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821 related items for PubMed ID: 29524628

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  • 2. Longitudinal assessment of metal concentrations and copper isotope ratios in the G93A SOD1 mouse model of amyotrophic lateral sclerosis.
    Enge TG, Ecroyd H, Jolley DF, Yerbury JJ, Dosseto A.
    Metallomics; 2017 Feb 22; 9(2):161-174. PubMed ID: 28067393
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  • 3. 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 Feb 22; 6():24. PubMed ID: 27340545
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  • 5. Differential effects of mutant SOD1 on protein structure of skeletal muscle and spinal cord of familial amyotrophic lateral sclerosis: role of chaperone network.
    Wei R, Bhattacharya A, Hamilton RT, Jernigan AL, Chaudhuri AR.
    Biochem Biophys Res Commun; 2013 Aug 16; 438(1):218-23. PubMed ID: 23886956
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  • 6. Galectin-1 deficiency improves axonal swelling of motor neurones in SOD1(G93A) transgenic mice.
    Kobayakawa Y, Sakumi K, Kajitani K, Kadoya T, Horie H, Kira J, Nakabeppu Y.
    Neuropathol Appl Neurobiol; 2015 Feb 16; 41(2):227-44. PubMed ID: 24707896
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  • 7. AAV-NRIP gene therapy ameliorates motor neuron degeneration and muscle atrophy in ALS model mice.
    Chen HH, Yeo HT, Huang YH, Tsai LK, Lai HJ, Tsao YP, Chen SL.
    Skelet Muscle; 2024 Jul 24; 14(1):17. PubMed ID: 39044305
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  • 9. Overexpression of Abeta is associated with acceleration of onset of motor impairment and superoxide dismutase 1 aggregation in an amyotrophic lateral sclerosis mouse model.
    Li QX, Mok SS, Laughton KM, McLean CA, Volitakis I, Cherny RA, Cheung NS, White AR, Masters CL.
    Aging Cell; 2006 Apr 24; 5(2):153-65. PubMed ID: 16626394
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  • 17. Microglia and motor neurons during disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis: changes in arginase1 and inducible nitric oxide synthase.
    Lewis KE, Rasmussen AL, Bennett W, King A, West AK, Chung RS, Chuah MI.
    J Neuroinflammation; 2014 Mar 23; 11():55. PubMed ID: 24655927
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  • 18. Axonal degeneration, distal collateral branching and neuromuscular junction architecture alterations occur prior to symptom onset in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Clark JA, Southam KA, Blizzard CA, King AE, Dickson TC.
    J Chem Neuroanat; 2016 Oct 23; 76(Pt A):35-47. PubMed ID: 27038603
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  • 19. Trehalose decreases mutant SOD1 expression and alleviates motor deficiency in early but not end-stage amyotrophic lateral sclerosis in a SOD1-G93A mouse model.
    Li Y, Guo Y, Wang X, Yu X, Duan W, Hong K, Wang J, Han H, Li C.
    Neuroscience; 2015 Jul 09; 298():12-25. PubMed ID: 25841320
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  • 20. Muscle-derived but not centrally derived transgene GDNF is neuroprotective in G93A-SOD1 mouse model of ALS.
    Li W, Brakefield D, Pan Y, Hunter D, Myckatyn TM, Parsadanian A.
    Exp Neurol; 2007 Feb 09; 203(2):457-71. PubMed ID: 17034790
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