-
1
-
-
0035516124
-
From Charcot to Lou Gehrig: Deciphering selective motor neuron death in ALS
-
D.W. Cleveland, and J.D. Rothstein From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS Nat Rev Neurosci 2 2001 806 819
-
(2001)
Nat Rev Neurosci
, vol.2
, pp. 806-819
-
-
Cleveland, D.W.1
Rothstein, J.D.2
-
2
-
-
0028915976
-
Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: Studies in yeast and neural cells
-
S. Rabizadeh, B.E. Gralla, D.R. Borchelt, R. Gwinn, J.S. Valentine, and S. Sisodia 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 U S A 92 1995 3024 3028
-
(1995)
Proc Natl Acad Sci U S a
, vol.92
, pp. 3024-3028
-
-
Rabizadeh, S.1
Gralla, B.E.2
Borchelt, D.R.3
Gwinn, R.4
Valentine, J.S.5
Sisodia, S.6
-
3
-
-
0030777650
-
Aggregation of mutant Cu/Zn superoxide dismutase proteins in a culture model of ALS
-
H.D. Durham, J. Roy, L. Dong, and D.A. Figlewicz Aggregation of mutant Cu/Zn superoxide dismutase proteins in a culture model of ALS J Neuropathol Exp Neurol 56 1997 523 530
-
(1997)
J Neuropathol Exp Neurol
, vol.56
, pp. 523-530
-
-
Durham, H.D.1
Roy, J.2
Dong, L.3
Figlewicz, D.A.4
-
4
-
-
0030831352
-
Mutant superoxide dismutase-1-linked familial amyotrophic lateral sclerosis: Molecular mechanisms of neuronal death and protection
-
G.D. Ghadge, J.P. Lee, V.P. Bindokas, J. Jordan, L. Ma, and R.J. Miller Mutant superoxide dismutase-1-linked familial amyotrophic lateral sclerosis: molecular mechanisms of neuronal death and protection J Neurosci 17 1997 8756 8766
-
(1997)
J Neurosci
, vol.17
, pp. 8756-8766
-
-
Ghadge, G.D.1
Lee, J.P.2
Bindokas, V.P.3
Jordan, J.4
Ma, L.5
Miller, R.J.6
-
5
-
-
0030943110
-
Effect of wild-type and mutated copper/zinc superoxide dismutase on neuronal survival and l-DOPA-induced toxicity in postnatal midbrain culture
-
M.A. Mena, U. Khan, D.M. Togasaki, D. Sulzer, C.J. Epstein, and S. Przedborski Effect of wild-type and mutated copper/zinc superoxide dismutase on neuronal survival and l-DOPA-induced toxicity in postnatal midbrain culture J Neurochem 69 1997 21 33
-
(1997)
J Neurochem
, vol.69
, pp. 21-33
-
-
Mena, M.A.1
Khan, U.2
Togasaki, D.M.3
Sulzer, D.4
Epstein, C.J.5
Przedborski, S.6
-
6
-
-
0035914342
-
Subcellular distribution of superoxide dismutases (SOD) in rat liver. Cu, Zn-SOD in mitochondria
-
A. Okado-Matsumoto, and I. Fridovich Subcellular distribution of superoxide dismutases (SOD) in rat liver. Cu, Zn-SOD in mitochondria J Biol Chem 276 2001 38388 38393
-
(2001)
J Biol Chem
, vol.276
, pp. 38388-38393
-
-
Okado-Matsumoto, A.1
Fridovich, I.2
-
7
-
-
0035851122
-
A fraction of yeast Cu,Zn-superoxide dismutase and its metallochaperone, CCS, localize to the intermembrane space of mitochondria. a physiological role for SOD1 in guarding against mitochondrial oxidative damage
-
L.A. Sturtz, K. Diekert, L.T. Jensen, R. Lill, and V.C. Culotta A fraction of yeast Cu,Zn-superoxide dismutase and its metallochaperone, CCS, localize to the intermembrane space of mitochondria. A physiological role for SOD1 in guarding against mitochondrial oxidative damage J Biol Chem 276 2001 38084 38089
-
(2001)
J Biol Chem
, vol.276
, pp. 38084-38089
-
-
Sturtz, L.A.1
Diekert, K.2
Jensen, L.T.3
Lill, R.4
Culotta, V.C.5
-
8
-
-
0037088793
-
Mutant Cu, Zn superoxide dismutase that causes motoneuron degeneration is present in mitochondria in the CNS
-
C.M.J. Higgins, C. Jung, H. Ding, and S. Xu Mutant Cu, Zn superoxide dismutase that causes motoneuron degeneration is present in mitochondria in the CNS J Neurosci 22 2002 RC215
-
(2002)
J Neurosci
, vol.22
, pp. 215
-
-
Higgins, C.M.J.1
Jung, C.2
Ding, H.3
Xu, S.4
-
9
-
-
0036176613
-
Mitochondrial involvement in amyotrophic lateral sclerosis
-
F.M. Menzies, P.G. Ince, and P.J. Shaw Mitochondrial involvement in amyotrophic lateral sclerosis Neurochem Int 40 2002 543 551
-
(2002)
Neurochem Int
, vol.40
, pp. 543-551
-
-
Menzies, F.M.1
Ince, P.G.2
Shaw, P.J.3
-
10
-
-
0034031598
-
Molecular factors underlying selective vulnerability of motor neurons to neurodegeneration in amyotrophic lateral sclerosis
-
P.J. Shaw, and C.J. Eggett Molecular factors underlying selective vulnerability of motor neurons to neurodegeneration in amyotrophic lateral sclerosis J Neurol 247 Suppl. 1 2000 I/17 I/27
-
(2000)
J Neurol
, vol.247
, Issue.1 SUPPL.
-
-
Shaw, P.J.1
Eggett, C.J.2
-
11
-
-
0028815433
-
Superoxide dismutase is an abundant component in cell bodies, dendrites, and axons of motor neurons and in a subset of other neurons
-
C.A. Pardo, Z. Xu, D.R. Borchelt, D.L. Price, S.S. Sisodia, and D.W. Cleveland Superoxide dismutase is an abundant component in cell bodies, dendrites, and axons of motor neurons and in a subset of other neurons Proc Natl Acad Sci U S A 92 1995 954 958
-
(1995)
Proc Natl Acad Sci U S a
, vol.92
, pp. 954-958
-
-
Pardo, C.A.1
Xu, Z.2
Borchelt, D.R.3
Price, D.L.4
Sisodia, S.S.5
Cleveland, D.W.6
-
12
-
-
0036488219
-
Increased mitochondrial antioxidative activity or decreased oxygen free radical propagation prevent mutant SOD1-mediated motor neuron cell death
-
R. Liu, B. Li, S.W. Flanagan, L.W. Oberley, D. Gozal, and M. Qiu Increased mitochondrial antioxidative activity or decreased oxygen free radical propagation prevent mutant SOD1-mediated motor neuron cell death J Neurochem 80 2002 488 500
-
(2002)
J Neurochem
, vol.80
, pp. 488-500
-
-
Liu, R.1
Li, B.2
Flanagan, S.W.3
Oberley, L.W.4
Gozal, D.5
Qiu, M.6
-
13
-
-
0036310142
-
Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis
-
F.M. Menzies, M.R. Cookson, R.W. Taylor, D.M. Turnbull, Z.M.A. Chrzanowska-Lightowlers, and L. Dong Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis Brain 125 2002 1522 1533
-
(2002)
Brain
, vol.125
, pp. 1522-1533
-
-
Menzies, F.M.1
Cookson, M.R.2
Taylor, R.W.3
Turnbull, D.M.4
Chrzanowska- Lightowlers, Z.M.A.5
Dong, L.6
-
14
-
-
0037458659
-
Analysis of the cytosolic proteome in a cell culture model of familial amyotrophic lateral sclerosis reveals alterations to the proteasome, antioxidant defenses, and nitric oxide synthetic pathways
-
S. Allen, P.R. Heath, J. Kirby, S.B. Wharton, M.R. Cookson, and F.M. Menzies Analysis of the cytosolic proteome in a cell culture model of familial amyotrophic lateral sclerosis reveals alterations to the proteasome, antioxidant defenses, and nitric oxide synthetic pathways J Biol Chem 278 2003 6371 6383
-
(2003)
J Biol Chem
, vol.278
, pp. 6371-6383
-
-
Allen, S.1
Heath, P.R.2
Kirby, J.3
Wharton, S.B.4
Cookson, M.R.5
Menzies, F.M.6
-
15
-
-
0026465350
-
Neuroblastoma × spinal cord (NSC) hybrid cell lines resemble developing motor neurons
-
N.R. Cashman, H.D. Durham, J.K. Blusztajn, K. Oda, T. Tabira, and I.T. Shaw Neuroblastoma × spinal cord (NSC) hybrid cell lines resemble developing motor neurons Dev Dyn 194 1992 209 221
-
(1992)
Dev Dyn
, vol.194
, pp. 209-221
-
-
Cashman, N.R.1
Durham, H.D.2
Blusztajn, J.K.3
Oda, K.4
Tabira, T.5
Shaw, I.T.6
-
16
-
-
0345825889
-
Expression of SOD1 G93A or wild-type SOD1 in primary cultures of astrocytes down-regulates the glutamate transporter GLT-1: Lack of involvement of oxidative stress
-
M. Tortarolo, A.J. Crossthwaite, L. Conforti, J.P. Spencer, R.J. Williams, and C. Bendotti Expression of SOD1 G93A or wild-type SOD1 in primary cultures of astrocytes down-regulates the glutamate transporter GLT-1: lack of involvement of oxidative stress J Neurochem 88 2004 481 493
-
(2004)
J Neurochem
, vol.88
, pp. 481-493
-
-
Tortarolo, M.1
Crossthwaite, A.J.2
Conforti, L.3
Spencer, J.P.4
Williams, R.J.5
Bendotti, C.6
-
17
-
-
12244297111
-
Mitochondrial dysfunction and death in motor neurons exposed to the glutathione-depleting agent ethacrynic acid
-
M. Rizzardini, M. Lupi, S. Bernasconi, A. Mangolini, and L. Cantoni Mitochondrial dysfunction and death in motor neurons exposed to the glutathione-depleting agent ethacrynic acid J Neurol Sci 207 2003 51 58
-
(2003)
J Neurol Sci
, vol.207
, pp. 51-58
-
-
Rizzardini, M.1
Lupi, M.2
Bernasconi, S.3
Mangolini, A.4
Cantoni, L.5
-
18
-
-
0030200643
-
Proteasome inhibition enhances the stability of mouse Cu/Zn superoxide dismutase with mutations linked to familial amyotrophic lateral sclerosis
-
E.K. Hoffman, H.M. Wilcox, R.W. Scott, and R. Siman Proteasome inhibition enhances the stability of mouse Cu/Zn superoxide dismutase with mutations linked to familial amyotrophic lateral sclerosis J Neurol Sci 139 1996 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
-
19
-
-
0028918657
-
A transient three-plasmid expression system for the production of high titer retroviral vectors
-
Y. Soneoka, P.M. Cannon, E.E. Ramsdale, J.C. Griffiths, G. Romano, and S.M. Kingsman A transient three-plasmid expression system for the production of high titer retroviral vectors Nucleic Acids Res 23 1995 628 633
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 628-633
-
-
Soneoka, Y.1
Cannon, P.M.2
Ramsdale, E.E.3
Griffiths, J.C.4
Romano, G.5
Kingsman, S.M.6
-
20
-
-
0034209229
-
Superoxide dismutase-1 mutation-related neurotoxicity in familial amyotrophic lateral sclerosis
-
N. Shibata, A. Hirano, T. Yamamoto, Y. Kato, and M. Kobayashi Superoxide dismutase-1 mutation-related neurotoxicity in familial amyotrophic lateral sclerosis Amyotroph Lateral Scler Other Mot Neuron Disord 1 2000 143 161
-
(2000)
Amyotroph Lateral Scler Other Mot Neuron Disord
, vol.1
, pp. 143-161
-
-
Shibata, N.1
Hirano, A.2
Yamamoto, T.3
Kato, Y.4
Kobayashi, M.5
-
21
-
-
15844429977
-
Superoxide dismutase activity is essential for stationary phase survival in Saccharomyces cerevisiae. Mitochondrial production of toxic oxygen species in vivo
-
V.D. Longo, E.B. Gralla, and J.S. Valentine Superoxide dismutase activity is essential for stationary phase survival in Saccharomyces cerevisiae. Mitochondrial production of toxic oxygen species in vivo J Biol Chem 271 1996 12275 12280
-
(1996)
J Biol Chem
, vol.271
, pp. 12275-12280
-
-
Longo, V.D.1
Gralla, E.B.2
Valentine, J.S.3
-
22
-
-
0038693216
-
The basic aspects of therapeutics in amyotrophic lateral sclerosis
-
M.J. Strong The basic aspects of therapeutics in amyotrophic lateral sclerosis Pharmacol Ther 98 2003 379 414
-
(2003)
Pharmacol Ther
, vol.98
, pp. 379-414
-
-
Strong, M.J.1
-
23
-
-
0035229427
-
The mitochondrion in apoptosis: How Pandora's box opens
-
N. Zanzami, and G. Kroemer The mitochondrion in apoptosis: how Pandora's box opens Nat Rev Mol Cell Biol 2 2001 67 71
-
(2001)
Nat Rev Mol Cell Biol
, vol.2
, pp. 67-71
-
-
Zanzami, N.1
Kroemer, G.2
-
25
-
-
0032731637
-
ALS-linked Cu/Zn SOD mutations increase vulnerability of motor neurons to excitotoxicity by a mechanism involving increased oxidative stress and perturbed calcium homeostasis
-
I.I. Kruman, W.A. Pedersen, J.E. Spriger, and M.P. Mattson ALS-linked Cu/Zn SOD mutations increase vulnerability of motor neurons to excitotoxicity by a mechanism involving increased oxidative stress and perturbed calcium homeostasis Exp Neurol 160 1999 28 39
-
(1999)
Exp Neurol
, vol.160
, pp. 28-39
-
-
Kruman, I.I.1
Pedersen, W.A.2
Spriger, J.E.3
Mattson, M.P.4
-
26
-
-
3042600245
-
Molecular basis for motor neuron selective damage induced by mutated SOD1: Distribution of the G93A mutant of SOD1 in mitochondria and mitochondrial structural alterations in motor neuron-like and in non-neuronal cellular models of ALS
-
A. Raimondi, A. Mangolini, C. Vanoni, L. Conforti, M. Francolini, and M. Rizzardini Molecular basis for motor neuron selective damage induced by mutated SOD1: distribution of the G93A mutant of SOD1 in mitochondria and mitochondrial structural alterations in motor neuron-like and in non-neuronal cellular models of ALS Amyotroph. Lateral Scler. Other Mot. Neuron Disord. 4 Suppl. 1 2003 150
-
(2003)
Amyotroph. Lateral Scler. Other Mot. Neuron Disord.
, vol.4
, Issue.1 SUPPL.
, pp. 150
-
-
Raimondi, A.1
Mangolini, A.2
Vanoni, C.3
Conforti, L.4
Francolini, M.5
Rizzardini, M.6
-
27
-
-
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
-
C. Bendotti, N. Calvaresi, L. Chiveri, A. Prelle, M. Moggio, and M. Braga 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 191 2001 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
-
28
-
-
0030026832
-
Ultrastructural evidence for altered calcium in motor nerve terminals in amyotrophic lateral sclerosis
-
L. Siklos, J. Engelhardt, Y. Harati, R.G. Smith, F. Joo, and S.H. Appel Ultrastructural evidence for altered calcium in motor nerve terminals in amyotrophic lateral sclerosis Ann Neurol 39 1996 203 216
-
(1996)
Ann Neurol
, vol.39
, pp. 203-216
-
-
Siklos, L.1
Engelhardt, J.2
Harati, Y.3
Smith, R.G.4
Joo, F.5
Appel, S.H.6
-
29
-
-
0023270442
-
Hepatic ultrastructural changes and liver dysfunction in amyotrophic lateral sclerosis
-
Y. Nakano, K. Hirayama, and K. Terao Hepatic ultrastructural changes and liver dysfunction in amyotrophic lateral sclerosis Arch Neurol 44 1987 103 106
-
(1987)
Arch Neurol
, vol.44
, pp. 103-106
-
-
Nakano, Y.1
Hirayama, K.2
Terao, K.3
-
30
-
-
0037424245
-
Mitochondrial complex I inhibitor rotenone induces apoptosis through enhancing mitochondrial reactive oxygen species production
-
N. Li, K. Ragheb, G. Lawler, J. Sturgis, B. Rajwa, and J.A. Melendez Mitochondrial complex I inhibitor rotenone induces apoptosis through enhancing mitochondrial reactive oxygen species production J Biol Chem 278 2003 8516 8525
-
(2003)
J Biol Chem
, vol.278
, pp. 8516-8525
-
-
Li, N.1
Ragheb, K.2
Lawler, G.3
Sturgis, J.4
Rajwa, B.5
Melendez, J.A.6
-
31
-
-
0036830072
-
Mitochondrial electron transport chain complex dysfunction in a transgenic mouse model for amyotrophic lateral sclerosis
-
C. Jung, C.M.J. Higgins, and S. Xu Mitochondrial electron transport chain complex dysfunction in a transgenic mouse model for amyotrophic lateral sclerosis J Neurochem 83 2002 535 545
-
(2002)
J Neurochem
, vol.83
, pp. 535-545
-
-
Jung, C.1
Higgins, C.M.J.2
Xu, S.3
-
32
-
-
0037119407
-
Mutated human SOD1 causes dysfunction of oxidative phosphorylation in mitochondria of transgenic mice
-
M. Mattiazzi, M. D'Aurelio, C.D. Gajewski, K. Martushova, M. Kiaei, and M.F. Beal Mutated human SOD1 causes dysfunction of oxidative phosphorylation in mitochondria of transgenic mice J Biol Chem 277 2002 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
-
33
-
-
0024996681
-
The oxidative inactivation of mitochondrial electron transport chain components and ATPase
-
Y. Zhang, O. Marcillat, C. Giulivi, L. Ernster, and K.J.A. Davies The oxidative inactivation of mitochondrial electron transport chain components and ATPase J Biol Chem 27 1990 16330 16336
-
(1990)
J Biol Chem
, vol.27
, pp. 16330-16336
-
-
Zhang, Y.1
Marcillat, O.2
Giulivi, C.3
Ernster, L.4
Davies, K.J.A.5
-
35
-
-
0042093555
-
Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine
-
S. Beretta, G. Sala, L. Mattavelli, C. Ceresa, A. Casciati, and A. Ferri Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine Neurobiol Dis 13 2003 213 221
-
(2003)
Neurobiol Dis
, vol.13
, pp. 213-221
-
-
Beretta, S.1
Sala, G.2
Mattavelli, L.3
Ceresa, C.4
Casciati, A.5
Ferri, A.6
-
36
-
-
0030478699
-
Neurodegenerative disorders: Clues from glutamate and energy metabolism
-
C. Ikonomidou, and L. Turski Neurodegenerative disorders: clues from glutamate and energy metabolism Crit Rev Neurobiol 10 1996 239 263
-
(1996)
Crit Rev Neurobiol
, vol.10
, pp. 239-263
-
-
Ikonomidou, C.1
Turski, L.2
-
37
-
-
0035863011
-
Mitochondrial respiratory chain-dependent generation of superoxide anion and its release into their intermembrane space
-
D. Han, E. Williams, and E. Cadenas Mitochondrial respiratory chain-dependent generation of superoxide anion and its release into their intermembrane space Biochem J 353 2001 411 416
-
(2001)
Biochem J
, vol.353
, pp. 411-416
-
-
Han, D.1
Williams, E.2
Cadenas, E.3
-
39
-
-
0037184999
-
Mitochondrial localization of mutant superoxide dismutase 1 triggers caspase-dependent cell death in a cellular model of familial amyotrophic lateral sclerosis
-
H. Takeuchi, Y. Kobayashi, S. Ishigaki, M. Doyu, and G. Sobue Mitochondrial localization of mutant superoxide dismutase 1 triggers caspase-dependent cell death in a cellular model of familial amyotrophic lateral sclerosis J Biol Chem 52 2002 50966 50972
-
(2002)
J Biol Chem
, vol.52
, pp. 50966-50972
-
-
Takeuchi, H.1
Kobayashi, Y.2
Ishigaki, S.3
Doyu, M.4
Sobue, G.5
-
40
-
-
0036071852
-
Overexpression of manganese superoxide dismutase attenuates neuronal death in human cells expressing mutant (G37R) Cu/Zn-superoxide dismutase
-
S.W. Flanagan, R.D. Anderson, M.A. Ross, and L.W. Oberley Overexpression of manganese superoxide dismutase attenuates neuronal death in human cells expressing mutant (G37R) Cu/Zn-superoxide dismutase J Neurochem 81 2002 170 177
-
(2002)
J Neurochem
, vol.81
, pp. 170-177
-
-
Flanagan, S.W.1
Anderson, R.D.2
Ross, M.A.3
Oberley, L.W.4
-
41
-
-
0034113695
-
Partial deficiency of manganese superoxide dismutase exacerbates a transgenic mouse model of amyotrophic lateral sclerosis
-
O.A. Andreassen, R.J. Ferrante, P. Klivenyi, A.M. Klein, L.A. Shinobu, and C.J. Epstein Partial deficiency of manganese superoxide dismutase exacerbates a transgenic mouse model of amyotrophic lateral sclerosis Ann Neurol 47 2000 447 455
-
(2000)
Ann Neurol
, vol.47
, pp. 447-455
-
-
Andreassen, O.A.1
Ferrante, R.J.2
Klivenyi, P.3
Klein, A.M.4
Shinobu, L.A.5
Epstein, C.J.6
-
42
-
-
0035896440
-
Intrathecal cyclosporin prolongs survival of late-stage ALS mice
-
M. Keep, E. Elmer, K.S.K. Fong, and K. Csiszar Intrathecal cyclosporin prolongs survival of late-stage ALS mice Brain Res 894 2001 327 331
-
(2001)
Brain Res
, vol.894
, pp. 327-331
-
-
Keep, M.1
Elmer, E.2
Fong, K.S.K.3
Csiszar, K.4
-
43
-
-
0037007645
-
Minocycline inhibits cytochrome c release and delays progression of amyotrophic lateral sclerosis in mice
-
S. Zhu, I.G. Stavrovskaya, M. Drozda, B.Y. Kim, V. Ona, and M. Li Minocycline inhibits cytochrome c release and delays progression of amyotrophic lateral sclerosis in mice Nature 417 2002 74 78
-
(2002)
Nature
, vol.417
, pp. 74-78
-
-
Zhu, S.1
Stavrovskaya, I.G.2
Drozda, M.3
Kim, B.Y.4
Ona, V.5
Li, M.6
-
44
-
-
0030756459
-
Bcl-2: Prolonging life in a transgenic mouse model of familial amyotrophic lateral sclerosis
-
V. Kostic, V. Jackson-Lewis, F. de Bilbao, M. Dubois-Dauphin, and S. Przedborski Bcl-2: prolonging life in a transgenic mouse model of familial amyotrophic lateral sclerosis Science 277 1997 559 562
-
(1997)
Science
, vol.277
, pp. 559-562
-
-
Kostic, V.1
Jackson-Lewis, V.2
De Bilbao, F.3
Dubois-Dauphin, M.4
Przedborski, S.5
-
45
-
-
0034922153
-
Effect of overexpression of wild-type and mutant Cu/Zn-superoxide dismutases on oxidative stress and cell death induced by hydrogen peroxide, 4-hydroxynonenal or serum deprivation: Potentiation of injury by ALS-related mutant superoxide dismutases and protection by bcl-2
-
M.H. Lee, D.-H. Hyun, B. Halliwell, and P. Jenner Effect of overexpression of wild-type and mutant Cu/Zn-superoxide dismutases on oxidative stress and cell death induced by hydrogen peroxide, 4-hydroxynonenal or serum deprivation: potentiation of injury by ALS-related mutant superoxide dismutases and protection by bcl-2 J Neurochem 78 2001 209 220
-
(2001)
J Neurochem
, vol.78
, pp. 209-220
-
-
Lee, M.H.1
Hyun, D.-H.2
Halliwell, B.3
Jenner, P.4
-
46
-
-
0034601439
-
N-acetyl-l-cysteine improves survival and preserves motor performance in an animal model of familial amyotrophic lateral sclerosis
-
O.A. Andreassen, A. Dedeoglu, P. Klivenyi, M.F. Beal, and A.I. Bush N-acetyl-l-cysteine improves survival and preserves motor performance in an animal model of familial amyotrophic lateral sclerosis Neuroreport 11 2000 2491 2493
-
(2000)
Neuroreport
, vol.11
, pp. 2491-2493
-
-
Andreassen, O.A.1
Dedeoglu, A.2
Klivenyi, P.3
Beal, M.F.4
Bush, A.I.5
|