-
1
-
-
27944505095
-
Postnatal phenotype and localization of spinal cord V1 derived interneurons
-
Alvarez FJ, Jonas PC, Sapir T, Hartley R, Berrocal MC, Geiman EJ, Todd AJ, Goulding M. Postnatal phenotype and localization of spinal cord V1 derived interneurons. J Comp Neurol 2005; 493: 177-192.
-
(2005)
J Comp Neurol
, vol.493
, pp. 177-192
-
-
Alvarez, F.J.1
Jonas, P.C.2
Sapir, T.3
Hartley, R.4
Berrocal, M.C.5
Geiman, E.J.6
Todd, A.J.7
Goulding, M.8
-
2
-
-
0031036896
-
Apoptosis and autophagy in nigral neurons of patients with Parkinson's disease
-
Anglade P, Vyas S, Javoy-Agid F, Herrero MT, Michel PP, Marguez J, Mouatt-Prigent A, Ruberg M, Hirsch EC, Agid Y. Apoptosis and autophagy in nigral neurons of patients with Parkinson's disease. Histol Histopathol 1997; 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
Marguez, J.6
Mouatt-Prigent, A.7
Ruberg, M.8
Hirsch, E.C.9
Agid, Y.10
-
3
-
-
0027293275
-
ALS, SOD and peroxynitrite
-
Beckman JS, Carson M, Smith CD, Koppenol WH. ALS, SOD and peroxynitrite. Nature 1993; 364: 548.
-
(1993)
Nature
, vol.364
, pp. 548
-
-
Beckman, J.S.1
Carson, M.2
Smith, C.D.3
Koppenol, W.H.4
-
4
-
-
0002770493
-
Superoxide dismutase and the death of motoneurons in ALS
-
Beckman JS, Estévez AG, Crow JP, Barbeito LH. Superoxide dismutase and the death of motoneurons in ALS. TINS 2001; 24 (Suppl): S15-S20.
-
(2001)
TINS
, vol.24
, Issue.SUPPL.
-
-
Beckman, J.S.1
Estévez, A.G.2
Crow, J.P.3
Barbeito, L.H.4
-
5
-
-
17644365438
-
Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability
-
Beilina A, Van Der Brug M, Ahmad R, Kesavapany S, Miller DW, Petsko GA, Cookson MR. Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability. Proc Natl Acad Sci USA 2005; 102: 5703-5708.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 5703-5708
-
-
Beilina, A.1
Van Der Brug, M.2
Ahmad, R.3
Kesavapany, S.4
Miller, D.W.5
Petsko, G.A.6
Cookson, M.R.7
-
6
-
-
0035886428
-
Early vacuolization and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity
-
Bendotti C, Calvaresi N, Chiveri L, Prelle A, Moggio M, Braga M, Silani V, De Biasi S. Early vacuolization and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity. J Neurol Sci 2001; 191: 25-33.
-
(2001)
J Neurol Sci
, vol.191
, pp. 25-33
-
-
Bendotti, C.1
Calvaresi, N.2
Chiveri, L.3
Prelle, A.4
Moggio, M.5
Braga, M.6
Silani, V.7
De Biasi, S.8
-
7
-
-
4043075622
-
Lessons from models of SOD1-linked familial ALS
-
Bendotti C, Carrì MT. Lessons from models of SOD1-linked familial ALS. Trends Mol Med 2004; 10: 393-400.
-
(2004)
Trends Mol Med
, vol.10
, pp. 393-400
-
-
Bendotti, C.1
Carrì, M.T.2
-
8
-
-
0037428241
-
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
-
Bonifati V, Rizzu P, van Baren MJ, Schaap O, Breedveld GJ, Krieger E, Dekker MC, Squitieri F, Ibanez P, Joosse M, van Dongen JW, Vanacore N, van Swieten JC, Brice A, Meco G, van Duijn CM, Oostra BA, Heutink P. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science 2003; 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
van Dongen, J.W.11
Vanacore, N.12
van Swieten, J.C.13
Brice, A.14
Meco, G.15
van Duijn, C.M.16
Oostra, B.A.17
Heutink, P.18
-
9
-
-
0027965073
-
Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity
-
Borchelt D R, Lee MK, Slunt HH, Guarnieri M, Xu Z-S, Wong PC, Brown RH Jr, Price DL, Sisodia SS, Cleveland DW. Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity. Proc Natl Acad Sci USA 1994; 91: 8292-8296.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 8292-8296
-
-
Borchelt, D.R.1
Lee, M.K.2
Slunt, H.H.3
Guarnieri, M.4
Xu, Z.-S.5
Wong, P.C.6
Brown Jr, R.H.7
Price, D.L.8
Sisodia, S.S.9
Cleveland, D.W.10
-
10
-
-
0037333666
-
Staging of brain pathology related to sporadic Parkinson's disease
-
Braak H, Del Tredici K, Rüb U, de Vos RAI, Jansen Steur ENH, Braak E. Staging of brain pathology related to sporadic Parkinson's disease. Neurobiol Aging 2003; 24: 197-211.
-
(2003)
Neurobiol Aging
, vol.24
, pp. 197-211
-
-
Braak, H.1
Del Tredici, K.2
Rüb, U.3
de Vos, R.A.I.4
Jansen Steur, E.N.H.5
Braak, E.6
-
11
-
-
0031051485
-
ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions
-
Bruijn LI, Becher MW, Lee MK, Anderson KL, Jenkins NA, Copeland NG, Sisodia SS, Rothstein JD, Borchelt DR, Price DL, Cleveland DW. ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions. Neuron 1997; 18: 327-338.
-
(1997)
Neuron
, vol.18
, pp. 327-338
-
-
Bruijn, L.I.1
Becher, M.W.2
Lee, M.K.3
Anderson, K.L.4
Jenkins, N.A.5
Copeland, N.G.6
Sisodia, S.S.7
Rothstein, J.D.8
Borchelt, D.R.9
Price, D.L.10
Cleveland, D.W.11
-
12
-
-
0032544674
-
Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1
-
Bruijn LI, Houseweart MK, Kato S, Anderson KL, Anderson SD, Ohama E, Reaume AG, Scott RW, Cleveland DW. Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1. Science 1998; 281: 1851-1854.
-
(1998)
Science
, vol.281
, pp. 1851-1854
-
-
Bruijn, L.I.1
Houseweart, M.K.2
Kato, S.3
Anderson, K.L.4
Anderson, S.D.5
Ohama, E.6
Reaume, A.G.7
Scott, R.W.8
Cleveland, D.W.9
-
13
-
-
3943102116
-
Unraveling the mechanisms involved in motor neuron degeneration in ALS
-
Bruijn LI, Miller TM, Cleveland DW. Unraveling the mechanisms involved in motor neuron degeneration in ALS. Annu Rev Neurosci 2004; 27: 723-749.
-
(2004)
Annu Rev Neurosci
, vol.27
, pp. 723-749
-
-
Bruijn, L.I.1
Miller, T.M.2
Cleveland, D.W.3
-
14
-
-
0037741021
-
Increased susceptibility of striatal mitochondria to calcium-induced permeability transition
-
Brustovetsky N, Brustovetsky T, Purl KJ, Capano M, Crompton M, Dubinsky JM. Increased susceptibility of striatal mitochondria to calcium-induced permeability transition. J Neurosci 2003; 23: 4858-4867.
-
(2003)
J Neurosci
, vol.23
, pp. 4858-4867
-
-
Brustovetsky, N.1
Brustovetsky, T.2
Purl, K.J.3
Capano, M.4
Crompton, M.5
Dubinsky, J.M.6
-
15
-
-
23844448652
-
Loss of ALS2 function is insufficient to trigger motor neuron degeneration in knock-out mice but predisposes neurons to oxidative stress
-
Cai H, Lin X, Xie C, Laird FM, Lai C, Wen H, Ching HC, Shim H, Farah MH, Hoke A, Price DL, Wong PC. Loss of ALS2 function is insufficient to trigger motor neuron degeneration in knock-out mice but predisposes neurons to oxidative stress. J Neurosci 2005; 25: 7567-7574.
-
(2005)
J Neurosci
, vol.25
, pp. 7567-7574
-
-
Cai, H.1
Lin, X.2
Xie, C.3
Laird, F.M.4
Lai, C.5
Wen, H.6
Ching, H.C.7
Shim, H.8
Farah, M.H.9
Hoke, A.10
Price, D.L.11
Wong, P.C.12
-
16
-
-
2942684871
-
The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization
-
Canet-Aviles RM, Wilson MA, Miller DW, Ahmad R, McLendon C, Bandyopadhyay S, Baptista MJ, Ringe D, Petsko GA, Cookson MR. The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization. Proc Natl Acad Sci USA 2004; 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
-
17
-
-
0037551741
-
Protofibrils, pores, fibril, and neurodegeneration: Separating the responsible protein aggregates from the innocent bystanders
-
Caughey B, Lansbury PT. Protofibrils, pores, fibril, and neurodegeneration: separating the responsible protein aggregates from the innocent bystanders. Annu Rev Neurosci 2003; 26: 267-298.
-
(2003)
Annu Rev Neurosci
, vol.26
, pp. 267-298
-
-
Caughey, B.1
Lansbury, P.T.2
-
18
-
-
6944227811
-
Double-knockout mice for α-and β-synucleins: Effects on synaptic functions
-
Chandra S, Fornai F, Kwon H-B, Yazdani U, Atasoy D, Liu X, Hammer RE, Battaglia G, German DC, Castillo PE, Südhof TC. Double-knockout mice for α-and β-synucleins: effects on synaptic functions. Proc Natl Acad Sci USA 2004; 101: 14966-14971.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 14966-14971
-
-
Chandra, S.1
Fornai, F.2
Kwon, H.-B.3
Yazdani, U.4
Atasoy, D.5
Liu, X.6
Hammer, R.E.7
Battaglia, G.8
German, D.C.9
Castillo, P.E.10
Südhof, T.C.11
-
19
-
-
27544507306
-
α-Synuclein cooperates with CSPα in preventing neurodegeneration
-
Chandra S, Gallardo G, Fernández-Chacón R, Schlüter OM, Südhof TC. α-Synuclein cooperates with CSPα in preventing neurodegeneration. Cell 2005; 123: 383-396.
-
(2005)
Cell
, vol.123
, pp. 383-396
-
-
Chandra, S.1
Gallardo, G.2
Fernández-Chacón, R.3
Schlüter, O.M.4
Südhof, T.C.5
-
20
-
-
20444367300
-
Age-dependent motor deficits and dopaminergic dysfunction in DJ-1 null mice
-
Chen L, Cagniard B, Mathews T, Jones S, Koh HC, Ding Y, Carvey PM, Ling Z, Kang UJ, Zhuang X. Age-dependent motor deficits and dopaminergic dysfunction in DJ-1 null mice. J Biol Chem 2005; 280: 21418-21426.
-
(2005)
J Biol Chem
, vol.280
, pp. 21418-21426
-
-
Chen, L.1
Cagniard, B.2
Mathews, T.3
Jones, S.4
Koh, H.C.5
Ding, Y.6
Carvey, P.M.7
Ling, Z.8
Kang, U.J.9
Zhuang, X.10
-
21
-
-
2442658908
-
-
Chen YZ, Bennett CL, Huynh HM, Blair IP, Puls I, Irobi J, Dierick I, Abel A, Kennerson ML, Rabin BA, Nicholson GA, Auer-Grumbach M, Wagner K, De Jonghe P, Griffin JW, Fishbeck KM, Timmerman V, Comblath DR, Chance PF. DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). Am J Hum Genet 2004; 74: 1128-1135.
-
Chen YZ, Bennett CL, Huynh HM, Blair IP, Puls I, Irobi J, Dierick I, Abel A, Kennerson ML, Rabin BA, Nicholson GA, Auer-Grumbach M, Wagner K, De Jonghe P, Griffin JW, Fishbeck KM, Timmerman V, Comblath DR, Chance PF. DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). Am J Hum Genet 2004; 74: 1128-1135.
-
-
-
-
22
-
-
33745131439
-
Senataxin, the yeast Sen1p orthologue: Characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease
-
Chen YZ, Hashemi SH, Anderson SK, Huang Y, Moreira MC, Lynch DR, Glass IA, Chance PF, Bennett CL. Senataxin, the yeast Sen1p orthologue: characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease. Neurobiol Dis 2006; 23: 97-108.
-
(2006)
Neurobiol Dis
, vol.23
, pp. 97-108
-
-
Chen, Y.Z.1
Hashemi, S.H.2
Anderson, S.K.3
Huang, Y.4
Moreira, M.C.5
Lynch, D.R.6
Glass, I.A.7
Chance, P.F.8
Bennett, C.L.9
-
23
-
-
0034681163
-
Acceleration of oligomerization, not fibrilization, is a shared property of both alpha-synuclein mutations linked to early-onset Parkinson's disease: Implications for pathogenesis and therapy
-
Conway KA, Lee SJ, Rochet JC, Ding TT, Williamson RE, Lansbury PT Jr. Acceleration of oligomerization, not fibrilization, is a shared property of both alpha-synuclein mutations linked to early-onset Parkinson's disease: implications for pathogenesis and therapy. Proc Natl Acad Sci USA 2000; 97: 571-576.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 571-576
-
-
Conway, K.A.1
Lee, S.J.2
Rochet, J.C.3
Ding, T.T.4
Williamson, R.E.5
Lansbury Jr., P.T.6
-
24
-
-
0027946294
-
Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis
-
Dal Canto MC, Gurney ME. Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis. Am J Pathol 1994; 145: 1271-1280.
-
(1994)
Am J Pathol
, vol.145
, pp. 1271-1280
-
-
Dal Canto, M.C.1
Gurney, M.E.2
-
25
-
-
0742323115
-
Mitochondrial calcium uptake stimulates nitric oxide production in mitochondria of bovine vascular endothelial cells
-
Dedkova EN, Ji X, Lipsius SL, Blatter LA. Mitochondrial calcium uptake stimulates nitric oxide production in mitochondria of bovine vascular endothelial cells. Am J Physiol Cell Physiol 2004; 286: C406-C415.
-
(2004)
Am J Physiol Cell Physiol
, vol.286
-
-
Dedkova, E.N.1
Ji, X.2
Lipsius, S.L.3
Blatter, L.A.4
-
26
-
-
0027426169
-
Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase
-
Deng H-X, Hentati A, Tainer JA, Iqbal Z, Cayabyab A, Hung W-Y, Getzoff ED, Hu P, Herzfeldt B, Roos RP, Warner C, Deng G, Soriano E, Smyth C, Parge HE, Ahmed A, Roses AD, Hallewell RA, Pericak-Vance MA, Siddique T. Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase. Science 1993; 261: 1047-1051.
-
(1993)
Science
, vol.261
, pp. 1047-1051
-
-
Deng, H.-X.1
Hentati, A.2
Tainer, J.A.3
Iqbal, Z.4
Cayabyab, A.5
Hung, W.-Y.6
Getzoff, E.D.7
Hu, P.8
Herzfeldt, B.9
Roos, R.P.10
Warner, C.11
Deng, G.12
Soriano, E.13
Smyth, C.14
Parge, H.E.15
Ahmed, A.16
Roses, A.D.17
Hallewell, R.A.18
Pericak-Vance, M.A.19
Siddique, T.20
more..
-
27
-
-
27144469287
-
Small interfering RNA targeting the PINK1 induces apoptosis in dopaminergic cells SH-SY5Y
-
Deng H, Jankovic J, Guo Y, Xie W, Le W. Small interfering RNA targeting the PINK1 induces apoptosis in dopaminergic cells SH-SY5Y. Biochem Biophys Res Commun 2005; 337: 1133-1138.
-
(2005)
Biochem Biophys Res Commun
, vol.337
, pp. 1133-1138
-
-
Deng, H.1
Jankovic, J.2
Guo, Y.3
Xie, W.4
Le, W.5
-
28
-
-
33745473350
-
-
Devon RS, Orban PC, Gerrow K, Barbieri MA, Schwab, Cao LP, Helm JR, Bissada N, Cruz-Aguado R, Davidson T-L, Winter J, Metzler M, Lam CK, Tezlaff W, Simpson EM, McMCaffery JM, El-Husseini AE, Leavitt BR, Hayden MR. Als2-deficient mice exhibit disturbances in endosome trafficking associated with motor behavioral abnormalities. Proc Natl Acad Sci USA 2006; 103: 9595-9600.
-
Devon RS, Orban PC, Gerrow K, Barbieri MA, Schwab, Cao LP, Helm JR, Bissada N, Cruz-Aguado R, Davidson T-L, Winter J, Metzler M, Lam CK, Tezlaff W, Simpson EM, McMCaffery JM, El-Husseini AE, Leavitt BR, Hayden MR. Als2-deficient mice exhibit disturbances in endosome trafficking associated with motor behavioral abnormalities. Proc Natl Acad Sci USA 2006; 103: 9595-9600.
-
-
-
-
29
-
-
20144379753
-
Cross-species characterization of the ALS2 gene and analysis of its pattern of expression in development and adulthood
-
Devon RS, Schwab C, Topp JD, Orban PC, Yang Y, Pape TD, Helm JR, Davidson T-L, Rogers DA, Gros-Louis F, Rouleau G, Harazdovsky BF, Leavitt BR, Hayden MR. Cross-species characterization of the ALS2 gene and analysis of its pattern of expression in development and adulthood. Neurobiol Dis 2005; 18: 243-257.
-
(2005)
Neurobiol Dis
, vol.18
, pp. 243-257
-
-
Devon, R.S.1
Schwab, C.2
Topp, J.D.3
Orban, P.C.4
Yang, Y.5
Pape, T.D.6
Helm, J.R.7
Davidson, T.-L.8
Rogers, D.A.9
Gros-Louis, F.10
Rouleau, G.11
Harazdovsky, B.F.12
Leavitt, B.R.13
Hayden, M.R.14
-
30
-
-
0039251419
-
Induction of nitric oxide-dependent apoptosis in motor neurons by zinc-deficient superoxide dismutase
-
Estévez, AG, Crow JP, Sampson JB, Reiter C, Zhuang Y, Richardson GJ, Tarpey MM, Barbeito L, Beckman JS. Induction of nitric oxide-dependent apoptosis in motor neurons by zinc-deficient superoxide dismutase. Science 1999; 286: 2498-2500.
-
(1999)
Science
, vol.286
, pp. 2498-2500
-
-
Estévez, A.G.1
Crow, J.P.2
Sampson, J.B.3
Reiter, C.4
Zhuang, Y.5
Richardson, G.J.6
Tarpey, M.M.7
Barbeito, L.8
Beckman, J.S.9
-
31
-
-
0032954386
-
Lack of involvement of neuronal nitric oxide synthase in the pathogenesis of a transgenic mouse model of familial amyotrophic lateral sclerosis
-
Facchinetti F, Sasaki M, Cutting FB, Zhai P, MacDonald JE, Reif D, Beal MF, Huang PL, Dawson TM, Gurney ME, Dawson VL. Lack of involvement of neuronal nitric oxide synthase in the pathogenesis of a transgenic mouse model of familial amyotrophic lateral sclerosis. Neuroscience 1999; 90: 1483-1492.
-
(1999)
Neuroscience
, vol.90
, pp. 1483-1492
-
-
Facchinetti, F.1
Sasaki, M.2
Cutting, F.B.3
Zhai, P.4
MacDonald, J.E.5
Reif, D.6
Beal, M.F.7
Huang, P.L.8
Dawson, T.M.9
Gurney, M.E.10
Dawson, V.L.11
-
32
-
-
33645790701
-
LRRK2 expression linked to dopamine-innervated areas
-
Galter D, Westerlund M, Carmine A, Lindqvist E, Sydow O, Olson L. LRRK2 expression linked to dopamine-innervated areas. Ann Neurol 2006; 59: 714-719.
-
(2006)
Ann Neurol
, vol.59
, pp. 714-719
-
-
Galter, D.1
Westerlund, M.2
Carmine, A.3
Lindqvist, E.4
Sydow, O.5
Olson, L.6
-
33
-
-
0034602442
-
Oxidative damage linked to neurodegeneration by selective alpha-synuclein nitration in synucleinopathy lesions
-
Giasson BI, Duda JE, Murray IVJ, Chen Q, Souza JM, Hurtig HI, Ischiropoulos H, Trojanowski JQ, Lee VM-Y. Oxidative damage linked to neurodegeneration by selective alpha-synuclein nitration in synucleinopathy lesions. Science 2000; 290: 985-989.
-
(2000)
Science
, vol.290
, pp. 985-989
-
-
Giasson, B.I.1
Duda, J.E.2
Murray, I.V.J.3
Chen, Q.4
Souza, J.M.5
Hurtig, H.I.6
Ischiropoulos, H.7
Trojanowski, J.Q.8
Lee, V.M.-Y.9
-
34
-
-
0037118259
-
Neuronal α-synucleinopathy with severe movement disorder in mice expressing A53T human α-synuclein
-
Giasson BI, Duda JE, Quinn SM, Zhang B, Trojanowski JQ, Lee WM-Y. Neuronal α-synucleinopathy with severe movement disorder in mice expressing A53T human α-synuclein. Neuron 2002; 34: 521-533.
-
(2002)
Neuron
, vol.34
, pp. 521-533
-
-
Giasson, B.I.1
Duda, J.E.2
Quinn, S.M.3
Zhang, B.4
Trojanowski, J.Q.5
Lee, W.M.-Y.6
-
35
-
-
77955397778
-
-
Ginsberg SD, Hemby SE, Mufson EJ, Martin LJ. Cell and tissue microdissection in combination with genomic and proteomic profiling. In: Zaborszky L, Wouterlood FG, Lanciego JL, eds. Neuroanatomical Tract-Tracing 3. Molecules, Neurons, and Systems. New York: Springer, 2006; 109-141.
-
Ginsberg SD, Hemby SE, Mufson EJ, Martin LJ. Cell and tissue microdissection in combination with genomic and proteomic profiling. In: Zaborszky L, Wouterlood FG, Lanciego JL, eds. Neuroanatomical Tract-Tracing 3. Molecules, Neurons, and Systems. New York: Springer, 2006; 109-141.
-
-
-
-
36
-
-
10744221260
-
Transgenic mice expressing mutant A53T human alpha-synuclein show neuronal dysfunction in the absence or aggregate formation
-
Gispert S, Del Turco D, Garrett L, Chen A, Bernard DJ, Hamm-Clement J, Korf HW, Deller T, Braak H, Auburger G, Nussbaum RL. Transgenic mice expressing mutant A53T human alpha-synuclein show neuronal dysfunction in the absence or aggregate formation. Mol Cell Neurosci 2003; 24: 419-429.
-
(2003)
Mol Cell Neurosci
, vol.24
, pp. 419-429
-
-
Gispert, S.1
Del Turco, D.2
Garrett, L.3
Chen, A.4
Bernard, D.J.5
Hamm-Clement, J.6
Korf, H.W.7
Deller, T.8
Braak, H.9
Auburger, G.10
Nussbaum, R.L.11
-
37
-
-
0037441389
-
Characterization and function of mitochondrial nitric oxide synthase
-
Giulivi C. Characterization and function of mitochondrial nitric oxide synthase. Free Radic Biol Med 2003; 34: 397-408.
-
(2003)
Free Radic Biol Med
, vol.34
, pp. 397-408
-
-
Giulivi, C.1
-
38
-
-
0035409575
-
Alpha-synuclein and neurodegenerative diseases
-
Goedert M. Alpha-synuclein and neurodegenerative diseases. Nat Rev Neurosci 2001; 2: 492-501.
-
(2001)
Nat Rev Neurosci
, vol.2
, pp. 492-501
-
-
Goedert, M.1
-
39
-
-
0141891953
-
Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons
-
Goldberg MS, Fleming SM, Palacino JJ, Capeda C, Lam HA, Bhatnagar A, Meloni EG, Wu N, Ackerson LC, Klapstein GJ, Gajendiram M, Roth BL, Chesselet MF, Maidment NT, Levine MS, Shen J. Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons. J Biol Chem 2003; 278: 43628-43635.
-
(2003)
J Biol Chem
, vol.278
, pp. 43628-43635
-
-
Goldberg, M.S.1
Fleming, S.M.2
Palacino, J.J.3
Capeda, C.4
Lam, H.A.5
Bhatnagar, A.6
Meloni, E.G.7
Wu, N.8
Ackerson, L.C.9
Klapstein, G.J.10
Gajendiram, M.11
Roth, B.L.12
Chesselet, M.F.13
Maidment, N.T.14
Levine, M.S.15
Shen, J.16
-
40
-
-
13844253723
-
Nigrostriatal dopaminergic deficits and hypokinesia caused by inactivation of the familial parkinsonism-linked gene DJ-1
-
Goldberg MS, Pisani A, Haburcak M, Vortherms TA, Kitada Y, Costa C, Tong Y, Martella G, Tscherter A, Martins A, Bernardi G, Roth BL, Pothos EN, Calabresi P, Shen J. Nigrostriatal dopaminergic deficits and hypokinesia caused by inactivation of the familial parkinsonism-linked gene DJ-1. Neuron 2005; 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, Y.5
Costa, C.6
Tong, Y.7
Martella, G.8
Tscherter, A.9
Martins, A.10
Bernardi, G.11
Roth, B.L.12
Pothos, E.N.13
Calabresi, P.14
Shen, J.15
-
41
-
-
17944374029
-
Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1
-
Grohmann K, Schuelke M, Diers A, Hoffmann K, Lucke B, Adams C, Bertini E, Leonhardt-Horti H, Muntoni F, Ouvrier R, Pfeufer A, Rossi R, Van Maldergem L, Wilmshurst JM, Wienker TF, Sendtner M, Rudnik-Schoneborn S, Zrres K, Hubner C. Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1. Nat Genet 2001; 29: 75-77.
-
(2001)
Nat Genet
, vol.29
, pp. 75-77
-
-
Grohmann, K.1
Schuelke, M.2
Diers, A.3
Hoffmann, K.4
Lucke, B.5
Adams, C.6
Bertini, E.7
Leonhardt-Horti, H.8
Muntoni, F.9
Ouvrier, R.10
Pfeufer, A.11
Rossi, R.12
Van Maldergem, L.13
Wilmshurst, J.M.14
Wienker, T.F.15
Sendtner, M.16
Rudnik-Schoneborn, S.17
Zrres, K.18
Hubner, C.19
-
42
-
-
0028284779
-
Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation
-
Gurney ME, Pu H, Chiu AY, Dal Canto MC, Polchow CY, Alexander DD, Caliendo J, Hentati A, Kwon YW, Deng HX, Chen W, Zhai P, Sufit RL, Siddique T. Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation. Science 1994; 264: 1772-1775.
-
(1994)
Science
, vol.264
, pp. 1772-1775
-
-
Gurney, M.E.1
Pu, H.2
Chiu, A.Y.3
Dal Canto, M.C.4
Polchow, C.Y.5
Alexander, D.D.6
Caliendo, J.7
Hentati, A.8
Kwon, Y.W.9
Deng, H.X.10
Chen, W.11
Zhai, P.12
Sufit, R.L.13
Siddique, T.14
-
43
-
-
0034785483
-
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
-
Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figelwicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH Jr, Scherer SW, Rouleau GA, Hayden MR, Ikead JE. A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. Nat Genet 2001; 29: 166-173.
-
(2001)
Nat Genet
, vol.29
, pp. 166-173
-
-
Hadano, S.1
Hand, C.K.2
Osuga, H.3
Yanagisawa, Y.4
Otomo, A.5
Devon, R.S.6
Miyamoto, N.7
Showguchi-Miyata, J.8
Okada, Y.9
Singaraja, R.10
Figelwicz, D.A.11
Kwiatkowski, T.12
Hosler, B.A.13
Sagie, T.14
Skaug, J.15
Nasir, J.16
Brown Jr, R.H.17
Scherer, S.W.18
Rouleau, G.A.19
Hayden, M.R.20
Ikead, J.E.21
more..
-
44
-
-
31144448704
-
Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking
-
Hadano S, Benn SC, Kakuta S, Otomo A, Sudo K, Kunita R, Suzuki-Utsunomiya K, Mizumura H, Shefner JM, Cox GA, Iwakura Y, Brown RH Jr, Ikeda JE. Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking. Hum Mol Genet 2006; 15: 233-250
-
(2006)
Hum Mol Genet
, vol.15
, pp. 233-250
-
-
Hadano, S.1
Benn, S.C.2
Kakuta, S.3
Otomo, A.4
Sudo, K.5
Kunita, R.6
Suzuki-Utsunomiya, K.7
Mizumura, H.8
Shefner, J.M.9
Cox, G.A.10
Iwakura, Y.11
Brown Jr, R.H.12
Ikeda, J.E.13
-
45
-
-
4444237208
-
Novel PINK1 mutations in early-onset parkinsonism
-
Hatano Y, Li Y, Sato K, Asakawa S, Yamamura Y, Tomiyama H, Yoshino H, Asahina M, Kobayashi S, Hassin-Baer S, Lu CS, Mg AR, Resales PL, Shimizu N, Toda T, Mizuno Y, Hattori N. Novel PINK1 mutations in early-onset parkinsonism. Ann Neurol 2004; 56: 424-427.
-
(2004)
Ann Neurol
, vol.56
, pp. 424-427
-
-
Hatano, Y.1
Li, Y.2
Sato, K.3
Asakawa, S.4
Yamamura, Y.5
Tomiyama, H.6
Yoshino, H.7
Asahina, M.8
Kobayashi, S.9
Hassin-Baer, S.10
Lu, C.S.11
Mg, A.R.12
Resales, P.L.13
Shimizu, N.14
Toda, T.15
Mizuno, Y.16
Hattori, N.17
-
46
-
-
0037734370
-
-
Hafezparast M, Klocke R, Ruhrberg C, Marquardt A, Ahmad-Annuar A, Bowen S, Lalli G, Witherden AS, Hummerich H, Nicholson S, Morgan J, Oozageer R, Priestley JV, Averill S, King V R, Ball S, Peters J, Toda T, Yammamoto A, Hiraoka Y, Augustin M, Korthaus D, Wattler S, Wabnitz P, Dickeite C, Lampel S, Boehme F, Peraus G, Popp A, Rudelius M, Schegel J, Fuchs H, de Angelis MH, Schiavo G, Shima DT, Russ AP, Stumm G, Martin JE, Fisher EMC. Mutations in dynein link motor neuron degeneration to defects in retrograde transport. Science 2003; 300: 808-812.
-
Hafezparast M, Klocke R, Ruhrberg C, Marquardt A, Ahmad-Annuar A, Bowen S, Lalli G, Witherden AS, Hummerich H, Nicholson S, Morgan J, Oozageer R, Priestley JV, Averill S, King V R, Ball S, Peters J, Toda T, Yammamoto A, Hiraoka Y, Augustin M, Korthaus D, Wattler S, Wabnitz P, Dickeite C, Lampel S, Boehme F, Peraus G, Popp A, Rudelius M, Schegel J, Fuchs H, de Angelis MH, Schiavo G, Shima DT, Russ AP, Stumm G, Martin JE, Fisher EMC. Mutations in dynein link motor neuron degeneration to defects in retrograde transport. Science 2003; 300: 808-812.
-
-
-
-
47
-
-
12944250987
-
Caspase-3: A vulnerability factor and final effector in apoptotic death of dopaminergic neurons in Parkinson's disease
-
Hartmann A, Hunot S, Michel PP, Muriel M-P, Vyas S, Faucheux BA, Mouatt-Prignet A, Turmel H, Srinivasan A, Ruberg M, Evan GI, Agid Y, Hirsch EC. Caspase-3: a vulnerability factor and final effector in apoptotic death of dopaminergic neurons in Parkinson's disease. Proc Natl Acad Sci USA 2000; 97: 2875-2880.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 2875-2880
-
-
Hartmann, A.1
Hunot, S.2
Michel, P.P.3
Muriel, M.-P.4
Vyas, S.5
Faucheux, B.A.6
Mouatt-Prignet, A.7
Turmel, H.8
Srinivasan, A.9
Ruberg, M.10
Evan, G.I.11
Agid, Y.12
Hirsch, E.C.13
-
48
-
-
0033625507
-
Motor neuron death in sporadic amyotrophic lateral sclerosis (ALS) is not apoptotic. A comparative study of ALS and chronic aluminum chloride neurotoxicity in New Zealand white rabbits
-
He BP, Strong MJ. Motor neuron death in sporadic amyotrophic lateral sclerosis (ALS) is not apoptotic. A comparative study of ALS and chronic aluminum chloride neurotoxicity in New Zealand white rabbits. Neuropath Appl Neurobiol 2000; 26: 150-160.
-
(2000)
Neuropath Appl Neurobiol
, vol.26
, pp. 150-160
-
-
He, B.P.1
Strong, M.J.2
-
50
-
-
0033890821
-
Alpha-synuclein promotes mitochondrial deficit and oxidative stress
-
Hsu LJ, Sagara Y, Arroyo A, Rockenstein E, Sisk A, Mallory M, Wong J, Takenouchi T, Hashimoto M, Masliah E. Alpha-synuclein promotes mitochondrial deficit and oxidative stress. Am J Pathol 2000; 157: 401-410.
-
(2000)
Am J Pathol
, vol.157
, pp. 401-410
-
-
Hsu, L.J.1
Sagara, Y.2
Arroyo, A.3
Rockenstein, E.4
Sisk, A.5
Mallory, M.6
Wong, J.7
Takenouchi, T.8
Hashimoto, M.9
Masliah, E.10
-
51
-
-
2942541204
-
How do Parkin mutations result in neurodegeneration?
-
Imai Y, Takahashi R. How do Parkin mutations result in neurodegeneration? Curr Opin Neurobiol 2004; 14: 384-389.
-
(2004)
Curr Opin Neurobiol
, vol.14
, pp. 384-389
-
-
Imai, Y.1
Takahashi, R.2
-
52
-
-
0038389681
-
Oxidative modification of alpha-synuclein
-
Ischiropoulos H. Oxidative modification of alpha-synuclein. Ann NY Acad Sci 2003; 991: 93-100.
-
(2003)
Ann NY Acad Sci
, vol.991
, pp. 93-100
-
-
Ischiropoulos, H.1
-
53
-
-
33750992481
-
The molecular genetics of non-ALS motor neuron diseases
-
James PA, Talbot K. The molecular genetics of non-ALS motor neuron diseases. Biochim Biophys Acta 2006; 1762: 986-1000.
-
(2006)
Biochim Biophys Acta
, vol.1762
, pp. 986-1000
-
-
James, P.A.1
Talbot, K.2
-
54
-
-
0033009205
-
Is there apoptosis in Lewy body disease?
-
Jellinger KA. Is there apoptosis in Lewy body disease? Acta Neuropathol 1999; 97: 413-415.
-
(1999)
Acta Neuropathol
, vol.97
, pp. 413-415
-
-
Jellinger, K.A.1
-
55
-
-
0037040491
-
Human α-synuclein overexpression increases intracellular reactive oxygen species levels and susceptibility to dopamine
-
Junn E, Mouradian MM. Human α-synuclein overexpression increases intracellular reactive oxygen species levels and susceptibility to dopamine. Neurosci Lett 2002; 320: 146-150.
-
(2002)
Neurosci Lett
, vol.320
, pp. 146-150
-
-
Junn, E.1
Mouradian, M.M.2
-
56
-
-
0034280435
-
Subcellular localization of wild-type and Parkinson's disease-associated mutant alpha-synuclein in human and transgenic mouse brain
-
Kahle PJ, Neumann M, Ozmen L, Muller V, Jacobsen H, Schindzielorz A, Okochi M, Leimer U, van der Putten H, Probst A, Kremmer E, Kretzschmar HA, Haass C. Subcellular localization of wild-type and Parkinson's disease-associated mutant alpha-synuclein in human and transgenic mouse brain. J Neurosci 2000; 20: 6365-6373.
-
(2000)
J Neurosci
, vol.20
, pp. 6365-6373
-
-
Kahle, P.J.1
Neumann, M.2
Ozmen, L.3
Muller, V.4
Jacobsen, H.5
Schindzielorz, A.6
Okochi, M.7
Leimer, U.8
van der Putten, H.9
Probst, A.10
Kremmer, E.11
Kretzschmar, H.A.12
Haass, C.13
-
57
-
-
2442463319
-
Alsin, the product of the ALS2 gene, suppresses SOD1 mutant neurotoxicity through RhoGEF domain by interacting with SOD1 mutants
-
Kanekura K, Hashimoto Y, Niikura T, Aiso S, Matsuoka M, Nishimoto I. Alsin, the product of the ALS2 gene, suppresses SOD1 mutant neurotoxicity through RhoGEF domain by interacting with SOD1 mutants. J Biol Chem 2004; 279: 19247-19256.
-
(2004)
J Biol Chem
, vol.279
, pp. 19247-19256
-
-
Kanekura, K.1
Hashimoto, Y.2
Niikura, T.3
Aiso, S.4
Matsuoka, M.5
Nishimoto, I.6
-
58
-
-
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, Shimizu N. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998; 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
-
59
-
-
0034537290
-
Autophagy as a regulated pathway of cellular degradation
-
Klionsky DJ, Emr SD. Autophagy as a regulated pathway of cellular degradation. Science 2000; 290: 1717-1721.
-
(2000)
Science
, vol.290
, pp. 1717-1721
-
-
Klionsky, D.J.1
Emr, S.D.2
-
60
-
-
0032079517
-
Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1
-
Kong J, Xu Z. Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1. J Neurosci 1998; 18: 3241-3250.
-
(1998)
J Neurosci
, vol.18
, pp. 3241-3250
-
-
Kong, J.1
Xu, Z.2
-
61
-
-
0031990490
-
Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease
-
Krüger R, Kuhn W, Müller T, Woitalla D, Graeber M, Kosel S, Przuntek H, Epplen JT, Schols L, Reiss O. Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease. Nat Genet 1998; 18: 106-108.
-
(1998)
Nat Genet
, vol.18
, pp. 106-108
-
-
Krüger, R.1
Kuhn, W.2
Müller, T.3
Woitalla, D.4
Graeber, M.5
Kosel, S.6
Przuntek, H.7
Epplen, J.T.8
Schols, L.9
Reiss, O.10
-
62
-
-
0242352419
-
Mitochondrial nitric oxide synthase is not eNOS, nNOS or iNOS
-
Lacza Z, Snipes JA, Zhang J, Horváth EM, Figueroa JP, Szabó C, Busija DW. Mitochondrial nitric oxide synthase is not eNOS, nNOS or iNOS. Free Radic Biol Med 2003; 35: 1217-1228.
-
(2003)
Free Radic Biol Med
, vol.35
, pp. 1217-1228
-
-
Lacza, Z.1
Snipes, J.A.2
Zhang, J.3
Horváth, E.M.4
Figueroa, J.P.5
Szabó, C.6
Busija, D.W.7
-
63
-
-
37749011188
-
-
Soc Neurosci Abstr
-
Laird FM, Ackerley S, Farah MH, Hoke A, Maragakis N, Rothstein J, Price DL, Martin LJ, Wong PC. Neuronal expression of an ALS-linked mutant dynactin p150glued in mice causes motor neuron disease. Soc Neurosci Abstr 2005; #131.1.
-
(2005)
Neuronal expression of an ALS-linked mutant dynactin p150glued in mice causes motor neuron disease
, Issue.131.1
-
-
Laird, F.M.1
Ackerley, S.2
Farah, M.H.3
Hoke, A.4
Maragakis, N.5
Rothstein, J.6
Price, D.L.7
Martin, L.J.8
Wong, P.C.9
-
64
-
-
0041903805
-
-
Lambrechts D, Storkebaum E, Morimoto M, Del-Favero J, Desmet F, Marklund SL, Wyns S, Thijs V, Andersson J, van Marion I, Al-Chalabi A, Bornes S, Musson R, Hansen V, Beckman L, Adolfsson A, Pall HS, Prats H, Vermeire S, Rutgeerts P, Katayama S, Awata T, LeighN, Lang-Lazdunski L, Dewerchin M, Shaw C, Moons L, Vlietinck R, Morrison KE, Robberecht W, Van Broeckhoven C, Collen D, Anderson PM, Carmeliet P. VEGF is a modifer of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death. Nat Genet 2003; 34: 383-394
-
Lambrechts D, Storkebaum E, Morimoto M, Del-Favero J, Desmet F, Marklund SL, Wyns S, Thijs V, Andersson J, van Marion I, Al-Chalabi A, Bornes S, Musson R, Hansen V, Beckman L, Adolfsson A, Pall HS, Prats H, Vermeire S, Rutgeerts P, Katayama S, Awata T, LeighN, Lang-Lazdunski L, Dewerchin M, Shaw C, Moons L, Vlietinck R, Morrison KE, Robberecht W, Van Broeckhoven C, Collen D, Anderson PM, Carmeliet P. VEGF is a modifer of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death. Nat Genet 2003; 34: 383-394
-
-
-
-
65
-
-
0036775723
-
Genetics of Parkinson's disease and biochemical studies of implicated gene products
-
Lansbury PT Jr, Brice A. Genetics of Parkinson's disease and biochemical studies of implicated gene products. Curr Opin Cell Biol 2002; 14: 653-660.
-
(2002)
Curr Opin Cell Biol
, vol.14
, pp. 653-660
-
-
Lansbury Jr, P.T.1
Brice, A.2
-
66
-
-
0032190090
-
The ubiquitin pathway in Parkinson's disease
-
Leroy E, Boyer R, Auburger G, Leube B, Ulm G, Mezey E, Harta G, Browstein MJ, Jonnalagada S, Chernova T, Dehejia A, Lavedan C, Gasser T, Steinbach PJ, Wilkinson KD, Polymeropoulos MH. The ubiquitin pathway in Parkinson's disease. Nature 1998; 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
Browstein, 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
-
67
-
-
0037173006
-
Human α-synuclein-harboring familial Parkinson's disease-linked Ala-53→Thr mutation causes neurodegenerative disease with α-synuclein aggregation in transgenic mice
-
Lee MK, Stirling W, Xu Y, Xu X, Qui D, Mandir AS, Dawson TM, Copeland NG, Jenkins NA, Price DL. Human α-synuclein-harboring familial Parkinson's disease-linked Ala-53→Thr mutation causes neurodegenerative disease with α-synuclein aggregation in transgenic mice. Proc Natl Acad Sci USA 2002; 99: 8968-8973.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 8968-8973
-
-
Lee, M.K.1
Stirling, W.2
Xu, Y.3
Xu, X.4
Qui, D.5
Mandir, A.S.6
Dawson, T.M.7
Copeland, N.G.8
Jenkins, N.A.9
Price, D.L.10
-
68
-
-
0041903805
-
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
-
Leigh N, Lang-Lazdunski L, Dewerchin M, Shaw C, Moons L, Vlietinck R, Morrison KE, Robberecht W, Van Broeckhoven C, Collen D, Andersen PM, Carmeliet P. VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death. Nat Genet 2003; 34: 383-394.
-
(2003)
Nat Genet
, vol.34
, pp. 383-394
-
-
Leigh, N.1
Lang-Lazdunski, L.2
Dewerchin, M.3
Shaw, C.4
Moons, L.5
Vlietinck, R.6
Morrison, K.E.7
Robberecht, W.8
Van Broeckhoven, C.9
Collen, D.10
Andersen, P.M.11
Carmeliet, P.12
-
69
-
-
0036127407
-
Long-term culture of mouse cortical neurons as a model for neuronal development, aging, and death
-
Lesuisse C, Martin LJ. Long-term culture of mouse cortical neurons as a model for neuronal development, aging, and death. J Neurobiol 2002; 51: 9-23.
-
(2002)
J Neurobiol
, vol.51
, pp. 9-23
-
-
Lesuisse, C.1
Martin, L.J.2
-
70
-
-
7244243876
-
Stabilization of alpha-synuclein protein with aging and familial Parkinson's disease-linked A53T mutation
-
Li W, Lesuisse C, Xu Y, Troncoso JC, Price DL, Lee MK. Stabilization of alpha-synuclein protein with aging and familial Parkinson's disease-linked A53T mutation. J Neurosci 2004; 24: 7400-7409.
-
(2004)
J Neurosci
, vol.24
, pp. 7400-7409
-
-
Li, W.1
Lesuisse, C.2
Xu, Y.3
Troncoso, J.C.4
Price, D.L.5
Lee, M.K.6
-
71
-
-
0347717732
-
Axonal transport of human alpha-synuclein slows with aging but is not affected by familial Parkinson's disease-linked mutations
-
Li W, Hoffman PN, Stirling W, Price DL, Lee MK. Axonal transport of human alpha-synuclein slows with aging but is not affected by familial Parkinson's disease-linked mutations. J Neurochem 2004; 88: 410-410.
-
(2004)
J Neurochem
, vol.88
, pp. 410-410
-
-
Li, W.1
Hoffman, P.N.2
Stirling, W.3
Price, D.L.4
Lee, M.K.5
-
72
-
-
0015197354
-
The axon reaction: A review of the principal features of perikaryal responses to axon injury
-
Lieberman AR. The axon reaction: a review of the principal features of perikaryal responses to axon injury. Int Rev Neurobiol 1971; 14: 49-124.
-
(1971)
Int Rev Neurobiol
, vol.14
, pp. 49-124
-
-
Lieberman, A.R.1
-
73
-
-
0038707391
-
-
Liochev SI, Fridovich I. Mutant Cu,Zn superoxide dismutases and familial amyotrophic lateral sclerosis: evaluation of oxidative hypotheses. Free Radic Biol Med 2003; 34: 1383-1389.
-
Liochev SI, Fridovich I. Mutant Cu,Zn superoxide dismutases and familial amyotrophic lateral sclerosis: evaluation of oxidative hypotheses. Free Radic Biol Med 2003; 34: 1383-1389.
-
-
-
-
74
-
-
0035953172
-
Motor neurons rapidly accumulate DNA single-strand breaks after in vitro exposure to nitric oxide and peroxynitrite and in vivo axotomy
-
Liu Z, Martin LJ. Motor neurons rapidly accumulate DNA single-strand breaks after in vitro exposure to nitric oxide and peroxynitrite and in vivo axotomy. J Comp Neurol 2001; 432: 35-60.
-
(2001)
J Comp Neurol
, vol.432
, pp. 35-60
-
-
Liu, Z.1
Martin, L.J.2
-
75
-
-
0000244524
-
Disorders of movement and system degeneration
-
Graham DI, Lantos PL, eds, London: Arnold
-
Lowe J, Lennox G, Leigh PN. Disorders of movement and system degeneration. In: Graham DI, Lantos PL, eds. Greenfields Neuropathology. London: Arnold, 1997; 281-366.
-
(1997)
Greenfields Neuropathology
, pp. 281-366
-
-
Lowe, J.1
Lennox, G.2
Leigh, P.N.3
-
76
-
-
0023722437
-
Synuclein: A neuron-specific protein localized to the nucleus and presynaptic nerve terminals
-
Maroteaux L, Campanelli JT, Scheller RH. Synuclein: a neuron-specific protein localized to the nucleus and presynaptic nerve terminals. J Neurosci 1988; 8: 2804-2815.
-
(1988)
J Neurosci
, vol.8
, pp. 2804-2815
-
-
Maroteaux, L.1
Campanelli, J.T.2
Scheller, R.H.3
-
77
-
-
0032896327
-
Neuronal death in amyotrophic lateral sclerosis is apoptosis: Possible contribution of a programmed cell death mechanism
-
Martin LJ. Neuronal death in amyotrophic lateral sclerosis is apoptosis: possible contribution of a programmed cell death mechanism. J Neuropathol Exp Neurol 1999; 58: 459-471.
-
(1999)
J Neuropathol Exp Neurol
, vol.58
, pp. 459-471
-
-
Martin, L.J.1
-
78
-
-
0034517935
-
p53 is abnormally elevated and active in the CNS of patients with amyotrophic lateral sclerosis
-
Martin LJ. p53 is abnormally elevated and active in the CNS of patients with amyotrophic lateral sclerosis. Neurobiol Dis 2000; 7: 613-622.
-
(2000)
Neurobiol Dis
, vol.7
, pp. 613-622
-
-
Martin, L.J.1
-
79
-
-
0035348408
-
Neuronal cell death in nervous system development, disease, and injury
-
Martin LJ. Neuronal cell death in nervous system development, disease, and injury. Int J Mol Med 2001; 7: 455-478.
-
(2001)
Int J Mol Med
, vol.7
, pp. 455-478
-
-
Martin, L.J.1
-
80
-
-
0032125488
-
Neurodegeneration in excitotoxicity, global cerebral ischemia, and target deprivation: A perspective on the contributions of apoptosis and necrosis
-
Martin LJ, Al-Abdulla NA, Brambrink AM, Kirsch JR, Sieber FE, Portera-Cailliau C. Neurodegeneration in excitotoxicity, global cerebral ischemia, and target deprivation: a perspective on the contributions of apoptosis and necrosis. Brain Res Bull 1998; 46: 281-309.
-
(1998)
Brain Res Bull
, vol.46
, pp. 281-309
-
-
Martin, L.J.1
Al-Abdulla, N.A.2
Brambrink, A.M.3
Kirsch, J.R.4
Sieber, F.E.5
Portera-Cailliau, C.6
-
81
-
-
0032864716
-
Motor neuron degeneration after sciatic nerve avulsion in adult rat evolves with oxidative stress and is apoptosis
-
Martin LJ, Kaiser A, Price AC. Motor neuron degeneration after sciatic nerve avulsion in adult rat evolves with oxidative stress and is apoptosis. J Neurobiol 1999; 40: 185-201.
-
(1999)
J Neurobiol
, vol.40
, pp. 185-201
-
-
Martin, L.J.1
Kaiser, A.2
Price, A.C.3
-
82
-
-
21844470751
-
Adult motor neuron apoptosis is mediated by nitric oxide and Fas death receptor linked by DNA damage and p53 activation
-
Martin LJ, Chen K, Liu Z. Adult motor neuron apoptosis is mediated by nitric oxide and Fas death receptor linked by DNA damage and p53 activation. J Neurosci 2005; 25: 6449-6459.
-
(2005)
J Neurosci
, vol.25
, pp. 6449-6459
-
-
Martin, L.J.1
Chen, K.2
Liu, Z.3
-
83
-
-
0037083204
-
Injury-induced spinal motor neuron apoptosis is preceded by DNA single-strand breaks and is p53- and Bax-dependent
-
Martin LJ, Liu Z. Injury-induced spinal motor neuron apoptosis is preceded by DNA single-strand breaks and is p53- and Bax-dependent. J Neurobiol 2002; 50: 181-197.
-
(2002)
J Neurobiol
, vol.50
, pp. 181-197
-
-
Martin, L.J.1
Liu, Z.2
-
84
-
-
0036807332
-
DNA damage profiling in motor neurons: A single-cell analysis by comet assay
-
Martin LJ, Liu Z. DNA damage profiling in motor neurons: a single-cell analysis by comet assay. Neurochem Res 2002; 27: 1089-1100.
-
(2002)
Neurochem Res
, vol.27
, pp. 1089-1100
-
-
Martin, L.J.1
Liu, Z.2
-
85
-
-
23744460521
-
Opportunities for neuroprotection in ALS using cell dealth mechanism rationales
-
Martin LJ, Liu Z. Opportunities for neuroprotection in ALS using cell dealth mechanism rationales. Drug Discov Today 2004; 1: 135-143.
-
(2004)
Drug Discov Today
, vol.1
, pp. 135-143
-
-
Martin, L.J.1
Liu, Z.2
-
86
-
-
33845410959
-
Neuronal cell death in human neurodegenerative diseases and their animal/cell models
-
Holcik M, LaCasse E, Korneluk R, MacKenzie A, eds, Cambridge: Cambridge University Press
-
Martin LJ, Liu Z, Troncoso JC, Price DL. Neuronal cell death in human neurodegenerative diseases and their animal/cell models. In: Holcik M, LaCasse E, Korneluk R, MacKenzie A, eds. Apoptosis in Health and Disease. Cambridge: Cambridge University Press, 2005; 242-315.
-
(2005)
Apoptosis in Health and Disease
, pp. 242-315
-
-
Martin, L.J.1
Liu, Z.2
Troncoso, J.C.3
Price, D.L.4
-
87
-
-
30644471051
-
Parkinson's disease α-synuclein transgenic mice develop neuronal mitochondrial degeneration and cell death
-
Martin LJ, Pan Y, Price AC, Sterling W, Copeland NG, Jenkins NA, Price DL, Lee MK. Parkinson's disease α-synuclein transgenic mice develop neuronal mitochondrial degeneration and cell death. J Neurosci 2006; 26: 41-50.
-
(2006)
J Neurosci
, vol.26
, pp. 41-50
-
-
Martin, L.J.1
Pan, Y.2
Price, A.C.3
Sterling, W.4
Copeland, N.G.5
Jenkins, N.A.6
Price, D.L.7
Lee, M.K.8
-
88
-
-
33845361630
-
Motor neuron degeneration in amyotrophic lateral sclerosis mutant superoxide dismutase-1 transgenic mice: Mechanisms of mitochondropathy and cell death
-
Martin LJ, Liu Z, Chen K, Price A, Pan Y, Swaby J, Golden WC. Motor neuron degeneration in amyotrophic lateral sclerosis mutant superoxide dismutase-1 transgenic mice: mechanisms of mitochondropathy and cell death. J Comp Neurol 2007; 500: 20-46.
-
(2007)
J Comp Neurol
, vol.500
, pp. 20-46
-
-
Martin, L.J.1
Liu, Z.2
Chen, K.3
Price, A.4
Pan, Y.5
Swaby, J.6
Golden, W.C.7
-
89
-
-
0034681471
-
Dopaminergic loss and inclusion body formation in α-synuclein mice: Implications for neurodegenerative disorders
-
Masliah E, Rockenstein E, Veinbergs I, Mallory M, Hashimoto M, Takeda A, Sagara Y, Sisk A, Mucke L. Dopaminergic loss and inclusion body formation in α-synuclein mice: implications for neurodegenerative disorders. Science 2000; 287: 1265-1269.
-
(2000)
Science
, vol.287
, pp. 1265-1269
-
-
Masliah, E.1
Rockenstein, E.2
Veinbergs, I.3
Mallory, M.4
Hashimoto, M.5
Takeda, A.6
Sagara, Y.7
Sisk, A.8
Mucke, L.9
-
90
-
-
0034979314
-
Lack of nigral pathology in transgenic mice expressing alpha-synuclein driven by the tyrosine hydroxylase promoter
-
Matsuoka Y, Vila M, Lincoln S, McCormack A, Picciano M, LaFrancois J, Yu X, Dickson D, Langston WJ, McGowan E, Farrer M, Hardy J, Duff K, Przedborski S, Di Monte DA. Lack of nigral pathology in transgenic mice expressing alpha-synuclein driven by the tyrosine hydroxylase promoter. Neurobiol Dis 2001; 8: 535-539.
-
(2001)
Neurobiol Dis
, vol.8
, pp. 535-539
-
-
Matsuoka, Y.1
Vila, M.2
Lincoln, S.3
McCormack, A.4
Picciano, M.5
LaFrancois, J.6
Yu, X.7
Dickson, D.8
Langston, W.J.9
McGowan, E.10
Farrer, M.11
Hardy, J.12
Duff, K.13
Przedborski, S.14
Di Monte, D.A.15
-
91
-
-
0037119407
-
Mutated human SOD1 causes dysfunction of oxidative phosphorylation in mitochondria of transgenic mice
-
Mattiazzi M, D'Aurelio M, Gajewski CD, Martushova K, Kiaei M, Beal MF, Manfredi G. Mutated human SOD1 causes dysfunction of oxidative phosphorylation in mitochondria of transgenic mice. J Biol Chem 2002; 277: 29626-29633.
-
(2002)
J Biol Chem
, vol.277
, pp. 29626-29633
-
-
Mattiazzi, M.1
D'Aurelio, M.2
Gajewski, C.D.3
Martushova, K.4
Kiaei, M.5
Beal, M.F.6
Manfredi, G.7
-
92
-
-
0036316947
-
Impairment of the ubiquitin-proteasome system causes dopaminergic cell death and inclusion body formation in ventral mesencephalic cultures
-
McNaught KS, Mytilineou C, Jnobaptiste R, Yabut J, Shahidharan P, Jennert P, Olanow CW. Impairment of the ubiquitin-proteasome system causes dopaminergic cell death and inclusion body formation in ventral mesencephalic cultures. J Neurochem 2002; 81: 301-306.
-
(2002)
J Neurochem
, vol.81
, pp. 301-306
-
-
McNaught, K.S.1
Mytilineou, C.2
Jnobaptiste, R.3
Yabut, J.4
Shahidharan, P.5
Jennert, P.6
Olanow, C.W.7
-
93
-
-
33646146878
-
Anatomical localization of leucine-rich repeat kinase 2 mouse brain
-
Melrose H, Lincoln S, Tyndall G, Dickson D, Farrer M. Anatomical localization of leucine-rich repeat kinase 2 mouse brain. Neuroscience 2006; 139: 791-794.
-
(2006)
Neuroscience
, vol.139
, pp. 791-794
-
-
Melrose, H.1
Lincoln, S.2
Tyndall, G.3
Dickson, D.4
Farrer, M.5
-
94
-
-
0141704202
-
L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system
-
Miller DW, Ahmad R, Hague S, Baptista MJ, Canet-Aviles R, McLendon C, Carter DM, Zhu PP, Stadler J, Chandran J, Klinefelter GR, Blackstone C, Cookson MR. L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system. J Biol Chem 2003; 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
Klinefelter, G.R.11
Blackstone, C.12
Cookson, M.R.13
-
95
-
-
10744230604
-
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2
-
Moreira MC, Klur S, Watanabe M, Nemeth AH, Le Ber I, Moniz JC, Tranchant C, Aubourg P, Tazir M, Schols L, Pandolfo M, Shoji M, Tanaka M, Izatt L, Shaw CE, M'Zahem A, Dunne E, Bomont P, Benhassine T, Bouslam N, Stevani G, Brice A, Guimaraes J, Mendonca P, Barbot C, Coutinho P, Sequeiros J, Durr A, Warter JM, Keonig M. Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. Nat Genet 2004; 36: 225-227.
-
(2004)
Nat Genet
, vol.36
, pp. 225-227
-
-
Moreira, M.C.1
Klur, S.2
Watanabe, M.3
Nemeth, A.H.4
Le Ber, I.5
Moniz, J.C.6
Tranchant, C.7
Aubourg, P.8
Tazir, M.9
Schols, L.10
Pandolfo, M.11
Shoji, M.12
Tanaka, M.13
Izatt, L.14
Shaw, C.E.15
M'Zahem, A.16
Dunne, E.17
Bomont, P.18
Benhassine, T.19
Bouslam, N.20
Stevani, G.21
Brice, A.22
Guimaraes, J.23
Mendonca, P.24
Barbot, C.25
Coutinho, P.26
Sequeiros, J.27
Durr, A.28
Warter, J.M.29
Keonig, M.30
more..
-
96
-
-
4143084861
-
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS
-
Münch C, Sedlmeier R, Meyer T, Homberg V, Sperfeld AD, Kurt A, Prudlo J, Peraus G, Hanemann CO, Stumm G, Ludolph AC. Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS. Neurology 2004; 63: 724-726.
-
(2004)
Neurology
, vol.63
, pp. 724-726
-
-
Münch, C.1
Sedlmeier, R.2
Meyer, T.3
Homberg, V.4
Sperfeld, A.D.5
Kurt, A.6
Prudlo, J.7
Peraus, G.8
Hanemann, C.O.9
Stumm, G.10
Ludolph, A.C.11
-
97
-
-
27644558934
-
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD
-
Münch C, Rosenbolm A, Sperfeld A-D, Uttner I, Reske S, Krause BJ, Sedlmeier R, Meyer T, Hanemann CO, Stumm G, Ludolph AC. Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD. Ann Neurol 2005; 58: 777-780.
-
(2005)
Ann Neurol
, vol.58
, pp. 777-780
-
-
Münch, C.1
Rosenbolm, A.2
Sperfeld, A.-D.3
Uttner, I.4
Reske, S.5
Krause, B.J.6
Sedlmeier, R.7
Meyer, T.8
Hanemann, C.O.9
Stumm, G.10
Ludolph, A.C.11
-
98
-
-
0034193399
-
Synucleins are developmentally expressed, and α-synuclein regulates the size of the presynaptic vesicular pool in primary hippocampal neurons
-
Murphy DD, Rueter SM, Trojanowski JQ, Lee VMY. Synucleins are developmentally expressed, and α-synuclein regulates the size of the presynaptic vesicular pool in primary hippocampal neurons. J Neurosci 2000; 20: 3214-3220.
-
(2000)
J Neurosci
, vol.20
, pp. 3214-3220
-
-
Murphy, D.D.1
Rueter, S.M.2
Trojanowski, J.Q.3
Lee, V.M.Y.4
-
99
-
-
0242321145
-
-
Nakajima A, Kataoka K, Hong M, Sakaguchi M, Huh NH. BRPK, a novel protein kinase showing increased expression in mouse cancer cell lines with higher metastatic potential. Cancer Lett 2003; 201: 195-201.
-
Nakajima A, Kataoka K, Hong M, Sakaguchi M, Huh NH. BRPK, a novel protein kinase showing increased expression in mouse cancer cell lines with higher metastatic potential. Cancer Lett 2003; 201: 195-201.
-
-
-
-
100
-
-
0033646422
-
Mice, the motor system, and human motor neuron pathology
-
Nicholson SJ, Witherden AS, Hafezparast M, Martin JE, Fisher EMC. Mice, the motor system, and human motor neuron pathology. Mamm Genome 2000; 11: 1041-1052.
-
(2000)
Mamm Genome
, vol.11
, pp. 1041-1052
-
-
Nicholson, S.J.1
Witherden, A.S.2
Hafezparast, M.3
Martin, J.E.4
Fisher, E.M.C.5
-
101
-
-
0033534788
-
Molecular cloning and characterization of mammalian homologues of vesicle-associated membrane protein-associated (VAMP-associated) proteins
-
Nishimura Y, Hayashi M, Inada H, Tanaka T. Molecular cloning and characterization of mammalian homologues of vesicle-associated membrane protein-associated (VAMP-associated) proteins. Biochem Biophys Res Commun 1999; 254: 21-26.
-
(1999)
Biochem Biophys Res Commun
, vol.254
, pp. 21-26
-
-
Nishimura, Y.1
Hayashi, M.2
Inada, H.3
Tanaka, T.4
-
102
-
-
6344257200
-
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atropny and amyotrophic lateral sclerosis
-
Nishimura AL, Mitne-Neto M, Silva HC, Richieri-Costa A, Middleton S, Cascia D, Kok F, Oliveira JR, Gillingwater T, Webb J, Skehel P, Zata M. A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atropny and amyotrophic lateral sclerosis. Am J Hum Genet 2004; 75: 822-831.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 822-831
-
-
Nishimura, A.L.1
Mitne-Neto, M.2
Silva, H.C.3
Richieri-Costa, A.4
Middleton, S.5
Cascia, D.6
Kok, F.7
Oliveira, J.R.8
Gillingwater, T.9
Webb, J.10
Skehel, P.11
Zata, M.12
-
103
-
-
0032936755
-
Etiology and pathogenesis of Parkinson's disease
-
Olanow CW, Tatton WG. Etiology and pathogenesis of Parkinson's disease. Annu Rev Neurosci 1999; 22: 123-144.
-
(1999)
Annu Rev Neurosci
, vol.22
, pp. 123-144
-
-
Olanow, C.W.1
Tatton, W.G.2
-
104
-
-
0034978562
-
-
Oosthuyse B, Moons L, Storkebaum E, Beck H, Nuyens D, Brusselmans K, Van Dorpe J, Hellings P, Gorselink M, Heymans S, Theilmeier G, Dewerchin M, Laudenbach V, Vermylen P, Raat H, Acker T, Vleminckx V, Van Den Bosch L, Cashman N, Fujisawa H, Drost MR, Sciot R, Bruyninckx F, Hicklin DJ, Ince C Gressens P, Lupu F, Plate KH, Robberecht W, Herbert JM, Collen D, Carmeliet P. Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration. Nat Genet 2001; 28: 131-138.
-
Oosthuyse B, Moons L, Storkebaum E, Beck H, Nuyens D, Brusselmans K, Van Dorpe J, Hellings P, Gorselink M, Heymans S, Theilmeier G, Dewerchin M, Laudenbach V, Vermylen P, Raat H, Acker T, Vleminckx V, Van Den Bosch L, Cashman N, Fujisawa H, Drost MR, Sciot R, Bruyninckx F, Hicklin DJ, Ince C Gressens P, Lupu F, Plate KH, Robberecht W, Herbert JM, Collen D, Carmeliet P. Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration. Nat Genet 2001; 28: 131-138.
-
-
-
-
105
-
-
0041308082
-
ALS2, a novel guanine nucleotide exchange factor for the small GTPase Rab5, is implicated in endosomal dynamics
-
Otomo A, Hadano S, Okada T, Mizumura H, Kunita R, Nishijama H, Showguchi-Miyata J, Yanagisawa Y, Kohiki E, Suga E, Yasuda M, Osuga H, Nishimoto T, Narumiya S, Ikeda JE. ALS2, a novel guanine nucleotide exchange factor for the small GTPase Rab5, is implicated in endosomal dynamics. Hum Mol Genet 2003; 12: 1671-1687.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1671-1687
-
-
Otomo, A.1
Hadano, S.2
Okada, T.3
Mizumura, H.4
Kunita, R.5
Nishijama, H.6
Showguchi-Miyata, J.7
Yanagisawa, Y.8
Kohiki, E.9
Suga, E.10
Yasuda, M.11
Osuga, H.12
Nishimoto, T.13
Narumiya, S.14
Ikeda, J.E.15
-
106
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
Paisán-Ruíz C, Jain S, Whitney Evans E, Gilks WP, Simón J, van der Brug M, López de Munain A, Aparicio S, Martínez-Gil A, Khan N, Johnson J, Ruiz Martinez J, Nicholl D, Marti Carrera I, Saénz Peňa A, de Silva R, Lees A, Martí- Massó JF, Pérez-Tur J, Wood NW, Singleton AB. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 2004; 44: 595-600.
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisán-Ruíz, C.1
Jain, S.2
Whitney Evans, E.3
Gilks, W.P.4
Simón, J.5
van der Brug, M.6
López de Munain, A.7
Aparicio, S.8
Martínez-Gil, A.9
Khan, N.10
Johnson, J.11
Ruiz Martinez, J.12
Nicholl, D.13
Marti Carrera, I.14
Saénz Peňa, A.15
de Silva, R.16
Lees, A.17
Martí- Massó, J.F.18
Pérez-Tur, J.19
Wood, N.W.20
Singleton, A.B.21
more..
-
107
-
-
2442481789
-
Mitochondrial dysfunction and oxidative damage in parkin-deficient mice
-
Palacino JJ, Sagi D, Goldberg MS, Krauss S, Motz C, Wacker M, Klose J, Shen J. Mitochondrial dysfunction and oxidative damage in parkin-deficient mice. J Biol Chem 2004; 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
-
108
-
-
0035887860
-
Induction of alpha-synuclein aggregation by intracellular nitrative insult
-
Paxinou E, Chen Q, Weisse M, Giasson BI, Norris EH, Rueter SM, Trojanowski JQ, L VM, Ischiropoulos H. Induction of alpha-synuclein aggregation by intracellular nitrative insult. J Neurosci 2001; 21: 8053-8061.
-
(2001)
J Neurosci
, vol.21
, pp. 8053-8061
-
-
Paxinou, E.1
Chen, Q.2
Weisse, M.3
Giasson, B.I.4
Norris, E.H.5
Rueter, S.M.6
Trojanowski, J.Q.7
VM, L.8
Ischiropoulos, H.9
-
109
-
-
13844313915
-
Parkin-deficient mice are not a robust model of parkinsonism
-
Perez FA, Palmiter RD. Parkin-deficient mice are not a robust model of parkinsonism. Proc Natl Acad Sci USA 2005; 102: 2174-2179.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 2174-2179
-
-
Perez, F.A.1
Palmiter, R.D.2
-
110
-
-
0242416191
-
Altered excitability of motor neurons in a transgenic mouse model of familial amyotrophic lateral sclerosis
-
Pieri M, Albo F, Gaetti C, Spalloni A, Bengston CP, Longone P, Cavalcanti S, Zona C. Altered excitability of motor neurons in a transgenic mouse model of familial amyotrophic lateral sclerosis. Neurosci Lett 2003; 351: 153-156.
-
(2003)
Neurosci Lett
, vol.351
, pp. 153-156
-
-
Pieri, M.1
Albo, F.2
Gaetti, C.3
Spalloni, A.4
Bengston, C.P.5
Longone, P.6
Cavalcanti, S.7
Zona, C.8
-
111
-
-
0030744876
-
Mutation in the α-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL. Mutation in the α-synuclein gene identified in families with Parkinson's disease. Science 1997; 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
Di Iorio, G.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
112
-
-
14744305520
-
Mitochondrial associated metabolic proteins are selectively oxidized in A30P α-synuclein transgenic mice - a model of familial Parkinson's disease
-
Poon HF, Frasier M, Shreve N, Calabrese V, Wolozin B, Butterfield DA. Mitochondrial associated metabolic proteins are selectively oxidized in A30P α-synuclein transgenic mice - a model of familial Parkinson's disease. Neurobiol Dis 2005; 18: 492-498.
-
(2005)
Neurobiol Dis
, vol.18
, pp. 492-498
-
-
Poon, H.F.1
Frasier, M.2
Shreve, N.3
Calabrese, V.4
Wolozin, B.5
Butterfield, D.A.6
-
113
-
-
0031029859
-
Excitotoxic neuronal death in the immature brain is an apoptosis-necrosis morphological continuum
-
Portera-Cailliau C, Price DL, Martin LJ. Excitotoxic neuronal death in the immature brain is an apoptosis-necrosis morphological continuum. J Comp Neurol 1997; 378: 70-87.
-
(1997)
J Comp Neurol
, vol.378
, pp. 70-87
-
-
Portera-Cailliau, C.1
Price, D.L.2
Martin, L.J.3
-
114
-
-
0031024876
-
Non-NMDA and NMDA receptor-mediated excitotoxic neuronal deaths in adult brain are morphologically distinct: Further evidence for an apoptosis-necrosis continuum
-
Portera-Cailliau C, Price DL, Martin LJ. Non-NMDA and NMDA receptor-mediated excitotoxic neuronal deaths in adult brain are morphologically distinct: further evidence for an apoptosis-necrosis continuum. J Comp Neurol 1997; 378: 88-104.
-
(1997)
J Comp Neurol
, vol.378
, pp. 88-104
-
-
Portera-Cailliau, C.1
Price, D.L.2
Martin, L.J.3
-
115
-
-
33845460959
-
Motor neuron diseases
-
Siegel GJ, Albers RW, Brady ST, Price DL, eds, New York: Elsevier
-
Price DL, Ackerly S, Martin LJ, Koliatsos V, Wong PC. Motor neuron diseases. In: Siegel GJ, Albers RW, Brady ST, Price DL, eds. Basic Neurochemistry: Molecular, Cellular, and Medical Aspects. New York: Elsevier, 2006; 731-743.
-
(2006)
Basic Neurochemistry: Molecular, Cellular, and Medical Aspects
, pp. 731-743
-
-
Price, D.L.1
Ackerly, S.2
Martin, L.J.3
Koliatsos, V.4
Wong, P.C.5
-
116
-
-
0037382240
-
Mutant dynactin in motor neuron disease
-
Puls I, Jonnakuty C, LaMonte BH, Holzbaur EL, Tokito M, Mann E, Floeter MK, Bidus K, Drayna D, Oh SJ, Brown RH Jr, Ludlow CL, Fischbeck KH. Mutant dynactin in motor neuron disease. Nat Genet 2003; 33: 455-456.
-
(2003)
Nat Genet
, vol.33
, pp. 455-456
-
-
Puls, I.1
Jonnakuty, C.2
LaMonte, B.H.3
Holzbaur, E.L.4
Tokito, M.5
Mann, E.6
Floeter, M.K.7
Bidus, K.8
Drayna, D.9
Oh, S.J.10
Brown Jr, R.H.11
Ludlow, C.L.12
Fischbeck, K.H.13
-
117
-
-
20944448536
-
Distal spinal and bulbar muscular atrophy caused by dynactin mutation
-
Puls I, Oh SJ, Sumner CJ, Wallace KE, Floeter MK, Mann EA, Kennedy WR, Wendelschafer-Crabb G, Votmeyer A, Powers R, Finnegan K, Holzbaur ELF, Fischbeck KH, Ludlow CL. Distal spinal and bulbar muscular atrophy caused by dynactin mutation. Ann Neurol 2005; 57: 687-694.
-
(2005)
Ann Neurol
, vol.57
, pp. 687-694
-
-
Puls, I.1
Oh, S.J.2
Sumner, C.J.3
Wallace, K.E.4
Floeter, M.K.5
Mann, E.A.6
Kennedy, W.R.7
Wendelschafer-Crabb, G.8
Votmeyer, A.9
Powers, R.10
Finnegan, K.11
Holzbaur, E.L.F.12
Fischbeck, K.H.13
Ludlow, C.L.14
-
118
-
-
2442624720
-
Monomeric Cu,Zn-superoxide dismutase is a common misfolding intermediate in the oxidation models of sporadic and familial amyotrophic sclerosis
-
Rakhit R, Crow JP, Lepock JR, Kondejewski LH, Cashman NR, Chakrabartty A. Monomeric Cu,Zn-superoxide dismutase is a common misfolding intermediate in the oxidation models of sporadic and familial amyotrophic sclerosis. J Biol Chem 2004; 279: 15499-15504.
-
(2004)
J Biol Chem
, vol.279
, pp. 15499-15504
-
-
Rakhit, R.1
Crow, J.P.2
Lepock, J.R.3
Kondejewski, L.H.4
Cashman, N.R.5
Chakrabartty, A.6
-
119
-
-
0037372292
-
Alterations in G1 to S phase cell-cycle regulators during amyotrophic lateral sclerosis
-
Ranganathan S, Bowser R. Alterations in G1 to S phase cell-cycle regulators during amyotrophic lateral sclerosis. Am J Pathol 2003; 162: 823-835.
-
(2003)
Am J Pathol
, vol.162
, pp. 823-835
-
-
Ranganathan, S.1
Bowser, R.2
-
120
-
-
0037068836
-
Motoneuron death triggered by a specific pathway downstream of Fas: Potentiation by ALS-linked SOD1 mutations
-
Raoul C, Estévez AG, Nishimune H, Cleveland DW, deLapeyriére O, Henderson CE, Hasse G, Pettmann B. Motoneuron death triggered by a specific pathway downstream of Fas: potentiation by ALS-linked SOD1 mutations. Neuron 2002; 35: 1067-1083.
-
(2002)
Neuron
, vol.35
, pp. 1067-1083
-
-
Raoul, C.1
Estévez, A.G.2
Nishimune, H.3
Cleveland, D.W.4
deLapeyriére, O.5
Henderson, C.E.6
Hasse, G.7
Pettmann, B.8
-
121
-
-
15844393658
-
Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury
-
Reaume AG, Elliott JL, Hoffman EK, Kowall NW, Ferrante RJ, Siwek DF, Wilcox HM, Flood DG, Beal MF, Brown RHJr, Scott RW, Snider WD. Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury. Nat Genet 1996; 13: 43-47.
-
(1996)
Nat Genet
, vol.13
, pp. 43-47
-
-
Reaume, A.G.1
Elliott, J.L.2
Hoffman, E.K.3
Kowall, N.W.4
Ferrante, R.J.5
Siwek, D.F.6
Wilcox, H.M.7
Flood, D.G.8
Beal, M.F.9
RHJr, B.10
Scott, R.W.11
Snider, W.D.12
-
122
-
-
0036245056
-
Behavioral and neurochemical effects of wild-type and mutated human alpha-synuclein in transgenic mice
-
Richfield EK Thiruchelvam MJ, Cory-Slechta DA, Wuetzer C, Gainetdinov RR, Caron MG, Di Monte DA, Federoff HJ. Behavioral and neurochemical effects of wild-type and mutated human alpha-synuclein in transgenic mice. Exp Neurol 2002; 175: 35-48.
-
(2002)
Exp Neurol
, vol.175
, pp. 35-48
-
-
Richfield, E.K.1
Thiruchelvam, M.J.2
Cory-Slechta, D.A.3
Wuetzer, C.4
Gainetdinov, R.R.5
Caron, M.G.6
Di Monte, D.A.7
Federoff, H.J.8
-
123
-
-
0027401203
-
-
Rosen DR, Siddique T, Patterson D, Figiewicz DA, Sapp P, Hentati A, Donalsson D, Goto J, O'Regan JP, Deng H-X, Rahmani Z, Krizus A, McKenna-Yasek D, Cayabyab A, Gaston AM, Berger R, Tanzi RE, Halperin JJ, Harzfeldt B, Van den Bergh R, Hung W-Y, Bird T, Deng G, Mulder DW, Smyth C, Laing NG, Soriano E, Pericak-Vance MA, Haines J, Rouleau GA, Gusella JS, Horvitz HR, Brown RH Jr. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993; 362: 59-62.
-
Rosen DR, Siddique T, Patterson D, Figiewicz DA, Sapp P, Hentati A, Donalsson D, Goto J, O'Regan JP, Deng H-X, Rahmani Z, Krizus A, McKenna-Yasek D, Cayabyab A, Gaston AM, Berger R, Tanzi RE, Halperin JJ, Harzfeldt B, Van den Bergh R, Hung W-Y, Bird T, Deng G, Mulder DW, Smyth C, Laing NG, Soriano E, Pericak-Vance MA, Haines J, Rouleau GA, Gusella JS, Horvitz HR, Brown RH Jr. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993; 362: 59-62.
-
-
-
-
124
-
-
0035978743
-
Amyotrophic lateral sclerosis
-
Rowland LP, Shneider NA. Amyotrophic lateral sclerosis. N Engl J Med 2001; 344: 1688-1700.
-
(2001)
N Engl J Med
, vol.344
, pp. 1688-1700
-
-
Rowland, L.P.1
Shneider, N.A.2
-
125
-
-
0034864628
-
-
Sathasivam S, Ince Shaw PJ. Apoptosis in amyotrophic lateral sclerosis: a review of the evidence. Neuropathol Appl Neurobiol 2001; 27: 257-274.
-
Sathasivam S, Ince PG, Shaw PJ. Apoptosis in amyotrophic lateral sclerosis: a review of the evidence. Neuropathol Appl Neurobiol 2001; 27: 257-274.
-
-
-
-
126
-
-
33744982893
-
Etiology of Parkinson's disease
-
Schapira AHV. Etiology of Parkinson's disease. Neurology 2006; 66 (Suppl 4): S10-S23.
-
(2006)
Neurology
, vol.66
, Issue.SUPPL. 4
-
-
Schapira, A.H.V.1
-
129
-
-
0034712918
-
Fiber diffraction of synthetic alpha synuclein filaments shows amyloid-like cross-beta conformation
-
Serpell LC, Berriman J, Jakes M, Goedert M, Crowther RA. Fiber diffraction of synthetic alpha synuclein filaments shows amyloid-like cross-beta conformation. Proc Natl Acad Sci USA 2000; 97: 4897-4902.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 4897-4902
-
-
Serpell, L.C.1
Berriman, J.2
Jakes, M.3
Goedert, M.4
Crowther, R.A.5
-
131
-
-
0035834274
-
Upregulation of the pro-apoptotic BH3-only peptide harakiri in spinal neurons of amyotrophic lateral sclerosis patients
-
Shinoe T, Wanaka A, Nikaido T, Kanazawa K, Shimizu J, Imaizumi K, Kanazawa I. Upregulation of the pro-apoptotic BH3-only peptide harakiri in spinal neurons of amyotrophic lateral sclerosis patients. Neurosci Lett 2001; 313: 153-157.
-
(2001)
Neurosci Lett
, vol.313
, pp. 153-157
-
-
Shinoe, T.1
Wanaka, A.2
Nikaido, T.3
Kanazawa, K.4
Shimizu, J.5
Imaizumi, K.6
Kanazawa, I.7
-
132
-
-
27944444154
-
Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism
-
Silvestri L, Caputo V, Bellacchio E, Atorino L, Dallapiccola B, Valente EM, Casari G. Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism. Hum Mol Genet 2005; 14: 3477-3492.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 3477-3492
-
-
Silvestri, L.1
Caputo, V.2
Bellacchio, E.3
Atorino, L.4
Dallapiccola, B.5
Valente, E.M.6
Casari, G.7
-
133
-
-
0242300619
-
Alpha-synuclein locus triplication causes Parkinson's disease
-
Singleton AB, Farrer M, Johnson J, Singleton A, Hague S, Kachergus J, Hulihan M, Peuralinna T, Dutra A, Nussbaum R, Lincoln S, Crawley A, Hanson M, Maraganore D, Adler C, Cookson MR, Muenter M, Baptista M, Miller D, Blancato J, Hardy J, Gwinn-Hardy K. Alpha-synuclein locus triplication causes Parkinson's disease. Science 2003; 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
Lincoln, S.11
Crawley, A.12
Hanson, M.13
Maraganore, D.14
Adler, C.15
Cookson, M.R.16
Muenter, M.17
Baptista, M.18
Miller, D.19
Blancato, J.20
Hardy, J.21
Gwinn-Hardy, K.22
more..
-
134
-
-
0033967492
-
Mouse VAP33 is associated with the endoplasmic reticulum and microtubules
-
Skehel PA, Fabian-Fine R, Kandel ER. Mouse VAP33 is associated with the endoplasmic reticulum and microtubules. Proc Natl Acad Sci USA 2000; 97: 1101-1106.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 1101-1106
-
-
Skehel, P.A.1
Fabian-Fine, R.2
Kandel, E.R.3
-
135
-
-
0034674652
-
Dityrosine cross-linking promotes formation of stable α-synuclein polymers
-
Souza JM, Giasson BI, Chen Q, Lee VM-Y, Ischiropoulos H. Dityrosine cross-linking promotes formation of stable α-synuclein polymers. J Biol Chem 2000; 265: 18344-18349.
-
(2000)
J Biol Chem
, vol.265
, pp. 18344-18349
-
-
Souza, J.M.1
Giasson, B.I.2
Chen, Q.3
Lee, V.M.-Y.4
Ischiropoulos, H.5
-
136
-
-
0035139227
-
Physiology of nitric oxide in skeletal muscle
-
Stamler JS, Meissner G. Physiology of nitric oxide in skeletal muscle. Physiol Rev 2001; 81: 209-237.
-
(2001)
Physiol Rev
, vol.81
, pp. 209-237
-
-
Stamler, J.S.1
Meissner, G.2
-
137
-
-
0036591852
-
Formation of hydrogen peroxide and hydroxyl radicals from Aβ and α-synuclein as a possible mechanism of cell death in Alzheimer's disease and Parkinson's disease
-
Tabner BJ, Turnbull S, El-Agnaf OM, Allsop D. Formation of hydrogen peroxide and hydroxyl radicals from Aβ and α-synuclein as a possible mechanism of cell death in Alzheimer's disease and Parkinson's disease. Free
-
(2002)
Free Radic Biol Med
, vol.32
, pp. 1076-1083
-
-
Tabner, B.J.1
Turnbull, S.2
El-Agnaf, O.M.3
Allsop, D.4
-
138
-
-
0034326816
-
Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicity
-
Tabrizi SJ, Orth M, Wilkinson JM, Taanman JW, Warner TT, Cooper JM, Schapira AH. Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicity. Hum Mol Genet 2000; 9: 2683-2689.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2683-2689
-
-
Tabrizi, S.J.1
Orth, M.2
Wilkinson, J.M.3
Taanman, J.W.4
Warner, T.T.5
Cooper, J.M.6
Schapira, A.H.7
-
139
-
-
2942700097
-
Reduced anti-oxidative stress activities of DJ-1 mutants found in Parkinson's disease patients
-
Takahashi-Niki K, Niki T, Taira T, Iguchi-Ariga SM, Ariga H. Reduced anti-oxidative stress activities of DJ-1 mutants found in Parkinson's disease patients. Biochem Biophys Res Commun 2004: 320: 389-397.
-
(2004)
Biochem Biophys Res Commun
, vol.320
, pp. 389-397
-
-
Takahashi-Niki, K.1
Niki, T.2
Taira, T.3
Iguchi-Ariga, S.M.4
Ariga, H.5
-
140
-
-
0031696403
-
A fluorescent double-labeling method to detect and confirm apoptotic nuclei in Parkinson's disease
-
Tatton NA, MaClean-Fraser A, Tatton WG, Perl DP, Olnanow CW. A fluorescent double-labeling method to detect and confirm apoptotic nuclei in Parkinson's disease. Ann Neurol 1998; 44: S142-S148.
-
(1998)
Ann Neurol
, vol.44
-
-
Tatton, N.A.1
MaClean-Fraser, A.2
Tatton, W.G.3
Perl, D.P.4
Olnanow, C.W.5
-
141
-
-
0037378897
-
-
Tatton WG, Chalmers-Redman R, Brown D, Tatton N. Apoptosis in Parkinson's disease: signals for neuronal degeneration. Ann Neurol 2003; 53: S61-S72.
-
Tatton WG, Chalmers-Redman R, Brown D, Tatton N. Apoptosis in Parkinson's disease: signals for neuronal degeneration. Ann Neurol 2003; 53: S61-S72.
-
-
-
-
143
-
-
0031013141
-
Apoptotic-like changes in Lewy-body-associated disorders and normal aging in substantia nigra neurons
-
Tompkins MM, Basgall EJ, Zamrini E, Hill WD. Apoptotic-like changes in Lewy-body-associated disorders and normal aging in substantia nigra neurons. Am J Pathol 1997; 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
-
145
-
-
0035873812
-
Alpha-synuclein implicated in Parkinson's disease catalyses the formation of hydrogen peroxide in vitro
-
Turnbull S, Tabner BJ, El-Agnaf OM, Moore S, Davies Y, Allsop D. Alpha-synuclein implicated in Parkinson's disease catalyses the formation of hydrogen peroxide in vitro. Free Radic Biol Med 2001; 30: 1163-1170.
-
(2001)
Free Radic Biol Med
, vol.30
, pp. 1163-1170
-
-
Turnbull, S.1
Tabner, B.J.2
El-Agnaf, O.M.3
Moore, S.4
Davies, Y.5
Allsop, D.6
-
146
-
-
0035958558
-
Growth-suppressive effects of BPOZ and RGR2, two genes involved in the PTEN signaling pathway
-
Unoki M, Nakamura Y. Growth-suppressive effects of BPOZ and RGR2, two genes involved in the PTEN signaling pathway. Oncogene 2001; 20: 4457-4465.
-
(2001)
Oncogene
, vol.20
, pp. 4457-4465
-
-
Unoki, M.1
Nakamura, Y.2
-
147
-
-
0033064535
-
Administration of nitric oxide synthase inhibitors does not alter disease course of amyotrophic lateral sclerosis SOD1 mutant transgenic mice
-
Upton-Rice MN, Cudkowicz ME, Mathew RK, Reif D, Brown RH Jr. Administration of nitric oxide synthase inhibitors does not alter disease course of amyotrophic lateral sclerosis SOD1 mutant transgenic mice. Ann Neurol 1999; 45: 413-414.
-
(1999)
Ann Neurol
, vol.45
, pp. 413-414
-
-
Upton-Rice, M.N.1
Cudkowicz, M.E.2
Mathew, R.K.3
Reif, D.4
Brown Jr., R.H.5
-
148
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
Valente EM, Abou-Sleiman PM, Caputo V, Muqit MM, Harvey K, Gispert A, Ali Z, Del Turco D, Bentivoglio AR, Healy DG, Albanese A, Nussbaum R, Gonzalez-Maldonado R, Deller T, Salvi S, Cortelli P, Gilks WP, Latchman DS, Harvey RJ, Dallapiccola B, Auburger G, Wood NW. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 2004; 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, A.6
Ali, Z.7
Del Turco, D.8
Bentivoglio, A.R.9
Healy, D.G.10
Albanese, A.11
Nussbaum, R.12
Gonzalez-Maldonado, R.13
Deller, T.14
Salvi, S.15
Cortelli, P.16
Gilks, W.P.17
Latchman, D.S.18
Harvey, R.J.19
Dallapiccola, B.20
Auburger, G.21
Wood, N.W.22
more..
-
149
-
-
0037675042
-
Indicence of Parkinson's disease: Variations by age, gender and race ethnicity
-
Van Den Eeden SK, Tanner CM, Bernstein AL, Fross RD, Leimpeter A, Bloch DA, Nelson LM. Indicence of Parkinson's disease: variations by age, gender and race ethnicity. Am J Epidemol 2003; 157: 1015-1022.
-
(2003)
Am J Epidemol
, vol.157
, pp. 1015-1022
-
-
Van Den Eeden, S.K.1
Tanner, C.M.2
Bernstein, A.L.3
Fross, R.D.4
Leimpeter, A.5
Bloch, D.A.6
Nelson, L.M.7
-
150
-
-
0034663176
-
Neuropathology in mice expressing human α-synuclein
-
van der Putten H, Wiederhold K-H, Probst A, Barbieri S, Mistl C, Danner S, Kauffmann S, Hofele K, Spooren WPJM, Ruegg MA, Lin S, Caroni P, Sommer B, Tolnay M, Bilbe G. Neuropathology in mice expressing human α-synuclein. J Neurosci 2000; 20: 6021-6029.
-
(2000)
J Neurosci
, vol.20
, pp. 6021-6029
-
-
van der Putten, H.1
Wiederhold, K.-H.2
Probst, A.3
Barbieri, S.4
Mistl, C.5
Danner, S.6
Kauffmann, S.7
Hofele, K.8
Spooren, W.P.J.M.9
Ruegg, M.A.10
Lin, S.11
Caroni, P.12
Sommer, B.13
Tolnay, M.14
Bilbe, G.15
-
151
-
-
18044371459
-
Mouse motor neuron disease caused by truncated SOD1 with or without C-terminal modification
-
Watanabe Y, Yasui K, Nakano T, Doi K, Fukada Y, Kitayama M, Ishimoto M, Kurihara S, Kawashima M, Fukuda H, Adachi Y, Inoue T, Nakashima K. Mouse motor neuron disease caused by truncated SOD1 with or without C-terminal modification. Mol Brain Res 2005; 135: 12-20.
-
(2005)
Mol Brain Res
, vol.135
, pp. 12-20
-
-
Watanabe, Y.1
Yasui, K.2
Nakano, T.3
Doi, K.4
Fukada, Y.5
Kitayama, M.6
Ishimoto, M.7
Kurihara, S.8
Kawashima, M.9
Fukuda, H.10
Adachi, Y.11
Inoue, T.12
Nakashima, K.13
-
152
-
-
0024461942
-
The neuron-specific protein PGP 9.5 is a ubiquitin carboxyl terminal hydrolase
-
Wilkinson KD, Lee KM, Deshpande S, Duerken-Hughes P, Boss JM, Pohl J. The neuron-specific protein PGP 9.5 is a ubiquitin carboxyl terminal hydrolase. Science 1989; 246: 670-673.
-
(1989)
Science
, vol.246
, pp. 670-673
-
-
Wilkinson, K.D.1
Lee, K.M.2
Deshpande, S.3
Duerken-Hughes, P.4
Boss, J.M.5
Pohl, J.6
-
153
-
-
0042130551
-
The 1.1-A resolution crystal structure of DJ-1, the protein mutated in autosomal recessive early onset Parkinson's disease
-
Wilson MA, Collins JL, Hod Y, Ringe D, Petsko GA. 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 2003; 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
-
154
-
-
0029053881
-
An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
-
Wong PC, Pardo CA, Borchelt DR, Lee MK, Copeland NG, Jenkins NA, Sisodia SS, Cleveland DW, Price DL. An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria. Neuron 1995; 14: 1105-1116.
-
(1995)
Neuron
, vol.14
, pp. 1105-1116
-
-
Wong, P.C.1
Pardo, C.A.2
Borchelt, D.R.3
Lee, M.K.4
Copeland, N.G.5
Jenkins, N.A.6
Sisodia, S.S.7
Cleveland, D.W.8
Price, D.L.9
-
155
-
-
0342331476
-
Cell death and apoptosis regulating proteins in Parkinson's disease - a cautionary note
-
Wüllner U, Kornhuber J, Weller M, Schulz JB, Loschmann PA, Riederer P, Klockgether T. Cell death and apoptosis regulating proteins in Parkinson's disease - a cautionary note. Acta Neuropathol 1999; 97: 408-412.
-
(1999)
Acta Neuropathol
, vol.97
, pp. 408-412
-
-
Wüllner, U.1
Kornhuber, J.2
Weller, M.3
Schulz, J.B.4
Loschmann, P.A.5
Riederer, P.6
Klockgether, T.7
-
156
-
-
0346734108
-
Unstable mutants in the peripheral endosomal membrane component ALS2 cause early-onset motor neuron disease
-
Yamanaka K, Vande VC, Eymard-Pierre E, Bertini E, Boespflug-Tanguy O, Cleveland DW. Unstable mutants in the peripheral endosomal membrane component ALS2 cause early-onset motor neuron disease. Proc Natl Acad Sci USA 2003; 100: 16041-6046.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 16041-16046
-
-
Yamanaka, K.1
Vande, V.C.2
Eymard-Pierre, E.3
Bertini, E.4
Boespflug-Tanguy, O.5
Cleveland, D.W.6
-
157
-
-
33745728401
-
Progressive spinal axonal degeneration and slowness in ALS2-deficient mice
-
Yamanaka K, Miller TM, McAlonis-Downes M, Chun SJ, Cleveland DW. Progressive spinal axonal degeneration and slowness in ALS2-deficient mice. Ann Neurol 2006; 60: 95-104
-
(2006)
Ann Neurol
, vol.60
, pp. 95-104
-
-
Yamanaka, K.1
Miller, T.M.2
McAlonis-Downes, M.3
Chun, S.J.4
Cleveland, D.W.5
-
158
-
-
85047699103
-
Is motoneuronal cell death in amyotrophic lateral sclerosis apoptosis?
-
Yamazaki M, Esumi E, Nakano I. Is motoneuronal cell death in amyotrophic lateral sclerosis apoptosis? Neuropathology 2005; 25: 381-387.
-
(2005)
Neuropathology
, vol.25
, pp. 381-387
-
-
Yamazaki, M.1
Esumi, E.2
Nakano, I.3
-
159
-
-
0034785509
-
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
-
Yang Y, Hentati A, Deng H-X, Dabbagh O, Sasaki T, Hirano M, Hung W-Y, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Pericak-Vaance M, Hentati F, Siddique T. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nat Genet 2001; 29: 160-165.
-
(2001)
Nat Genet
, vol.29
, pp. 160-165
-
-
Yang, Y.1
Hentati, A.2
Deng, H.-X.3
Dabbagh, O.4
Sasaki, T.5
Hirano, M.6
Hung, W.-Y.7
Ouahchi, K.8
Yan, J.9
Azim, A.C.10
Cole, N.11
Gascon, G.12
Yagmour, A.13
Ben-Hamida, M.14
Pericak-Vaance, M.15
Hentati, F.16
Siddique, T.17
-
163
-
-
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 RJ, Calne DB, Stoessi J, Pfeiffer RF, Patenge N, Carballo Carbajal I, Vieregge P, Asmus F, Müller-Myhsok B, Dickson DW, Meitinger T, Storm TM, Wszolek ZK, Gasser T. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron 2004; 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
Calne, D.B.10
Stoessi, J.11
Pfeiffer, R.F.12
Patenge, N.13
Carballo Carbajal, I.14
Vieregge, P.15
Asmus, F.16
Müller-Myhsok, B.17
Dickson, D.W.18
Meitinger, T.19
Storm, T.M.20
Wszolek, Z.K.21
Gasser, T.22
more..
|