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Journal Abstract Search

250 related items for PubMed ID: 9689132

  • 21.
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  • 22. Reduction of axonal caliber does not alleviate motor neuron disease caused by mutant superoxide dismutase 1.
    Nguyen MD, Larivière RC, Julien JP.
    Proc Natl Acad Sci U S A; 2000 Oct 24; 97(22):12306-11. PubMed ID: 11050249
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  • 24. p38alpha stress-activated protein kinase phosphorylates neurofilaments and is associated with neurofilament pathology in amyotrophic lateral sclerosis.
    Ackerley S, Grierson AJ, Banner S, Perkinton MS, Brownlees J, Byers HL, Ward M, Thornhill P, Hussain K, Waby JS, Anderton BH, Cooper JD, Dingwall C, Leigh PN, Shaw CE, Miller CC.
    Mol Cell Neurosci; 2004 Jun 24; 26(2):354-64. PubMed ID: 15207859
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  • 28. Mutant copper-zinc superoxide dismutase (SOD1) induces protein secretion pathway alterations and exosome release in astrocytes: implications for disease spreading and motor neuron pathology in amyotrophic lateral sclerosis.
    Basso M, Pozzi S, Tortarolo M, Fiordaliso F, Bisighini C, Pasetto L, Spaltro G, Lidonnici D, Gensano F, Battaglia E, Bendotti C, Bonetto V.
    J Biol Chem; 2013 May 31; 288(22):15699-711. PubMed ID: 23592792
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  • 31. Elevated free nitrotyrosine levels, but not protein-bound nitrotyrosine or hydroxyl radicals, throughout amyotrophic lateral sclerosis (ALS)-like disease implicate tyrosine nitration as an aberrant in vivo property of one familial ALS-linked superoxide dismutase 1 mutant.
    Bruijn LI, Beal MF, Becher MW, Schulz JB, Wong PC, Price DL, Cleveland DW.
    Proc Natl Acad Sci U S A; 1997 Jul 08; 94(14):7606-11. PubMed ID: 9207139
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  • 32. Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.
    Ince PG, Tomkins J, Slade JY, Thatcher NM, Shaw PJ.
    J Neuropathol Exp Neurol; 1998 Oct 08; 57(10):895-904. PubMed ID: 9786240
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  • 34. Neurofilaments in health and disease.
    Julien JP, Mushynski WE.
    Prog Nucleic Acid Res Mol Biol; 1998 Oct 08; 61():1-23. PubMed ID: 9752717
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  • 38. 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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  • 40. Mutant SOD1 in cell types other than motor neurons and oligodendrocytes accelerates onset of disease in ALS mice.
    Yamanaka K, Boillee S, Roberts EA, Garcia ML, McAlonis-Downes M, Mikse OR, Cleveland DW, Goldstein LS.
    Proc Natl Acad Sci U S A; 2008 May 27; 105(21):7594-9. PubMed ID: 18492803
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