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Journal Abstract Search

220 related items for PubMed ID: 8830861

  • 1. Instability of mutant Cu/Zn superoxide dismutase (Ala4Thr) associated with familial amyotrophic lateral sclerosis.
    Nakano R, Inuzuka T, Kikugawa K, Takahashi H, Sakimura K, Fujii J, Taniguchi N, Tsuji S.
    Neurosci Lett; 1996 Jun 21; 211(2):129-31. PubMed ID: 8830861
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  • 2. 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, Sakoda S.
    Eur J Neurosci; 2001 Dec 21; 14(12):2032-6. PubMed ID: 11860498
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  • 4. 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 21; 1042():303-13. PubMed ID: 15965076
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  • 6. Familial amyotrophic lateral sclerosis.
    Siddique T, Nijhawan D, Hentati A.
    J Neural Transm Suppl; 1997 May 21; 49():219-33. PubMed ID: 9266431
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  • 7. 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 21; 3(6):981-7. PubMed ID: 7951249
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  • 8. Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis.
    Boukaftane Y, Khoris J, Moulard B, Salachas F, Meininger V, Malafosse A, Camu W, Rouleau GA.
    Can J Neurol Sci; 1998 Aug 21; 25(3):192-6. PubMed ID: 9706719
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  • 10. A novel SOD1 mutation in amyotrophic lateral sclerosis with a distinct clinical phenotype.
    Hu J, Chen K, Ni B, Li L, Chen G, Shi S.
    Amyotroph Lateral Scler; 2012 Jan 21; 13(1):149-54. PubMed ID: 22185396
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  • 12. Wild-type Cu/Zn superoxide dismutase (SOD1) does not facilitate, but impedes the formation of protein aggregates of amyotrophic lateral sclerosis causing mutant SOD1.
    Witan H, Gorlovoy P, Kaya AM, Koziollek-Drechsler I, Neumann H, Behl C, Clement AM.
    Neurobiol Dis; 2009 Nov 21; 36(2):331-42. PubMed ID: 19660548
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  • 13. Cu/Zn superoxide dismutase (SOD1) mutations associated with familial amyotrophic lateral sclerosis (ALS) affect cellular free radical release in the presence of oxidative stress.
    Cookson MR, Menzies FM, Manning P, Eggett CJ, Figlewicz DA, McNeil CJ, Shaw PJ.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Jun 21; 3(2):75-85. PubMed ID: 12215229
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  • 16. Mutant SOD1 alters the motor neuronal transcriptome: implications for familial ALS.
    Kirby J, Halligan E, Baptista MJ, Allen S, Heath PR, Holden H, Barber SC, Loynes CA, Wood-Allum CA, Lunec J, Shaw PJ.
    Brain; 2005 Jul 21; 128(Pt 7):1686-706. PubMed ID: 15872021
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  • 20. Enhanced oxidative damage by the familial amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutants.
    Kang JH, Eum WS.
    Biochim Biophys Acta; 2000 Dec 15; 1524(2-3):162-70. PubMed ID: 11113563
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