204 related articles for article (PubMed ID: 12390515)
1. Mitochondrial electron transport chain complex dysfunction in a transgenic mouse model for amyotrophic lateral sclerosis.
Jung C; Higgins CM; Xu Z
J Neurochem; 2002 Nov; 83(3):535-45. PubMed ID: 12390515
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Mitochondrial DNA and respiratory chain function in spinal cords of ALS patients.
Wiedemann FR; Manfredi G; Mawrin C; Beal MF; Schon EA
J Neurochem; 2002 Feb; 80(4):616-25. PubMed ID: 11841569
[TBL] [Abstract][Full Text] [Related]
5. Cytochrome c association with the inner mitochondrial membrane is impaired in the CNS of G93A-SOD1 mice.
Kirkinezos IG; Bacman SR; Hernandez D; Oca-Cossio J; Arias LJ; Perez-Pinzon MA; Bradley WG; Moraes CT
J Neurosci; 2005 Jan; 25(1):164-72. PubMed ID: 15634778
[TBL] [Abstract][Full Text] [Related]
6. Early mitochondrial dysfunction occurs in motor cortex and spinal cord at the onset of disease in the Wobbler mouse.
Dave KR; Bradley WG; Pérez-Pinzón MA
Exp Neurol; 2003 Aug; 182(2):412-20. PubMed ID: 12895451
[TBL] [Abstract][Full Text] [Related]
7. Early vacuolization and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity.
Bendotti C; Calvaresi N; Chiveri L; Prelle A; Moggio M; Braga M; Silani V; De Biasi S
J Neurol Sci; 2001 Oct; 191(1-2):25-33. PubMed ID: 11676989
[TBL] [Abstract][Full Text] [Related]
8. A quantitative histochemical assay for activities of mitochondrial electron transport chain complexes in mouse spinal cord sections.
Jung C; Higgins CM; Xu Z
J Neurosci Methods; 2002 Mar; 114(2):165-72. PubMed ID: 11856567
[TBL] [Abstract][Full Text] [Related]
9. Mutant Cu, Zn superoxide dismutase that causes motoneuron degeneration is present in mitochondria in the CNS.
Higgins CM; Jung C; Ding H; Xu Z
J Neurosci; 2002 Mar; 22(6):RC215. PubMed ID: 11886899
[TBL] [Abstract][Full Text] [Related]
10. Knocking down metabotropic glutamate receptor 1 improves survival and disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
Milanese M; Giribaldi F; Melone M; Bonifacino T; Musante I; Carminati E; Rossi PI; Vergani L; Voci A; Conti F; Puliti A; Bonanno G
Neurobiol Dis; 2014 Apr; 64():48-59. PubMed ID: 24361555
[TBL] [Abstract][Full Text] [Related]
11. Expression of a familial amyotrophic lateral sclerosis-associated mutant human superoxide dismutase in yeast leads to decreased mitochondrial electron transport.
Gunther MR; Vangilder R; Fang J; Beattie DS
Arch Biochem Biophys; 2004 Nov; 431(2):207-14. PubMed ID: 15488469
[TBL] [Abstract][Full Text] [Related]
12. [Assay of biochemical activity (respiratory complex activity, pyruvate dehydrogenase complex activity etc)for diagnosis of mitochondrial diseases].
Kanamori T; Ohta S
Nihon Rinsho; 2002 Apr; 60 Suppl 4():256-60. PubMed ID: 12013860
[No Abstract] [Full Text] [Related]
13. The accumulation of enzymatically inactive cuproenzymes is a CNS-specific phenomenon of the SOD1
Hilton JB; Kysenius K; White AR; Crouch PJ
Exp Neurol; 2018 Sep; 307():118-128. PubMed ID: 29906423
[TBL] [Abstract][Full Text] [Related]
14. Increased phospho-adducin immunoreactivity in a murine model of amyotrophic lateral sclerosis.
Shan X; Hu JH; Cayabyab FS; Krieger C
Neuroscience; 2005; 134(3):833-46. PubMed ID: 15994023
[TBL] [Abstract][Full Text] [Related]
15. Focal dysfunction of the proteasome: a pathogenic factor in a mouse model of amyotrophic lateral sclerosis.
Kabashi E; Agar JN; Taylor DM; Minotti S; Durham HD
J Neurochem; 2004 Jun; 89(6):1325-35. PubMed ID: 15189335
[TBL] [Abstract][Full Text] [Related]
16. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues.
Watanabe M; Dykes-Hoberg M; Culotta VC; Price DL; Wong PC; Rothstein JD
Neurobiol Dis; 2001 Dec; 8(6):933-41. PubMed ID: 11741389
[TBL] [Abstract][Full Text] [Related]
17. Ablation of P2X7 receptor exacerbates gliosis and motoneuron death in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
Apolloni S; Amadio S; Montilli C; Volonté C; D'Ambrosi N
Hum Mol Genet; 2013 Oct; 22(20):4102-16. PubMed ID: 23736299
[TBL] [Abstract][Full Text] [Related]
18. Aggregate formation in the spinal cord of mutant SOD1 transgenic mice is reversible and mediated by proteasomes.
Puttaparthi K; Wojcik C; Rajendran B; DeMartino GN; Elliott JL
J Neurochem; 2003 Nov; 87(4):851-60. PubMed ID: 14622116
[TBL] [Abstract][Full Text] [Related]
19. Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues.
Birch-Machin MA; Turnbull DM
Methods Cell Biol; 2001; 65():97-117. PubMed ID: 11381612
[No Abstract] [Full Text] [Related]
20. Oxidative damage to mitochondrial DNA in spinal motoneurons of transgenic ALS mice.
Warita H; Hayashi T; Murakami T; Manabe Y; Abe K
Brain Res Mol Brain Res; 2001 Apr; 89(1-2):147-52. PubMed ID: 11311985
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
