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Journal Abstract Search

118 related items for PubMed ID: 16856153

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  • 2. Amyloid precursor protein (APP) contributes to pathology in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Bryson JB, Hobbs C, Parsons MJ, Bosch KD, Pandraud A, Walsh FS, Doherty P, Greensmith L.
    Hum Mol Genet; 2012 Sep 01; 21(17):3871-82. PubMed ID: 22678056
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  • 4. Inhibition of amyloid precursor protein beta-secretase cleavage site affects survival and motor functions of amyotrophic lateral sclerosis transgenic mice.
    Rabinovich-Toidman P, Becker M, Barbiro B, Solomon B.
    Neurodegener Dis; 2012 Sep 01; 10(1-4):30-3. PubMed ID: 22269310
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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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  • 7. Sex-dependent effects of amyloid precursor-like protein 2 in the SOD1-G37R transgenic mouse model of MND.
    Truong PH, Crouch PJ, Hilton JBW, McLean CA, Cappai R, Ciccotosto GD.
    Cell Mol Life Sci; 2021 Oct 16; 78(19-20):6605-6630. PubMed ID: 34476545
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  • 8. L-carnitine suppresses the onset of neuromuscular degeneration and increases the life span of mice with familial amyotrophic lateral sclerosis.
    Kira Y, Nishikawa M, Ochi A, Sato E, Inoue M.
    Brain Res; 2006 Jan 27; 1070(1):206-14. PubMed ID: 16412993
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  • 9. Early detection of denervated muscle fibers in hindlimb muscles after sciatic nerve transection in wild type mice and in the G93A mouse model of amyotrophic lateral sclerosis.
    Gordon T, Ly V, Hegedus J, Tyreman N.
    Neurol Res; 2009 Feb 27; 31(1):28-42. PubMed ID: 18768111
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  • 10. Coincident thresholds of mutant protein for paralytic disease and protein aggregation caused by restrictively expressed superoxide dismutase cDNA.
    Wang J, Xu G, Slunt HH, Gonzales V, Coonfield M, Fromholt D, Copeland NG, Jenkins NA, Borchelt DR.
    Neurobiol Dis; 2005 Dec 27; 20(3):943-52. PubMed ID: 16046140
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  • 11. Gene expression profiles of APP and BACE1 in Tg SOD1G93A cortical cells.
    Spadoni O, Crestini A, Piscopo P, Malvezzi-Campeggi L, Carunchio I, Pieri M, Zona C, Confaloni A.
    Cell Mol Neurobiol; 2009 Jul 27; 29(5):635-41. PubMed ID: 19214738
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  • 14. 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 27; 8(6):933-41. PubMed ID: 11741389
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  • 15. 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 Dec 27; 1782(7-8):462-8. PubMed ID: 18485920
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  • 18. Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS).
    Howland DS, Liu J, She Y, Goad B, Maragakis NJ, Kim B, Erickson J, Kulik J, DeVito L, Psaltis G, DeGennaro LJ, Cleveland DW, Rothstein JD.
    Proc Natl Acad Sci U S A; 2002 Feb 05; 99(3):1604-9. PubMed ID: 11818550
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  • 19. A soluble activin type IIB receptor improves function in a mouse model of amyotrophic lateral sclerosis.
    Morrison BM, Lachey JL, Warsing LC, Ting BL, Pullen AE, Underwood KW, Kumar R, Sako D, Grinberg A, Wong V, Colantuoni E, Seehra JS, Wagner KR.
    Exp Neurol; 2009 Jun 05; 217(2):258-68. PubMed ID: 19285073
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  • 20. Relationship of oxygen radical-induced lipid peroxidative damage to disease onset and progression in a transgenic model of familial ALS.
    Hall ED, Andrus PK, Oostveen JA, Fleck TJ, Gurney ME.
    J Neurosci Res; 1998 Jul 01; 53(1):66-77. PubMed ID: 9670993
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