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138 related items for PubMed ID: 15833433

  • 1. Properties of slow- and fast-twitch muscle fibres in a mouse model of amyotrophic lateral sclerosis.
    Atkin JD, Scott RL, West JM, Lopes E, Quah AK, Cheema SS.
    Neuromuscul Disord; 2005 May; 15(5):377-88. PubMed ID: 15833433
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  • 2. Functional over-load saves motor units in the SOD1-G93A transgenic mouse model of amyotrophic lateral sclerosis.
    Gordon T, Tyreman N, Li S, Putman CT, Hegedus J.
    Neurobiol Dis; 2010 Feb; 37(2):412-22. PubMed ID: 19879358
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  • 3. 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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  • 4. Skeletal muscle properties in a transgenic mouse model for amyotrophic lateral sclerosis: effects of creatine treatment.
    Derave W, Van Den Bosch L, Lemmens G, Eijnde BO, Robberecht W, Hespel P.
    Neurobiol Dis; 2003 Aug 15; 13(3):264-72. PubMed ID: 12901841
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  • 6. Treatment with a coinducer of the heat shock response delays muscle denervation in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
    Kalmar B, Edet-Amana E, Greensmith L.
    Amyotroph Lateral Scler; 2012 Jun 15; 13(4):378-92. PubMed ID: 22591194
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  • 7. Muscle fiber-type specific terminal Schwann cell pathology leads to sprouting deficits following partial denervation in SOD1G93A mice.
    Harrison JM, Rafuse VF.
    Neurobiol Dis; 2020 Nov 15; 145():105052. PubMed ID: 32827689
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  • 8. MicroRNA-206: a potential circulating biomarker candidate for amyotrophic lateral sclerosis.
    Toivonen JM, Manzano R, Oliván S, Zaragoza P, García-Redondo A, Osta R.
    PLoS One; 2014 Nov 15; 9(2):e89065. PubMed ID: 24586506
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  • 9. Analysis of Ca2+ and Sr2+ activation characteristics in skinned muscle fibre preparations with different proportions of myofibrillar isoforms.
    Lynch GS, Stephenson DG, Williams DA.
    J Muscle Res Cell Motil; 1995 Feb 15; 16(1):65-78. PubMed ID: 7751406
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  • 15. Preservation of neuromuscular function in symptomatic SOD1-G93A mice by peripheral infusion of methylene blue.
    Talbot JD, Barrett JN, Nonner D, Zhang Z, Wicomb K, Barrett EF.
    Exp Neurol; 2016 Nov 15; 285(Pt A):96-107. PubMed ID: 27567739
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  • 16. Altered in vitro proliferation of mouse SOD1-G93A skeletal muscle satellite cells.
    Manzano R, Toivonen JM, Calvo AC, Oliván S, Zaragoza P, Rodellar C, Montarras D, Osta R.
    Neurodegener Dis; 2013 Nov 15; 11(3):153-64. PubMed ID: 22797053
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  • 17. Progressive motor unit loss in the G93A mouse model of amyotrophic lateral sclerosis is unaffected by gender.
    Hegedus J, Putman CT, Gordon T.
    Muscle Nerve; 2009 Mar 15; 39(3):318-27. PubMed ID: 19208415
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  • 20. Length-dependent axo-terminal degeneration at the neuromuscular synapses of type II muscle in SOD1 mice.
    Tallon C, Russell KA, Sakhalkar S, Andrapallayal N, Farah MH.
    Neuroscience; 2016 Jan 15; 312():179-89. PubMed ID: 26592719
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