137 related articles for article (PubMed ID: 12039658)
21. Cu/Zn superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis.
Robberecht W; Sapp P; Viaene MK; Rosen D; McKenna-Yasek D; Haines J; Horvitz R; Theys P; Brown R
J Neurochem; 1994 Jan; 62(1):384-7. PubMed ID: 8263541
[TBL] [Abstract][Full Text] [Related]
22. A SOD1 gene mutation in a patient with slowly progressing familial ALS.
Penco S; Schenone A; Bordo D; Bolognesi M; Abbruzzese M; Bugiani O; Ajmar F; Garrè C
Neurology; 1999 Jul; 53(2):404-6. PubMed ID: 10430435
[TBL] [Abstract][Full Text] [Related]
23. [Familial amyotrophic lateral sclerosis and mutations in the Cu/Zn superoxide dismutase gene].
Nakano R
Rinsho Shinkeigaku; 1995 Dec; 35(12):1546-8. PubMed ID: 8752459
[TBL] [Abstract][Full Text] [Related]
24. Amyotrophic lateral sclerosis with mutation of the Cu/Zn superoxide dismutase gene (SOD1) in a patient with Down syndrome.
Marucci G; Morandi L; Bartolomei I; Salvi F; Pession A; Righi A; Lauria G; Foschini MP
Neuromuscul Disord; 2007 Oct; 17(9-10):673-6. PubMed ID: 17624778
[TBL] [Abstract][Full Text] [Related]
25. Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene.
Kawata A; Kato S; Hayashi H; Hirai S
J Neurol Sci; 1997 Dec; 153(1):82-5. PubMed ID: 9455983
[TBL] [Abstract][Full Text] [Related]
26. 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
Hum Mol Genet; 1994 Feb; 3(2):363-4. PubMed ID: 8004110
[No Abstract] [Full Text] [Related]
27. Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.
Giess R; Holtmann B; Braga M; Grimm T; Müller-Myhsok B; Toyka KV; Sendtner M
Am J Hum Genet; 2002 May; 70(5):1277-86. PubMed ID: 11951178
[TBL] [Abstract][Full Text] [Related]
28. 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
Nature; 1993 Mar; 362(6415):59-62. PubMed ID: 8446170
[TBL] [Abstract][Full Text] [Related]
29. A new variant Cu/Zn superoxide dismutase (Val7-->Glu) deduced from lymphocyte mRNA sequences from Japanese patients with familial amyotrophic lateral sclerosis.
Hirano M; Fujii J; Nagai Y; Sonobe M; Okamoto K; Araki H; Taniguchi N; Ueno S
Biochem Biophys Res Commun; 1994 Oct; 204(2):572-7. PubMed ID: 7980516
[TBL] [Abstract][Full Text] [Related]
30. SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.
Rouleau GA; Clark AW; Rooke K; Pramatarova A; Krizus A; Suchowersky O; Julien JP; Figlewicz D
Ann Neurol; 1996 Jan; 39(1):128-31. PubMed ID: 8572658
[TBL] [Abstract][Full Text] [Related]
31. Absence of mutations in the Mn superoxide dismutase or catalase genes in familial amyotrophic lateral sclerosis.
Parboosingh JS; Rouleau GA; Meninger V; McKenna-Yasek D; Brown RH; Figlewicz DA
Neuromuscul Disord; 1995 Jan; 5(1):7-10. PubMed ID: 7719145
[TBL] [Abstract][Full Text] [Related]
32. Identification of three mutations in the Cu,Zn-superoxide dismutase (Cu,Zn-SOD) gene with familial amyotrophic lateral sclerosis: transduction of human Cu,Zn-SOD into PC12 cells by HIV-1 TAT protein basic domain.
Chou CM; Huang CJ; Shih CM; Chen YP; Liu TP; Chen CT
Ann N Y Acad Sci; 2005 May; 1042():303-13. PubMed ID: 15965076
[TBL] [Abstract][Full Text] [Related]
33. A gain-of-function of an amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutant: An enhancement of free radical formation due to a decrease in Km for hydrogen peroxide.
Yim MB; Kang JH; Yim HS; Kwak HS; Chock PB; Stadtman ER
Proc Natl Acad Sci U S A; 1996 Jun; 93(12):5709-14. PubMed ID: 8650157
[TBL] [Abstract][Full Text] [Related]
34. Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation.
Tan CF; Piao YS; Hayashi S; Obata H; Umeda Y; Sato M; Fukushima T; Nakano R; Tsuji S; Takahashi H
Acta Neuropathol; 2004 Oct; 108(4):332-6. PubMed ID: 15235802
[TBL] [Abstract][Full Text] [Related]
35. Identification of two novel mutations in the Cu/Zn superoxide dismutase gene with familial amyotrophic lateral sclerosis: mass spectrometric and genomic analyses.
Sato T; Yamamoto Y; Nakanishi T; Fukada K; Sugai F; Zhou Z; Okuno T; Nagano S; Hirata S; Shimizu A; Sakoda S
J Neurol Sci; 2004 Mar; 218(1-2):79-83. PubMed ID: 14759637
[TBL] [Abstract][Full Text] [Related]
36. [Identification of the mutation of SOD1 gene in a familial amyotrophic lateral sclerosis].
Shi SG; Li LS; Chen KN; Liu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):149-52. PubMed ID: 15079798
[TBL] [Abstract][Full Text] [Related]
37. A novel two-base mutation in the Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis in Japan.
Morita M; Aoki M; Abe K; Hasegawa T; Sakuma R; Onodera Y; Ichikawa N; Nishizawa M; Itoyama Y
Neurosci Lett; 1996 Feb; 205(2):79-82. PubMed ID: 8907321
[TBL] [Abstract][Full Text] [Related]
38. The free radical-generating function of a familial amyotrophic lateral sclerosis-associated D90A Cu,Zn-superoxide dismutase mutant.
Kim SM; Eum WS; Kwon OB; Kang JH
Biochem Mol Biol Int; 1998 Dec; 46(6):1191-200. PubMed ID: 9891852
[TBL] [Abstract][Full Text] [Related]
39. A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis.
Rosen DR; Bowling AC; Patterson D; Usdin TB; Sapp P; Mezey E; McKenna-Yasek D; O'Regan J; Rahmani Z; Ferrante RJ
Hum Mol Genet; 1994 Jun; 3(6):981-7. PubMed ID: 7951249
[TBL] [Abstract][Full Text] [Related]
40. A second ALS patient having an L67P mutation in exon 3 of the Cu/Zn superoxide dismutase gene.
Krieger C; Haase S; Scott P
Amyotroph Lateral Scler; 2011 Nov; 12(6):466-7. PubMed ID: 21692663
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]