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164 related items for PubMed ID: 18485920

  • 1. Presymptomatic biochemical changes in hindlimb muscle of G93A human Cu/Zn superoxide dismutase 1 transgenic mouse model of amyotrophic lateral sclerosis.
    Park KH, Vincent I.
    Biochim Biophys Acta; 2008; 1782(7-8):462-8. PubMed ID: 18485920
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  • 2. Progressive impairment of CaV1.1 function in the skeletal muscle of mice expressing a mutant type 1 Cu/Zn superoxide dismutase (G93A) linked to amyotrophic lateral sclerosis.
    Beqollari D, Romberg CF, Dobrowolny G, Martini M, Voss AA, Musarò A, Bannister RA.
    Skelet Muscle; 2016; 6():24. PubMed ID: 27340545
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  • 3. Pre-symptomatic detection of chronic motor deficits and genotype prediction in congenic B6.SOD1(G93A) ALS mouse model.
    Hayworth CR, Gonzalez-Lima F.
    Neuroscience; 2009 Dec 15; 164(3):975-85. PubMed ID: 19699279
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  • 4. Assessment of metal concentrations in the SOD1G93A mouse model of amyotrophic lateral sclerosis and its potential role in muscular denervation, with particular focus on muscle tissue.
    Enge TG, Ecroyd H, Jolley DF, Yerbury JJ, Kalmar B, Dosseto A.
    Mol Cell Neurosci; 2018 Apr 15; 88():319-329. PubMed ID: 29524628
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  • 7. Preferential motor unit loss in the SOD1 G93A transgenic mouse model of amyotrophic lateral sclerosis.
    Hegedus J, Putman CT, Tyreman N, Gordon T.
    J Physiol; 2008 Jul 15; 586(14):3337-51. PubMed ID: 18467368
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  • 8. Elevated levels of amyloid precursor protein in muscle of patients with amyotrophic lateral sclerosis and a mouse model of the disease.
    Koistinen H, Prinjha R, Soden P, Harper A, Banner SJ, Pradat PF, Loeffler JP, Dingwall C.
    Muscle Nerve; 2006 Oct 15; 34(4):444-50. PubMed ID: 16856153
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  • 11. Neuromuscular accumulation of mutant superoxide dismutase 1 aggregates in a transgenic mouse model of familial amyotrophic lateral sclerosis.
    Turner BJ, Lopes EC, Cheema SS.
    Neurosci Lett; 2003 Oct 23; 350(2):132-6. PubMed ID: 12972170
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  • 12. Transient recovery in a rat model of familial amyotrophic lateral sclerosis after transplantation of motor neurons derived from mouse embryonic stem cells.
    López-González R, Kunckles P, Velasco I.
    Cell Transplant; 2009 Oct 23; 18(10):1171-81. PubMed ID: 19660174
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  • 13. Molecular signatures of amyotrophic lateral sclerosis disease progression in hind and forelimb muscles of an SOD1(G93A) mouse model.
    Capitanio D, Vasso M, Ratti A, Grignaschi G, Volta M, Moriggi M, Daleno C, Bendotti C, Silani V, Gelfi C.
    Antioxid Redox Signal; 2012 Nov 15; 17(10):1333-50. PubMed ID: 22563797
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  • 14. Local expression of mIgf-1 modulates ubiquitin, caspase and CDK5 expression in skeletal muscle of an ALS mouse model.
    Dobrowolny G, Aucello M, Molinaro M, Musarò A.
    Neurol Res; 2008 Mar 15; 30(2):131-6. PubMed ID: 18397603
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  • 15. 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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  • 16. Toll-Like Receptor-4 Inhibitor TAK-242 Attenuates Motor Dysfunction and Spinal Cord Pathology in an Amyotrophic Lateral Sclerosis Mouse Model.
    Fellner A, Barhum Y, Angel A, Perets N, Steiner I, Offen D, Lev N.
    Int J Mol Sci; 2017 Aug 01; 18(8):. PubMed ID: 28763002
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  • 17. Complement C5a-C5aR1 signalling drives skeletal muscle macrophage recruitment in the hSOD1G93A mouse model of amyotrophic lateral sclerosis.
    Wang HA, Lee JD, Lee KM, Woodruff TM, Noakes PG.
    Skelet Muscle; 2017 Jun 01; 7(1):10. PubMed ID: 28571586
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  • 18. MRI detects early hindlimb muscle atrophy in Gly93Ala superoxide dismutase-1 (G93A SOD1) transgenic mice, an animal model of familial amyotrophic lateral sclerosis.
    Brooks KJ, Hill MD, Hockings PD, Reid DG.
    NMR Biomed; 2004 Feb 01; 17(1):28-32. PubMed ID: 15011248
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  • 19. Dysregulation of Rac or Rho elicits death of motor neurons and activation of these GTPases is altered in the G93A mutant hSOD1 mouse model of amyotrophic lateral sclerosis.
    Stankiewicz TR, Pena C, Bouchard RJ, Linseman DA.
    Neurobiol Dis; 2020 Mar 01; 136():104743. PubMed ID: 31931138
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  • 20. Evolution of the neurochemical profiles in the G93A-SOD1 mouse model of amyotrophic lateral sclerosis.
    Lei H, Dirren E, Poitry-Yamate C, Schneider BL, Gruetter R, Aebischer P.
    J Cereb Blood Flow Metab; 2019 Jul 01; 39(7):1283-1298. PubMed ID: 29400109
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