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Journal Abstract Search

352 related items for PubMed ID: 12077179

  • 1. Accumulation of SOD1 mutants in postnatal motoneurons does not cause motoneuron pathology or motoneuron disease.
    Lino MM, Schneider C, Caroni P.
    J Neurosci; 2002 Jun 15; 22(12):4825-32. PubMed ID: 12077179
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 3. Ablation of P2X7 receptor exacerbates gliosis and motoneuron death in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
    Apolloni S, Amadio S, Montilli C, Volonté C, D'Ambrosi N.
    Hum Mol Genet; 2013 Oct 15; 22(20):4102-16. PubMed ID: 23736299
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  • 4. Early Hypoexcitability in a Subgroup of Spinal Motoneurons in Superoxide Dismutase 1 Transgenic Mice, a Model of Amyotrophic Lateral Sclerosis.
    Filipchuk A, Pambo-Pambo A, Gaudel F, Liabeuf S, Brocard C, Gueritaud JP, Durand J.
    Neuroscience; 2021 May 21; 463():337-353. PubMed ID: 33556455
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  • 5. Glycine receptor channels in spinal motoneurons are abnormal in a transgenic mouse model of amyotrophic lateral sclerosis.
    Chang Q, Martin LJ.
    J Neurosci; 2011 Feb 23; 31(8):2815-27. PubMed ID: 21414903
    [Abstract] [Full Text] [Related]

  • 6. Knocking down metabotropic glutamate receptor 1 improves survival and disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Milanese M, Giribaldi F, Melone M, Bonifacino T, Musante I, Carminati E, Rossi PI, Vergani L, Voci A, Conti F, Puliti A, Bonanno G.
    Neurobiol Dis; 2014 Apr 23; 64():48-59. PubMed ID: 24361555
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  • 7. Transcriptomic indices of fast and slow disease progression in two mouse models of amyotrophic lateral sclerosis.
    Nardo G, Iennaco R, Fusi N, Heath PR, Marino M, Trolese MC, Ferraiuolo L, Lawrence N, Shaw PJ, Bendotti C.
    Brain; 2013 Nov 23; 136(Pt 11):3305-32. PubMed ID: 24065725
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  • 8. Stabilization of mutant Cu/Zn superoxide dismutase (SOD1) protein by coexpressed wild SOD1 protein accelerates the disease progression in familial amyotrophic lateral sclerosis mice.
    Fukada K, Nagano S, Satoh M, Tohyama C, Nakanishi T, Shimizu A, Yanagihara T, Sakoda S.
    Eur J Neurosci; 2001 Dec 23; 14(12):2032-6. PubMed ID: 11860498
    [Abstract] [Full Text] [Related]

  • 9. Altered postnatal maturation of electrical properties in spinal motoneurons in a mouse model of amyotrophic lateral sclerosis.
    Quinlan KA, Schuster JE, Fu R, Siddique T, Heckman CJ.
    J Physiol; 2011 May 01; 589(Pt 9):2245-60. PubMed ID: 21486770
    [Abstract] [Full Text] [Related]

  • 10. Dysregulation of astrocyte-motoneuron cross-talk in mutant superoxide dismutase 1-related amyotrophic lateral sclerosis.
    Ferraiuolo L, Higginbottom A, Heath PR, Barber S, Greenald D, Kirby J, Shaw PJ.
    Brain; 2011 Sep 01; 134(Pt 9):2627-41. PubMed ID: 21908873
    [Abstract] [Full Text] [Related]

  • 11. Wild-type microglia extend survival in PU.1 knockout mice with familial amyotrophic lateral sclerosis.
    Beers DR, Henkel JS, Xiao Q, Zhao W, Wang J, Yen AA, Siklos L, McKercher SR, Appel SH.
    Proc Natl Acad Sci U S A; 2006 Oct 24; 103(43):16021-6. PubMed ID: 17043238
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  • 15. Dismutase-competent SOD1 mutant accumulation in myelinating Schwann cells is not detrimental to normal or transgenic ALS model mice.
    Turner BJ, Ackerley S, Davies KE, Talbot K.
    Hum Mol Genet; 2010 Mar 01; 19(5):815-24. PubMed ID: 20008901
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  • 16. The vulnerability of spinal motoneurons and soma size plasticity in a mouse model of amyotrophic lateral sclerosis.
    Dukkipati SS, Garrett TL, Elbasiouny SM.
    J Physiol; 2018 May 01; 596(9):1723-1745. PubMed ID: 29502344
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  • 17. Motoneuron subtypes show specificity in glycine receptor channel abnormalities in a transgenic mouse model of amyotrophic lateral sclerosis.
    Chang Q, Martin LJ.
    Channels (Austin); 2011 May 01; 5(4):299-303. PubMed ID: 21558795
    [Abstract] [Full Text] [Related]

  • 18. Chronic infusion of SOD1G93A astrocyte-secreted factors induces spinal motoneuron degeneration and neuromuscular dysfunction in healthy rats.
    Ramírez-Jarquín UN, Rojas F, van Zundert B, Tapia R.
    J Cell Physiol; 2017 Oct 01; 232(10):2610-2615. PubMed ID: 28128448
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