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261 related items for PubMed ID: 35216298

  • 21. Neurovascular unit pathology is observed very early in disease progression in the mutant SOD1G93A mouse model of amyotrophic lateral sclerosis.
    Yoshikawa M, Aizawa S, Oppenheim RW, Milligan C.
    Exp Neurol; 2022 Jul; 353():114084. PubMed ID: 35439439
    [Abstract] [Full Text] [Related]

  • 22. Proteomics analysis indicates the involvement of immunity and inflammation in the onset stage of SOD1-G93A mouse model of ALS.
    Chen L, Wang N, Zhang Y, Li D, He C, Li Z, Zhang J, Guo Y.
    J Proteomics; 2023 Feb 10; 272():104776. PubMed ID: 36423857
    [Abstract] [Full Text] [Related]

  • 23. Increased surface P2X4 receptors by mutant SOD1 proteins contribute to ALS pathogenesis in SOD1-G93A mice.
    Bertin E, Martinez A, Fayoux A, Carvalho K, Carracedo S, Fernagut PO, Koch-Nolte F, Blum D, Bertrand SS, Boué-Grabot E.
    Cell Mol Life Sci; 2022 Jul 19; 79(8):431. PubMed ID: 35852606
    [Abstract] [Full Text] [Related]

  • 24. 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]

  • 25. Excitatory action of low frequency depolarizing GABA/glycine synaptic inputs is prevalent in prenatal spinal SOD1G93A motoneurons.
    Zhu H, Dalvi U, Cazenave W, Cattaert D, Branchereau P.
    J Physiol; 2024 Mar 01; 602(5):913-932. PubMed ID: 38345477
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. 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 15; 5(2):153-65. PubMed ID: 16626394
    [Abstract] [Full Text] [Related]

  • 28. RNS60 exerts therapeutic effects in the SOD1 ALS mouse model through protective glia and peripheral nerve rescue.
    Vallarola A, Sironi F, Tortarolo M, Gatto N, De Gioia R, Pasetto L, De Paola M, Mariani A, Ghosh S, Watson R, Kalmes A, Bonetto V, Bendotti C.
    J Neuroinflammation; 2018 Mar 01; 15(1):65. PubMed ID: 29495962
    [Abstract] [Full Text] [Related]

  • 29. Plasma neurofilament heavy chain levels correlate to markers of late stage disease progression and treatment response in SOD1(G93A) mice that model ALS.
    Lu CH, Petzold A, Kalmar B, Dick J, Malaspina A, Greensmith L.
    PLoS One; 2012 Mar 01; 7(7):e40998. PubMed ID: 22815892
    [Abstract] [Full Text] [Related]

  • 30. CNS-derived extracellular vesicles from superoxide dismutase 1 (SOD1)G93A ALS mice originate from astrocytes and neurons and carry misfolded SOD1.
    Silverman JM, Christy D, Shyu CC, Moon KM, Fernando S, Gidden Z, Cowan CM, Ban Y, Stacey RG, Grad LI, McAlary L, Mackenzie IR, Foster LJ, Cashman NR.
    J Biol Chem; 2019 Mar 08; 294(10):3744-3759. PubMed ID: 30635404
    [Abstract] [Full Text] [Related]

  • 31. CD4 T-cell aging exacerbates neuroinflammation in a late-onset mouse model of amyotrophic lateral sclerosis.
    Zaccai S, Nemirovsky A, Lerner L, Alfahel L, Eremenko E, Israelson A, Monsonego A.
    J Neuroinflammation; 2024 Jan 11; 21(1):17. PubMed ID: 38212835
    [Abstract] [Full Text] [Related]

  • 32. PACAP signaling exerts opposing effects on neuroprotection and neuroinflammation during disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Ringer C, Büning LS, Schäfer MK, Eiden LE, Weihe E, Schütz B.
    Neurobiol Dis; 2013 Jun 11; 54():32-42. PubMed ID: 23466699
    [Abstract] [Full Text] [Related]

  • 33. Actions of the antihistaminergic clemastine on presymptomatic SOD1-G93A mice ameliorate ALS disease progression.
    Apolloni S, Fabbrizio P, Amadio S, Volonté C.
    J Neuroinflammation; 2016 Aug 22; 13(1):191. PubMed ID: 27549088
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  • 34. 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]

  • 35. In-vivo genetic ablation of metabotropic glutamate receptor type 5 slows down disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis.
    Bonifacino T, Provenzano F, Gallia E, Ravera S, Torazza C, Bossi S, Ferrando S, Puliti A, Van Den Bosch L, Bonanno G, Milanese M.
    Neurobiol Dis; 2019 Sep 23; 129():79-92. PubMed ID: 31102766
    [Abstract] [Full Text] [Related]

  • 36. Over-expression of Hsp27 does not influence disease in the mutant SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Krishnan J, Vannuvel K, Andries M, Waelkens E, Robberecht W, Van Den Bosch L.
    J Neurochem; 2008 Sep 23; 106(5):2170-83. PubMed ID: 18624915
    [Abstract] [Full Text] [Related]

  • 37. Abnormal Upregulation of GPR17 Receptor Contributes to Oligodendrocyte Dysfunction in SOD1 G93A Mice.
    Bonfanti E, Bonifacino T, Raffaele S, Milanese M, Morgante E, Bonanno G, Abbracchio MP, Fumagalli M.
    Int J Mol Sci; 2020 Mar 31; 21(7):. PubMed ID: 32244295
    [Abstract] [Full Text] [Related]

  • 38. Activation of the Notch Signaling Pathway and Cellular Localization of Notch Signaling Molecules in the Spinal Cord of SOD1-G93A ALS Model Mice.
    Liu C, Li D, Lv C, Gao Z, Qi Y, Wu H, Tian Y, Guo Y.
    Neuroscience; 2020 Apr 15; 432():84-93. PubMed ID: 32114100
    [Abstract] [Full Text] [Related]

  • 39. The distribution and function of GDE2, a regulator of spinal motor neuron survival, are disrupted in Amyotrophic Lateral Sclerosis.
    Westerhaus A, Joseph T, Meyers AJ, Jang Y, Na CH, Cave C, Sockanathan S.
    Acta Neuropathol Commun; 2022 May 12; 10(1):73. PubMed ID: 35550203
    [Abstract] [Full Text] [Related]

  • 40. A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model.
    Post J, Kogel V, Schaffrath A, Lohmann P, Shah NJ, Langen KJ, Willbold D, Willuweit A, Kutzsche J.
    Molecules; 2021 Mar 13; 26(6):. PubMed ID: 33805709
    [Abstract] [Full Text] [Related]

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