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Journal Abstract Search

424 related items for PubMed ID: 9547233

  • 1. Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1.
    Kong J, Xu Z.
    J Neurosci; 1998 May 01; 18(9):3241-50. PubMed ID: 9547233
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  • 2. 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 01; 7(6 Pt B):623-43. PubMed ID: 11114261
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  • 4. Nuclear localization of human SOD1 and mutant SOD1-specific disruption of survival motor neuron protein complex in transgenic amyotrophic lateral sclerosis mice.
    Gertz B, Wong M, Martin LJ.
    J Neuropathol Exp Neurol; 2012 Feb 01; 71(2):162-77. PubMed ID: 22249462
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  • 5. 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 Feb 01; 18(2):115-36. PubMed ID: 17593875
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  • 6. 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 15; 191(1-2):25-33. PubMed ID: 11676989
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  • 7. Delayed disease onset and extended survival in the SOD1G93A rat model of amyotrophic lateral sclerosis after suppression of mutant SOD1 in the motor cortex.
    Thomsen GM, Gowing G, Latter J, Chen M, Vit JP, Staggenborg K, Avalos P, Alkaslasi M, Ferraiuolo L, Likhite S, Kaspar BK, Svendsen CN.
    J Neurosci; 2014 Nov 19; 34(47):15587-600. PubMed ID: 25411487
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  • 8. Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice.
    Clement AM, Nguyen MD, Roberts EA, Garcia ML, Boillée S, Rule M, McMahon AP, Doucette W, Siwek D, Ferrante RJ, Brown RH, Julien JP, Goldstein LS, Cleveland DW.
    Science; 2003 Oct 03; 302(5642):113-7. PubMed ID: 14526083
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  • 9. Spinal inhibitory interneuron pathology follows motor neuron degeneration independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS mice.
    Hossaini M, Cardona Cano S, van Dis V, Haasdijk ED, Hoogenraad CC, Holstege JC, Jaarsma D.
    J Neuropathol Exp Neurol; 2011 Aug 03; 70(8):662-77. PubMed ID: 21760539
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  • 10. Sensory involvement in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
    Guo YS, Wu DX, Wu HR, Wu SY, Yang C, Li B, Bu H, Zhang YS, Li CY.
    Exp Mol Med; 2009 Mar 31; 41(3):140-50. PubMed ID: 19293633
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  • 11. Human superoxide dismutase 1 overexpression in motor neurons of Caenorhabditis elegans causes axon guidance defect and neurodegeneration.
    Li J, Li T, Zhang X, Tang Y, Yang J, Le W.
    Neurobiol Aging; 2014 Apr 31; 35(4):837-46. PubMed ID: 24126158
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  • 12. The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease.
    Mourelatos Z, Gonatas NK, Stieber A, Gurney ME, Dal Canto MC.
    Proc Natl Acad Sci U S A; 1996 May 28; 93(11):5472-7. PubMed ID: 8643599
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  • 13. 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 28; 64():48-59. PubMed ID: 24361555
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  • 16. Mutant SOD1G93A triggers mitochondrial fragmentation in spinal cord motor neurons: neuroprotection by SIRT3 and PGC-1α.
    Song W, Song Y, Kincaid B, Bossy B, Bossy-Wetzel E.
    Neurobiol Dis; 2013 Mar 28; 51():72-81. PubMed ID: 22819776
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  • 20. Transcriptional profiling in the lumbar spinal cord of a mouse model of amyotrophic lateral sclerosis: a role for wild-type superoxide dismutase 1 in sporadic disease?
    D'Arrigo A, Colavito D, Peña-Altamira E, Fabris M, Dam M, Contestabile A, Leon A.
    J Mol Neurosci; 2010 Jul 28; 41(3):404-15. PubMed ID: 20177826
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