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315 related items for PubMed ID: 21486770

  • 21. The effect of peripheral nerve injury on disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Sharp PS, Dick JR, Greensmith L.
    Neuroscience; 2005; 130(4):897-910. PubMed ID: 15652988
    [Abstract] [Full Text] [Related]

  • 22. 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; 6():24. PubMed ID: 27340545
    [Abstract] [Full Text] [Related]

  • 23. Mutant SOD1-expressing astrocytes release toxic factors that trigger motoneuron death by inducing hyperexcitability.
    Fritz E, Izaurieta P, Weiss A, Mir FR, Rojas P, Gonzalez D, Rojas F, Brown RH, Madrid R, van Zundert B.
    J Neurophysiol; 2013 Jun; 109(11):2803-14. PubMed ID: 23486205
    [Abstract] [Full Text] [Related]

  • 24. 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; 5(2):153-65. PubMed ID: 16626394
    [Abstract] [Full Text] [Related]

  • 25. Novel behavioural characteristics of the superoxide dismutase 1 G93A (SOD1G93A ) mouse model of amyotrophic lateral sclerosis include sex-dependent phenotypes.
    Kreilaus F, Guerra S, Masanetz R, Menne V, Yerbury J, Karl T.
    Genes Brain Behav; 2020 Feb; 19(2):e12604. PubMed ID: 31412164
    [Abstract] [Full Text] [Related]

  • 26. 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; 134(Pt 9):2627-41. PubMed ID: 21908873
    [Abstract] [Full Text] [Related]

  • 27. Altered development in GABA co-release shapes glycinergic synaptic currents in cultured spinal slices of the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Medelin M, Rancic V, Cellot G, Laishram J, Veeraraghavan P, Rossi C, Muzio L, Sivilotti L, Ballerini L.
    J Physiol; 2016 Jul 01; 594(13):3827-40. PubMed ID: 27098371
    [Abstract] [Full Text] [Related]

  • 28. Cytotoxic CD8+ T lymphocytes expressing ALS-causing SOD1 mutant selectively trigger death of spinal motoneurons.
    Coque E, Salsac C, Espinosa-Carrasco G, Varga B, Degauque N, Cadoux M, Crabé R, Virenque A, Soulard C, Fierle JK, Brodovitch A, Libralato M, Végh AG, Venteo S, Scamps F, Boucraut J, Laplaud D, Hernandez J, Gergely C, Vincent T, Raoul C.
    Proc Natl Acad Sci U S A; 2019 Feb 05; 116(6):2312-2317. PubMed ID: 30674678
    [Abstract] [Full Text] [Related]

  • 29. Progressive changes in synaptic inputs to motoneurons in adult sacral spinal cord of a mouse model of amyotrophic lateral sclerosis.
    Jiang M, Schuster JE, Fu R, Siddique T, Heckman CJ.
    J Neurosci; 2009 Dec 02; 29(48):15031-8. PubMed ID: 19955354
    [Abstract] [Full Text] [Related]

  • 30. Calcium-permeable AMPA receptors promote misfolding of mutant SOD1 protein and development of amyotrophic lateral sclerosis in a transgenic mouse model.
    Tateno M, Sadakata H, Tanaka M, Itohara S, Shin RM, Miura M, Masuda M, Aosaki T, Urushitani M, Misawa H, Takahashi R.
    Hum Mol Genet; 2004 Oct 01; 13(19):2183-96. PubMed ID: 15294873
    [Abstract] [Full Text] [Related]

  • 31. Early abnormalities in transgenic mouse models of amyotrophic lateral sclerosis.
    Durand J, Amendola J, Bories C, Lamotte d'Incamps B.
    J Physiol Paris; 2006 Oct 01; 99(2-3):211-20. PubMed ID: 16448809
    [Abstract] [Full Text] [Related]

  • 32. Increase in presynaptic territory of C-terminals on lumbar motoneurons of G93A SOD1 mice during disease progression.
    Pullen AH, Athanasiou D.
    Eur J Neurosci; 2009 Feb 01; 29(3):551-61. PubMed ID: 19187267
    [Abstract] [Full Text] [Related]

  • 33. 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 01; 64():48-59. PubMed ID: 24361555
    [Abstract] [Full Text] [Related]

  • 34. Compensatory changes in degenerating spinal motoneurons sustain functional sparing in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
    Giusto E, Codrich M, de Leo G, Francardo V, Coradazzi M, Parenti R, Gulisano M, Vicario N, Gulino R, Leanza G.
    J Comp Neurol; 2020 Feb 01; 528(2):231-243. PubMed ID: 31364764
    [Abstract] [Full Text] [Related]

  • 35. Electrical and Morphological Properties of Developing Motoneurons in Postnatal Mice and Early Abnormalities in SOD1 Transgenic Mice.
    Durand J, Filipchuk A.
    Adv Neurobiol; 2022 Feb 01; 28():353-373. PubMed ID: 36066832
    [Abstract] [Full Text] [Related]

  • 36. Postnatal dendritic development in lumbar motoneurons in mutant superoxide dismutase 1 mouse model of amyotrophic lateral sclerosis.
    Filipchuk AA, Durand J.
    Neuroscience; 2012 May 03; 209():144-54. PubMed ID: 22387111
    [Abstract] [Full Text] [Related]

  • 37. Autophagy activation and neuroprotection by progesterone in the G93A-SOD1 transgenic mouse model of amyotrophic lateral sclerosis.
    Kim J, Kim TY, Cho KS, Kim HN, Koh JY.
    Neurobiol Dis; 2013 Nov 03; 59():80-5. PubMed ID: 23891729
    [Abstract] [Full Text] [Related]

  • 38. 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
    [Abstract] [Full Text] [Related]

  • 39. Different human copper-zinc superoxide dismutase mutants, SOD1G93A and SOD1H46R, exert distinct harmful effects on gross phenotype in mice.
    Pan L, Yoshii Y, Otomo A, Ogawa H, Iwasaki Y, Shang HF, Hadano S.
    PLoS One; 2012 Oct 15; 7(3):e33409. PubMed ID: 22438926
    [Abstract] [Full Text] [Related]

  • 40. Intrinsic properties of lumbar motor neurones in the adult G127insTGGG superoxide dismutase-1 mutant mouse in vivo: evidence for increased persistent inward currents.
    Meehan CF, Moldovan M, Marklund SL, Graffmo KS, Nielsen JB, Hultborn H.
    Acta Physiol (Oxf); 2010 Dec 15; 200(4):361-76. PubMed ID: 20874803
    [Abstract] [Full Text] [Related]

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