-
1
-
-
0032497504
-
Parkinson's disease. First of two parts
-
Lang, A.E. and Lozano, A.M. (1998) Parkinson's disease. First of two parts. N. Engl. J. Med., 339, 1044-1053.
-
(1998)
N. Engl. J. Med.
, vol.339
, pp. 1044-1053
-
-
Lang, A.E.1
Lozano, A.M.2
-
2
-
-
0032531924
-
Parkinson's disease. Second of two parts
-
Lang, A.E. and Lozano, A.M. (1998) Parkinson's disease. Second of two parts. N. Engl. J. Med., 339, 1130-1143.
-
(1998)
N. Engl. J. Med.
, vol.339
, pp. 1130-1143
-
-
Lang, A.E.1
Lozano, A.M.2
-
3
-
-
0036100742
-
Environment, mitochondria, and Parkinson's disease
-
Sherer, T.B., Betarbet, R. and Greenamyre, J.T. (2002) Environment, mitochondria, and Parkinson's disease. Neuroscientist, 8, 192-197.
-
(2002)
Neuroscientist
, vol.8
, pp. 192-197
-
-
Sherer, T.B.1
Betarbet, R.2
Greenamyre, J.T.3
-
4
-
-
0031684326
-
Mitochondria in the etiology and pathogenesis of Parkinson's disease
-
Schapira, A.H., Go, M., Taanman, J.W., Tabrizi, S.J., Seaton, T., Cleeter, M. and Cooper, J.M. (1998) Mitochondria in the etiology and pathogenesis of Parkinson's disease. Ann. Neurol., 44, S89-S98.
-
(1998)
Ann. Neurol.
, vol.44
-
-
Schapira, A.H.1
Go, M.2
Taanman, J.W.3
Tabrizi, S.J.4
Seaton, T.5
Cleeter, M.6
Cooper, J.M.7
-
5
-
-
0036182026
-
Mitochondrial involvement in Parkinson's disease
-
Orth, M. and Schapira, A.H. (2002) Mitochondrial involvement in Parkinson's disease. Neurochem. Int., 40, 533-541.
-
(2002)
Neurochem. Int.
, vol.40
, pp. 533-541
-
-
Orth, M.1
Schapira, A.H.2
-
6
-
-
0023924828
-
An electron microscopic study of MPTP-induced inclusion bodies in an old monkey
-
Forno, L.S., Langston, J.W., DeLanney, L.E. and Irwin, I. (1988) An electron microscopic study of MPTP-induced inclusion bodies in an old monkey. Brain Res., 448, 150-157.
-
(1988)
Brain Res.
, vol.448
, pp. 150-157
-
-
Forno, L.S.1
Langston, J.W.2
DeLanney, L.E.3
Irwin, I.4
-
7
-
-
0038205745
-
Targeting programmed cell death in neurodegenerative diseases
-
Vila, M. and Przedborski, S. (2003) Targeting programmed cell death in neurodegenerative diseases. Nat. Rev. Neurosci., 4, 365-375.
-
(2003)
Nat. Rev. Neurosci.
, vol.4
, pp. 365-375
-
-
Vila, M.1
Przedborski, S.2
-
8
-
-
0034671469
-
The nigrostriatal dopaminergic system as a preferential target of repeated exposures to combined paraquat and maneb: Implications for Parkinson's disease
-
Thiruchelvam, M., Richfield, E.K., Baggs, R.B., Tank, A.W. and Cory-Slechta, D.A. (2000) The nigrostriatal dopaminergic system as a preferential target of repeated exposures to combined paraquat and maneb: Implications for Parkinson's disease. J. Neurosci., 20 9207-9214.
-
(2000)
J. Neurosci.
, vol.20
, pp. 9207-9214
-
-
Thiruchelvam, M.1
Richfield, E.K.2
Baggs, R.B.3
Tank, A.W.4
Cory-Slechta, D.A.5
-
9
-
-
0033681149
-
Chronic systemic pesticide exposure reproduces features of Parkinson's disease
-
Betarbet, R., Sherer, T.B., MacKenzie, G., Garcia-Osuna, M., Panov, A.V. and Greenamyre, J.T. (2000) Chronic systemic pesticide exposure reproduces features of Parkinson's disease. Nat. Neurosci., 3 1301-1306.
-
(2000)
Nat. Neurosci.
, vol.3
, pp. 1301-1306
-
-
Betarbet, R.1
Sherer, T.B.2
MacKenzie, G.3
Garcia-Osuna, M.4
Panov, A.V.5
Greenamyre, J.T.6
-
10
-
-
0242363670
-
Molecular pathways of neurodegeneration in Parkinson's disease
-
Dawson, T.M. and Dawson, V.L. (2003) Molecular pathways of neurodegeneration in Parkinson's disease. Science, 302, 819-822.
-
(2003)
Science
, vol.302
, pp. 819-822
-
-
Dawson, T.M.1
Dawson, V.L.2
-
11
-
-
0037240325
-
Rare genetic mutations shed light on the pathogenesis of Parkinson's disease
-
Dawson, T.M. and Dawson, V.L. (2003) Rare genetic mutations shed light on the pathogenesis of Parkinson's disease. J. Clin. Invest., 111, 145-151.
-
(2003)
J. Clin. Invest.
, vol.111
, pp. 145-151
-
-
Dawson, T.M.1
Dawson, V.L.2
-
12
-
-
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. et al. (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
-
13
-
-
0242300619
-
Alpha-Synuclein locus triplication causes Parkinson's disease
-
Singleton, A.B., Farrer, M., Johnson, J., Singleton, A., Hague, S., Kachergus, J., Hulihan, M., Peuralinna, T., Dutra, A., Nussbaum, R. et al. (2003) alpha-Synuclein locus triplication causes Parkinson's disease. Science, 302, 841.
-
(2003)
Science
, vol.302
, pp. 841
-
-
Singleton, A.B.1
Farrer, M.2
Johnson, J.3
Singleton, A.4
Hague, S.5
Kachergus, J.6
Hulihan, M.7
Peuralinna, T.8
Dutra, A.9
Nussbaum, R.10
-
14
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
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 juvenile parkinsonism. 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
-
15
-
-
0037428241
-
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
-
Bonifati, V., Rizzu, P., van Baren, M.J., Schaap, O., Breedveld, G.J., Krieger, E., Dekker, M.C., Squitieri, F., Ibanez, P., Joosse, M. et al. (2003) Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science, 299, 256-259.
-
(2003)
Science
, vol.299
, pp. 256-259
-
-
Bonifati, V.1
Rizzu, P.2
van Baren, M.J.3
Schaap, O.4
Breedveld, G.J.5
Krieger, E.6
Dekker, M.C.7
Squitieri, F.8
Ibanez, P.9
Joosse, M.10
-
16
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
Valente, E.M., Abou-Sleiman, P.M., Caputo, V., Muqit, M.M., Harvey, K., Gispert, S., Ali, Z., Del Turco, D., Bentivoglio, A.R., Mealy, D.G. et al. (2004) Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science, 304, 1158-1160.
-
(2004)
Science
, vol.304
, pp. 1158-1160
-
-
Valente, E.M.1
Abou-Sleiman, P.M.2
Caputo, V.3
Muqit, M.M.4
Harvey, K.5
Gispert, S.6
Ali, Z.7
Del Turco, D.8
Bentivoglio, A.R.9
Mealy, D.G.10
-
17
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
Paisan-Ruiz, C., Jain, S., Evans, E.W., Gilks, W.P., Simon, J., van der Brug, M., de Munain, A.L., Aparicio, S., Gil, A.M., Khan, N. et al. (2004) Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron, 44, 595-600.
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisan-Ruiz, C.1
Jain, S.2
Evans, E.W.3
Gilks, W.P.4
Simon, J.5
van der Brug, M.6
de Munain, A.L.7
Aparicio, S.8
Gil, A.M.9
Khan, N.10
-
18
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
Zimprich, A., Biskup, S., Leitner, P., Lichtner, P., Farrer, M., Lincoln, S., Kachergus, J.. Hulihan, M., Uitti, R.J., Caine, D.B. et al. (2004) Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron, 44, 601-607.
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
Lichtner, P.4
Farrer, M.5
Lincoln, S.6
Kachergus, J.7
Hulihan, M.8
Uitti, R.J.9
Caine, D.B.10
-
19
-
-
0242497815
-
Crystal structures of human DJ-1 and Escherichia coli Hsp31, which share an evolutionarily conserved domain
-
Lee, S.J., Kim, S.J., Kim, I.K., Ko, J., Jeong, C.S., Kim, G.H., Park, C., Kang, S.O., Suh, P.G., Lee, H. S. et al. (2003) Crystal structures of human DJ-1 and Escherichia coli Hsp31, which share an evolutionarily conserved domain. J. Biol. Chem., 278, 44552-44559.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 44552-44559
-
-
Lee, S.J.1
Kim, S.J.2
Kim, I.K.3
Ko, J.4
Jeong, C.S.5
Kim, G.H.6
Park, C.7
Kang, S.O.8
Suh, P.G.9
Lee, H.S.10
-
20
-
-
13944267769
-
DJ-1 is a redox-dependent molecular chaperone that inhibits alpha-Synuclein aggregate formation
-
Shendelman, S., Jonason, A., Martinat, C., Leete, T. and Abeliovich, A. (2004) DJ-1 is a redox-dependent molecular chaperone that inhibits alpha-Synuclein aggregate formation. PLoS Biol., 2, 1764-1773.
-
(2004)
PLoS Biol.
, vol.2
, pp. 1764-1773
-
-
Shendelman, S.1
Jonason, A.2
Martinat, C.3
Leete, T.4
Abeliovich, A.5
-
21
-
-
0042130551
-
The 1.1-A resolution crystal structure of DJ-1, the protein mutated in autosomal recessive early onset Parkinson's disease
-
Wilson, M.A., Collins, J.L., Hod, Y., Ringe, D. and Petsko, G.A. (2003) The 1.1-A resolution crystal structure of DJ-1, the protein mutated in autosomal recessive early onset Parkinson's disease. Proc. Natl Acad. Sci. USA, 100, 9256-9261.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 9256-9261
-
-
Wilson, M.A.1
Collins, J.L.2
Hod, Y.3
Ringe, D.4
Petsko, G.A.5
-
22
-
-
1242274611
-
The 1.8-A resolution crystal structure of YDR533Cp from Saccharomyces cerevisiae: A member of the DJ-1/ThiJ/PfpI superfamily
-
Wilson, M.A., St Amour, C.V., Collins, J.L., Ringe, D. and Petsko, G.A. (2004) The 1.8-A resolution crystal structure of YDR533Cp from Saccharomyces cerevisiae: A member of the DJ-1/ThiJ/PfpI superfamily. Proc. Natl Acad. Sci. USA, 101, 1531-1536.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 1531-1536
-
-
Wilson, M.A.1
St Amour, C.V.2
Collins, J.L.3
Ringe, D.4
Petsko, G.A.5
-
23
-
-
1642527499
-
DJ-1 has a role in antioxidative stress to prevent cell death
-
Taira, T., Saito, Y., Niki, T., Iguchi-Ariga, S.M., Takahashi, K. and Ariga, H. (2004) DJ-1 has a role in antioxidative stress to prevent cell death. EMBO Rep., 5, 213-218.
-
(2004)
EMBO Rep.
, vol.5
, pp. 213-218
-
-
Taira, T.1
Saito, Y.2
Niki, T.3
Iguchi-Ariga, S.M.4
Takahashi, K.5
Ariga, H.6
-
24
-
-
0141704202
-
L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system
-
Miller, D.W., Ahmad, R., Hague, S., Baptista, M.J., Canet-Aviles, R., McLendon, C., Carter, D.M., Zhu, P.P., Stadler, J., Chandran, J. et al. (2003) L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system. J. Biol. Chem., 278, 36588-36595.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 36588-36595
-
-
Miller, D.W.1
Ahmad, R.2
Hague, S.3
Baptista, M.J.4
Canet-Aviles, R.5
McLendon, C.6
Carter, D.M.7
Zhu, P.P.8
Stadler, J.9
Chandran, J.10
-
25
-
-
0242524434
-
The DJ-IL166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexes
-
Macedo, M.G., Anar, B., Bronner, I.F., Cannella, M., Squitieri, F., Bonifati, V., Hoogeveen, A., Heutink, P. and Rizzu, P. (2003) The DJ-IL166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexes. Hum. Mol. Genet., 12, 2807-2816.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2807-2816
-
-
Macedo, M.G.1
Anar, B.2
Bronner, I.F.3
Cannella, M.4
Squitieri, F.5
Bonifati, V.6
Hoogeveen, A.7
Heutink, P.8
Rizzu, P.9
-
26
-
-
1342346572
-
Differential effects of Parkinson's disease-associated mutations on stability and folding of DJ-1
-
Gorner, K., Holtorf, E., Odoy, S., Nuscher, B., Yamamoto, A., Regula, J.T., Beyer, K., Haass, C. and Kahle, P.J. (2004) Differential effects of Parkinson's disease-associated mutations on stability and folding of DJ-1. J. Biol. Chem., 279, 6943-6951.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 6943-6951
-
-
Gorner, K.1
Holtorf, E.2
Odoy, S.3
Nuscher, B.4
Yamamoto, A.5
Regula, J.T.6
Beyer, K.7
Haass, C.8
Kahle, P.J.9
-
27
-
-
1542349213
-
Familial Parkinson's disease-associated L166P mutation disrupts DJ-1 protein folding and function
-
Olzmann, J.A., Brown, K., Wilkinson, K.D., Rees, H.D., Huai, Q., Ke, H., Levey, A.L, Li, L. and Chin, L.S. (2004) Familial Parkinson's disease-associated L166P mutation disrupts DJ-1 protein folding and function. J. Biol. Chem., 279, 8506-8515.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 8506-8515
-
-
Olzmann, J.A.1
Brown, K.2
Wilkinson, K.D.3
Rees, H.D.4
Huai, Q.5
Ke, H.6
Levey, A.L.7
Li, L.8
Chin, L.S.9
-
28
-
-
0346434141
-
A missense mutation (L166P) in DJ-1, linked to familial Parkinson's disease, confers reduced protein stability and impairs homo-oligomerization
-
Moore, D.J., Zhang, L., Dawson, T.M. and Dawson, V.L. (2003) A missense mutation (L166P) in DJ-1, linked to familial Parkinson's disease, confers reduced protein stability and impairs homo-oligomerization. J. Neurochem., 87, 1558-1567.
-
(2003)
J. Neurochem.
, vol.87
, pp. 1558-1567
-
-
Moore, D.J.1
Zhang, L.2
Dawson, T.M.3
Dawson, V.L.4
-
29
-
-
0142217556
-
DJ-1(PARK7), a novel gene for autosomal recessive, early onset Parkinsonism
-
Bonifati, V., Rizzu, P., Squitieri, F., Krieger, E., Vanacore, N., van Swieten, J.C., Brice, A., van Duijn, C.M.. Oostra, B., Meco, G. et al. (2003) DJ-1(PARK7), a novel gene for autosomal recessive, early onset Parkinsonism. Neurol. Sci., 24, 159-160.
-
(2003)
Neurol. Sci.
, vol.24
, pp. 159-160
-
-
Bonifati, V.1
Rizzu, P.2
Squitieri, F.3
Krieger, E.4
Vanacore, N.5
van Swieten, J.C.6
Brice, A.7
van Duijn, C.M.8
Oostra, B.9
Meco, G.10
-
30
-
-
2942684871
-
The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization
-
Canet-Aviles, R.M., Wilson, M.A., Miller, D.W., Ahmad, R., McLendon, C., Bandyopadhyay, S., Baptista, M.J., Ringe, D., Petsko, G.A. and Cookson, M.R. (2004) The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization. Proc. Natl Acad. Sci. USA, 101, 9103-9108.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 9103-9108
-
-
Canet-Aviles, R.M.1
Wilson, M.A.2
Miller, D.W.3
Ahmad, R.4
McLendon, C.5
Bandyopadhyay, S.6
Baptista, M.J.7
Ringe, D.8
Petsko, G.A.9
Cookson, M.R.10
-
31
-
-
0020955120
-
Synapsin I (protein I), a nerve terminal-specific phosphoprotein. III. Its association with synaptic vesicles studied in a highly purified synaptic vesicle preparation
-
Huttner, W.B., Schiebler, W., Greengard, P. and De Camilli, P. (1983) Synapsin I (protein I), a nerve terminal-specific phosphoprotein. III. Its association with synaptic vesicles studied in a highly purified synaptic vesicle preparation. J Cell Biol., 96, 1374-1388.
-
(1983)
J. Cell. Biol.
, vol.96
, pp. 1374-1388
-
-
Huttner, W.B.1
Schiebler, W.2
Greengard, P.3
De Camilli, P.4
-
32
-
-
0029900136
-
Organization of AMPA receptor subunits at a glutamate synapse: A quantitative immunogold analysis of hair cell synapses in the rat organ of Corti
-
Matsubara, A., Laake, J.H., Davanger, S., Usami, S. and Ottersen, O.P. (1996) Organization of AMPA receptor subunits at a glutamate synapse: A quantitative immunogold analysis of hair cell synapses in the rat organ of Corti. J. Neurosci., 16, 4457-4467.
-
(1996)
J. Neurosci.
, vol.16
, pp. 4457-4467
-
-
Matsubara, A.1
Laake, J.H.2
Davanger, S.3
Usami, S.4
Ottersen, O.P.5
-
33
-
-
10744224951
-
Novel monoclonal antibodies demonstrate biochemical variation of brain parkin with age
-
Pawlyk, A.C., Giasson, B.I., Sampathu, D.M., Perez, F.A., Lim, K.L., Dawson, V.L., Dawson, T.M., Palmiter, R.D., Trojanowski, J.Q. and Lee, V.M. (2003) Novel monoclonal antibodies demonstrate biochemical variation of brain parkin with age. J. Biol. Chem., 278, 48120-48128.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 48120-48128
-
-
Pawlyk, A.C.1
Giasson, B.I.2
Sampathu, D.M.3
Perez, F.A.4
Lim, K.L.5
Dawson, V.L.6
Dawson, T.M.7
Palmiter, R.D.8
Trojanowski, J.Q.9
Lee, V.M.10
-
34
-
-
0023722437
-
Synuclein: A neuron-specific protein localized to the nucleus and presynaptic nerve terminal
-
Maroteaux, L., Campanelli, J.T. and Scheller, R.H. (1988) Synuclein: A neuron-specific protein localized to the nucleus and presynaptic nerve terminal. J. Neurosci., 8, 2804-2815.
-
(1988)
J. Neurosci.
, vol.8
, pp. 2804-2815
-
-
Maroteaux, L.1
Campanelli, J.T.2
Scheller, R.H.3
-
35
-
-
0037386532
-
Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants
-
Greene, J.C., Whitworth, A.J., Kuo, I., Andrews, L.A., Feany, M.B. and Pallanck, L.J. (2003) Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants. Proc. Natl Acad. Sci. USA, 100, 4078-4083.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 4078-4083
-
-
Greene, J.C.1
Whitworth, A.J.2
Kuo, I.3
Andrews, L.A.4
Feany, M.B.5
Pallanck, L.J.6
-
36
-
-
0037338634
-
Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death
-
Darios, F., Corti, O., Lucking, C.B., Hampe, C., Muriel, M.P., Abbas, N., Gu, W.J., Hirsch, E.C., Rooney, T., Ruberg, M. et al. (2003) Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death. Hum. Mol. Genet., 12, 517-526.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 517-526
-
-
Darios, F.1
Corti, O.2
Lucking, C.B.3
Hampe, C.4
Muriel, M.P.5
Abbas, N.6
Gu, W.J.7
Hirsch, E.C.8
Rooney, T.9
Ruberg, M.10
-
37
-
-
2442481789
-
Mitochondrial dysfunction and oxidative damage in parkin-deficient mice
-
Palacino, J.J., Sagi, D., Goldberg, M.S., Krauss, S., Motz, C., Wacker, M., Klose, J. and Shen, J. (2004) Mitochondrial dysfunction and oxidative damage in parkin-deficient mice. J. Biol. Chem., 279 18614-18622.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 18614-18622
-
-
Palacino, J.J.1
Sagi, D.2
Goldberg, M.S.3
Krauss, S.4
Motz, C.5
Wacker, M.6
Klose, J.7
Shen, J.8
-
38
-
-
0035870881
-
Inducible expression of mutant alpha-synuclein decreases proteasome activity and increases sensitivity to mitochondria-dependent apoptosis
-
Tanaka, Y., Engelender, S., Igarashi, S., Rao, R.K., Wanner, T., Tanzi, R.E., Sawa, A., Dawson, V.L., Dawson, T.M. and Ross, C.A. (2001) Inducible expression of mutant alpha-synuclein decreases proteasome activity and increases sensitivity to mitochondria-dependent apoptosis. Hum. Mol. Genet., 10, 919-926.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 919-926
-
-
Tanaka, Y.1
Engelender, S.2
Igarashi, S.3
Rao, R.K.4
Wanner, T.5
Tanzi, R.E.6
Sawa, A.7
Dawson, V.L.8
Dawson, T.M.9
Ross, C.A.10
-
39
-
-
13844253723
-
Nigrostriatal dopaminergic deficits and hypokinesia caused by inactivation of the familial Parkinsonism-linked gene DJ-1
-
Goldberg, M.S., Pisani, A., Haburcak, M., Vortherms, T.A., Kitada, T., Costa, C., Tong, Y., Martella, G., Tscherter, A., Martins, A. et al. (2005) Nigrostriatal dopaminergic deficits and hypokinesia caused by inactivation of the familial Parkinsonism-linked gene DJ-1. Neuron 45, 489-496.
-
(2005)
Neuron
, vol.45
, pp. 489-496
-
-
Goldberg, M.S.1
Pisani, A.2
Haburcak, M.3
Vortherms, T.A.4
Kitada, T.5
Costa, C.6
Tong, Y.7
Martella, G.8
Tscherter, A.9
Martins, A.10
-
40
-
-
1842740232
-
Cysteine-106 of DJ-1 is the most sensitive cysteine residue to hydrogen peroxide-mediated oxidation in vivo in human umbilical vein endothelial cells
-
Kinumi, T., Kimata, J., Taira, T., Ariga, H. and Niki, E. (2004) Cysteine-106 of DJ-1 is the most sensitive cysteine residue to hydrogen peroxide-mediated oxidation in vivo in human umbilical vein endothelial cells. Biochem. Biophys. Res. Commun., 317, 722-728.
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.317
, pp. 722-728
-
-
Kinumi, T.1
Kimata, J.2
Taira, T.3
Ariga, H.4
Niki, E.5
-
41
-
-
0345357664
-
Down regulation of DJ-1 enhances cell death by oxidative stress, ER stress, and proteasome inhibition
-
Yokota, T., Sugawara, K., Ito, K., Takahashi, R., Ariga, H. and Mizusawa, H. (2003) Down regulation of DJ-1 enhances cell death by oxidative stress, ER stress, and proteasome inhibition. Biochem. Biophys. Res. Commun., 312, 1342-1348.
-
(2003)
Biochem. Biophys. Res. Commun.
, vol.312
, pp. 1342-1348
-
-
Yokota, T.1
Sugawara, K.2
Ito, K.3
Takahashi, R.4
Ariga, H.5
Mizusawa, H.6
-
42
-
-
20144389422
-
Hypersensitivity of DJ-1-deficient mice to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrindine (MPTP) and oxidative stress
-
Kim, R.H., Smith, P.D., Aleyasin, H., Hayley, S., Mount, M.P., Pownall, S., Wakeham, A., You-Ten, A.J., Kalia, S.K., Home, P. et al. (2005) Hypersensitivity of DJ-1-deficient mice to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrindine (MPTP) and oxidative stress. Proc. Natl Acad. Sci. USA, 102, 5215-5220.
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 5215-5220
-
-
Kim, R.H.1
Smith, P.D.2
Aleyasin, H.3
Hayley, S.4
Mount, M.P.5
Pownall, S.6
Wakeham, A.7
You-Ten, A.J.8
Kalia, S.K.9
Home, P.10
-
43
-
-
15544384294
-
Effects of DJ-1 mutations and polymorphisms on protein stability and subcellular localization
-
Blackinton, J., Ahmad, R., Miller, D.W., van der Brug, M.P., Canet-Aviles, R.M., Hague, S.M., Kaleem, M. and Cookson, M.R. (2005) Effects of DJ-1 mutations and polymorphisms on protein stability and subcellular localization. Brain Res. Mol. Brain Res., 134, 76-83.
-
(2005)
Brain Res. Mol. Brain Res.
, vol.134
, pp. 76-83
-
-
Blackinton, J.1
Ahmad, R.2
Miller, D.W.3
van der Brug, M.P.4
Canet-Aviles, R.M.5
Hague, S.M.6
Kaleem, M.7
Cookson, M.R.8
-
44
-
-
12344251678
-
Association of DJ-1 and parkin mediated by pathogenic DJ-1 mutations and oxidative stress
-
Moore, D.J., Zhang, L., Troncoso, J., Lee, M.K., Hattori, N., Mizuno, Y., Dawson, T.M. and Dawson, V.L. (2005) Association of DJ-1 and parkin mediated by pathogenic DJ-1 mutations and oxidative stress. Hum. Mol. Genet., 14, 71-84.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 71-84
-
-
Moore, D.J.1
Zhang, L.2
Troncoso, J.3
Lee, M.K.4
Hattori, N.5
Mizuno, Y.6
Dawson, T.M.7
Dawson, V.L.8
-
45
-
-
0029034511
-
Widespread expression of Huntington's disease gene (IT15) protein product
-
Sharp, A.H., Loev, S.J., Schilling. G., Li, S.H., Li, X.J., Bao, J., Wagster, M.V., Kotzuk, J.A., Steiner, J.P., Lo, A. et al. (1995) Widespread expression of Huntington's disease gene (IT15) protein product. Neuron, 14, 1065-1074.
-
(1995)
Neuron
, vol.14
, pp. 1065-1074
-
-
Sharp, A.H.1
Loev, S.J.2
Schilling, G.3
Li, S.H.4
Li, X.J.5
Bao, J.6
Wagster, M.V.7
Kotzuk, J.A.8
Steiner, J.P.9
Lo, A.10
-
46
-
-
0002055740
-
Intact Rat Brain Mitochondria from a Single Animal: Preparation and Properties
-
Academic Press Inc., New York
-
Lee, C.P., Sciamanna, M. and Peterson, P.L. (1993) Intact Rat Brain Mitochondria from a Single Animal: Preparation and Properties. Methods in Toxicology. Academic Press Inc., New York, vol. 2, pp. 41-50.
-
(1993)
Methods in Toxicology
, vol.2
, pp. 41-50
-
-
Lee, C.P.1
Sciamanna, M.2
Peterson, P.L.3
-
47
-
-
0025091897
-
Improved methods to isolate and subfractionate rat liver mitochondria. Lipid composition of the inter and outer membrane
-
Hovius, R., Lambrechts, H., Nicolay, K. and de Kruijff, B. (1990) Improved methods to isolate and subfractionate rat liver mitochondria. Lipid composition of the inter and outer membrane. Biochim. Biophys. Acta, 1021, 217-226.
-
(1990)
Biochim. Biophys. Acta
, vol.1021
, pp. 217-226
-
-
Hovius, R.1
Lambrechts, H.2
Nicolay, K.3
de Kruijff, B.4
-
48
-
-
0037067317
-
Mediation of poly(ADP-ribose) polymerase-1-dependent cell death by apoptosis-inducing factor
-
Yu, S.W., Wang, H., Poitras, M.F., Coombs, C., Bowers, W.J., Federoff, H.J., Poirier, G.G., Dawson, T.M. and Dawson, V.L. (2002) Mediation of poly(ADP-ribose) polymerase-1-dependent cell death by apoptosis-inducing factor. Science, 297, 259-263.
-
(2002)
Science
, vol.297
, pp. 259-263
-
-
Yu, S.W.1
Wang, H.2
Poitras, M.F.3
Coombs, C.4
Bowers, W.J.5
Federoff, H.J.6
Poirier, G.G.7
Dawson, T.M.8
Dawson, V.L.9
-
49
-
-
0342375000
-
Different modes of expression of AMPA and NMDA receptors in hippocampal synapses
-
Takumi, Y., Ramirez-Leon, V., Laake, P., Rinvik, E. and Ottersen, O.P. (1999) Different modes of expression of AMPA and NMDA receptors in hippocampal synapses. Nat. Neurosci., 2, 618-624.
-
(1999)
Nat. Neurosci.
, vol.2
, pp. 618-624
-
-
Takumi, Y.1
Ramirez-Leon, V.2
Laake, P.3
Rinvik, E.4
Ottersen, O.P.5
|