-
1
-
-
0027401203
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
Rosen DR, Siddique T, Patterson D, et al. 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
-
2
-
-
0028918944
-
Identification of new mutations in the Cu/Zn Superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis
-
Pramatarova A, Figlewicz DA, Krizus A, et al. Identification of new mutations in the Cu/Zn Superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis. Am J Hum Genet 1995;56:592-96
-
(1995)
Am J Hum Genet
, vol.56
, pp. 592-596
-
-
Pramatarova, A.1
Figlewicz, D.A.2
Krizus, A.3
-
3
-
-
0028067985
-
A two basepair deletion in the SOD 1 gene causes familial amyotrophic lateral sclerosis
-
Pramatarova A, Goto J, Nanba E, et al. A two basepair deletion in the SOD 1 gene causes familial amyotrophic lateral sclerosis. Hum Mol Genet 1994;3:2061-62
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2061-2062
-
-
Pramatarova, A.1
Goto, J.2
Nanba, E.3
-
4
-
-
0030014299
-
Amyotrophic lateral sclerosis: Recent advances in understanding disease mechanisms
-
De Belleroche J, Orrell RW, Virgo L. Amyotrophic lateral sclerosis: Recent advances in understanding disease mechanisms. J Neuropathol Exp Neurol 1996;55:747-57
-
(1996)
J Neuropathol Exp Neurol
, vol.55
, pp. 747-757
-
-
De Belleroche, J.1
Orrell, R.W.2
Virgo, L.3
-
5
-
-
0028284779
-
Motor neuron degeneration in mice that express a human Cu, Zn Superoxide dismutase mutation
-
Gurney ME, Pu H, Chiu AY, et al. Motor neuron degeneration in mice that express a human Cu, Zn Superoxide dismutase mutation. Science 1994;264:1772-75
-
(1994)
Science
, vol.264
, pp. 1772-1775
-
-
Gurney, M.E.1
Pu, H.2
Chiu, A.Y.3
-
6
-
-
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, et al. An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria. Neuron 1995;14:1105-16
-
(1995)
Neuron
, vol.14
, pp. 1105-1116
-
-
Wong, P.C.1
Pardo, C.A.2
Borchelt, D.R.3
-
7
-
-
0028888945
-
Transgenic mice expressing an altered murine Superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis
-
Ripps ME, Huntley GW, Hof PR, Morrison JH, Gordon JW. Transgenic mice expressing an altered murine Superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis. Proc Natl Acad Sci USA 1995;92:689-93
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 689-693
-
-
Ripps, M.E.1
Huntley, G.W.2
Hof, P.R.3
Morrison, J.H.4
Gordon, J.W.5
-
8
-
-
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 VMY. 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.Y.6
-
9
-
-
0030022780
-
Activation of protein kinase C induces neurofilament fragmentation, hyperphosphorylation of perikaryal neurofilaments and proximal dendritic swellings in cultured motor neurons
-
Doroudchi MM, Durham HD. Activation of protein kinase C induces neurofilament fragmentation, hyperphosphorylation of perikaryal neurofilaments and proximal dendritic swellings in cultured motor neurons. J Neuropathol Exp Neurol 1996;55:246-56
-
(1996)
J Neuropathol Exp Neurol
, vol.55
, pp. 246-256
-
-
Doroudchi, M.M.1
Durham, H.D.2
-
10
-
-
0024364748
-
Size distribution of rhodamine-labelled microspheres retrogradely transported in cultured neurons
-
Hollander H, Egensperger R, Dirlich G. Size distribution of rhodamine-labelled microspheres retrogradely transported in cultured neurons. J Neurosci Meth 1989;29:1-4
-
(1989)
J Neurosci Meth
, vol.29
, pp. 1-4
-
-
Hollander, H.1
Egensperger, R.2
Dirlich, G.3
-
11
-
-
0027965073
-
Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity
-
Borchelt DR, Lee MK, Slunt HS, et al. Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity. Proc Natl Acad Sci USA 1994;91:8292-96
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 8292-8296
-
-
Borchelt, D.R.1
Lee, M.K.2
Slunt, H.S.3
-
12
-
-
0028915976
-
Mutations associated with amyotrophic lateral sclerosis convert Superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: Studies in yeast and neural cells
-
Rabizadeh S, Gralla EB, Borchelt DR, et al. Mutations associated with amyotrophic lateral sclerosis convert Superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: Studies in yeast and neural cells. Proc Natl Acad Sci USA 1995;92:3024-28
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3024-3028
-
-
Rabizadeh, S.1
Gralla, E.B.2
Borchelt, D.R.3
-
13
-
-
0030034545
-
SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis
-
Rouleau GA, Clark AW, Rooke K, et al. SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis. Ann Neurol 1996;39:128-31
-
(1996)
Ann Neurol
, vol.39
, pp. 128-131
-
-
Rouleau, G.A.1
Clark, A.W.2
Rooke, K.3
-
14
-
-
0023738527
-
Accumulation of phosphorylated neurofilaments in anterior horn motoneurons of amyotrophic lateral sclerosis
-
Munoz DG, Greene C, Perl DP, Selkoe DJ. Accumulation of phosphorylated neurofilaments in anterior horn motoneurons of amyotrophic lateral sclerosis. J Neuropathol Exp Neurol 1988;47:9-18
-
(1988)
J Neuropathol Exp Neurol
, vol.47
, pp. 9-18
-
-
Munoz, D.G.1
Greene, C.2
Perl, D.P.3
Selkoe, D.J.4
-
15
-
-
0028001606
-
Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis
-
Figlewicz DA, Krizus A, Martinoli MG, et al. Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis. Hum Mol Genet 1994;3:1757-61
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1757-1761
-
-
Figlewicz, D.A.1
Krizus, A.2
Martinoli, M.G.3
-
16
-
-
0027426169
-
Amyotrophic lateral sclerosis and structural defects in Cu,Zn Superoxide dismutase
-
Deng H-X, Hentati A, Tainer JA, et al. 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
-
17
-
-
0029035120
-
Superoxide dismutase activity in lymphoblastoid cells from motor neurone disease/ amyotrophic lateral sclerosis (MND/ALS) patients
-
Garofalo O, Figlewicz DA, Thomas SM, et al. Superoxide dismutase activity in lymphoblastoid cells from motor neurone disease/ amyotrophic lateral sclerosis (MND/ALS) patients. J Neurol Sci 1995;129Suppl.:90-92
-
(1995)
J Neurol Sci
, vol.129
, Issue.SUPPL.
, pp. 90-92
-
-
Garofalo, O.1
Figlewicz, D.A.2
Thomas, S.M.3
-
18
-
-
0027952571
-
Cu/Zn Superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis
-
Robberecht W, Sapp P, Viaene MK, et al. Cu/Zn Superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis. J Neurochem 1994;62:384-87
-
(1994)
J Neurochem
, vol.62
, pp. 384-387
-
-
Robberecht, W.1
Sapp, P.2
Viaene, M.K.3
-
19
-
-
0027359334
-
Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis
-
Bowling AC, Schulz JB, Brown RH, Jr., Beal MF. Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis. J Neurochem 1993;61:2322-25
-
(1993)
J Neurochem
, vol.61
, pp. 2322-2325
-
-
Bowling, A.C.1
Schulz, J.B.2
Brown Jr., R.H.3
Beal, M.F.4
-
20
-
-
0028940996
-
Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis
-
Bowling AC, Barkowski EE, McKenna-Yasek D, et al. Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis. J Neurochem 1995;64:2366-69
-
(1995)
J Neurochem
, vol.64
, pp. 2366-2369
-
-
Bowling, A.C.1
Barkowski, E.E.2
McKenna-Yasek, D.3
-
21
-
-
0029671220
-
Altered reactivity of Superoxide dismutase in amyotrophic lateral sclerosis
-
Wiedau-Pazos M, Goto JJ, Rabizadeh S, et al. Altered reactivity of Superoxide dismutase in amyotrophic lateral sclerosis. Science 1996;271:515-18
-
(1996)
Science
, vol.271
, pp. 515-518
-
-
Wiedau-Pazos, M.1
Goto, J.J.2
Rabizadeh, S.3
-
23
-
-
0029927679
-
Intense Superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement
-
Shibata N, Hirano A, Kobayashi M, et al. Intense Superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement. J Neuropathol Exp Neurol 1996;55:481-90
-
(1996)
J Neuropathol Exp Neurol
, vol.55
, pp. 481-490
-
-
Shibata, N.1
Hirano, A.2
Kobayashi, M.3
-
24
-
-
0029991827
-
Colocalization of NOS and SOD1 in neurofilament accumulation within motor neurons of amyotrophic lateral sclerosis: An immunohistochemical study
-
Chou SM, Wang HS, Komai K. Colocalization of NOS and SOD1 in neurofilament accumulation within motor neurons of amyotrophic lateral sclerosis: An immunohistochemical study. J Chem Neuroanat 1996;10:249-58
-
(1996)
J Chem Neuroanat
, vol.10
, pp. 249-258
-
-
Chou, S.M.1
Wang, H.S.2
Komai, K.3
-
25
-
-
0029840428
-
Familial amyotrophic laterals sclerosis with a two base pair deletion in Superoxide dismutase 1 gene: Multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes
-
Kato S, Shimoda M, Watanabe Y, Nakashima K, Takahashi K, Ohama E. Familial amyotrophic laterals sclerosis with a two base pair deletion in Superoxide dismutase 1 gene: Multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes. J Neuropathol Exp Neurol 1996;55:1089-1101
-
(1996)
J Neuropathol Exp Neurol
, vol.55
, pp. 1089-1101
-
-
Kato, S.1
Shimoda, M.2
Watanabe, Y.3
Nakashima, K.4
Takahashi, K.5
Ohama, E.6
-
26
-
-
0028031495
-
Copper-dependent metabolism of Cu,Zn-superoxide dismutase in human K562 cells. Lack of specific transcriptional activation and accumulation of a partially inactivated enzyme
-
Steinkühler C, Carri MT, Micheli G, Knoepfel L, Weser U, Rotilio G. Copper-dependent metabolism of Cu,Zn-superoxide dismutase in human K562 cells. Lack of specific transcriptional activation and accumulation of a partially inactivated enzyme. Biochem J 1994;302:687-94
-
(1994)
Biochem J
, vol.302
, pp. 687-694
-
-
Steinkühler, C.1
Carri, M.T.2
Micheli, G.3
Knoepfel, L.4
Weser, U.5
Rotilio, G.6
-
27
-
-
0025358959
-
Superoxide dismutase undergoes proteolysis and fragmentation following oxidative modification and inactivation
-
Salo DC, Pacifici RE, Lin SW, Giulivi C, Davies KJA. Superoxide dismutase undergoes proteolysis and fragmentation following oxidative modification and inactivation. J Biol Chem 1990;265:11919-27
-
(1990)
J Biol Chem
, vol.265
, pp. 11919-11927
-
-
Salo, D.C.1
Pacifici, R.E.2
Lin, S.W.3
Giulivi, C.4
Davies, K.J.A.5
|