-
1
-
-
0029010496
-
Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase
-
Andersen P. M., Nilsson P., Ala-Hurula V., Keranen M. L., Tarvainen I., Haltia T., Nilsson L., Binzer M., Forsgren L. and Marklund S. L. (1995) Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase. Nat. Genet. 10, 61-66.
-
(1995)
Nat. Genet.
, vol.10
, pp. 61-66
-
-
Andersen, P.M.1
Nilsson, P.2
Ala-Hurula, V.3
Keranen, M.L.4
Tarvainen, I.5
Haltia, T.6
Nilsson, L.7
Binzer, M.8
Forsgren, L.9
Marklund, S.L.10
-
2
-
-
29244480266
-
EFNS task force on management of amyotrophic lateral sclerosis: Guidelines for diagnosing and clinical care of patients and relatives
-
Andersen P. M., Borasio G. D., Dengler R., Hardiman O., Kollewe K., Leigh P. N., Pradat P. F., Silani V. and Tomik B. (2005) EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relatives. Eur. J. Neurol. 12, 921-938.
-
(2005)
Eur. J. Neurol.
, vol.12
, pp. 921-938
-
-
Andersen, P.M.1
Borasio, G.D.2
Dengler, R.3
Hardiman, O.4
Kollewe, K.5
Leigh, P.N.6
Pradat, P.F.7
Silani, V.8
Tomik, B.9
-
3
-
-
10744229692
-
Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families
-
DOI 10.1007/s00401-003-0763-5
-
Arisato T., Okubo R., Arata H. et al. (2003) Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families. Acta Neuropathol. 106, 561-568. (Pubitemid 37441613)
-
(2003)
Acta Neuropathologica
, vol.106
, Issue.6
, pp. 561-568
-
-
Arisato, T.1
Okubo, R.2
Arata, H.3
Abe, K.4
Fukada, K.5
Sakoda, S.6
Shimizu, A.7
Qin, X.H.8
Izumo, S.9
Osame, M.10
Nakagawa, M.11
-
4
-
-
9144261759
-
The unusually stable quaternary structure of human Cu,Zn-superoxide dismutase 1 is controlled by both metal occupancy and disulfide status
-
Arnesano F., Banci L., Bertini I., Martinelli M., Furukawa Y. and O'Halloran T. V. (2004) The unusually stable quaternary structure of human Cu,Zn-superoxide dismutase 1 is controlled by both metal occupancy and disulfide status. J. Biol. Chem. 279, 47998-48003.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 47998-48003
-
-
Arnesano, F.1
Banci, L.2
Bertini, I.3
Martinelli, M.4
Furukawa, Y.5
O'Halloran, T.V.6
-
5
-
-
77958519939
-
Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS
-
Bosco D. A., Morfini G., Karabacak N. M. et al. (2010) Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS. Nat. Neurosci. 13, 1396-1403.
-
(2010)
Nat. Neurosci.
, vol.13
, pp. 1396-1403
-
-
Bosco, D.A.1
Morfini, G.2
Karabacak, N.M.3
-
6
-
-
0027359334
-
Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis
-
DOI 10.1111/j.1471-4159.1993.tb07478.x
-
Bowling A. C., Schulz J. B., Brown Jr R. H. and Beal M. F. (1993) Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis. J. Neurochem. 61, 2322-2325. (Pubitemid 23354097)
-
(1993)
Journal of Neurochemistry
, vol.61
, Issue.6
, pp. 2322-2325
-
-
Bowling, A.C.1
Schulz, J.B.2
Brown Jr., R.H.3
Beal, M.F.4
-
7
-
-
79952571109
-
Template-directed misfolding of SOD1 in vitro: A model for ALS propagation?
-
20th International Symposium on ALS/MND, Berlin, Germany
-
Cashman N., Yanai A. and Grad L. (2009) Template-directed misfolding of SOD1 in vitro: A model for ALS propagation? 20th International Symposium on ALS/MND, Berlin, Germany. Amyotroph. Lateral Scler. 10(Suppl 11), 19.
-
(2009)
Amyotroph. Lateral Scler.
, vol.10
, Issue.SUPPL. 11
, pp. 19
-
-
Cashman, N.1
Yanai, A.2
Grad, L.3
-
8
-
-
77956270117
-
Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis
-
Chia R., Tattum M. H., Jones S., Collinge J., Fisher E. M. and Jackson G. S. (2010) Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis. PLoS ONE 5, e10627.
-
(2010)
PLoS ONE
, vol.5
-
-
Chia, R.1
Tattum, M.H.2
Jones, S.3
Collinge, J.4
Fisher, E.M.5
Jackson, G.S.6
-
9
-
-
34250177650
-
Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation
-
DOI 10.1111/j.1471-4159.2007.04531.x
-
Ezzi S. A., Urushitani M. and Julien J. P. (2007) Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation. J. Neurochem. 102, 170-178. (Pubitemid 46906269)
-
(2007)
Journal of Neurochemistry
, vol.102
, Issue.1
, pp. 170-178
-
-
Ezzi, S.A.1
Urushitani, M.2
Julien, J.-P.3
-
10
-
-
77955352066
-
Novel antibodies reveal inclusions containing non-native SOD1 in sporadic ALS patients
-
Forsberg K., Jonsson P. A., Andersen P. M., Bergemalm D., Graffmo K. S., Hultdin M., Jacobsson J., Rosquist R., Marklund S. L. and Brannstrom T. (2010) Novel antibodies reveal inclusions containing non-native SOD1 in sporadic ALS patients. PLoS ONE 5, e11552.
-
(2010)
PLoS ONE
, vol.5
-
-
Forsberg, K.1
Jonsson, P.A.2
Andersen, P.M.3
Bergemalm, D.4
Graffmo, K.S.5
Hultdin, M.6
Jacobsson, J.7
Rosquist, R.8
Marklund, S.L.9
Brannstrom, T.10
-
11
-
-
0035783937
-
Stabilization of mutant Cu/Zn superoxide dismutase (SOD1) protein by coexpressed wild SOD1 protein accelerates the disease progression in familial amyotrophic lateral sclerosis mice
-
Fukada K., Nagano S., Satoh M., Tohyama C., Nakanishi T., Shimizu A., Yanagihara T. and Sakoda S. (2001) Stabilization of mutant Cu/Zn superoxide dismutase (SOD1) protein by coexpressed wild SOD1 protein accelerates the disease progression in familial amyotrophic lateral sclerosis mice. Eur. J. Neurosci. 14, 2032-2036.
-
(2001)
Eur. J. Neurosci.
, vol.14
, pp. 2032-2036
-
-
Fukada, K.1
Nagano, S.2
Satoh, M.3
Tohyama, C.4
Nakanishi, T.5
Shimizu, A.6
Yanagihara, T.7
Sakoda, S.8
-
12
-
-
77951924183
-
Intracerebroventricular infusion of monoclonal antibody or its derived Fab fragment against misfolded forms of SOD1 mutant delays mortality in a mouse model of ALS
-
Gros-Louis F., Soucy G., Lariviere R. and Julien J. P. (2010) Intracerebroventricular infusion of monoclonal antibody or its derived Fab fragment against misfolded forms of SOD1 mutant delays mortality in a mouse model of ALS. J. Neurochem. 113, 1188-1199.
-
(2010)
J. Neurochem.
, vol.113
, pp. 1188-1199
-
-
Gros-Louis, F.1
Soucy, G.2
Lariviere, R.3
Julien, J.P.4
-
13
-
-
33646588005
-
Widespread sensorimotor and frontal cortical atrophy in Amyotrophic Lateral Sclerosis
-
Grosskreutz J., Kaufmann J., Fradrich J., Dengler R., Heinze H. J. and Peschel T. (2006) Widespread sensorimotor and frontal cortical atrophy in Amyotrophic Lateral Sclerosis. BMC Neurol. 6, 17.
-
(2006)
BMC Neurol.
, vol.6
, pp. 17
-
-
Grosskreutz, J.1
Kaufmann, J.2
Fradrich, J.3
Dengler, R.4
Heinze, H.J.5
Peschel, T.6
-
14
-
-
0028284779
-
Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation
-
Gurney M. E., Pu H., Chiu A. Y. et al. (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
-
15
-
-
74049164709
-
Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond
-
Ilieva H., Polymenidou M. and Cleveland D. W. (2009) Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond. J. Cell Biol. 187, 761-772.
-
(2009)
J. Cell Biol.
, vol.187
, pp. 761-772
-
-
Ilieva, H.1
Polymenidou, M.2
Cleveland, D.W.3
-
16
-
-
0034520591
-
Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1
-
Jaarsma D., Haasdijk E. D., Grashorn J. A. C., Hawkins R., van Duijn W., Verspaget H. W., London J. and Holstege J. C. (2000) Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1. Neurobiol. Dis. 7, 623-643.
-
(2000)
Neurobiol. Dis.
, vol.7
, pp. 623-643
-
-
Jaarsma, D.1
Haasdijk, E.D.2
Grashorn, J.A.C.3
Hawkins, R.4
Van Duijn, W.5
Verspaget, H.W.6
London, J.7
Holstege, J.C.8
-
17
-
-
0034956740
-
Superoxide dismutase in CSF from amyotrophic lateral sclerosis patients with and without CuZn-superoxide dismutase mutations
-
Jacobsson J., Jonsson P. A., Andersen P. M., Forsgren L. and Marklund S. L. (2001) Superoxide dismutase in CSF from amyotrophic lateral sclerosis patients with and without CuZn-superoxide dismutase mutations. Brain 124, 1461-1466. (Pubitemid 32606106)
-
(2001)
Brain
, vol.124
, Issue.7
, pp. 1461-1466
-
-
Jacobsson, J.1
Jonsson, P.A.2
Andersen, P.M.3
Forsgren, L.4
Marklund, S.L.5
-
18
-
-
0347358915
-
Minute quantities of misfolded mutant superoxide dismutase-1 cause amyotrophic lateral sclerosis
-
DOI 10.1093/brain/awh005
-
Jonsson P. A., Ernhill K., Andersen P. M., Bergemalm D., Brannstrom T., Gredal O., Nilsson P. and Marklund S. L. (2004) Minute quantities of misfolded mutant superoxide dismutase-1 cause amyotrophic lateral sclerosis. Brain 127, 73-88. (Pubitemid 38055347)
-
(2004)
Brain
, vol.127
, Issue.1
, pp. 73-88
-
-
Jonsson, P.A.1
Ernhill, K.2
Andersen, P.M.3
Bergemalm, D.4
Brannstrom, T.5
Gredal, O.6
Nilsson, P.7
Marklund, S.L.8
-
19
-
-
31544467869
-
Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis models
-
DOI 10.1093/brain/awh704
-
Jonsson P. A., Graffmo K. S., Andersen P. M., Brannstrom T., Lindberg M., Oliveberg M. and Marklund S. L. (2006) Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis models. Brain 129, 451-464. (Pubitemid 43164368)
-
(2006)
Brain
, vol.129
, Issue.2
, pp. 451-464
-
-
Jonsson, P.A.1
Graffmo, K.S.2
Andersen, P.M.3
Brannstrom, T.4
Lindberg, M.5
Oliveberg, M.6
Marklund, S.L.7
-
20
-
-
70350344061
-
Superoxide dismutase in amyotrophic lateral sclerosis patients homozygous for the D90A mutation
-
Jonsson P. A., Graffmo K. S., Andersen P. M., Marklund S. L. and Brannstrom T. (2009) Superoxide dismutase in amyotrophic lateral sclerosis patients homozygous for the D90A mutation. Neurobiol. Dis. 36, 421-424.
-
(2009)
Neurobiol. Dis.
, vol.36
, pp. 421-424
-
-
Jonsson, P.A.1
Graffmo, K.S.2
Andersen, P.M.3
Marklund, S.L.4
Brannstrom, T.5
-
21
-
-
0034209203
-
New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: Inclusions containing SOD1 in neurons and astrocytes
-
Kato S., Takikawa M., Nakashima K., Hirano A., Cleveland D. W., Kusaka H., Shibata N., Kato M., Nakano I. and Ohama E. (2000) New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes. Amyotroph. Lateral Scler. Other Motor Neuron Disord. 1, 163-184.
-
(2000)
Amyotroph. Lateral Scler. Other Motor Neuron Disord.
, vol.1
, pp. 163-184
-
-
Kato, S.1
Takikawa, M.2
Nakashima, K.3
Hirano, A.4
Cleveland, D.W.5
Kusaka, H.6
Shibata, N.7
Kato, M.8
Nakano, I.9
Ohama, E.10
-
22
-
-
0037168643
-
Common denominator of Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis: Decreased stability of the apo state
-
Lindberg M. J., Tibell L. and Oliveberg M. (2002) Common denominator of Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis: decreased stability of the apo state. Proc. Natl Acad. Sci. USA 99, 16607-16612.
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 16607-16612
-
-
Lindberg, M.J.1
Tibell, L.2
Oliveberg, M.3
-
23
-
-
0030749689
-
Normal binding and reactivity of copper in mutant superoxide dismutase isolated from amyotrophic lateral sclerosis patients
-
Marklund S. L., Andersen P. M., Forsgren L., Nilsson P., Ohlsson P. I., Wikander G. and Oberg A. (1997) Normal binding and reactivity of copper in mutant superoxide dismutase isolated from amyotrophic lateral sclerosis patients. J. Neurochem. 69, 675-681. (Pubitemid 27327970)
-
(1997)
Journal of Neurochemistry
, vol.69
, Issue.2
, pp. 675-681
-
-
Marklund, S.L.1
Andersen, P.M.2
Forsgren, L.3
Nilsson, P.4
Ohlsson, P.-I.5
Wikander, G.6
Oberg, A.7
-
24
-
-
0042477834
-
Physiology of the cerebrospinal fluid
-
(Milhorat T. H., ed.), Neuroscience Society of New York, New York
-
Milhorat T. H. (1987) Physiology of the cerebrospinal fluid, in Cerebrospinal Fluid and the Brain Edemas (Milhorat T. H., ed.), pp. 39-73. Neuroscience Society of New York, New York.
-
(1987)
Cerebrospinal Fluid and the Brain Edemas
, pp. 39-73
-
-
Milhorat, T.H.1
-
25
-
-
0029884093
-
Evidence for secretion of cytosolic CuZn superoxide dismutase by Hep G2 cells and human fibroblasts
-
Mondola P., Annella T., Santillo M. and Santangelo F. (1996) Evidence for secretion of cytosolic CuZn superoxide dismutase by Hep G2 cells and human fibroblasts. Int. J. Biochem. Cell Biol. 28, 677-681.
-
(1996)
Int. J. Biochem. Cell Biol.
, vol.28
, pp. 677-681
-
-
Mondola, P.1
Annella, T.2
Santillo, M.3
Santangelo, F.4
-
26
-
-
0028982454
-
Reduction of beta-amyloid peptide42 in the cerebrospinal fluid of patients with Alzheimer's disease
-
Motter R., Vigo-Pelfrey C., Kholodenko D. et al. (1995) Reduction of beta-amyloid peptide42 in the cerebrospinal fluid of patients with Alzheimer's disease. Ann. Neurol. 38, 643-648.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 643-648
-
-
Motter, R.1
Vigo-Pelfrey, C.2
Kholodenko, D.3
-
27
-
-
2442624720
-
Monomeric Cu, Zn-superoxide dismutase is a common misfolding intermediate in the oxidation models of sporadic and familial amyotrophic lateral sclerosis
-
Rakhit R., Crow J. P., Lepock J. R., Kondejewski L. H., Cashman N. R. and Chakrabartty A. (2004) Monomeric Cu, Zn-superoxide dismutase is a common misfolding intermediate in the oxidation models of sporadic and familial amyotrophic lateral sclerosis. J. Biol. Chem. 279, 15499-15504.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 15499-15504
-
-
Rakhit, R.1
Crow, J.P.2
Lepock, J.R.3
Kondejewski, L.H.4
Cashman, N.R.5
Chakrabartty, A.6
-
28
-
-
0027401203
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
DOI 10.1038/362059a0
-
Rosen D. R., Siddique T., Patterson D. et al. (1993) Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 362, 59-62. (Pubitemid 23087289)
-
(1993)
Nature
, vol.362
, Issue.6415
, 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
-
29
-
-
12144249923
-
Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis
-
DOI 10.1523/JNEUROSCI.4253-04.2005
-
Turner B. J., Atkin J. D., Farg M. A., Zang D. W., Rembach A., Lopes E. C., Patch J. D., Hill A. F. and Cheema S. S. (2005) Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis. J. Neurosci. 25, 108-117. (Pubitemid 40110771)
-
(2005)
Journal of Neuroscience
, vol.25
, Issue.1
, pp. 108-117
-
-
Turner, B.J.1
Atkin, J.D.2
Farg, M.A.3
Da, W.Z.4
Rembach, A.5
Lopes, E.C.6
Patch, J.D.7
Hill, A.F.8
Cheema, S.S.9
-
30
-
-
29444443348
-
Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis
-
Urushitani M., Sik A., Sakurai T., Nukina N., Takahashi R. and Julien J. P. (2006) Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis. Nat. Neurosci. 9, 108-118.
-
(2006)
Nat. Neurosci.
, vol.9
, pp. 108-118
-
-
Urushitani, M.1
Sik, A.2
Sakurai, T.3
Nukina, N.4
Takahashi, R.5
Julien, J.P.6
-
31
-
-
33847787621
-
Therapeutic effects of immunization with mutant superoxide dismutase in mice models of amyotrophic lateral sclerosis
-
Urushitani M., Ezzi S. A. and Julien J. P. (2007) Therapeutic effects of immunization with mutant superoxide dismutase in mice models of amyotrophic lateral sclerosis. Proc. Natl Acad. Sci. USA 104, 2495-2500.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 2495-2500
-
-
Urushitani, M.1
Ezzi, S.A.2
Julien, J.P.3
-
32
-
-
0035068562
-
Japanese familial amyotrophic lateral sclerosis family with a two-base deletion in the superoxide dismutase-1 gene
-
DOI 10.1046/j.1440-1789.2001.00360.x
-
Watanabe Y., Adachi Y. and Nakashima K. (2001) Japanese familial amyotrophic lateral sclerosis family with a two-base deletion in the superoxide dismutase-1 gene. Neuropathology 21, 61-66. (Pubitemid 32280389)
-
(2001)
Neuropathology
, vol.21
, Issue.1
, pp. 61-66
-
-
Watanabe, Y.1
Adachi, Y.2
Nakashima, K.3
-
33
-
-
48249151156
-
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
-
Wroe R., Wai-Ling Butler A., Andersen P. M., Powell J. F. and Al-Chalabi A. (2008) ALSOD: the Amyotrophic Lateral Sclerosis Online Database. Amyotroph. Lateral Scler. 9, 249-250.
-
(2008)
Amyotroph. Lateral Scler.
, vol.9
, pp. 249-250
-
-
Wroe, R.1
Wai-Ling Butler, A.2
Andersen, P.M.3
Powell, J.F.4
Al-Chalabi, A.5
-
34
-
-
70249096265
-
Optimization of procedures for collecting and storing of CSF for studying the metabolome in ALS
-
Wuolikainen A., Hedenstrom M., Moritz T., Marklund S. L., Antti H. and Andersen P. M. (2009) Optimization of procedures for collecting and storing of CSF for studying the metabolome in ALS. Amyotroph. Lateral Scler. 10, 229-236.
-
(2009)
Amyotroph. Lateral Scler.
, vol.10
, pp. 229-236
-
-
Wuolikainen, A.1
Hedenstrom, M.2
Moritz, T.3
Marklund, S.L.4
Antti, H.5
Andersen, P.M.6
-
35
-
-
35348874857
-
Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models
-
Zetterstrom P., Stewart H. G., Bergemalm D., Jonsson P. A., Graffmo K. S., Andersen P. M., Brannstrom T., Oliveberg M. and Marklund S. L. (2007) Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models. Proc. Natl Acad. Sci. USA 104, 14157-14162.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 14157-14162
-
-
Zetterstrom, P.1
Stewart, H.G.2
Bergemalm, D.3
Jonsson, P.A.4
Graffmo, K.S.5
Andersen, P.M.6
Brannstrom, T.7
Oliveberg, M.8
Marklund, S.L.9
-
36
-
-
73149105494
-
Extracellular mutant SOD1 induces microglial-mediated motoneuron injury
-
Zhao W., Beers D. R., Henkel J. S., Zhang W., Urushitani M., Julien J. P. and Appel S. H. (2010) Extracellular mutant SOD1 induces microglial-mediated motoneuron injury. Glia 58, 231-243.
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(2010)
Glia
, vol.58
, pp. 231-243
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Zhao, W.1
Beers, D.R.2
Henkel, J.S.3
Zhang, W.4
Urushitani, M.5
Julien, J.P.6
Appel, S.H.7
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