-
1
-
-
0026002405
-
Molecular genetics of familial amyotrophic lateral sclerosis
-
Siddique T. Molecular genetics of familial amyotrophic lateral sclerosis. Adv Neurol 1991; 56: 227-31
-
(1991)
Adv Neurol
, vol.56
, pp. 227-231
-
-
Siddique, T.1
-
2
-
-
0020392683
-
Familial motor neuron diseases
-
Emery AE, Holloway S. Familial motor neuron diseases. Adv Neurol 1982; 36; 139-47
-
(1982)
Adv Neurol
, vol.36
, pp. 139-147
-
-
Emery, A.E.1
Holloway, S.2
-
3
-
-
0027401203
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J, O'Regan JP, Deng HX, Rahmani Z, Krizus A, McKenna-Yasek D, Cayabyab A, Gaston SM, Berger R, Tanzi RE, Halperin JJ, Herzfeldt 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, Horvitx HR, Brown RH. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993; 362: 59-62
-
(1993)
Nature
, vol.362
, pp. 59-62
-
-
Rosen, D.R.1
Siddique, T.2
Patterson, D.3
Figlewicz, D.A.4
Sapp, P.5
Hentati, A.6
Donaldson, D.7
Goto, J.8
O'Regan, J.P.9
Deng, H.X.10
Rahmani, Z.11
Krizus, A.12
McKenna-Yasek, D.13
Cayabyab, A.14
Gaston, S.M.15
Berger, R.16
Tanzi, R.E.17
Halperin, J.J.18
Herzfeldt, B.19
Van Den Bergh, R.20
Hung, W.-Y.21
Bird, T.22
Deng, G.23
Mulder, D.W.24
Smyth, C.25
Laing, N.G.26
Soriano, E.27
Pericak-Vance, M.A.28
Haines, J.29
Rouleau, G.A.30
Gusella, J.S.31
Horvitx, H.R.32
Brown, R.H.33
more..
-
4
-
-
0027426169
-
Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase
-
Deng HX, Hentati A, Tainer JA, Iqbal Z, Cayabyab A, Hung WY, 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: 1047-51
-
(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..
-
5
-
-
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: 1772-5
-
(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
-
6
-
-
0029890685
-
The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease
-
Mourelatos Z, Gonatas NK, Stieber A, Gurney ME, Dal Canto MC. The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease. Proc Natl Acad Sci USA 1996; 93: 5472-7
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 5472-5477
-
-
Mourelatos, Z.1
Gonatas, N.K.2
Stieber, A.3
Gurney, M.E.4
Dal Canto, M.C.5
-
7
-
-
0028000273
-
Rous-Whipple Award Lecture. Contributions to the physiology and pathology of the Golgi apparatus
-
Gonatas NK. Rous-Whipple Award Lecture. Contributions to the physiology and pathology of the Golgi apparatus. Am J Pathol 1994; 145: 751-61
-
(1994)
Am J Pathol
, vol.145
, pp. 751-761
-
-
Gonatas, N.K.1
-
8
-
-
0030910404
-
Oxidative stress, mutant SOD1, and neurofilament pathology in transgenic mouse models of human motor neuron disease
-
Tu PH, Gurney ME, Julien JP, Lee VM, Trojanowski JQ. Oxidative stress, mutant SOD1, and neurofilament pathology in transgenic mouse models of human motor neuron disease. Lab Invest 1997; 76: 441-56
-
(1997)
Lab Invest
, vol.76
, pp. 441-456
-
-
Tu, P.H.1
Gurney, M.E.2
Julien, J.P.3
Lee, V.M.4
Trojanowski, J.Q.5
-
9
-
-
0029808008
-
Molecular genetic basis of familial ALS
-
discussion S34-5
-
Siddique T, Nijhawan D, Hentati A. Molecular genetic basis of familial ALS. Neurology 1996; 47: S27-34; discussion S34-5.
-
(1996)
Neurology
, vol.47
-
-
Siddique, T.1
Nijhawan, D.2
Hentati, A.3
-
10
-
-
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 RH Jr, 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: 43-7
-
(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
Brown Jr., R.H.10
Scott, R.W.11
Snider, W.D.12
-
11
-
-
0035936804
-
Amyotrophic lateral sclerosis unfolding the toxicity of the misfolded
-
Julien JP. Amyotrophic lateral sclerosis unfolding the toxicity of the misfolded. Cell 2001; 104: 581-91
-
(2001)
Cell
, vol.104
, pp. 581-591
-
-
Julien, J.P.1
-
12
-
-
0029966363
-
Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions
-
Tu PH, Raju P, Robinson KA, Gurney ME, Trojanowski JQ, Lee VM. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions. Proc Natl Acad Sci USA 1996; 93: 3155-60
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 3155-3160
-
-
Tu, P.H.1
Raju, P.2
Robinson, K.A.3
Gurney, M.E.4
Trojanowski, J.Q.5
Lee, V.M.6
-
13
-
-
0033962285
-
Aggregation of ubiquitin and a mutant ALS-linked SOD1 protein correlate with disease progression and fragmentation of the Golgi apparatus
-
Stieber A, Gonatas JO, Gonatas NK. Aggregation of ubiquitin and a mutant ALS-linked SOD1 protein correlate with disease progression and fragmentation of the Golgi apparatus. J Neurol Sci 2000; 173: 53-62
-
(2000)
J Neurol Sci
, vol.173
, pp. 53-62
-
-
Stieber, A.1
Gonatas, J.O.2
Gonatas, N.K.3
-
14
-
-
0033823740
-
Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation
-
Kato S, Horiuchi S, Liu J, Cleveland DW, Shibata N, Nakashima K, Nagai R, Hirano A, Takikawa M, Kato M, Nakano I, Ohama E. Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation. Acta Neuropathol (Berl) 2000; 100: 490-505
-
(2000)
Acta Neuropathol (Berl)
, vol.100
, pp. 490-505
-
-
Kato, S.1
Horiuchi, S.2
Liu, J.3
Cleveland, D.W.4
Shibata, N.5
Nakashima, K.6
Nagai, R.7
Hirano, A.8
Takikawa, M.9
Kato, M.10
Nakano, I.11
Ohama, E.12
-
15
-
-
0030200643
-
Proteasome inhibition enhances the stability of mouse Cu/Zn superoxide dismutase with mutations linked to familial amyotrophic lateral sclerosis
-
Hoffman EK, Wilcox HM, Scott RW, Siman R. Proteasome inhibition enhances the stability of mouse Cu/Zn superoxide dismutase with mutations linked to familial amyotrophic lateral sclerosis. J Neurol Sci 1996; 139: 15-20
-
(1996)
J Neurol Sci
, vol.139
, pp. 15-20
-
-
Hoffman, E.K.1
Wilcox, H.M.2
Scott, R.W.3
Siman, R.4
-
16
-
-
0030596537
-
Instability of mutant Cu/Zn superoxide dismutase (Ala4Thr) associated with familial amyotrophic lateral sclerosis
-
Nakano R, Inuzuka T, Kikugawa K, Takahashi H, Sakimura K, Fujii J, Taniguchi N, Tsuji S. Instability of mutant Cu/Zn superoxide dismutase (Ala4Thr) associated with familial amyotrophic lateral sclerosis. Neurosci Lett 1996; 211: 129-31
-
(1996)
Neurosci Lett
, vol.211
, pp. 129-131
-
-
Nakano, R.1
Inuzuka, T.2
Kikugawa, K.3
Takahashi, H.4
Sakimura, K.5
Fujii, J.6
Taniguchi, N.7
Tsuji, S.8
-
17
-
-
0033749379
-
Formation of high molecular weight complexes of mutant Cu,Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis
-
Johnston JA, Dalton MJ, Gurney ME, Kopito RR. Formation of high molecular weight complexes of mutant Cu,Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis. Proc Natl Acad Sci USA 2000; 97: 12571-6
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 12571-12576
-
-
Johnston, J.A.1
Dalton, M.J.2
Gurney, M.E.3
Kopito, R.R.4
-
18
-
-
0036892683
-
Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis
-
Urushitani M, Kurisu J, Tsukita K, Takahashi R. Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis. J Neurochem 2002; 83: 1030-42
-
(2002)
J Neurochem
, vol.83
, pp. 1030-1042
-
-
Urushitani, M.1
Kurisu, J.2
Tsukita, K.3
Takahashi, R.4
-
19
-
-
0037184063
-
Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity
-
Niwa J, Ishigaki S, Hishikawa N, Yamamoto M, Doyu M, Murata S, Tanaka K, Taniguchi N, Sobue G. Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity. J Biol Chem 2002; 277: 36793-8
-
(2002)
J Biol Chem
, vol.277
, pp. 36793-36798
-
-
Niwa, J.1
Ishigaki, S.2
Hishikawa, N.3
Yamamoto, M.4
Doyu, M.5
Murata, S.6
Tanaka, K.7
Taniguchi, N.8
Sobue, G.9
-
20
-
-
0034065822
-
Ubiquitin-mediated proteolysis: Biological regulation via destruction
-
Ciechanover A, Orian A, Schwartz AL. Ubiquitin-mediated proteolysis: biological regulation via destruction. Bioessays 2000; 22: 442-51
-
(2000)
Bioessays
, vol.22
, pp. 442-451
-
-
Ciechanover, A.1
Orian, A.2
Schwartz, A.L.3
-
23
-
-
0024992208
-
Ubiquitin, cell stress and diseases of the nervous system
-
Lowe J, Mayer RJ. Ubiquitin, cell stress and diseases of the nervous system. Neuropathol Appl Neurobiol 1990; 16: 281-91
-
(1990)
Neuropathol Appl Neurobiol
, vol.16
, pp. 281-291
-
-
Lowe, J.1
Mayer, R.J.2
-
24
-
-
0035947372
-
Impairment of the ubiquitin-proteasome system by protein aggregation
-
Bence NF, Sampat RM, Kopito RR. Impairment of the ubiquitin-proteasome system by protein aggregation. Science 2001; 292: 1552-5
-
(2001)
Science
, vol.292
, pp. 1552-1555
-
-
Bence, N.F.1
Sampat, R.M.2
Kopito, R.R.3
-
25
-
-
0035336658
-
Altered proteasomal function due to the expression of polyglutamine-expanded truncated N-terminal huntingtin induces apoptosis by caspase activation through mitochondrial cytochrome c release
-
Jana NR, Zemskov EA, Wang G, Nukina N. Altered proteasomal function due to the expression of polyglutamine-expanded truncated N-terminal huntingtin induces apoptosis by caspase activation through mitochondrial cytochrome c release. Hum Mol Genet 2001; 10: 1049-59
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1049-1059
-
-
Jana, N.R.1
Zemskov, E.A.2
Wang, G.3
Nukina, N.4
-
26
-
-
0038413759
-
Aggregated and monomeric alpha-synuclein bind to the S6′ proteasomal protein and inhibit proteasomal function
-
Snyder H, Mensah K, Theisler C, Lee J, Matouschek A, Wolozin B. Aggregated and monomeric alpha-synuclein bind to the S6′ proteasomal protein and inhibit proteasomal function. J Biol Chem 2003; 278: 11753-9
-
(2003)
J Biol Chem
, vol.278
, pp. 11753-11759
-
-
Snyder, H.1
Mensah, K.2
Theisler, C.3
Lee, J.4
Matouschek, A.5
Wolozin, B.6
-
27
-
-
0034895295
-
Parkin and Parkinson's disease
-
Mizuno Y, Hattori N, Mod H, Suzuki T, Tanaka K. Parkin and Parkinson's disease. Curr Opin Neurol 2001; 14: 477-82
-
(2001)
Curr Opin Neurol
, vol.14
, pp. 477-482
-
-
Mizuno, Y.1
Hattori, N.2
Mod, H.3
Suzuki, T.4
Tanaka, K.5
-
28
-
-
0032190090
-
The ubiquitin pathway in Parkinson's disease
-
Leroy E, Boyer R, Auburger G, Leube B, Ulm G, Mezey E, Harta G, Brownstein 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: 451-2
-
(1998)
Nature
, vol.395
, pp. 451-452
-
-
Leroy, E.1
Boyer, R.2
Auburger, G.3
Leube, B.4
Ulm, G.5
Mezey, E.6
Harta, G.7
Brownstein, M.J.8
Jonnalagada, S.9
Chernova, T.10
Dehejia, A.11
Lavedan, C.12
Gasser, T.13
Steinbach, P.J.14
Wilkinson, K.D.15
Polymeropoulos, M.H.16
-
29
-
-
0034864346
-
No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease
-
Levecque C, Destee A, Mouroux V, Becquet E, Defebvre L, Amouyel P, Chartier-Harlin MC. No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease. J Neural Transm 2001; 108: 979-84
-
(2001)
J Neural Transm
, vol.108
, pp. 979-984
-
-
Levecque, C.1
Destee, A.2
Mouroux, V.3
Becquet, E.4
Defebvre, L.5
Amouyel, P.6
Chartier-Harlin, M.C.7
-
30
-
-
0036135090
-
Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms
-
Momose Y, Murata M, Kobayashi K, Tachikawa M, Nakabayashi Y, Kanazawa I, Toda T. Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms. Ann Neurol 2002; 51: 133-6
-
(2002)
Ann Neurol
, vol.51
, pp. 133-136
-
-
Momose, Y.1
Murata, M.2
Kobayashi, K.3
Tachikawa, M.4
Nakabayashi, Y.5
Kanazawa, I.6
Toda, T.7
-
31
-
-
0035881339
-
A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population
-
Satoh J, Kuroda Y. A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population. J Neurol Sci 2001; 189: 113-7
-
(2001)
J Neurol Sci
, vol.189
, pp. 113-117
-
-
Satoh, J.1
Kuroda, Y.2
-
32
-
-
0036654541
-
ACT and UCH-L1 polymorphisms in Parkinson's disease and age of onset
-
Wang J, Zhao CY, Si YM, Liu ZL, Chen B, YuL. ACT and UCH-L1 polymorphisms in Parkinson's disease and age of onset. Mov Disord 2002; 17: 767-71
-
(2002)
Mov Disord
, vol.17
, pp. 767-771
-
-
Wang, J.1
Zhao, C.Y.2
Si, Y.M.3
Liu, Z.L.4
Chen, B.5
Yu, L.6
-
33
-
-
0037466510
-
Alterations of structure and hydrolase activity of parkinsonism- associated human ubiquitin carboxyl-terminal hydrolase L1 variants
-
Nishikawa K, Li H, Kawamura R, Osaka H, Wang YL, Kara Y, Hirokawa T, Manage Y, Amano T, Noda M, Aoki S, Wada K. Alterations of structure and hydrolase activity of parkinsonism-associated human ubiquitin carboxyl-terminal hydrolase L1 variants. Biochem Biophys Res Commun 2003; 304: 176-83
-
(2003)
Biochem Biophys Res Commun
, vol.304
, pp. 176-183
-
-
Nishikawa, K.1
Li, H.2
Kawamura, R.3
Osaka, H.4
Wang, Y.L.5
Kara, Y.6
Hirokawa, T.7
Manage, Y.8
Amano, T.9
Noda, M.10
Aoki, S.11
Wada, K.12
-
34
-
-
0033544368
-
Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease
-
Maraganore DM, Farrer MJ, Hardy JA, Lincoln SJ, McDonnell SK, Rocca WA. Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease. Neurology 1999; 53: 1858-60
-
(1999)
Neurology
, vol.53
, pp. 1858-1860
-
-
Maraganore, D.M.1
Farrer, M.J.2
Hardy, J.A.3
Lincoln, S.J.4
McDonnell, S.K.5
Rocca, W.A.6
-
35
-
-
0032846416
-
Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice
-
Saigoh K, Wang YL, Suh JG, Yamanishi T, Sakai Y, Kiyosawa H, Harada T, Ichihara N, Wakana S, Kikuchi T, Wada K. Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice. Nat Genet 1999; 23: 47-51
-
(1999)
Nat Genet
, vol.23
, pp. 47-51
-
-
Saigoh, K.1
Wang, Y.L.2
Suh, J.G.3
Yamanishi, T.4
Sakai, Y.5
Kiyosawa, H.6
Harada, T.7
Ichihara, N.8
Wakana, S.9
Kikuchi, T.10
Wada, K.11
-
36
-
-
0036842130
-
Synaptic defects in ataxia mice result from a mutation in Usp14. Encoding a ubiquitin-specific protease
-
Wilson SM, Bhattacharyya B, Rachel RA, Coppola V, Tessarollo L, Householder DB, Fletcher CF, Miller RJ, Copeland NG, Jenkins NA. Synaptic defects in ataxia mice result from a mutation in Usp14. encoding a ubiquitin-specific protease. Nat Genet 2002; 32: 420-5
-
(2002)
Nat Genet
, vol.32
, pp. 420-425
-
-
Wilson, S.M.1
Bhattacharyya, B.2
Rachel, R.A.3
Coppola, V.4
Tessarollo, L.5
Householder, D.B.6
Fletcher, C.F.7
Miller, R.J.8
Copeland, N.G.9
Jenkins, N.A.10
-
37
-
-
0347298778
-
Spongiform degeneration in mahoganoid mutant mice
-
He L, Lu XY, Jolly AF, Eldridge AG, Watson SJ, Jackson PK, Barsh GS, Gunn TM. Spongiform degeneration in mahoganoid mutant mice. Science 2003; 299: 710-2
-
(2003)
Science
, vol.299
, pp. 710-712
-
-
He, L.1
Lu, X.Y.2
Jolly, A.F.3
Eldridge, A.G.4
Watson, S.J.5
Jackson, P.K.6
Barsh, G.S.7
Gunn, T.M.8
-
38
-
-
0030457014
-
Ubiquitin-dependent protein degradation
-
Hochstrasser M. Ubiquitin-dependent protein degradation. Annu Rev Genet 1996; 30: 405-39
-
(1996)
Annu Rev Genet
, vol.30
, pp. 405-439
-
-
Hochstrasser, M.1
-
39
-
-
0024514688
-
A multiubiquitin chain is confined to specific lysine in a targeted short-lived protein
-
Chau V, Tobias JW, Bachmair A, Marriott D, Ecker DJ, Gonda DK, Varshavsky A. A multiubiquitin chain is confined to specific lysine in a targeted short-lived protein. Science 1989; 243: 1576-83
-
(1989)
Science
, vol.243
, pp. 1576-1583
-
-
Chau, V.1
Tobias, J.W.2
Bachmair, A.3
Marriott, D.4
Ecker, D.J.5
Gonda, D.K.6
Varshavsky, A.7
-
40
-
-
0029119522
-
A proteolytic pathway that recognizes ubiquitin as a degradation signal
-
Johnson ES, Ma PC, Ota JM, Varshavsky A. A proteolytic pathway that recognizes ubiquitin as a degradation signal. J Biol Chem 1995; 270: 17442-56
-
(1995)
J Biol Chem
, vol.270
, pp. 17442-17456
-
-
Johnson, E.S.1
Ma, P.C.2
Ota, J.M.3
Varshavsky, A.4
-
41
-
-
0033525589
-
A novel ubiquitination factor, E4, is involved in multiubiquitin chain assembly
-
Koegl M, Hoppe T, Schlenker S, Ulrich HD, Mayer TU, Jentsch S. A novel ubiquitination factor, E4, is involved in multiubiquitin chain assembly. Cell 1999; 96: 635-44
-
(1999)
Cell
, vol.96
, pp. 635-644
-
-
Koegl, M.1
Hoppe, T.2
Schlenker, S.3
Ulrich, H.D.4
Mayer, T.U.5
Jentsch, S.6
-
43
-
-
0030863993
-
Inhibition of the 26 S proteasome by polyubiquitin chains synthesized to have defined lengths
-
Piotrowski J, Beal R, Hoffman L, Wilkinson KD, Cohen RE, Pickart CM. Inhibition of the 26 S proteasome by polyubiquitin chains synthesized to have defined lengths. J Biol Chem 1997; 272: 23712-21
-
(1997)
J Biol Chem
, vol.272
, pp. 23712-23721
-
-
Piotrowski, J.1
Beal, R.2
Hoffman, L.3
Wilkinson, K.D.4
Cohen, R.E.5
Pickart, C.M.6
-
44
-
-
0034959450
-
Analysis of ubiquitination in vivo using a transgenic mouse model
-
Tsirigotis M, Thurig S, Dube M, Vanderhyden BC, Zhang M, Gray DA. Analysis of ubiquitination in vivo using a transgenic mouse model. Biotechniques 2001; 31: 120-6,128,130
-
(2001)
Biotechniques
, vol.31
, pp. 120-126
-
-
Tsirigotis, M.1
Thurig, S.2
Dube, M.3
Vanderhyden, B.C.4
Zhang, M.5
Gray, D.A.6
-
45
-
-
0037663945
-
Effects of mutant ubiquitin on ts1 retrovirus-mediated neuropathology
-
Zhang M, Thurig S, Tsirigotis M, Wong PK, Reuhl KR, Gray DA. Effects of mutant ubiquitin on ts1 retrovirus-mediated neuropathology. J Virol 2003; 77: 7193-201
-
(2003)
J Virol
, vol.77
, pp. 7193-7201
-
-
Zhang, M.1
Thurig, S.2
Tsirigotis, M.3
Wong, P.K.4
Reuhl, K.R.5
Gray, D.A.6
-
46
-
-
0344844526
-
Expression of a K48R mutant ubiquitin protects mouse testis from cryptorchid injury and aging
-
Rasoulpour RJ, Schoenfeld HA, Gray DA, Boekelheide K. Expression of a K48R mutant ubiquitin protects mouse testis from cryptorchid injury and aging. Am J Pathol 2003;163:2595-603
-
(2003)
Am J Pathol
, vol.163
, pp. 2595-2603
-
-
Rasoulpour, R.J.1
Schoenfeld, H.A.2
Gray, D.A.3
Boekelheide, K.4
-
47
-
-
0035824651
-
Sensitivity of mammalian cells expressing mutant ubiquitin to protein-damaging agents
-
Tsirigotis M, Zhang M, Chiu RK, Wouters BG, Gray DA. Sensitivity of mammalian cells expressing mutant ubiquitin to protein-damaging agents. J Biol Chem 2001; 276: 46073-8
-
(2001)
J Biol Chem
, vol.276
, pp. 46073-46078
-
-
Tsirigotis, M.1
Zhang, M.2
Chiu, R.K.3
Wouters, B.G.4
Gray, D.A.5
-
49
-
-
0025283268
-
Immunocytochemical visualization of the Golgi apparatus in several species, including human, and tissues with an antiserum against MG-160, a sialoglyco-protein of rat Golgi apparatus
-
Croul S, Mezitis SG, Stieber A, Chen YJ, Gonatas JO, Goud B, Gonatas NK. Immunocytochemical visualization of the Golgi apparatus in several species, including human, and tissues with an antiserum against MG-160, a sialoglyco-protein of rat Golgi apparatus. J Histochem Cytochem 1990; 38: 957-63
-
(1990)
J Histochem Cytochem
, vol.38
, pp. 957-963
-
-
Croul, S.1
Mezitis, S.G.2
Stieber, A.3
Chen, Y.J.4
Gonatas, J.O.5
Goud, B.6
Gonatas, N.K.7
-
50
-
-
0024534135
-
MG-160. A novel sialoglycoprotein of the medial cisternae of the Golgi apparatus
-
Gonatas JO, Mezitis SG, Stieber A, Fleischer B, Gonatas NK. MG-160. A novel sialoglycoprotein of the medial cisternae of the Golgi apparatus published erratum appears in J Biol Chem 1989 March 5; 264 (7):4264. J Biol Chem 1989; 264: 646-53
-
(1989)
J Biol Chem
, vol.264
, pp. 646-653
-
-
Gonatas, J.O.1
Mezitis, S.G.2
Stieber, A.3
Fleischer, B.4
Gonatas, N.K.5
-
51
-
-
0024534135
-
-
published erratum appears March 5
-
Gonatas JO, Mezitis SG, Stieber A, Fleischer B, Gonatas NK. MG-160. A novel sialoglycoprotein of the medial cisternae of the Golgi apparatus published erratum appears in J Biol Chem 1989 March 5; 264 (7):4264. J Biol Chem 1989; 264: 646-53
-
(1989)
J Biol Chem
, vol.264
, Issue.7
, pp. 4264
-
-
-
52
-
-
0028941319
-
MG-160, a membrane sialoglycoprotein of the medial cisternae of the rat Golgi apparatus, binds basic fibroblast growth factor and exhibits a high level of sequence identity to a chicken fibroblast growth factor receptor
-
Gonatas JO, Mourelatos Z, Stieber A, Lane WS, Brosius J, Gonatas NK. MG-160, a membrane sialoglycoprotein of the medial cisternae of the rat Golgi apparatus, binds basic fibroblast growth factor and exhibits a high level of sequence identity to a chicken fibroblast growth factor receptor. J Cell Sci 1995; 108 (Pt 2): 457-67
-
(1995)
J Cell Sci
, vol.108
, Issue.PART 2
, pp. 457-467
-
-
Gonatas, J.O.1
Mourelatos, Z.2
Stieber, A.3
Lane, W.S.4
Brosius, J.5
Gonatas, N.K.6
-
53
-
-
0032125587
-
Relationship of microglial and astrocytic activation to disease onset and progression in a transgenic model of familial ALS
-
Hall ED, Oostveen JA, Gurney ME. Relationship of microglial and astrocytic activation to disease onset and progression in a transgenic model of familial ALS. Glia 1998; 23: 249-56
-
(1998)
Glia
, vol.23
, pp. 249-256
-
-
Hall, E.D.1
Oostveen, J.A.2
Gurney, M.E.3
-
54
-
-
0033485920
-
Astrocytes interact intimately with degenerating motor neurons in mouse amyotrophic lateral sclerosis (ALS)
-
Levine JB, Kong J, Nadler M, Xu Z. Astrocytes interact intimately with degenerating motor neurons in mouse amyotrophic lateral sclerosis (ALS). Glia 1999; 28: 215-24
-
(1999)
Glia
, vol.28
, pp. 215-224
-
-
Levine, J.B.1
Kong, J.2
Nadler, M.3
Xu, Z.4
-
55
-
-
0028146192
-
Inhibition of proteolysis and cell cycle progression in a multiubiquitination-deficient yeast mutant
-
Finley D, Sadis S, Monia BP, Boucher P, Ecker DJ, Crooke ST, Chau V. Inhibition of proteolysis and cell cycle progression in a multiubiquitination- deficient yeast mutant. Mol Cell Biol 1994: 14: 5501-9
-
(1994)
Mol Cell Biol
, vol.14
, pp. 5501-5509
-
-
Finley, D.1
Sadis, S.2
Monia, B.P.3
Boucher, P.4
Ecker, D.J.5
Crooke, S.T.6
Chau, V.7
-
56
-
-
0344507132
-
Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosis
-
Bruening W, Roy J, Giasson B, Figlewicz DA, Mushynski WE, Durham HD. Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosis. J Neurochem 1999; 72: 693-9
-
(1999)
J Neurochem
, vol.72
, pp. 693-699
-
-
Bruening, W.1
Roy, J.2
Giasson, B.3
Figlewicz, D.A.4
Mushynski, W.E.5
Durham, H.D.6
-
57
-
-
0033499931
-
Analysis of the role of heat shock protein (Hsp) molecular chaperones in polyglutamine disease
-
Chai Y, Koppenhafer SL, Bonini NM, Paulson HL. Analysis of the role of heat shock protein (Hsp) molecular chaperones in polyglutamine disease. J Neurosci 1999; 19: 10338-47
-
(1999)
J Neurosci
, vol.19
, pp. 10338-10347
-
-
Chai, Y.1
Koppenhafer, S.L.2
Bonini, N.M.3
Paulson, H.L.4
-
58
-
-
0032727617
-
Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70
-
Warrick JM, Chan HY, Gray-Board GL, Chai Y, Paulson HL, Bonini NM. Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70. Nat Genet 1999; 23: 425-8
-
(1999)
Nat Genet
, vol.23
, pp. 425-428
-
-
Warrick, J.M.1
Chan, H.Y.2
Gray-Board, G.L.3
Chai, Y.4
Paulson, H.L.5
Bonini, N.M.6
-
59
-
-
0034951251
-
Damage control - A possible non-proteolytic role for ubiquitin in limiting neurodegeneration
-
Gray DA. Damage control - a possible non-proteolytic role for ubiquitin in limiting neurodegeneration. Neuropathol Appl Neurobiol 2001; 27: 89-94
-
(2001)
Neuropathol Appl Neurobiol
, vol.27
, pp. 89-94
-
-
Gray, D.A.1
-
60
-
-
0344609220
-
Beneficial effects of lysine acetylsalicylate, a soluble salt of aspirin, on motor performance in a transgenic model of amyotrophic lateral sclerosis
-
Barneoud P, Curet O. Beneficial effects of lysine acetylsalicylate, a soluble salt of aspirin, on motor performance in a transgenic model of amyotrophic lateral sclerosis. Exp Neurol 1999; 155: 243-51
-
(1999)
Exp Neurol
, vol.155
, pp. 243-251
-
-
Barneoud, P.1
Curet, O.2
-
61
-
-
0034773568
-
Presymptomatic motor neuron loss and reactive astrocytosis in the SOD1 mouse model of amyotrophic lateral sclerosis
-
Feeney SJ, McKelvie PA, Austin L, Jean-Francois MJ, Kapsa R, Tombs SM, Byrne E. Presymptomatic motor neuron loss and reactive astrocytosis in the SOD1 mouse model of amyotrophic lateral sclerosis. Muscle Nerve 2001; 24: 1510-9
-
(2001)
Muscle Nerve
, vol.24
, pp. 1510-1519
-
-
Feeney, S.J.1
McKelvie, P.A.2
Austin, L.3
Jean-Francois, M.J.4
Kapsa, R.5
Tombs, S.M.6
Byrne, E.7
-
62
-
-
0034653512
-
Fragmentation of the Golgi apparatus of the anterior horn cells in patients with familial amyotrophic lateral sclerosis with SOD1 mutations and posterior column involvement
-
Fujita Y, Okamoto K, Sakurai A, Gonatas NK, Hirano A. Fragmentation of the Golgi apparatus of the anterior horn cells in patients with familial amyotrophic lateral sclerosis with SOD1 mutations and posterior column involvement. J Neurol Sci 2000; 174: 137-40
-
(2000)
J Neurol Sci
, vol.174
, pp. 137-140
-
-
Fujita, Y.1
Okamoto, K.2
Sakurai, A.3
Gonatas, N.K.4
Hirano, A.5
-
63
-
-
0026529968
-
Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis
-
Gonatas NK, Stieber A, Mourelatos Z, Chen Y, Gonatas JO, Appel SH, Hays AP, Hickey WF, Hauw JJ. Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis. Am J Pathol 1992; 140: 731-7
-
(1992)
Am J Pathol
, vol.140
, pp. 731-737
-
-
Gonatas, N.K.1
Stieber, A.2
Mourelatos, Z.3
Chen, Y.4
Gonatas, J.O.5
Appel, S.H.6
Hays, A.P.7
Hickey, W.F.8
Hauw, J.J.9
-
64
-
-
0034194338
-
Caspase-2 is localized at the Golgi complex and cleaves golgin-160 during apoptosis
-
Mancini M, Machamer CE, Roy S, Nicholson DW, Thornberry NA, Casciola-Rosen LA, Rosen A. Caspase-2 is localized at the Golgi complex and cleaves golgin-160 during apoptosis. J Cell Biol 2000; 149: 603-12
-
(2000)
J Cell Biol
, vol.149
, pp. 603-612
-
-
Mancini, M.1
Machamer, C.E.2
Roy, S.3
Nicholson, D.W.4
Thornberry, N.A.5
Casciola-Rosen, L.A.6
Rosen, A.7
-
65
-
-
0035839187
-
Impaired retrograde axonal transport of adenovirus-mediated E. coli LacZ gene in the mice carrying mutant SOD1 gene
-
Murakami T, Nagano I, Hayashi T, Manabe Y, Shoji M, Setoguchi Y, Abe K. Impaired retrograde axonal transport of adenovirus-mediated E. coli LacZ gene in the mice carrying mutant SOD1 gene. Neurosci Lett 2001; 308: 149-52
-
(2001)
Neurosci Lett
, vol.308
, pp. 149-152
-
-
Murakami, T.1
Nagano, I.2
Hayashi, T.3
Manabe, Y.4
Shoji, M.5
Setoguchi, Y.6
Abe, K.7
-
66
-
-
0033366384
-
Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons
-
Williamson TL, Cleveland DW. Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons. Nat Neurosci 1999; 2: 50-6
-
(1999)
Nat Neurosci
, vol.2
, pp. 50-56
-
-
Williamson, T.L.1
Cleveland, D.W.2
-
67
-
-
0032502573
-
Expression of adenovirus-mediated E. coli lacZ gene in skeletal muscles and spinal motor neurons of transgenic mice with a mutant superoxide dismutase gene
-
Warita H, Abe K, Setoguchi Y, Itoyama Y. Expression of adenovirus-mediated E. coli lacZ gene in skeletal muscles and spinal motor neurons of transgenic mice with a mutant superoxide dismutase gene. Neurosci Lett 1998; 246: 153-6
-
(1998)
Neurosci Lett
, vol.246
, pp. 153-156
-
-
Warita, H.1
Abe, K.2
Setoguchi, Y.3
Itoyama, Y.4
-
68
-
-
0032126386
-
Axonal transport of mutant superoxide dismutase 1 and focal axonal abnormalities in the proximal axons of transgenic mice
-
Borchelt DR, Wong PC, Becher MW, Pardo CA, Lee MK, Xu ZS, Thinakaran G, Jenkins NA, Copeland NG, Sisodia SS, Cleveland DW, Price DL, Hoffman PN. Axonal transport of mutant superoxide dismutase 1 and focal axonal abnormalities in the proximal axons of transgenic mice. Neurobiol Dis 1998; 5: 27-35
-
(1998)
Neurobiol Dis
, vol.5
, pp. 27-35
-
-
Borchelt, D.R.1
Wong, P.C.2
Becher, M.W.3
Pardo, C.A.4
Lee, M.K.5
Xu, Z.S.6
Thinakaran, G.7
Jenkins, N.A.8
Copeland, N.G.9
Sisodia, S.S.10
Cleveland, D.W.11
Price, D.L.12
Hoffman, P.N.13
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