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884 related items for PubMed ID: 17403682

  • 1. 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 01; 282(22):16691-9. PubMed ID: 17403682
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  • 2. Effects of ALS-related SOD1 mutants on dynein- and KIF5-mediated retrograde and anterograde axonal transport.
    Shi P, Ström AL, Gal J, Zhu H.
    Biochim Biophys Acta; 2010 Sep 01; 1802(9):707-16. PubMed ID: 20510358
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  • 3. Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis.
    Turner BJ, Atkin JD, Farg MA, Zang DW, Rembach A, Lopes EC, Patch JD, Hill AF, Cheema SS.
    J Neurosci; 2005 Jan 05; 25(1):108-17. PubMed ID: 15634772
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  • 4. Interaction of amyotrophic lateral sclerosis (ALS)-related mutant copper-zinc superoxide dismutase with the dynein-dynactin complex contributes to inclusion formation.
    Ström AL, Shi P, Zhang F, Gal J, Kilty R, Hayward LJ, Zhu H.
    J Biol Chem; 2008 Aug 15; 283(33):22795-805. PubMed ID: 18515363
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  • 5. 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 15; 8(6):933-41. PubMed ID: 11741389
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  • 6. 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 15; 7(6 Pt B):623-43. PubMed ID: 11114261
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  • 7. 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 18; 281(5384):1851-4. PubMed ID: 9743498
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  • 12. Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells.
    Oh YK, Shin KS, Yuan J, Kang SJ.
    J Neurochem; 2008 Feb 18; 104(4):993-1005. PubMed ID: 18233996
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  • 14. Modulation of mutant superoxide dismutase 1 aggregation by co-expression of wild-type enzyme.
    Prudencio M, Durazo A, Whitelegge JP, Borchelt DR.
    J Neurochem; 2009 Feb 18; 108(4):1009-18. PubMed ID: 19077113
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  • 16. 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 18; 43(6):581-6. PubMed ID: 22089637
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  • 18. Absence of neurofilaments reduces the selective vulnerability of motor neurons and slows disease caused by a familial amyotrophic lateral sclerosis-linked superoxide dismutase 1 mutant.
    Williamson TL, Bruijn LI, Zhu Q, Anderson KL, Anderson SD, Julien JP, Cleveland DW.
    Proc Natl Acad Sci U S A; 1998 Aug 04; 95(16):9631-6. PubMed ID: 9689132
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