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Journal Abstract Search

260 related items for PubMed ID: 37508478

  • 1. CXCR2 Is Deregulated in ALS Spinal Cord and Its Activation Triggers Apoptosis in Motor Neuron-Like Cells Overexpressing hSOD1-G93A.
    La Cognata V, D'Amico AG, Maugeri G, Morello G, Guarnaccia M, Magrì B, Aronica E, D'Agata V, Cavallaro S.
    Cells; 2023 Jul 09; 12(14):. PubMed ID: 37508478
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  • 2. CXCR2 increases in ALS cortical neurons and its inhibition prevents motor neuron degeneration in vitro and improves neuromuscular function in SOD1G93A mice.
    La Cognata V, Golini E, Iemmolo R, Balletta S, Morello G, De Rosa C, Villari A, Marinelli S, Vacca V, Bonaventura G, Dell'Albani P, Aronica E, Mammano F, Mandillo S, Cavallaro S.
    Neurobiol Dis; 2021 Dec 09; 160():105538. PubMed ID: 34743985
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  • 3. Nuclear Localization of Human SOD1 in Motor Neurons in Mouse Model and Patient Amyotrophic Lateral Sclerosis: Possible Links to Cholinergic Phenotype, NADPH Oxidase, Oxidative Stress, and DNA Damage.
    Martin LJ, Koh SJ, Price A, Park D, Kim BW.
    Int J Mol Sci; 2024 Aug 22; 25(16):. PubMed ID: 39201793
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  • 4. The Overexpression of TDP-43 Protein in the Neuron and Oligodendrocyte Cells Causes the Progressive Motor Neuron Degeneration in the SOD1 G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis.
    Lu Y, Tang C, Zhu L, Li J, Liang H, Zhang J, Xu R.
    Int J Biol Sci; 2016 Aug 22; 12(9):1140-9. PubMed ID: 27570488
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  • 6. NRF2 activation suppresses motor neuron ferroptosis induced by the SOD1G93A mutation and exerts neuroprotection in amyotrophic lateral sclerosis.
    Yang B, Pan J, Zhang XN, Wang H, He L, Rong X, Li X, Peng Y.
    Neurobiol Dis; 2023 Aug 22; 184():106210. PubMed ID: 37352984
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  • 9. GPX4 deficiency-dependent phospholipid peroxidation drives motor deficits of ALS.
    Tu LF, Zhang TZ, Zhou YF, Zhou QQ, Gong HB, Liang L, Hai LN, You NX, Su Y, Chen YJ, Mo XK, Shi CZ, Luo LP, Sun WY, Duan WJ, Kurihara H, Li YF, He RR.
    J Adv Res; 2023 Jan 22; 43():205-218. PubMed ID: 36585109
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  • 10. The alteration of serine transporter activity in a cell line model of amyotrophic lateral sclerosis (ALS).
    Lee NY, Kim Y, Ryu H, Kang YS.
    Biochem Biophys Res Commun; 2017 Jan 29; 483(1):135-141. PubMed ID: 28043791
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  • 11. 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 29; 64():48-59. PubMed ID: 24361555
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  • 12. Cdk5 inhibition in the SOD1G93A transgenic mouse model of amyotrophic lateral sclerosis suppresses neurodegeneration and extends survival.
    Kim A, Lee DY, Sung JJ.
    J Neurochem; 2024 Sep 29; 168(9):2908-2925. PubMed ID: 38934222
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  • 13. The ε-Isozyme of Protein Kinase C (PKCε) Is Impaired in ALS Motor Cortex and Its Pulse Activation by Bryostatin-1 Produces Long Term Survival in Degenerating SOD1-G93A Motor Neuron-like Cells.
    La Cognata V, D'Amico AG, Maugeri G, Morello G, Guarnaccia M, Magrì B, Aronica E, Alkon DL, D'Agata V, Cavallaro S.
    Int J Mol Sci; 2023 Aug 15; 24(16):. PubMed ID: 37629005
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  • 15. c-Abl inhibition delays motor neuron degeneration in the G93A mouse, an animal model of amyotrophic lateral sclerosis.
    Katsumata R, Ishigaki S, Katsuno M, Kawai K, Sone J, Huang Z, Adachi H, Tanaka F, Urano F, Sobue G.
    PLoS One; 2012 Aug 15; 7(9):e46185. PubMed ID: 23049975
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  • 16. Persistent NRG1 Type III Overexpression in Spinal Motor Neurons Has No Therapeutic Effect on ALS-Related Pathology in SOD1G93A Mice.
    Hernández S, Salvany S, Casanovas A, Piedrafita L, Soto-Bernardini MC, Tarabal O, Blasco A, Gras S, Gatius A, Schwab MH, Calderó J, Esquerda JE.
    Neurotherapeutics; 2023 Oct 15; 20(6):1820-1834. PubMed ID: 37733208
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  • 17. Comparing effects of microgravity and amyotrophic lateral sclerosis in the mouse ventral lumbar spinal cord.
    Yoshikawa M, Ishikawa C, Li H, Kudo T, Shiba D, Shirakawa M, Muratani M, Takahashi S, Aizawa S, Shiga T.
    Mol Cell Neurosci; 2022 Jul 15; 121():103745. PubMed ID: 35660087
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  • 18. 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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  • 19. Aberrant DNA and RNA Methylation Occur in Spinal Cord and Skeletal Muscle of Human SOD1 Mouse Models of ALS and in Human ALS: Targeting DNA Methylation Is Therapeutic.
    Martin LJ, Adams DA, Niedzwiecki MV, Wong M.
    Cells; 2022 Oct 31; 11(21):. PubMed ID: 36359844
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  • 20. 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 31; 602(5):913-932. PubMed ID: 38345477
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