Jellinger, K., Pantucek, F., Zöchling, R., Boissl, K.W., and Reichmann, H. (1994). Unaltered aconitase activity, but decreased complex I activity in Substantia nigra pars compacta of patients with Parkinson's disease. Neurosci. Lett. 169, 126-128.
-
(1994)
Neurosci. Lett.
, vol.169
, pp. 126-128
-
-
Janetzky, B.1
Hauck, S.2
Youdim, M.B.H.3
Riederer, P.4
Jellinger, K.5
Pantucek, F.6
Zöchling, R.7
Boissl, K.W.8
Reichmann, H.9
-
18
-
-
0031401865
-
Cloning of the human cDNA sequence encoding the NADH:ubiquinone oxidoreductase MLRQ subunit
-
Kim, J.W., Lee, Y., Kang, H.B., Chose, Y.K., Chung, T.W., Chang, S.Y., Lee, K.S., Choe, I.S. (1997). Cloning of the human cDNA sequence encoding the NADH:ubiquinone oxidoreductase MLRQ subunit. Biochem. Mol. Biol. Int.43, 669-675.
-
(1997)
Biochem. Mol. Biol. Int.
, vol.43
, pp. 669-675
-
-
Kim, J.W.1
Lee, Y.2
Kang, H.B.3
Chose, Y.K.4
Chung, T.W.5
Chang, S.Y.6
Lee, K.S.7
Choe, I.S.8
-
19
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenileparkinsonism
-
Kitada, T., Asakawa, S., Hattori, N., Matsumine, H., Yamamura, Y., Minoshima, S., Yokochi, M., Mizuno, Y., and Shimizu, N. (1998). Mutations in the parkin gene cause autosomal recessive juvenileparkinsonism. Nature 392, 605-608.
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
Minoshima, S.6
Yokochi, M.7
Mizuno, Y.8
Shimizu, N.9
-
20
-
-
0030931581
-
The common deletion in not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction
-
Kösel, S., Egensperger, R., Schnopp, N.M., and Graeber, M.B. (1997a). The common deletion in not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction. Movement Disorders 12, 639-645.
-
(1997)
Movement Disorders
, vol.12
, pp. 639-645
-
-
Kösel, S.1
Egensperger, R.2
Schnopp, N.M.3
Graeber, M.B.4
-
21
-
-
1842297607
-
On the question of apoptosis in the parkinsonian substantia nigra
-
Kösel, S., Egensperger, R., von Eitzen, U., Mehraein, P., and Graeber, M.B. (1997b). On the question of apoptosis in the parkinsonian substantia nigra. Acta Neuropathol. 93, 105-108.
-
(1997)
Acta Neuropathol.
, vol.93
, pp. 105-108
-
-
Kösel, S.1
Egensperger, R.2
Von Eitzen, U.3
Mehraein, P.4
Graeber, M.B.5
-
22
-
-
0032008669
-
Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease
-
Kösel, S., Grasbon-Frodl, E.M., Mautsch, U., Egensperger, R., von Eitzen, U., Frishman, D., Hofmann, S., Gerbitz, K.-D., Mehraein, P., and Graeber, M.B. (1998). Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease. Neurogenetics 1, 197-204.
-
(1998)
Neurogenetics
, vol.1
, pp. 197-204
-
-
Kösel, S.1
Grasbon-Frodl, E.M.2
Mautsch, U.3
Egensperger, R.4
Von Eitzen, U.5
Frishman, D.6
Hofmann, S.7
Gerbitz, K.-D.8
Mehraein, P.9
Graeber, M.B.10
-
23
-
-
0026484964
-
Platelet mitochondrial function in Parkinson's disease
-
Krige, D., Carroll, M.T., Cooper, J.M., Marsden, C.D., and Schapira, A.H. (1992). Platelet mitochondrial function in Parkinson's disease. Ann. Neurol. 32, 782-788.
-
(1992)
Ann. Neurol.
, vol.32
, pp. 782-788
-
-
Krige, D.1
Carroll, M.T.2
Cooper, J.M.3
Marsden, C.D.4
Schapira, A.H.5
-
24
-
-
0031990490
-
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
-
Krüger, R., Kühn, W., Müller, T., Woitalla, D., Graeber, M., Kösel, S., Przuntek, H., Epplen, J.T., Schols, L., and Riess, O. (1998). Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. Nature Genet. 18, 106-108.
-
(1998)
Nature Genet.
, vol.18
, pp. 106-108
-
-
Krüger, R.1
Kühn, W.2
Müller, T.3
Woitalla, D.4
Graeber, M.5
Kösel, S.6
Przuntek, H.7
Epplen, J.T.8
Schols, L.9
Riess, O.10
-
25
-
-
0020680904
-
Chronic parkinsonism in humans due to a product of meperidine-analog synthesis
-
Langston, J.W., Ballard, P., Tetrud, J.W., and Irwin, I. (1983). Chronic parkinsonism in humans due to a product of meperidine-analog synthesis. Anal. Biochem. 219, 979-980.
-
(1983)
Anal. Biochem.
, vol.219
, pp. 979-980
-
-
Langston, J.W.1
Ballard, P.2
Tetrud, J.W.3
Irwin, I.4
-
26
-
-
0032504568
-
The mitochondrial permeability transition in cell death: A common mechanism in necrosis, apoptosis and autophagy
-
Lemasters, J.J., Nieminen, A.L., Quian, T., Trost, L.C., Elmore, S.P., Nishimura, Y., Crowe, R.A., Cascio, W.E., Bradham, C.A., Brenner, D.A., and Herman, B. (1998). The mitochondrial permeability transition in cell death: a common mechanism in necrosis, apoptosis and autophagy. Biochim. Biophys. Acta 1366, 177-196.
-
(1998)
Biochim. Biophys. Acta
, vol.1366
, pp. 177-196
-
-
Lemasters, J.J.1
Nieminen, A.L.2
Quian, T.3
Trost, L.C.4
Elmore, S.P.5
Nishimura, Y.6
Crowe, R.A.7
Cascio, W.E.8
Bradham, C.A.9
Brenner, D.A.10
Herman, B.11
-
27
-
-
0032190090
-
The ubiquitin pathway in Parkinson's disease
-
Leroy, E., Boyer, R., Auburger, G., Leube, B., Ulm, G., Mezey, E., Harta, G., Brownstein, M.J., Jonnalagada, S., Chernova, T., Dehejia, A., Lavedan, C., Gasser, T., Steinbach, P.J., Wilkinson, K.D., and Polymeropoulos, M.H. (1998). The ubiquitin pathway in Parkinson's disease. Nature 395, 451-452.
-
(1998)
Nature
, vol.395
, pp. 451-452
-
-
Leroy, E.1
Boyer, R.2
Auburger, G.3
Leube, B.4
Ulm, G.5
Mezey, E.6
Harta, G.7
Brownstein, M.J.8
Jonnalagada, S.9
Chernova, T.10
Dehejia, A.11
Lavedan, C.12
Gasser, T.13
Steinbach, P.J.14
Wilkinson, K.D.15
Polymeropoulos, M.H.16
-
28
-
-
0025047351
-
Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defect
-
Lestienne, P., Nelson, J., Riederer, P., Jellinger, K., and Reichmann, H. (1990). Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defect. J. Neurochem. 55, 1810-1812.
-
(1990)
J. Neurochem.
, vol.55
, pp. 1810-1812
-
-
Lestienne, P.1
Nelson, J.2
Riederer, P.3
Jellinger, K.4
Reichmann, H.5
-
29
-
-
0032564235
-
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on genetic susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group
-
Lucking, C.B., Abbas, N., Durr, A., Bonifati, V., Bonnet, A.M., de Broucker, T., De Michele, G., Wood, N.W., Agid, Y., and Brice, A. (1998). Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on genetic susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group. Lancet 352, 1355-1356.
-
(1998)
Lancet
, vol.352
, pp. 1355-1356
-
-
Lucking, C.B.1
Abbas, N.2
Durr, A.3
Bonifati, V.4
Bonnet, A.M.5
De Broucker, T.6
De Michele, G.7
Wood, N.W.8
Agid, Y.9
Brice, A.10
-
30
-
-
0026548217
-
Quantitation of mitochondrial DNA deletion in Parkinson's disease
-
Mann, V.M., Cooper, J.M., and Schapira, A.H.V. (1992). Quantitation of mitochondrial DNA deletion in Parkinson's disease. FEBS Lett. 299, 218-222.
-
(1992)
FEBS Lett.
, vol.299
, pp. 218-222
-
-
Mann, V.M.1
Cooper, J.M.2
Schapira, A.H.V.3
-
31
-
-
0030070870
-
Effects of isoquinoline derivates structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) on mitochondrial respiration
-
McNaught, K.S., Thull, U., Carrupt, P.A., Altomare, C., Cellamare, S., Carotti, A., Testa, B., Jenner, P., and Marsden, C.D. (1996). Effects of isoquinoline derivates structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) on mitochondrial respiration. Biochem. Pharmacol. 51, 1503-1511.
-
(1996)
Biochem. Pharmacol.
, vol.51
, pp. 1503-1511
-
-
McNaught, K.S.1
Thull, U.2
Carrupt, P.A.3
Altomare, C.4
Cellamare, S.5
Carotti, A.6
Testa, B.7
Jenner, P.8
Marsden, C.D.9
-
32
-
-
0024330311
-
Deficiencies in complex I subunits of the respiratory chain in Parkinson's disease
-
Mizuno, Y., Ohta, S. Tanaka, M., Takamiya, S., Suzuki, K., Sato, T., Oya, H., Ozawa, T., and Kagawa, Y. (1989). Deficiencies in complex I subunits of the respiratory chain in Parkinson's disease. Biochem. Biophys. Res. Commun. 163, 1450-1455.
-
(1989)
Biochem. Biophys. Res. Commun.
, vol.163
, pp. 1450-1455
-
-
Mizuno, Y.1
Ohta, S.2
Tanaka, M.3
Takamiya, S.4
Suzuki, K.5
Sato, T.6
Oya, H.7
Ozawa, T.8
Kagawa, Y.9
-
33
-
-
0029942337
-
Histochemical detection of apoptosis in Parkinson's disease
-
Mochizuki, H., Goto, K., Mori, H., and Mizuno, Y. (1996). Histochemical detection of apoptosis in Parkinson's disease. J. Neurol. Sci. 137, 120-123.
-
(1996)
J. Neurol. Sci.
, vol.137
, pp. 120-123
-
-
Mochizuki, H.1
Goto, K.2
Mori, H.3
Mizuno, Y.4
-
34
-
-
0025149002
-
Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by kinetic PCR analysis
-
Ozawa, T., Tanaka, M., Ikebe, S., Ohno, K., Kondo, T., and Mizuno, Y. (1990). Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by kinetic PCR analysis. Biochem. Biophys. Res. Commun. 172, 483-489.
-
(1990)
Biochem. Biophys. Res. Commun.
, vol.172
, pp. 483-489
-
-
Ozawa, T.1
Tanaka, M.2
Ikebe, S.3
Ohno, K.4
Kondo, T.5
Mizuno, Y.6
-
35
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos, M.H., Lavedan, C., Leroy, E., Ide, S.E., Dehejia, A., Dutra, A., Pike, B., Root, H., Rubenstein, J., Boyer, R., Stenroos, E.S., Chandrasekharappa, S., Athanassiadou, A., Papapetropoulos, T., Johnson, W.G., Lazzarini, A.M., Duvoisin, R.C., Diiorio, G., Golbe, L.I., and Nussbaum, R.L. (1997). Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 276, 2045-2047.
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
Pike, B.7
Root, H.8
Rubenstein, J.9
Boyer, R.10
Stenroos, E.S.11
Chandrasekharappa, S.12
Athanassiadou, A.13
Papapetropoulos, T.14
Johnson, W.G.15
Lazzarini, A.M.16
Duvoisin, R.C.17
Diiorio, G.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
36
-
-
0030631582
-
Cloning of the human NADH: Ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15
-
Russell, M.W., du Manoir, S., Collins, F.S., Brody, L.C. (1997). Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15. Mamm. Genome 8, 60-61.
-
(1997)
Mamm. Genome
, vol.8
, pp. 60-61
-
-
Russell, M.W.1
Du Manoir, S.2
Collins, F.S.3
Brody, L.C.4
-
37
-
-
0024390719
-
Mitochondrial complex I deficiency in Parkinson's disease
-
Schapira, A.H.V., Cooper, J.M., Dexter, D., Jenner, P., Clark, J.B., and Marsden, C.D. (1989). Mitochondrial complex I deficiency in Parkinson's disease. Lancet 1, 1269.
-
(1989)
Lancet
, vol.1
, pp. 1269
-
-
Schapira, A.H.V.1
Cooper, J.M.2
Dexter, D.3
Jenner, P.4
Clark, J.B.5
Marsden, C.D.6
-
38
-
-
0025640845
-
Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease
-
Schapira, A.H.V., Mann, V.M., Cooper, J.M., Dexter, D., Daniel, S.E., Jenner, P., Clark, J.B., and Marsden, C.D. (1990). Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease. J. Neurochem. 55, 2142-2145.
-
(1990)
J. Neurochem.
, vol.55
, pp. 2142-2145
-
-
Schapira, A.H.V.1
Mann, V.M.2
Cooper, J.M.3
Dexter, D.4
Daniel, S.E.5
Jenner, P.6
Clark, J.B.7
Marsden, C.D.8
-
39
-
-
0027200741
-
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
-
Shoffner, J.M., Brown, M.D., Torrini, A., Lott, M.T., Cabell, M.F., Mirra, S.S., Beal, M.F., Yang, C.-C., Gearing, M., Salvo, R., Watts, R.L., Juncos, J.L., Hansen, L.A., Crain, B.J., Fayed, M., Reckord, C.L., and Wallace, D.C. (1993). Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. Genomics 17, 171-184.
-
(1993)
Genomics
, vol.17
, pp. 171-184
-
-
Shoffner, J.M.1
Brown, M.D.2
Torrini, A.3
Lott, M.T.4
Cabell, M.F.5
Mirra, S.S.6
Beal, M.F.7
Yang, C.-C.8
Gearing, M.9
Salvo, R.10
Watts, R.L.11
Juncos, J.L.12
Hansen, L.A.13
Crain, B.J.14
Fayed, M.15
Reckord, C.L.16
Wallace, D.C.17
-
40
-
-
0028075410
-
Alterations in glutathione levels in Parkinson's disease and other neurodegenerative disorders affecting basal ganglia
-
Sian, J., Dexter, D.T., Lees, A.J., Daniel, S., Agid, Y., Javoy Agid, F., Jenner, P., and Marsden, C.D. (1994). Alterations in glutathione levels in Parkinson's disease and other neurodegenerative disorders affecting basal ganglia. Ann. Neurol. 36, 348-355.
-
(1994)
Ann. Neurol.
, vol.36
, pp. 348-355
-
-
Sian, J.1
Dexter, D.T.2
Lees, A.J.3
Daniel, S.4
Agid, Y.5
Javoy Agid, F.6
Jenner, P.7
Marsden, C.D.8
-
41
-
-
0032504575
-
Mitochondria as regulators of apoptosis: Doubt no more
-
Susin, S.A., Zamzami, N., and Kroemer, G. (1998). Mitochondria as regulators of apoptosis: doubt no more. Biochim. Biophys. Acta 1366, 151-165.
-
(1998)
Biochim. Biophys. Acta
, vol.1366
, pp. 151-165
-
-
Susin, S.A.1
Zamzami, N.2
Kroemer, G.3
-
42
-
-
0029908226
-
Origin and functional consequences of the complex I defect in Parkinson's disease
-
Swerdlow, R.H., Parks, J.K., Miller, S.W., Tuttle, J.B., Trimmer, P.A., Sheehan, J.P., Bennett, J.P., Davis, R.E., and Parker, W.D. (1996). Origin and functional consequences of the complex I defect in Parkinson's disease. Ann. Neurol. 40, 663-671.
-
(1996)
Ann. Neurol.
, vol.40
, pp. 663-671
-
-
Swerdlow, R.H.1
Parks, J.K.2
Miller, S.W.3
Tuttle, J.B.4
Trimmer, P.A.5
Sheehan, J.P.6
Bennett, J.P.7
Davis, R.E.8
Parker, W.D.9
-
43
-
-
0031792679
-
Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family
-
Swerdlow, R.H., Parks, J.K., Davis, J.N., Cassarino, D.S., Trimmer, P.A., Currie, L.J., Dougherty, J., Bridges, W.S., Bennett, J.P., Wooten, G.F., and Parker, W.D. (1998). Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family. Ann. Neurol. 44, 873-881.
-
(1998)
Ann. Neurol.
, vol.44
, pp. 873-881
-
-
Swerdlow, R.H.1
Parks, J.K.2
Davis, J.N.3
Cassarino, D.S.4
Trimmer, P.A.5
Currie, L.J.6
Dougherty, J.7
Bridges, W.S.8
Bennett, J.P.9
Wooten, G.F.10
Parker, W.D.11
-
44
-
-
0031857366
-
Mitochondrial-DNA in focal dystonia - A cybrid analysis
-
Tabrizi, S.J., Cooper, J.M., and Schapira, A.H.V. (1998). Mitochondrial-DNA in focal dystonia - a cybrid analysis. Ann. Neurol. 44, 258-261.
-
(1998)
Ann. Neurol.
, vol.44
, pp. 258-261
-
-
Tabrizi, S.J.1
Cooper, J.M.2
Schapira, A.H.V.3
-
45
-
-
0031013141
-
Apoptotic-like changes in Lewy-body-associated disorders and normal aging in substantia nigra neurons
-
Tompkins, M.M., Basgall, E.J., Zamrini, E., and Hill, W.D. (1997). Apoptotic-like changes in Lewy-body-associated disorders and normal aging in substantia nigra neurons. Am. J. Pathol. 150, 119-131.
-
(1997)
Am. J. Pathol.
, vol.150
, pp. 119-131
-
-
Tompkins, M.M.1
Basgall, E.J.2
Zamrini, E.3
Hill, W.D.4
-
46
-
-
0033546640
-
Parkinson disease in twins: A follow-up study
-
in press
-
Vieregge, P., Hagenah, J., Heberlein, I., Klein, C., and Ludin, H.-P. (1999). Parkinson disease in twins: A follow-up study. Neurology, in press.
-
(1999)
Neurology
-
-
Vieregge, P.1
Hagenah, J.2
Heberlein, I.3
Klein, C.4
Ludin, H.-P.5
-
47
-
-
0026624980
-
Diseases of the mitochondrial DNA
-
Wallace, D.C. (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
-
48
-
-
1842335744
-
Maternal inheritance in Parkinson's disease
-
Wooten, G.F., Currie, L.J., Bennett, J.P., Harrison, M.B., Trugman, J.M., and Parker, W.D. (1997). Maternal inheritance in Parkinson's disease. Ann. Neurol. 41, 265-268.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 265-268
-
-
Wooten, G.F.1
Currie, L.J.2
Bennett, J.P.3
Harrison, M.B.4
Trugman, J.M.5
Parker, W.D.6
|