179 related articles for article (PubMed ID: 22089637)
1. Mitochondria in motor nerve terminals: function in health and in mutant superoxide dismutase 1 mouse models of familial ALS.
Barrett EF; Barrett JN; David G
J Bioenerg Biomembr; 2011 Dec; 43(6):581-6. PubMed ID: 22089637
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial dysfunction in familial amyotrophic lateral sclerosis.
Faes L; Callewaert G
J Bioenerg Biomembr; 2011 Dec; 43(6):587-92. PubMed ID: 22072073
[TBL] [Abstract][Full Text] [Related]
3. Interaction between familial amyotrophic lateral sclerosis (ALS)-linked SOD1 mutants and the dynein complex.
Zhang F; Ström AL; Fukada K; Lee S; Hayward LJ; Zhu H
J Biol Chem; 2007 Jun; 282(22):16691-9. PubMed ID: 17403682
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Repetitive nerve stimulation transiently opens the mitochondrial permeability transition pore in motor nerve terminals of symptomatic mutant SOD1 mice.
Nguyen KT; Barrett JN; García-Chacón L; David G; Barrett EF
Neurobiol Dis; 2011 Jun; 42(3):381-90. PubMed ID: 21310237
[TBL] [Abstract][Full Text] [Related]
6. Enhancing mitochondrial calcium buffering capacity reduces aggregation of misfolded SOD1 and motor neuron cell death without extending survival in mouse models of inherited amyotrophic lateral sclerosis.
Parone PA; Da Cruz S; Han JS; McAlonis-Downes M; Vetto AP; Lee SK; Tseng E; Cleveland DW
J Neurosci; 2013 Mar; 33(11):4657-71. PubMed ID: 23486940
[TBL] [Abstract][Full Text] [Related]
7. The Psi(m) depolarization that accompanies mitochondrial Ca2+ uptake is greater in mutant SOD1 than in wild-type mouse motor terminals.
Nguyen KT; García-Chacón LE; Barrett JN; Barrett EF; David G
Proc Natl Acad Sci U S A; 2009 Feb; 106(6):2007-11. PubMed ID: 19174508
[TBL] [Abstract][Full Text] [Related]
8. Mutant SOD1 in neuronal mitochondria causes toxicity and mitochondrial dynamics abnormalities.
Magrané J; Hervias I; Henning MS; Damiano M; Kawamata H; Manfredi G
Hum Mol Genet; 2009 Dec; 18(23):4552-64. PubMed ID: 19779023
[TBL] [Abstract][Full Text] [Related]
9. Transgenic mice with human mutant genes causing Parkinson's disease and amyotrophic lateral sclerosis provide common insight into mechanisms of motor neuron selective vulnerability to degeneration.
Martin LJ
Rev Neurosci; 2007; 18(2):115-36. PubMed ID: 17593875
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The human G93A-superoxide dismutase-1 mutation, mitochondrial glutathione and apoptotic cell death.
Muyderman H; Hutson PG; Matusica D; Rogers ML; Rush RA
Neurochem Res; 2009 Oct; 34(10):1847-56. PubMed ID: 19399611
[TBL] [Abstract][Full Text] [Related]
12. Phenotype of transgenic mice carrying a very low copy number of the mutant human G93A superoxide dismutase-1 gene associated with amyotrophic lateral sclerosis.
Deitch JS; Alexander GM; Bensinger A; Yang S; Jiang JT; Heiman-Patterson TD
PLoS One; 2014; 9(6):e99879. PubMed ID: 24945277
[TBL] [Abstract][Full Text] [Related]
13. Enhancing NAD+ Salvage Pathway Reverts the Toxicity of Primary Astrocytes Expressing Amyotrophic Lateral Sclerosis-linked Mutant Superoxide Dismutase 1 (SOD1).
Harlan BA; Pehar M; Sharma DR; Beeson G; Beeson CC; Vargas MR
J Biol Chem; 2016 May; 291(20):10836-46. PubMed ID: 27002158
[TBL] [Abstract][Full Text] [Related]
14. CuZn superoxide dismutase (SOD1) accumulates in vacuolated mitochondria in transgenic mice expressing amyotrophic lateral sclerosis-linked SOD1 mutations.
Jaarsma D; Rognoni F; van Duijn W; Verspaget HW; Haasdijk ED; Holstege JC
Acta Neuropathol; 2001 Oct; 102(4):293-305. PubMed ID: 11603803
[TBL] [Abstract][Full Text] [Related]
15. Cu/Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of mitochondria and perturbs Ca2+ homeostasis in SOD1G93A mice.
Jaiswal MK; Keller BU
Mol Pharmacol; 2009 Mar; 75(3):478-89. PubMed ID: 19060114
[TBL] [Abstract][Full Text] [Related]
16. Cell culture models to investigate the selective vulnerability of motoneuronal mitochondria to familial ALS-linked G93ASOD1.
Raimondi A; Mangolini A; Rizzardini M; Tartari S; Massari S; Bendotti C; Francolini M; Borgese N; Cantoni L; Pietrini G
Eur J Neurosci; 2006 Jul; 24(2):387-99. PubMed ID: 16903849
[TBL] [Abstract][Full Text] [Related]
17. A drosophila model for amyotrophic lateral sclerosis reveals motor neuron damage by human SOD1.
Watson MR; Lagow RD; Xu K; Zhang B; Bonini NM
J Biol Chem; 2008 Sep; 283(36):24972-81. PubMed ID: 18596033
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial dysfunction in SOD1G93A-bearing astrocytes promotes motor neuron degeneration: prevention by mitochondrial-targeted antioxidants.
Cassina P; Cassina A; Pehar M; Castellanos R; Gandelman M; de León A; Robinson KM; Mason RP; Beckman JS; Barbeito L; Radi R
J Neurosci; 2008 Apr; 28(16):4115-22. PubMed ID: 18417691
[TBL] [Abstract][Full Text] [Related]
19. In vivo pathogenic role of mutant SOD1 localized in the mitochondrial intermembrane space.
Igoudjil A; Magrané J; Fischer LR; Kim HJ; Hervias I; Dumont M; Cortez C; Glass JD; Starkov AA; Manfredi G
J Neurosci; 2011 Nov; 31(44):15826-37. PubMed ID: 22049426
[TBL] [Abstract][Full Text] [Related]
20. Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation.
Gurney ME; Pu H; Chiu AY; Dal Canto MC; Polchow CY; Alexander DD; Caliendo J; Hentati A; Kwon YW; Deng HX
Science; 1994 Jun; 264(5166):1772-5. PubMed ID: 8209258
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]