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Journal Abstract Search

687 related items for PubMed ID: 25932674

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  • 2. Current hypotheses for the underlying biology of amyotrophic lateral sclerosis.
    Rothstein JD.
    Ann Neurol; 2009 Jan; 65 Suppl 1():S3-9. PubMed ID: 19191304
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  • 4. TDP-43 in differential diagnosis of motor neuron disorders.
    Dickson DW, Josephs KA, Amador-Ortiz C.
    Acta Neuropathol; 2007 Jul; 114(1):71-9. PubMed ID: 17569066
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  • 5. Altered distribution and levels of cathepsinD and cystatins in amyotrophic lateral sclerosis transgenic mice: possible roles in motor neuron survival.
    Wootz H, Weber E, Korhonen L, Lindholm D.
    Neuroscience; 2006 Dec 01; 143(2):419-30. PubMed ID: 16973300
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  • 7. 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 01; 8(6):933-41. PubMed ID: 11741389
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  • 8. TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.
    Turner BJ, Bäumer D, Parkinson NJ, Scaber J, Ansorge O, Talbot K.
    BMC Neurosci; 2008 Oct 28; 9():104. PubMed ID: 18957104
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  • 9. TDP-43 modification in the hSOD1(G93A) amyotrophic lateral sclerosis mouse model.
    Cai M, Lee KW, Choi SM, Yang EJ.
    Neurol Res; 2015 Mar 28; 37(3):253-62. PubMed ID: 25213598
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  • 11. Molecular biology of amyotrophic lateral sclerosis: insights from genetics.
    Pasinelli P, Brown RH.
    Nat Rev Neurosci; 2006 Sep 28; 7(9):710-23. PubMed ID: 16924260
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  • 15. Bromocriptine methylate suppresses glial inflammation and moderates disease progression in a mouse model of amyotrophic lateral sclerosis.
    Tanaka K, Kanno T, Yanagisawa Y, Yasutake K, Hadano S, Yoshii F, Ikeda JE.
    Exp Neurol; 2011 Nov 28; 232(1):41-52. PubMed ID: 21867702
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  • 16. Increased survival and function of SOD1 mice after glial cell-derived neurotrophic factor gene therapy.
    Acsadi G, Anguelov RA, Yang H, Toth G, Thomas R, Jani A, Wang Y, Ianakova E, Mohammad S, Lewis RA, Shy ME.
    Hum Gene Ther; 2002 Jun 10; 13(9):1047-59. PubMed ID: 12067438
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  • 18. Dysfunction of endocytic kinase AAK1 in ALS.
    Shi B, Conner SD, Liu J.
    Int J Mol Sci; 2014 Dec 10; 15(12):22918-32. PubMed ID: 25514244
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  • 19. VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model.
    Azzouz M, Ralph GS, Storkebaum E, Walmsley LE, Mitrophanous KA, Kingsman SM, Carmeliet P, Mazarakis ND.
    Nature; 2004 May 27; 429(6990):413-7. PubMed ID: 15164063
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  • 20. Overexpression of metallothionein-I, a copper-regulating protein, attenuates intracellular copper dyshomeostasis and extends lifespan in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase-1.
    Tokuda E, Okawa E, Watanabe S, Ono S.
    Hum Mol Genet; 2014 Mar 01; 23(5):1271-85. PubMed ID: 24163136
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