-
1
-
-
3943102116
-
Unraveling the mechanisms involved in motor neuron degeneration in ALS
-
DOI 10.1146/annurev.neuro.27.070203.144244
-
Bruijn LI, Miller TM, Cleveland DW (2004) Unraveling the mechanisms involved in motor neuron degeneration in ALS. Annu Rev Neurosci 27:723-749 (Pubitemid 39050419)
-
(2004)
Annual Review of Neuroscience
, vol.27
, pp. 723-749
-
-
Bruijn, L.I.1
Miller, T.M.2
Cleveland, D.W.3
-
2
-
-
30344442440
-
Disease progression of human SOD1 (G93A) transgenic ALS model rats
-
DOI 10.1002/jnr.20708
-
Matsumoto A, Okada Y, Nakamichi M, Nakamura M, Toyama Y, Sobue G, Nagai M, Aoki M, Itoyama Y, Okano H (2006) Disease progression of human SOD1 (G93A) transgenic ALS model rats. J Neurosci Res 83:119-133 (Pubitemid 43062016)
-
(2006)
Journal of Neuroscience Research
, vol.83
, Issue.1
, pp. 119-133
-
-
Matsumoto, A.1
Okada, Y.2
Nakamichi, M.3
Nakamura, M.4
Toyama, Y.5
Sobue, G.6
Nagai, M.7
Aoki, M.8
Itoyama, Y.9
Okano, H.10
-
3
-
-
42049091220
-
Molecular insights and therapeutic targets in amyotrophic lateral sclerosis
-
DOI 10.2174/187152708783885110
-
Tripathi VB, Al-Chalabi A (2008) Molecular insights and therapeutic targets in amyotrophic lateral sclerosis. CNS Neurol Disord Drug Targets 7:11-19 (Pubitemid 351516212)
-
(2008)
CNS and Neurological Disorders - Drug Targets
, vol.7
, Issue.1
, pp. 11-19
-
-
Tripathi, V.B.1
Al-Chalabi, A.2
-
4
-
-
69049087653
-
The human G93A-superoxide dismutase-1 mutation, mitochondrial glutathione and apoptotic cell death
-
Muyderman H, Hutson PG, Matusica D, Rogers ML, Rush RA (2009) The human G93A-superoxide dismutase-1 mutation, mitochondrial glutathione and apoptotic cell death. Neurochem Res 34: 1847-1856
-
(2009)
Neurochem Res
, vol.34
, pp. 1847-1856
-
-
Muyderman, H.1
Hutson, P.G.2
Matusica, D.3
Rogers, M.L.4
Rush, R.A.5
-
5
-
-
0028093154
-
New pathological findings in amyotrophic lateral sclerosis
-
Lowe J (1994) New pathological findings in amyotrophic lateral sclerosis. J Neurol Sci 124(Suppl):38-51
-
(1994)
J Neurol Sci
, vol.124
, Issue.SUPPL.
, pp. 38-51
-
-
Lowe, J.1
-
6
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
DOI 10.1126/science.1134108
-
Neumann M, Sampathu DM, Kwong LK et al (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314:130-133 (Pubitemid 44547757)
-
(2006)
Science
, vol.314
, Issue.5796
, pp. 130-133
-
-
Neumann, M.1
Sampathu, D.M.2
Kwong, L.K.3
Truax, A.C.4
Micsenyi, M.C.5
Chou, T.T.6
Bruce, J.7
Schuck, T.8
Grossman, M.9
Clark, C.M.10
McCluskey, L.F.11
Miller, B.L.12
Masliah, E.13
Mackenzie, I.R.14
Feldman, H.15
Feiden, W.16
Kretzschmar, H.A.17
Trojanowski, J.Q.18
Lee, V.M.-Y.19
-
7
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
DOI 10.1126/science.1154584
-
Sreedharan J, Blair IP, Tripathi VB et al (2008) TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319: 1668-1672 (Pubitemid 351432505)
-
(2008)
Science
, vol.319
, Issue.5870
, pp. 1668-1672
-
-
Sreedharan, J.1
Blair, I.P.2
Tripathi, V.B.3
Hu, X.4
Vance, C.5
Rogelj, B.6
Ackerley, S.7
Durnall, J.C.8
Williams, K.L.9
Buratti, E.10
Baralle, F.11
De Belleroche, J.12
Mitchell, J.D.13
Leigh, P.N.14
Al-Chalabi, A.15
Miller, C.C.16
Nicholson, G.17
Shaw, C.E.18
-
8
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
Vance C, Rogelj B, Hortobagyi T et al (2009) Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 323:1208-1211
-
(2009)
Science
, vol.323
, pp. 1208-1211
-
-
Vance, C.1
Rogelj, B.2
Hortobagyi, T.3
-
9
-
-
84871219249
-
The C9ORF72 expansionmutation is a common cause of ALS+/-FTD in Europe and has a single founder
-
Smith BN, Newhouse S, Shatunov A et al (2013) The C9ORF72 expansionmutation is a common cause of ALS+/-FTD in Europe and has a single founder. Eur J Hum Genet 21:102-108
-
(2013)
Eur J Hum Genet
, vol.21
, pp. 102-108
-
-
Smith, B.N.1
Newhouse, S.2
Shatunov, A.3
-
10
-
-
80052580969
-
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
-
Deng HX, Chen W, Hong ST et al (2011) Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature 477:211-215
-
(2011)
Nature
, vol.477
, pp. 211-215
-
-
Deng, H.X.1
Chen, W.2
Hong, S.T.3
-
11
-
-
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 (1994) Motor neuron degeneration in mice that express a human Cu, Zn superoxide dismutase mutation. Science 264:1772-1775 (Pubitemid 24227760)
-
(1994)
Science
, vol.264
, Issue.5166
, pp. 1772-1775
-
-
Gurney, M.E.1
Pu, H.2
Chiu, A.Y.3
Dal, C.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
-
12
-
-
34548157024
-
Microarray analysis of the cellular pathways involved in the adaptation to and progression of motor neuron injury in the SOD1 G93A mouse model of familial ALS
-
DOI 10.1523/JNEUROSCI.1470-07.2007
-
Ferraiuolo L, Heath PR, Holden H, Kasher P, Kirby J, Shaw PJ (2007) Microarray analysis of the cellular pathways involved in the adaptation to and progression of motor neuron injury in the SOD1 G93A mouse model of familial ALS. J Neurosci 27:9201-9219 (Pubitemid 47312070)
-
(2007)
Journal of Neuroscience
, vol.27
, Issue.34
, pp. 9201-9219
-
-
Ferraiuolo, L.1
Heath, P.R.2
Holden, H.3
Kasher, P.4
Kirby, J.5
Shaw, P.J.6
-
13
-
-
33645225597
-
Pathogenic superoxide dismutase structure, folding, aggregation and turnover
-
Hart PJ (2006) Pathogenic superoxide dismutase structure, folding, aggregation and turnover. Curr Opin Chem Biol 10:131-138
-
(2006)
Curr Opin Chem Biol
, vol.10
, pp. 131-138
-
-
Hart, P.J.1
-
14
-
-
0037077040
-
Toxic proteins in neurodegenerative disease
-
DOI 10.1126/science.1067122
-
Taylor JP, Hardy J, Fischbeck KH (2002) Toxic proteins in neurodegenerative disease. Science 296:1991-1995 (Pubitemid 34627514)
-
(2002)
Science
, vol.296
, Issue.5575
, pp. 1991-1995
-
-
Taylor, J.P.1
Hardy, J.2
Fischbeck, K.H.3
-
15
-
-
0033743320
-
Protein disulfide isomerase in Alzheimer disease
-
Kim HT, Russell RL, Raina AK, Harris PL, Siedlak SL, Zhu X, Petersen RB, Shimohama S, Smith MA, Perry G (2000) Protein disulfide isomerase in Alzheimer disease. Antioxid Redox Signal 2:485-489
-
(2000)
Antioxid Redox Signal
, vol.2
, pp. 485-489
-
-
Kim, H.T.1
Russell, R.L.2
Raina, A.K.3
Harris, P.L.4
Siedlak, S.L.5
Zhu, X.6
Petersen, R.B.7
Shimohama, S.8
Smith, M.A.9
Perry, G.10
-
16
-
-
36749094065
-
S-nitrosylation of peroxiredoxin 2 promotes oxidative stress-induced neuronal cell death in Parkinson's disease
-
DOI 10.1073/pnas.0705904104
-
Fang J, Nakamura T, Cho DH, Gu Z, Lipton SA (2007) Snitrosylation of peroxiredoxin 2 promotes oxidative stress-induced neuronal cell death in Parkinson's disease. Proc Natl Acad Sci U S A 104:18742-18747 (Pubitemid 350210767)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.47
, pp. 18742-18747
-
-
Fang, J.1
Nakamura, T.2
Cho, D.-H.3
Gu, Z.4
Lipton, S.A.5
-
17
-
-
62449244004
-
Cell death: Protein misfolding and neurodegenerative diseases
-
Nakamura T, Lipton SA (2009) Cell death: protein misfolding and neurodegenerative diseases. Apoptosis 14:455-468
-
(2009)
Apoptosis
, vol.14
, pp. 455-468
-
-
Nakamura, T.1
Lipton, S.A.2
-
18
-
-
77957358299
-
Mitochondrial dynamics in cell death and neurodegeneration
-
Cho DH, Nakamura T, Lipton SA (2010)Mitochondrial dynamics in cell death and neurodegeneration. Cell Mol Life Sci 67:3435-3447
-
(2010)
Cell Mol Life Sci
, vol.67
, pp. 3435-3447
-
-
Cho, D.H.1
Nakamura, T.2
Lipton, S.A.3
-
19
-
-
77955653927
-
Protein disulfide isomerase-immunopositive inclusions in patients with Alzheimer disease
-
Honjo Y, Ito H, Horibe T, Takahashi R, Kawakami K (2010) Protein disulfide isomerase-immunopositive inclusions in patients with Alzheimer disease. Brain Res 1349:90-96
-
(2010)
Brain Res
, vol.1349
, pp. 90-96
-
-
Honjo, Y.1
Ito, H.2
Horibe, T.3
Takahashi, R.4
Kawakami, K.5
-
20
-
-
77955432558
-
S-nitrosylation of Drp1 links excessive mitochondrial fission to neuronal injury in neurodegeneration
-
Nakamura T, Cieplak P, Cho DH, Godzik A, Lipton SA (2010) S-nitrosylation of Drp1 links excessive mitochondrial fission to neuronal injury in neurodegeneration. Mitochondrion 10:573-578
-
(2010)
Mitochondrion
, vol.10
, pp. 573-578
-
-
Nakamura, T.1
Cieplak, P.2
Cho, D.H.3
Godzik, A.4
Lipton, S.A.5
-
21
-
-
84862001706
-
Protein disulfide isomerase regulates endoplasmic reticulum stress and the apoptotic process during prion infection and PrP mutant-induced cytotoxicity
-
Wang SB, Shi Q, Xu Y, Xie WL, Zhang J, Tian C, Guo Y, Wang K, Zhang BY, Chen C, Gao C, Dong XP (2012) Protein disulfide isomerase regulates endoplasmic reticulum stress and the apoptotic process during prion infection and PrP mutant-induced cytotoxicity. PLoS One 7:e38221
-
(2012)
PLoS One
, vol.7
-
-
Wang, S.B.1
Shi, Q.2
Xu, Y.3
Xie, W.L.4
Zhang, J.5
Tian, C.6
Guo, Y.7
Wang, K.8
Zhang, B.Y.9
Chen, C.10
Gao, C.11
Dong, X.P.12
-
22
-
-
33749563294
-
Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1
-
DOI 10.1074/jbc.M603393200
-
Atkin JD, Farg MA, Turner BJ, Tomas D, Lysaght JA, Nunan J, Rembach A, Nagley P, Beart PM, Cheema SS, Horne MK (2006) Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1. J Biol Chem 281:30152-30165 (Pubitemid 44537023)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.40
, pp. 30152-30165
-
-
Atkin, J.D.1
Farg, M.A.2
Turner, B.J.3
Tomas, D.4
Lysaght, J.A.5
Nunan, J.6
Rembach, A.7
Nagley, P.8
Beart, P.M.9
Cheema, S.S.10
Horne, M.K.11
-
23
-
-
43649100018
-
Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis
-
Atkin JD, Farg MA, Walker AK, McLean C, Tomas D, Horne MK (2008) Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis. Neurobiol Dis 30:400-407
-
(2008)
Neurobiol Dis
, vol.30
, pp. 400-407
-
-
Atkin, J.D.1
Farg, M.A.2
Walker, A.K.3
McLean, C.4
Tomas, D.5
Horne, M.K.6
-
24
-
-
4444237848
-
Identification of the protein disulfide isomerase family member PDIp in experimental Parkinson's disease and Lewy body pathology
-
DOI 10.1016/j.brainres.2004.07.026, PII S0006899304010911
-
Conn KJ, Gao W, McKee A, Lan MS, Ullman MD, Eisenhauer PB, Fine RE, Wells JM (2004) Identification of the protein disulfide isomerase family member PDIp in experimental Parkinson's disease and Lewy body pathology. Brain Res 1022:164-172 (Pubitemid 39194996)
-
(2004)
Brain Research
, vol.1022
, Issue.1-2
, pp. 164-172
-
-
Conn, K.J.1
Gao, W.2
McKee, A.3
Lan, M.S.4
Ullman, M.D.5
Eisenhauer, P.B.6
Fine, R.E.7
Wells, J.M.8
-
25
-
-
33745821631
-
Posttranslational modifications in Cu,Zn-superoxide dismutase and mutations associated with amyptrophic lateral sclerosis
-
DOI 10.1089/ars.2006.8.847
-
Furukawa Y, O'Halloran TV (2006) Posttranslational modifications in Cu, Zn-superoxide dismutase andmutations associatedwith amyotrophic lateral sclerosis. Antioxid Redox Signal 8:847-867 (Pubitemid 44036502)
-
(2006)
Antioxidants and Redox Signaling
, vol.8
, Issue.5-6
, pp. 847-867
-
-
Furukawa, Y.1
O'Halloran, T.V.2
-
26
-
-
66749133370
-
Aggregation of copper-zinc superoxide dismutase in familial and sporadic ALS
-
Chattopadhyay M, Valentine JS (2009) Aggregation of copper-zinc superoxide dismutase in familial and sporadic ALS. Antioxid Redox Signal 11:1603-1614
-
(2009)
Antioxid Redox Signal
, vol.11
, pp. 1603-1614
-
-
Chattopadhyay, M.1
Valentine, J.S.2
-
27
-
-
70349759885
-
Immature copper-zinc superoxide dismutase and familial amyotrophic lateral sclerosis
-
Maywood
-
Seetharaman SV, Prudencio M, Karch C, Holloway SP, Borchelt DR, Hart PJ (2009) Immature copper-zinc superoxide dismutase and familial amyotrophic lateral sclerosis. Exp Biol Med (Maywood) 234:1140-1154
-
(2009)
Exp Biol Med
, vol.234
, pp. 1140-1154
-
-
Seetharaman, S.V.1
Prudencio, M.2
Karch, C.3
Holloway, S.P.4
Borchelt, D.R.5
Hart, P.J.6
-
28
-
-
3543029884
-
Oxygen-induced maturation of SOD1: A key role for disulfide formation by the copper chaperone CCS
-
DOI 10.1038/sj.emboj.7600276
-
Furukawa Y, Torres AS, O'Halloran TV (2004) Oxygen-induced maturation of SOD1: a key role for disulfide formation by the copper chaperone CCS. EMBO J 23:2872-2881 (Pubitemid 39013559)
-
(2004)
EMBO Journal
, vol.23
, Issue.14
, pp. 2872-2881
-
-
Furukawa, Y.1
Torres, A.S.2
O'Halloran, T.V.3
-
29
-
-
33645798615
-
Spinal cord endoplasmic reticulum stress associated with a microsomal accumulation of mutant superoxide dismutase-1 in an ALS model
-
Kikuchi H, Almer G, Yamashita S, Guegan C, Nagai M, Xu Z, Sosunov AA, McKhann GM 2nd, Przedborski S (2006) Spinal cord endoplasmic reticulum stress associated with a microsomal accumulation of mutant superoxide dismutase-1 in an ALS model. Proc Natl Acad Sci U S A 103:6025-6030
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 6025-6030
-
-
Kikuchi, H.1
Almer, G.2
Yamashita, S.3
Guegan, C.4
Nagai, M.5
Xu, Z.6
Sosunov, A.A.7
McKhann II, G.M.8
Przedborski, S.9
-
30
-
-
36248949141
-
The endoplasmic reticulum and the unfolded protein response
-
DOI 10.1016/j.semcdb.2007.09.003, PII S1084952107001498, Degredation of Misfolded Glycoproteins
-
Malhotra JD, Kaufman RJ (2007) The endoplasmic reticulumand the unfolded protein response. Semin Cell Dev Biol 18:716-731 (Pubitemid 350138453)
-
(2007)
Seminars in Cell and Developmental Biology
, vol.18
, Issue.6
, pp. 716-731
-
-
Malhotra, J.D.1
Kaufman, R.J.2
-
31
-
-
70449377144
-
Reticulon-4A (Nogo-A) redistributes protein disulfide isomerase to protect mice from SOD1-dependent amyotrophic lateral sclerosis
-
Yang YS, Harel NY, Strittmatter SM (2009) Reticulon-4A (Nogo-A) redistributes protein disulfide isomerase to protect mice from SOD1-dependent amyotrophic lateral sclerosis. J Neurosci 29: 13850-13859
-
(2009)
J Neurosci
, vol.29
, pp. 13850-13859
-
-
Yang, Y.S.1
Harel, N.Y.2
Strittmatter, S.M.3
-
32
-
-
78649246847
-
Inhibitors of protein disulfide isomerase suppress apoptosis induced by misfolded proteins
-
Hoffstrom BG, Kaplan A, Letso R, Schmid RS, Turmel GJ, Lo DC, Stockwell BR (2010) Inhibitors of protein disulfide isomerase suppress apoptosis induced by misfolded proteins. Nat Chem Biol 6: 900-906
-
(2010)
Nat Chem Biol
, vol.6
, pp. 900-906
-
-
Hoffstrom, B.G.1
Kaplan, A.2
Letso, R.3
Schmid, R.S.4
Turmel, G.J.5
Lo, D.C.6
Stockwell, B.R.7
-
33
-
-
74249084267
-
Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis
-
Walker AK, Farg MA, Bye CR, McLean CA, Horne MK, Atkin JD (2010) Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis. Brain 133:105-116
-
(2010)
Brain
, vol.133
, pp. 105-116
-
-
Walker, A.K.1
Farg, M.A.2
Bye, C.R.3
McLean, C.A.4
Horne, M.K.5
Atkin, J.D.6
-
34
-
-
0037144597
-
Role of ubiquilin associated with protein-disulfide isomerase in the endoplasmic reticulum in stress-induced apoptotic cell death
-
Ko HS, Uehara T, Nomura Y (2002) Role of ubiquilin associated with protein-disulfide isomerase in the endoplasmic reticulum in stress-induced apoptotic cell death. J Biol Chem 277:35386-35392
-
(2002)
J Biol Chem
, vol.277
, pp. 35386-35392
-
-
Ko, H.S.1
Uehara, T.2
Nomura, Y.3
-
35
-
-
7744232493
-
Misfolded proteins, endoplasmic reticulum stress and neurodegeneration
-
DOI 10.1016/j.ceb.2004.09.012, PII S0955067404001486
-
Rao RV, Bredesen DE (2004) Misfolded proteins, endoplasmic reticulum stress and neurodegeneration. Curr Opin Cell Biol 16:653-662 (Pubitemid 39463116)
-
(2004)
Current Opinion in Cell Biology
, vol.16
, Issue.6
, pp. 653-662
-
-
Rao, R.V.1
Bredesen, D.E.2
-
36
-
-
15244361681
-
The disulfide isomerase Grp58 is a protective factor against prion neurotoxicity
-
DOI 10.1523/JNEUROSCI.4090-04.2005
-
Hetz C, Russelakis-Carneiro M, Walchli S, Carboni S, Vial-Knecht E, Maundrell K, Castilla J, Soto C (2005) The disulfide isomerase Grp58 is a protective factor against prion neurotoxicity. J Neurosci 25:2793-2802 (Pubitemid 40389237)
-
(2005)
Journal of Neuroscience
, vol.25
, Issue.11
, pp. 2793-2802
-
-
Hetz, C.1
Russelakis-Carneiro, M.2
Walchli, S.3
Carboni, S.4
Vial-Knecht, E.5
Maundrell, K.6
Castilla, J.7
Soto, C.8
-
37
-
-
33745315287
-
S-Nitrosylated protein-disulphide isomerase links protein misfolding to neurodegeneration
-
DOI 10.1038/nature04782, PII NATURE04782
-
Uehara T, Nakamura T, Yao D, Shi ZQ, Gu Z, Ma Y, Masliah E, Nomura Y, Lipton SA (2006) S-nitrosylated protein-disulphide isomerase links protein misfolding to neurodegeneration. Nature 441: 513-517 (Pubitemid 44050153)
-
(2006)
Nature
, vol.441
, Issue.7092
, pp. 513-517
-
-
Uehara, T.1
Nakamura, T.2
Yao, D.3
Shi, Z.-Q.4
Gu, Z.5
Ma, Y.6
Masliah, E.7
Nomura, Y.8
Lipton, S.A.9
-
38
-
-
70049083635
-
Protein S-nitrosylation in health and disease: A current perspective
-
Foster MW, Hess DT, Stamler JS (2009) Protein S-nitrosylation in health and disease: a current perspective. Trends Mol Med 15:391-404
-
(2009)
Trends Mol Med
, vol.15
, pp. 391-404
-
-
Foster, M.W.1
Hess, D.T.2
Stamler, J.S.3
-
39
-
-
80051781073
-
Redox modulation by S-nitrosylation contributes to protein misfolding, mitochondrial dynamics, and neuronal synaptic damage in neurodegenerative diseases
-
Nakamura T, Lipton SA (2011) Redox modulation by S-nitrosylation contributes to protein misfolding, mitochondrial dynamics, and neuronal synaptic damage in neurodegenerative diseases. Cell Death Differ 18:1478-1486
-
(2011)
Cell Death Differ
, vol.18
, pp. 1478-1486
-
-
Nakamura, T.1
Lipton, S.A.2
-
40
-
-
0037119624
-
S-nitrosylation of matrix metalloproteinases: Signaling pathway to neuronal cell death
-
DOI 10.1126/science.1073634
-
Gu Z, Kaul M, Yan B, Kridel SJ, Cui J, Strongin A, Smith JW, Liddington RC, Lipton SA (2002) S-nitrosylation of matrix metalloproteinases: signaling pathway to neuronal cell death. Science 297: 1186-1190 (Pubitemid 36193354)
-
(2002)
Science
, vol.297
, Issue.5584
, pp. 1186-1190
-
-
Gu, Z.1
Kaul, M.2
Yan, B.3
Kridel, S.J.4
Cui, J.5
Strongin, A.6
Smith, J.W.7
Liddington, R.C.8
Lipton, S.A.9
-
41
-
-
2542534741
-
S-nitrosylation of parkin regulates ubiquitination and compromises parkin's protective function
-
DOI 10.1126/science.1093891
-
Chung KK, Thomas B, Li X, Pletnikova O, Troncoso JC, Marsh L, Dawson VL, Dawson TM (2004) S-nitrosylation of parkin regulates ubiquitination and compromises Parkin's protective function. Science 304:1328-1331 (Pubitemid 38697430)
-
(2004)
Science
, vol.304
, Issue.5675
, pp. 1328-1331
-
-
Chung, K.K.K.1
Thomas, B.2
Li, X.3
Pletnikova, O.4
Troncoso, J.C.5
Marsh, L.6
Dawson, V.L.7
Dawson, T.M.8
-
42
-
-
3242733689
-
Nitrosative stress linked to sporadic Parkinson's disease: S-nitrosylation of parkin regulates its E3 ubiquitin ligase activity
-
DOI 10.1073/pnas.0404161101
-
Yao D, Gu Z, Nakamura T, Shi Z-Q, Ma Y, Gaston B, Palmer LA, Rockenstein EM, Zhang Z, Masliah E, Uehara T, Lipton SA (2004) Nitrosative stress linked to sporadic Parkinson's disease: S - nitrosylation of parkin regulates it E3 ligase activity. Proc Natl Acad Sci U S A 101:10810-10814 (Pubitemid 38955824)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.29
, pp. 10810-10814
-
-
Yao, D.1
Gu, Z.2
Nakamura, T.3
Shi, Z.-Q.4
Ma, Y.5
Gaston, B.6
Palmer, L.A.7
Rockenstein, E.M.8
Zhang, Z.9
Masliah, E.10
Uehara, T.11
Lipton, S.A.12
-
43
-
-
34248998027
-
Nitrosative stress in the ER: A new role for S-nitrosylation in neurodegenerative diseases
-
Benhar M, Forrester MT, Stamler JS (2006) Nitrosative stress in the ER: a new role for S-nitrosylation in neurodegenerative diseases. ACS Chem Biol 1:355-358
-
(2006)
ACS Chem Biol
, vol.1
, pp. 355-358
-
-
Benhar, M.1
Forrester, M.T.2
Stamler, J.S.3
-
44
-
-
36148975760
-
Emerging roles of S-nitrosylation in protein misfolding and neurodegenerative diseases
-
DOI 10.1089/ars.2007.1858
-
Nakamura T, Lipton SA (2008) Emerging roles of S-nitrosylation in protein misfolding and neurodegenerative diseases. Antioxid Redox Signal 10:87-101 (Pubitemid 350115990)
-
(2008)
Antioxidants and Redox Signaling
, vol.10
, Issue.1
, pp. 87-101
-
-
Nakamura, T.1
Lipton, S.A.2
-
45
-
-
64249133725
-
S-nitrosylation of Drp1 mediates beta-amyloid-related mitochondrial fission and neuronal injury
-
Cho DH, Nakamura T, Fang J, Cieplak P, Godzik A, Gu Z, Lipton SA (2009) S-nitrosylation of Drp1 mediates beta-amyloid-related mitochondrial fission and neuronal injury. Science 324:102-105
-
(2009)
Science
, vol.324
, pp. 102-105
-
-
Cho, D.H.1
Nakamura, T.2
Fang, J.3
Cieplak, P.4
Godzik, A.5
Gu, Z.6
Lipton, S.A.7
-
46
-
-
77955085868
-
Redox reactions induced by nitrosative stress mediate protein misfolding and mitochondrial dysfunction in neurodegenerative diseases
-
Gu Z, Nakamura T, Lipton SA (2010) Redox reactions induced by nitrosative stress mediate protein misfolding and mitochondrial dysfunction in neurodegenerative diseases. Mol Neurobiol 41:55-72
-
(2010)
Mol Neurobiol
, vol.41
, pp. 55-72
-
-
Gu, Z.1
Nakamura, T.2
Lipton, S.A.3
-
47
-
-
84870953719
-
S-nitrosylated protein disulfide isomerase contributes to mutant SOD1 aggregates in amyotrophic lateral sclerosis
-
Chen X, Zhang X, Li C, Guan T, Shang H, Cui L, Li XM, Kong J (2013) S-nitrosylated protein disulfide isomerase contributes to mutant SOD1 aggregates in amyotrophic lateral sclerosis. J Neurochem 124:45-58
-
(2013)
J Neurochem
, vol.124
, pp. 45-58
-
-
Chen, X.1
Zhang, X.2
Li, C.3
Guan, T.4
Shang, H.5
Cui, L.6
Li, X.M.7
Kong, J.8
-
48
-
-
0034705057
-
Mitochondrial and extramitochondrial apoptotic signaling pathways in cerebrocortical neurons
-
DOI 10.1073/pnas.100121097
-
Budd SL, Tenneti L, Lishnak T, Lipton SA (2000)Mitochondrial and extramitochondrial apoptotic signaling pathways in cerebrocortical neurons. Proc Natl Acad Sci U S A 97:6161-6166 (Pubitemid 30367540)
-
(2000)
Proceedings of the National Academy of Sciences of the United States of America
, vol.97
, Issue.11
, pp. 6161-6166
-
-
Budd, S.L.1
Tenneti, L.2
Lishnak, T.3
Lipton, S.A.4
-
49
-
-
0037133620
-
Dominant-interfering forms of MEF2 generated by caspase cleavage contribute to NMDA-induced neuronal apoptosis
-
DOI 10.1073/pnas.022036399
-
Okamoto S, Li Z, Ju C, Scholzke MN, Mathews E, Cui J, Salvesen GS, Bossy-Wetzel E, Lipton SA (2002) Dominant-interfering forms of MEF2 generated by caspase cleavage contribute to NMDA-induced neuronal apoptosis. Proc Natl Acad Sci U S A 99:3974-3979 (Pubitemid 34252215)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.6
, pp. 3974-3979
-
-
Okamoto, S.-I.1
Li, Z.2
Ju, C.3
Scholzke, M.N.4
Mathews, E.5
Cui, J.6
Salvesen, G.S.7
Bossy-Wetzel, E.8
Lipton, S.A.9
-
50
-
-
84864610364
-
The neuroprotective effect of the GSK-3â inhibitor and influence on the extrinsic apoptosis in the ALS transgenic mice
-
Ahn SW, Kim JE, Park KS, Choi WJ, Hong YH, Kim SM, Kim SH, Lee KW, Sung JJ (2012) The neuroprotective effect of the GSK-3â inhibitor and influence on the extrinsic apoptosis in the ALS transgenic mice. J Neurol Sci 320:1-5
-
(2012)
J Neurol Sci
, vol.320
, pp. 1-5
-
-
Ahn, S.W.1
Kim, J.E.2
Park, K.S.3
Choi, W.J.4
Hong, Y.H.5
Kim, S.M.6
Kim, S.H.7
Lee, K.W.8
Sung, J.J.9
-
51
-
-
0022387362
-
Sequence of protein disulphide isomerase and implications of its relationship to thioredoxin
-
DOI 10.1038/317267a0
-
Edman JC, Ellis L, Blacher RW, Roth RA, Rutter WJ (1985) Sequence of protein disulfide isomerase and implications of its relationship to thioredoxin. Nature 317:267-270 (Pubitemid 16246506)
-
(1985)
Nature
, vol.317
, Issue.6034
, pp. 267-270
-
-
Edman, J.C.1
Ellis, L.2
Blacher, R.W.3
-
52
-
-
33644976621
-
Enhancement of protein secretion in Pichia pastoris by overexpression of protein disulfide isomerase
-
Inan M, Aryasomayajula D, Sinha J, Meagher MM (2006) Enhancement of protein secretion in Pichia pastoris by overexpression of protein disulfide isomerase. Biotechnol Bioeng 93:771-778
-
(2006)
Biotechnol Bioeng
, vol.93
, pp. 771-778
-
-
Inan, M.1
Aryasomayajula, D.2
Sinha, J.3
Meagher, M.M.4
-
53
-
-
29444443348
-
Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis
-
DOI 10.1038/nn1603
-
Urushitani M, Sik A, Sakurai T, Nukina N, Takahashi R, Julien JP (2006) Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis. Nat Neurosci 9:108-118 (Pubitemid 43011916)
-
(2006)
Nature Neuroscience
, vol.9
, Issue.1
, pp. 108-118
-
-
Urushitani, M.1
Sik, A.2
Sakurai, T.3
Nukina, N.4
Takahashi, R.5
Julien, J.-P.6
-
54
-
-
77749319356
-
Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein
-
Bauer PO, Goswami A, Wong HK, Okuno M, Kurosawa M, Yamada M, Miyazaki H, Matsumoto G, Kino Y, Nagai Y, Nukina N (2010) Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein. Nat Biotechnol 28:256-263
-
(2010)
Nat Biotechnol
, vol.28
, pp. 256-263
-
-
Bauer, P.O.1
Goswami, A.2
Wong, H.K.3
Okuno, M.4
Kurosawa, M.5
Yamada, M.6
Miyazaki, H.7
Matsumoto, G.8
Kino, Y.9
Nagai, Y.10
Nukina, N.11
-
55
-
-
0029146852
-
Independence of the chaperone activity of protein disulfide isomerase from its thioredoxin-like active site
-
Quan H, Fan G, Wang CC (1995) Independence of the chaperone activity of protein disulfide isomerase from its thioredoxin-like active site. J Biol Chem 270:17078-17080
-
(1995)
J Biol Chem
, vol.270
, pp. 17078-17080
-
-
Quan, H.1
Fan, G.2
Wang, C.C.3
-
56
-
-
57049117856
-
Cell death and endoplasmic reticulum stress: Disease relevance and therapeutic opportunities
-
Kim I, Xu W, Reed JC (2008) Cell death and endoplasmic reticulum stress: disease relevance and therapeutic opportunities. Nat Rev Drug Discov 7:1013-1030
-
(2008)
Nat Rev Drug Discov
, vol.7
, pp. 1013-1030
-
-
Kim, I.1
Xu, W.2
Reed, J.C.3
-
57
-
-
77952680368
-
Bacitracin is not a specific inhibitor of protein disulfide isomerase
-
Karala AR, Ruddock LW(2010) Bacitracin is not a specific inhibitor of protein disulfide isomerase. FEBS J 277:2454-2462
-
(2010)
FEBS J
, vol.277
, pp. 2454-2462
-
-
Karala, A.R.1
Ruddock, L.W.2
-
58
-
-
37149031347
-
Increased ER stress during motor neuron degeneration in a transgenic mouse model of amyotrophic lateral sclerosis
-
DOI 10.1179/016164107X229803
-
Nagata T, Ilieva H, Murakami T, Shiote M, Narai H, Ohta Y, Hayashi T, Shoji M, Abe K (2007) Increased ER stress during motor neuron degeneration in a transgenic mouse model of amyotrophic lateral sclerosis. Neurol Res 29:767-771 (Pubitemid 350255148)
-
(2007)
Neurological Research
, vol.29
, Issue.8
, pp. 767-771
-
-
Nagata, T.1
Ilieva, H.2
Murakami, T.3
Shiote, M.4
Narai, H.5
Ohta, Y.6
Hayashi, T.7
Shoji, M.8
Abe, K.9
-
59
-
-
66149156941
-
ER stress and un-folded protein response in amyotrophic lateral sclerosis
-
Kanekura K, Suzuki H, Aiso S, Matsuoka M (2009) ER stress and un-folded protein response in amyotrophic lateral sclerosis. Mol Neurobiol 39:81-89
-
(2009)
Mol Neurobiol
, vol.39
, pp. 81-89
-
-
Kanekura, K.1
Suzuki, H.2
Aiso, S.3
Matsuoka, M.4
-
60
-
-
67349164383
-
A role for motoneuron subty-peselective ER stress in disease manifestations of FALS mice
-
Saxena S, Cabuy E, Caroni P (2009) A role for motoneuron subty-peselective ER stress in disease manifestations of FALS mice. Nat Neurosci 12:627-636
-
(2009)
Nat Neurosci
, vol.12
, pp. 627-636
-
-
Saxena, S.1
Cabuy, E.2
Caroni, P.3
-
61
-
-
77955786575
-
Gold nanoparticle enrichment method for identifying S-nitrosylation and S-glutathionylation sites in proteins
-
Faccenda A, Bonham CA, Vacratsis PO, Zhang X, Mutus B (2010) Gold nanoparticle enrichment method for identifying S-nitrosylation and S-glutathionylation sites in proteins. J Am Chem Soc 132: 11392-11394
-
(2010)
J Am Chem Soc
, vol.132
, pp. 11392-11394
-
-
Faccenda, A.1
Bonham, C.A.2
Vacratsis, P.O.3
Zhang, X.4
Mutus, B.5
-
62
-
-
80055031464
-
Protein disulfide isomerase-immunopositive inclusions in patients with amyotrophic lateral sclerosis
-
Honjo Y, Kaneko S, Ito H, Horibe T, Nagashima M, Nakamura M, Fujita K, Takahashi R, Kusaka H, Kawakami K (2011) Protein disulfide isomerase- immunopositive inclusions in patients with amyotrophic lateral sclerosis. Amyotroph Lateral Scler 12:444-450
-
(2011)
Amyotroph Lateral Scler
, vol.12
, pp. 444-450
-
-
Honjo, Y.1
Kaneko, S.2
Ito, H.3
Horibe, T.4
Nagashima, M.5
Nakamura, M.6
Fujita, K.7
Takahashi, R.8
Kusaka, H.9
Kawakami, K.10
|