-
2
-
-
0014691242
-
Superoxide dismutase: An enzymic function for erythrocuprein (hemocuprein)
-
McCord JM, Fridovich I. Superoxide dismutase: An enzymic function for erythrocuprein (hemocuprein). J Biol Chem 1969;244:6049-55
-
(1969)
J Biol Chem
, vol.244
, pp. 6049-6055
-
-
McCord, J.M.1
Fridovich, I.2
-
3
-
-
0015694842
-
Mitochondrial superoxide dismutase: Site of synthesis and intramitochondrial localization
-
Weisiger RA, Fridovich I. Mitochondrial superoxide dismutase: Site of synthesis and intramitochondrial localization. J Biol Chem 1973;248:4793-96
-
(1973)
J Biol Chem
, vol.248
, pp. 4793-4796
-
-
Weisiger, R.A.1
Fridovich, I.2
-
5
-
-
0024334904
-
Linkage analysis in familial amyotrophic lateral sclerosis
-
Siddique T, Pericak-Vance MA, Brooks BR, et al. Linkage analysis in familial amyotrophic lateral sclerosis. Neurology 1989;39:919-25
-
(1989)
Neurology
, vol.39
, pp. 919-925
-
-
Siddique, T.1
Pericak-Vance, M.A.2
Brooks, B.R.3
-
6
-
-
12044249765
-
Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity
-
Siddique T, Figlewicz DA, Pericak-Vance MA, et al. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. N Engl J Med 1991;324:1381-84
-
(1991)
N Engl J Med
, vol.324
, pp. 1381-1384
-
-
Siddique, T.1
Figlewicz, D.A.2
Pericak-Vance, M.A.3
-
7
-
-
0021921322
-
Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase
-
Levanon D, Lieman-Hurwitz J, Dafni N, et al. Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase. EMBO J 1985;4:77-84
-
(1985)
EMBO J
, vol.4
, pp. 77-84
-
-
Levanon, D.1
Lieman-Hurwitz, J.2
Dafni, N.3
-
8
-
-
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
-
9
-
-
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
-
10
-
-
0027452090
-
Mild ALS in Japan associated with novel SOD mutation
-
Ogasawara M, Matsubara Y, Narisawa K, et al. Mild ALS in Japan associated with novel SOD mutation. Nature Genet 1993;5:323-24
-
(1993)
Nature Genet
, vol.5
, pp. 323-324
-
-
Ogasawara, M.1
Matsubara, Y.2
Narisawa, K.3
-
11
-
-
0028168971
-
Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: A possible new subtype of familial ALS
-
Aoki M, Ogasawara M, Matsubara Y, et al. Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: A possible new subtype of familial ALS. J Neurol Sci 1994;126:77-83
-
(1994)
J Neurol Sci
, vol.126
, pp. 77-83
-
-
Aoki, M.1
Ogasawara, M.2
Matsubara, Y.3
-
12
-
-
0028123297
-
Identification of a new missense point mutation in exon 4 of the Cu/Zn superoxide dismutase (SOD-1) gene in a family with amyotrophic lateral sclerosis
-
Elshafey A, Lanyon WG, Connor JM. Identification of a new missense point mutation in exon 4 of the Cu/Zn superoxide dismutase (SOD-1) gene in a family with amyotrophic lateral sclerosis. Hum Mol Genet 1994;3:363-64
-
(1994)
Hum Mol Genet
, vol.3
, pp. 363-364
-
-
Elshafey, A.1
Lanyon, W.G.2
Connor, J.M.3
-
13
-
-
0028244477
-
Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis
-
Esteban J, Rosen DR, Bowling AC, et al. Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis. Hum Mol Genet 1994;3:997-98
-
(1994)
Hum Mol Genet
, vol.3
, pp. 997-998
-
-
Esteban, J.1
Rosen, D.R.2
Bowling, A.C.3
-
14
-
-
0028132231
-
7 → Glu) deduced from lymphocyte mRNA sequences from Japanese patients with familial amyotrophic lateral sclerosis
-
7 → Glu) deduced from lymphocyte mRNA sequences from Japanese patients with familial amyotrophic lateral sclerosis. Biochem Biophys Res Commun 1994;204:572-77
-
(1994)
Biochem Biophys Res Commun
, vol.204
, pp. 572-577
-
-
Hirano, M.1
Fijii, J.2
Nagai, Y.3
-
15
-
-
0028771134
-
106 → Val (CTC → GTC) mutation of superoxide dismutase-1 gene in patient with familial amyotrophic lateral sclerosis in Japan
-
106 → Val (CTC → GTC) mutation of superoxide dismutase-1 gene in patient with familial amyotrophic lateral sclerosis in Japan. Lancet 1994;343:1501
-
(1994)
Lancet
, vol.343
, pp. 1501
-
-
Kawamata, J.1
Hasegawa, H.2
Shimohama, S.3
Kimura, J.4
Tanaka, S.5
Ueda, K.6
-
16
-
-
0028601342
-
Autosomal dominant amyotrophic lateral sclerosis: A novel mutation in the Cu/Zn superoxide dismutase-1 gene
-
Kostrzewa M, Burck-Lehmann U, Müller U. Autosomal dominant amyotrophic lateral sclerosis: A novel mutation in the Cu/Zn superoxide dismutase-1 gene. Hum Mol Genet 1994;3:2261-62
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2261-2262
-
-
Kostrzewa, M.1
Burck-Lehmann, U.2
Müller, U.3
-
17
-
-
0028204413
-
A novel mutation in Cu/Zn superoxide dismutase gene in Japanese familial amyotrophic lateral sclerosis
-
Nakano R, Sato S, Inuzuka T, et al. A novel mutation in Cu/Zn superoxide dismutase gene in Japanese familial amyotrophic lateral sclerosis. Biochem Biophys Res Commun 1994;200:695-703
-
(1994)
Biochem Biophys Res Commun
, vol.200
, pp. 695-703
-
-
Nakano, R.1
Sato, S.2
Inuzuka, T.3
-
18
-
-
0028199849
-
SOD1 missense mutation in an Italian family with ALS
-
Rainero I, Pinessi L, Tsuda T, et al. SOD1 missense mutation in an Italian family with ALS. Neurology 1994;44:347-49
-
(1994)
Neurology
, vol.44
, pp. 347-349
-
-
Rainero, I.1
Pinessi, L.2
Tsuda, T.3
-
19
-
-
0029002286
-
Cu, Zn SOD in German families with ALS
-
Bachus R, Claus A, Megow D, et al. Cu, Zn SOD in German families with ALS. J Neurol Sci 1995;129 (Suppl):93-95
-
(1995)
J Neurol Sci
, vol.129
, Issue.SUPPL.
, pp. 93-95
-
-
Bachus, R.1
Claus, A.2
Megow, D.3
-
20
-
-
0028941313
-
A novel SOD mutant and ALS
-
Orrell R, De Belleroche J, Marklund S, Bowe F, Hallewell R. A novel SOD mutant and ALS. Nature 1995;374:504-5
-
(1995)
Nature
, vol.374
, pp. 504-505
-
-
Orrell, R.1
De Belleroche, J.2
Marklund, S.3
Bowe, F.4
Hallewell, R.5
-
21
-
-
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
-
22
-
-
0029003428
-
Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis
-
Deng H-X, Tainer JA, Mitsumoto H, et al. Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis. Hum Mol Genet 1995;4:1113-16
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1113-1116
-
-
Deng, H.-X.1
Tainer, J.A.2
Mitsumoto, H.3
-
23
-
-
0028067985
-
A two basepair deletion in the SOD1 gene causes familial amyotrophic lateral sclerosis
-
Pramatarova A, Goto J, Nanba E, et al. A two basepair deletion in the SOD1 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
-
24
-
-
0029020394
-
Abnormality of Cu/Zn superoxide dismutase (SOD1) activity in Japanese familial amyotrophic lateral sclerosis with two base pair deletion in the SOD1 gene
-
Nakashima K, Watanabe Y, Kuno N, Nanba E, Takahashi K. Abnormality of Cu/Zn superoxide dismutase (SOD1) activity in Japanese familial amyotrophic lateral sclerosis with two base pair deletion in the SOD1 gene. Neurology 1995;45:1019-20
-
(1995)
Neurology
, vol.45
, pp. 1019-1020
-
-
Nakashima, K.1
Watanabe, Y.2
Kuno, N.3
Nanba, E.4
Takahashi, K.5
-
25
-
-
0015419721
-
Hereditary amyotrophic lateral sclerosis. Histochemical and electron microscopic study of hyaline inclusions in motor neurons
-
Takahashi K, Nakamura H, Okada E. Hereditary amyotrophic lateral sclerosis. Histochemical and electron microscopic study of hyaline inclusions in motor neurons. Arch Neurol 1972;27:292-99
-
(1972)
Arch Neurol
, vol.27
, pp. 292-299
-
-
Takahashi, K.1
Nakamura, H.2
Okada, E.3
-
26
-
-
13344257516
-
An inherited disease similar to amyotrophic lateral sclerosis with a pattern of posterior column involvement. An intermediate form?
-
Engel WK, Kurland LT, Klatzo I. An inherited disease similar to amyotrophic lateral sclerosis with a pattern of posterior column involvement. An intermediate form? Brain 1959;82:203-20
-
(1959)
Brain
, vol.82
, pp. 203-220
-
-
Engel, W.K.1
Kurland, L.T.2
Klatzo, I.3
-
27
-
-
0014063240
-
Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells
-
Hirano A, Kurland LT, Sayre GP. Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells. Arch Neurol 1967;16:232-43
-
(1967)
Arch Neurol
, vol.16
, pp. 232-243
-
-
Hirano, A.1
Kurland, L.T.2
Sayre, G.P.3
-
28
-
-
0016257871
-
Wetherbee Ail. Documentation of a neurological disease in a Vermont family 90 years later
-
Powers JM, Horoupian DS, Schaumburg HH. Wetherbee Ail. Documentation of a neurological disease in a Vermont family 90 years later. Can J Neurol Sci 1974;1:139-40
-
(1974)
Can J Neurol Sci
, vol.1
, pp. 139-140
-
-
Powers, J.M.1
Horoupian, D.S.2
Schaumburg, H.H.3
-
29
-
-
0002565942
-
Familial amyotrophic lateral sclerosis. Neuropathology of two brothers in American "C" family
-
Tokyo
-
Nakano I, Hirano A, Kurland LT, Mulder DW, Holley PW, Saccomanno G. Familial amyotrophic lateral sclerosis. Neuropathology of two brothers in American "C" family. Neurol Med (Tokyo) 1984;20:458-71
-
(1984)
Neurol Med
, vol.20
, pp. 458-471
-
-
Nakano, I.1
Hirano, A.2
Kurland, L.T.3
Mulder, D.W.4
Holley, P.W.5
Saccomanno, G.6
-
30
-
-
0023201688
-
Asymmetric involvement of the spinal cord involving both large and small anterior horn cells in a case of familial amyotrophic lateral sclerosis
-
Kato T, Hirano A, Kurland LT. Asymmetric involvement of the spinal cord involving both large and small anterior horn cells in a case of familial amyotrophic lateral sclerosis. Clin Neuropathol 1987;6:67-70
-
(1987)
Clin Neuropathol
, vol.6
, pp. 67-70
-
-
Kato, T.1
Hirano, A.2
Kurland, L.T.3
-
31
-
-
0024314656
-
Immunocytochemical and ultrastructural study of Lewy body-like hyaline inclusions in familial amyotrophic lateral sclerosis
-
Murayama S, Ookawa Y, Mori H, et al. Immunocytochemical and ultrastructural study of Lewy body-like hyaline inclusions in familial amyotrophic lateral sclerosis. Acta Neuropathol 1989;78:143-52
-
(1989)
Acta Neuropathol
, vol.78
, pp. 143-152
-
-
Murayama, S.1
Ookawa, Y.2
Mori, H.3
-
32
-
-
0028106044
-
Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn superoxide dismutase gene
-
Takahashi H, Makifuchi T, Nakano R, et al. Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn superoxide dismutase gene. Acta Neuropathol 1994;88:185-88
-
(1994)
Acta Neuropathol
, vol.88
, pp. 185-188
-
-
Takahashi, H.1
Makifuchi, T.2
Nakano, R.3
-
33
-
-
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
-
34
-
-
0024419525
-
Inclusion bodies in motor cortex and brainstem of patients with motor neurone disease are detected by immunocytochemical localisation of ubiquitin
-
Lowe J, Aldridge F, Lennox G, et al. Inclusion bodies in motor cortex and brainstem of patients with motor neurone disease are detected by immunocytochemical localisation of ubiquitin. Neurosci Lett 1989;105:7-13
-
(1989)
Neurosci Lett
, vol.105
, pp. 7-13
-
-
Lowe, J.1
Aldridge, F.2
Lennox, G.3
-
35
-
-
1842283922
-
Hyaline and skein-like inclusions in amyotrophic lateral sclerosis
-
Mizusawa H. Hyaline and skein-like inclusions in amyotrophic lateral sclerosis. Neuropathology 1993;13:201-8
-
(1993)
Neuropathology
, vol.13
, pp. 201-208
-
-
Mizusawa, H.1
-
36
-
-
0021278273
-
Familial amyotrophic lateral sclerosis: Features of multisystem degeneration
-
Tanaka J, Nakamura H, Tabuchi Y, Takahashi K. Familial amyotrophic lateral sclerosis: Features of multisystem degeneration. Acta Neuropathol 1984;64:22-29
-
(1984)
Acta Neuropathol
, vol.64
, pp. 22-29
-
-
Tanaka, J.1
Nakamura, H.2
Tabuchi, Y.3
Takahashi, K.4
-
37
-
-
84944967464
-
Amyotrophic lateral sclerosis and related conditions. A clinical analysis
-
Swank RL, Putnam TJ. Amyotrophic lateral sclerosis and related conditions. A clinical analysis. Arch Neurol Psychiatry 1943;49: 151-77
-
(1943)
Arch Neurol Psychiatry
, vol.49
, pp. 151-177
-
-
Swank, R.L.1
Putnam, T.J.2
-
38
-
-
85015880852
-
Neuropathology in amyotrophic lateral sclerosis patients on respirators: Uniformity and diversity in 13 cases
-
Kato S, Oda M, Hayashi H. Neuropathology in amyotrophic lateral sclerosis patients on respirators: Uniformity and diversity in 13 cases. Neuropathology 1993;13:229-36
-
(1993)
Neuropathology
, vol.13
, pp. 229-236
-
-
Kato, S.1
Oda, M.2
Hayashi, H.3
-
39
-
-
0026720809
-
Sporadic amyotrophic lateral sclerosis with extensive neurological involvement
-
Sasaki S, Tsutsumi Y, Yamane K, Sakuma H, Mayuyama S. Sporadic amyotrophic lateral sclerosis with extensive neurological involvement. Acta Neuropathol 1992;84:211-15
-
(1992)
Acta Neuropathol
, vol.84
, pp. 211-215
-
-
Sasaki, S.1
Tsutsumi, Y.2
Yamane, K.3
Sakuma, H.4
Mayuyama, S.5
-
40
-
-
0026675219
-
Amyotrophic lateral sclerosis with ophthalmoplegia and multisystem degeneration in patients on long-term use of respirators
-
Mizutani T, Sakamaki S, Tsuchiya N, et al. Amyotrophic lateral sclerosis with ophthalmoplegia and multisystem degeneration in patients on long-term use of respirators. Acta Neuropathol 1992;84: 372-77
-
(1992)
Acta Neuropathol
, vol.84
, pp. 372-377
-
-
Mizutani, T.1
Sakamaki, S.2
Tsuchiya, N.3
-
41
-
-
0345104080
-
Clinicopathological study of two respirator-assisted long survival cases of amyotrophic lateral sclerosis
-
Hashizume Y, Yoshida M, Murakami N. Clinicopathological study of two respirator-assisted long survival cases of amyotrophic lateral sclerosis. Neuropathology 1993;13:237-41
-
(1993)
Neuropathology
, vol.13
, pp. 237-241
-
-
Hashizume, Y.1
Yoshida, M.2
Murakami, N.3
-
42
-
-
0342905524
-
Clinicopathological study of two cases of sporadic amyotrophic lateral sclerosis with long survival
-
Tokyo
-
Nakano I, Hirano A. Clinicopathological study of two cases of sporadic amyotrophic lateral sclerosis with long survival. Neurol Med (Tokyo) 1981;15:45-53
-
(1981)
Neurol Med
, vol.15
, pp. 45-53
-
-
Nakano, I.1
Hirano, A.2
-
43
-
-
0003138098
-
Immunohistochemistry of glutamine synthetase of the mouse and human brain: A preliminary study on pathogenesis of hepatic gliopathy
-
Oda M, Ikeda K, Yamamoto T. Immunohistochemistry of glutamine synthetase of the mouse and human brain: A preliminary study on pathogenesis of hepatic gliopathy. Neuropathology 1983;4:19-30
-
(1983)
Neuropathology
, vol.4
, pp. 19-30
-
-
Oda, M.1
Ikeda, K.2
Yamamoto, T.3
-
44
-
-
0021062674
-
Recognition of myelin-associated glycoprotein by the monoclonal antibody HNK-1
-
McGarry RC, Helfand SL, Quarles RH, Roder JC. Recognition of myelin-associated glycoprotein by the monoclonal antibody HNK-1. Nature 1983;306:376-78
-
(1983)
Nature
, vol.306
, pp. 376-378
-
-
McGarry, R.C.1
Helfand, S.L.2
Quarles, R.H.3
Roder, J.C.4
-
45
-
-
0025999502
-
Argyrophilic ubiquitinated cytoplasmic inclusions of Leu-7-positive glial cells in olivopontocerebellar atrophy (multiple system atrophy)
-
Kato S, Nakamura H, Hirano A, Ito H, Llena JF, Yen S-H. Argyrophilic ubiquitinated cytoplasmic inclusions of Leu-7-positive glial cells in olivopontocerebellar atrophy (multiple system atrophy). Acta Neuropathol 1991;82:488-93
-
(1991)
Acta Neuropathol
, vol.82
, pp. 488-493
-
-
Kato, S.1
Nakamura, H.2
Hirano, A.3
Ito, H.4
Llena, J.F.5
Yen, S.-H.6
-
46
-
-
0021157469
-
Fine structural study of neurofibrillary changes in a family with amyotrophic lateral sclerosis
-
Hirano A, Nakano I, Kurland LT, Mulder DW, Holley PW, Saccomanno G. Fine structural study of neurofibrillary changes in a family with amyotrophic lateral sclerosis. J Neuropathol Exp Neurol 1984;43:471-80
-
(1984)
J Neuropathol Exp Neurol
, vol.43
, pp. 471-480
-
-
Hirano, A.1
Nakano, I.2
Kurland, L.T.3
Mulder, D.W.4
Holley, P.W.5
Saccomanno, G.6
-
47
-
-
85015902212
-
Immunohistochemical demonstration of Cu/Zn superoxide dismutase in the spinal cord of patients with familial amyotrophic lateral sclerosis
-
Shibata N, Hirano A, Kobayashi M, et al. Immunohistochemical demonstration of Cu/Zn superoxide dismutase in the spinal cord of patients with familial amyotrophic lateral sclerosis. Acta Histochem Cytochem 1993;26:619-22
-
(1993)
Acta Histochem Cytochem
, vol.26
, pp. 619-622
-
-
Shibata, N.1
Hirano, A.2
Kobayashi, M.3
-
48
-
-
0030052114
-
Mutant enzyme provides new insights into the cause of ALS
-
Marx J. Mutant enzyme provides new insights into the cause of ALS. Science 1996;271:446-47
-
(1996)
Science
, vol.271
, pp. 446-447
-
-
Marx, J.1
-
49
-
-
0029671220
-
Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis
-
Wiedau-Pazos M, Goto JJ, Rabizadeh S, et al. Altered reactivity of superoxide dismutase in familial 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
-
50
-
-
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
-
51
-
-
0027946294
-
Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis
-
Dal Canto MC, Gurney ME. Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis. Am J Pathol 1994;145:1271-79
-
(1994)
Am J Pathol
, vol.145
, pp. 1271-1279
-
-
Dal Canto, M.C.1
Gurney, M.E.2
-
52
-
-
0021383547
-
Joint purification of mangano and cuprozinc superoxide dismutases from a single source: A simplified method
-
Asayama K, Burr IM. Joint purification of mangano and cuprozinc superoxide dismutases from a single source: A simplified method. Anal Biochem 1984;136:336-39
-
(1984)
Anal Biochem
, vol.136
, pp. 336-339
-
-
Asayama, K.1
Burr, I.M.2
-
53
-
-
0022149366
-
Selective induction of manganous superoxide dismutase in human monocytes
-
Asayama K, Janco RL, Burr IM. Selective induction of manganous superoxide dismutase in human monocytes. Am J Physiol 1985;249:C393-97
-
(1985)
Am J Physiol
, vol.249
-
-
Asayama, K.1
Janco, R.L.2
Burr, I.M.3
-
54
-
-
0024591280
-
A study of infantile motor neuron disease with neurofilament and ubiquitin immunocytochemistry
-
Lee S, Park YD, Yen S-H, Ksiezak-Reding H, Goldman JE, Dickson DW. A study of infantile motor neuron disease with neurofilament and ubiquitin immunocytochemistry. Neuropediatrics 1989;20:107-11
-
(1989)
Neuropediatrics
, vol.20
, pp. 107-111
-
-
Lee, S.1
Park, Y.D.2
Yen, S.-H.3
Ksiezak-Reding, H.4
Goldman, J.E.5
Dickson, D.W.6
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