176 related articles for article (PubMed ID: 10795881)
1. Oxidative stress in amyotrophic lateral sclerosis.
Robberecht W
J Neurol; 2000 Mar; 247 Suppl 1():I1-6. PubMed ID: 10795881
[TBL] [Abstract][Full Text] [Related]
2. Partial deficiency of manganese superoxide dismutase exacerbates a transgenic mouse model of amyotrophic lateral sclerosis.
Andreassen OA; Ferrante RJ; Klivenyi P; Klein AM; Shinobu LA; Epstein CJ; Beal MF
Ann Neurol; 2000 Apr; 47(4):447-55. PubMed ID: 10762155
[TBL] [Abstract][Full Text] [Related]
3. Expression of N19S-SOD1, an SOD1 mutant found in sporadic amyotrophic lateral sclerosis patients, induces low-grade motoneuronal toxicity.
Obata Y; Niikura T; Kanekura K; Hashimoto Y; Kawasumi M; Kita Y; Aiso S; Matsuoka M; Nishimoto I
J Neurosci Res; 2005 Sep; 81(5):720-9. PubMed ID: 16035108
[TBL] [Abstract][Full Text] [Related]
4. Oxidative stress in ALS: key role in motor neuron injury and therapeutic target.
Barber SC; Shaw PJ
Free Radic Biol Med; 2010 Mar; 48(5):629-41. PubMed ID: 19969067
[TBL] [Abstract][Full Text] [Related]
5. Hypoxia causes autophagic stress and derangement of metabolic adaptation in a cell model of amyotrophic lateral sclerosis.
Cimini S; Rizzardini M; Biella G; Cantoni L
J Neurochem; 2014 May; 129(3):413-25. PubMed ID: 24359187
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis.
Menzies FM; Cookson MR; Taylor RW; Turnbull DM; Chrzanowska-Lightowlers ZM; Dong L; Figlewicz DA; Shaw PJ
Brain; 2002 Jul; 125(Pt 7):1522-33. PubMed ID: 12077002
[TBL] [Abstract][Full Text] [Related]
7. Oxidative stress: its role in the pathogenesis of amyotrophic lateral sclerosis.
Bergeron C
J Neurol Sci; 1995 May; 129 Suppl():81-4. PubMed ID: 7595629
[TBL] [Abstract][Full Text] [Related]
8. Detection method of the adjacent motor neuronal death in an in vitro co-culture model of familial ALS-associated Cu/Zn superoxide dismutase.
Park KS; Kim HJ; Choi WJ; Kim M; Lee KW
Biotechnol Lett; 2004 Aug; 26(15):1201-5. PubMed ID: 15289674
[TBL] [Abstract][Full Text] [Related]
9. Early decrease of redox factor-1 in spinal motor neurons of presymptomatic transgenic mice with a mutant SOD1 gene.
Manabe Y; Warita H; Murakami T; Shiote M; Hayashi T; Nagano I; Shoji M; Abe K
Brain Res; 2001 Oct; 915(1):104-7. PubMed ID: 11578626
[TBL] [Abstract][Full Text] [Related]
10. Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading.
Subramaniam JR; Lyons WE; Liu J; Bartnikas TB; Rothstein J; Price DL; Cleveland DW; Gitlin JD; Wong PC
Nat Neurosci; 2002 Apr; 5(4):301-7. PubMed ID: 11889469
[TBL] [Abstract][Full Text] [Related]
11. Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1.
Bruijn LI; Houseweart MK; Kato S; Anderson KL; Anderson SD; Ohama E; Reaume AG; Scott RW; Cleveland DW
Science; 1998 Sep; 281(5384):1851-4. PubMed ID: 9743498
[TBL] [Abstract][Full Text] [Related]
12. 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; 3(2):75-85. PubMed ID: 12215229
[TBL] [Abstract][Full Text] [Related]
13. [Superoxide dismutase-1 (SOD-1) gene mutation-dependent mechanisms of neural degeneration in amyotrophic lateral sclerosis].
Iłzecka J
Neurol Neurochir Pol; 2001; 35(3):461-9. PubMed ID: 11732268
[TBL] [Abstract][Full Text] [Related]
14. Current hypotheses for the underlying biology of amyotrophic lateral sclerosis.
Rothstein JD
Ann Neurol; 2009 Jan; 65 Suppl 1():S3-9. PubMed ID: 19191304
[TBL] [Abstract][Full Text] [Related]
15. Neurodegeneration induced by complex I inhibition in a cellular model of familial amyotrophic lateral sclerosis.
Rizzardini M; Lupi M; Mangolini A; Babetto E; Ubezio P; Cantoni L
Brain Res Bull; 2006 Apr; 69(4):465-74. PubMed ID: 16624679
[TBL] [Abstract][Full Text] [Related]
16. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions.
Tu PH; Raju P; Robinson KA; Gurney ME; Trojanowski JQ; Lee VM
Proc Natl Acad Sci U S A; 1996 Apr; 93(7):3155-60. PubMed ID: 8610185
[TBL] [Abstract][Full Text] [Related]
17. Transcriptomic indices of fast and slow disease progression in two mouse models of amyotrophic lateral sclerosis.
Nardo G; Iennaco R; Fusi N; Heath PR; Marino M; Trolese MC; Ferraiuolo L; Lawrence N; Shaw PJ; Bendotti C
Brain; 2013 Nov; 136(Pt 11):3305-32. PubMed ID: 24065725
[TBL] [Abstract][Full Text] [Related]
18. Nonoxidative protein glycation is implicated in familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation.
Shibata N; Nagai R; Miyata S; Jono T; Horiuchi S; Hirano A; Kato S; Sasaki S; Asayama K; Kobayashi M
Acta Neuropathol; 2000 Sep; 100(3):275-84. PubMed ID: 10965797
[TBL] [Abstract][Full Text] [Related]
19. Mutant SOD1 mediated pathogenesis of Amyotrophic Lateral Sclerosis.
Kaur SJ; McKeown SR; Rashid S
Gene; 2016 Feb; 577(2):109-18. PubMed ID: 26657039
[TBL] [Abstract][Full Text] [Related]
20. 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 ED; Grashorn JA; Hawkins R; van Duijn W; Verspaget HW; London J; Holstege JC
Neurobiol Dis; 2000 Dec; 7(6 Pt B):623-43. PubMed ID: 11114261
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
