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251 related items for PubMed ID: 20653686

  • 21. Early pathogenesis in the adult-onset neurodegenerative disease amyotrophic lateral sclerosis.
    van Zundert B, Izaurieta P, Fritz E, Alvarez FJ.
    J Cell Biochem; 2012 Nov; 113(11):3301-12. PubMed ID: 22740507
    [Abstract] [Full Text] [Related]

  • 22. Altered presymptomatic AMPA and cannabinoid receptor trafficking in motor neurons of ALS model mice: implications for excitotoxicity.
    Zhao P, Ignacio S, Beattie EC, Abood ME.
    Eur J Neurosci; 2008 Feb; 27(3):572-9. PubMed ID: 18279310
    [Abstract] [Full Text] [Related]

  • 23.
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  • 24. Cellular changes in motoneurons in a transgenic mouse model for amyotrophic lateral sclerosis as revealed by monoclonal antibody Py.
    Joosten EA, Van Westerlaak MG, Biesheuvel C, Woodhams PL, Brook GA, Veldman H, Bär PR.
    Brain Res Dev Brain Res; 2001 Nov 26; 131(1-2):153-9. PubMed ID: 11718846
    [Abstract] [Full Text] [Related]

  • 25. Voltage-gated calcium channels are abnormal in cultured spinal motoneurons in the G93A-SOD1 transgenic mouse model of ALS.
    Chang Q, Martin LJ.
    Neurobiol Dis; 2016 Sep 26; 93():78-95. PubMed ID: 27151771
    [Abstract] [Full Text] [Related]

  • 26. Early intrinsic hyperexcitability does not contribute to motoneuron degeneration in amyotrophic lateral sclerosis.
    Leroy F, Lamotte d'Incamps B, Imhoff-Manuel RD, Zytnicki D.
    Elife; 2014 Oct 14; 3():. PubMed ID: 25313866
    [Abstract] [Full Text] [Related]

  • 27. Differential vulnerability of cranial motoneurons in mouse models with motor neuron degeneration.
    Haenggeli C, Kato AC.
    Neurosci Lett; 2002 Dec 19; 335(1):39-43. PubMed ID: 12457737
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. Excitatory to inhibitory synaptic ratios are unchanged at presymptomatic stages in multiple models of ALS.
    Bonthron C, Burley S, Broadhead MJ, Metodieva V, Grant SGN, Chandran S, Miles GB.
    PLoS One; 2024 Oct 15; 19(8):e0306423. PubMed ID: 39088455
    [Abstract] [Full Text] [Related]

  • 30. Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 mice.
    Maatkamp A, Vlug A, Haasdijk E, Troost D, French PJ, Jaarsma D.
    Eur J Neurosci; 2004 Jul 15; 20(1):14-28. PubMed ID: 15245475
    [Abstract] [Full Text] [Related]

  • 31. Postsynaptic alteration of NR2A subunit and defective autophosphorylation of alphaCaMKII at threonine-286 contribute to abnormal plasticity and morphology of upper motor neurons in presymptomatic SOD1G93A mice, a murine model for amyotrophic lateral sclerosis.
    Spalloni A, Origlia N, Sgobio C, Trabalza A, Nutini M, Berretta N, Bernardi G, Domenici L, Ammassari-Teule M, Longone P.
    Cereb Cortex; 2011 Apr 15; 21(4):796-805. PubMed ID: 20732897
    [Abstract] [Full Text] [Related]

  • 32. Degeneration of axons in spinal white matter in G93A mSOD1 mouse characterized by NFL and α-internexin immunoreactivity.
    King AE, Blizzard CA, Southam KA, Vickers JC, Dickson TC.
    Brain Res; 2012 Jul 17; 1465():90-100. PubMed ID: 22609817
    [Abstract] [Full Text] [Related]

  • 33. Toll-Like Receptor-4 Inhibitor TAK-242 Attenuates Motor Dysfunction and Spinal Cord Pathology in an Amyotrophic Lateral Sclerosis Mouse Model.
    Fellner A, Barhum Y, Angel A, Perets N, Steiner I, Offen D, Lev N.
    Int J Mol Sci; 2017 Aug 01; 18(8):. PubMed ID: 28763002
    [Abstract] [Full Text] [Related]

  • 34. Nrf2 activation in astrocytes protects against neurodegeneration in mouse models of familial amyotrophic lateral sclerosis.
    Vargas MR, Johnson DA, Sirkis DW, Messing A, Johnson JA.
    J Neurosci; 2008 Dec 10; 28(50):13574-81. PubMed ID: 19074031
    [Abstract] [Full Text] [Related]

  • 35. Motor neuron degeneration in amyotrophic lateral sclerosis mutant superoxide dismutase-1 transgenic mice: mechanisms of mitochondriopathy and cell death.
    Martin LJ, Liu Z, Chen K, Price AC, Pan Y, Swaby JA, Golden WC.
    J Comp Neurol; 2007 Jan 01; 500(1):20-46. PubMed ID: 17099894
    [Abstract] [Full Text] [Related]

  • 36. Altered reaction of facial motoneurons to axonal damage in the presymptomatic phase of a murine model of familial amyotrophic lateral sclerosis.
    Mariotti R, Cristino L, Bressan C, Boscolo S, Bentivoglio M.
    Neuroscience; 2002 Jan 01; 115(2):331-5. PubMed ID: 12421599
    [Abstract] [Full Text] [Related]

  • 37. Calcitonin gene-related peptide expression levels predict motor neuron vulnerability in the superoxide dismutase 1-G93A mouse model of amyotrophic lateral sclerosis.
    Ringer C, Weihe E, Schütz B.
    Neurobiol Dis; 2012 Jan 01; 45(1):547-54. PubMed ID: 21964254
    [Abstract] [Full Text] [Related]

  • 38. Neonatal neuronal circuitry shows hyperexcitable disturbance in a mouse model of the adult-onset neurodegenerative disease amyotrophic lateral sclerosis.
    van Zundert B, Peuscher MH, Hynynen M, Chen A, Neve RL, Brown RH, Constantine-Paton M, Bellingham MC.
    J Neurosci; 2008 Oct 22; 28(43):10864-74. PubMed ID: 18945894
    [Abstract] [Full Text] [Related]

  • 39. Degeneration of proprioceptive sensory nerve endings in mice harboring amyotrophic lateral sclerosis-causing mutations.
    Vaughan SK, Kemp Z, Hatzipetros T, Vieira F, Valdez G.
    J Comp Neurol; 2015 Dec 01; 523(17):2477-94. PubMed ID: 26136049
    [Abstract] [Full Text] [Related]

  • 40. Defects in synapse structure and function precede motor neuron degeneration in Drosophila models of FUS-related ALS.
    Shahidullah M, Le Marchand SJ, Fei H, Zhang J, Pandey UB, Dalva MB, Pasinelli P, Levitan IB.
    J Neurosci; 2013 Dec 11; 33(50):19590-8. PubMed ID: 24336723
    [Abstract] [Full Text] [Related]

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