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251 related items for PubMed ID: 20653686

  • 1. Reduction in the motoneuron inhibitory/excitatory synaptic ratio in an early-symptomatic mouse model of amyotrophic lateral sclerosis.
    Sunico CR, Domínguez G, García-Verdugo JM, Osta R, Montero F, Moreno-López B.
    Brain Pathol; 2011 Jan; 21(1):1-15. PubMed ID: 20653686
    [Abstract] [Full Text] [Related]

  • 2. Imbalanced excitatory to inhibitory synaptic input precedes motor neuron degeneration in an animal model of amyotrophic lateral sclerosis.
    Schütz B.
    Neurobiol Dis; 2005 Oct; 20(1):131-40. PubMed ID: 16137574
    [Abstract] [Full Text] [Related]

  • 3. Early signs of motoneuron vulnerability in a disease model system: Characterization of transverse slice cultures of spinal cord isolated from embryonic ALS mice.
    Avossa D, Grandolfo M, Mazzarol F, Zatta M, Ballerini L.
    Neuroscience; 2006 Oct; 138(4):1179-94. PubMed ID: 16442737
    [Abstract] [Full Text] [Related]

  • 4. Inhibitory synaptic regulation of motoneurons: a new target of disease mechanisms in amyotrophic lateral sclerosis.
    Martin LJ, Chang Q.
    Mol Neurobiol; 2012 Feb; 45(1):30-42. PubMed ID: 22072396
    [Abstract] [Full Text] [Related]

  • 5. 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; 7(6 Pt B):623-43. PubMed ID: 11114261
    [Abstract] [Full Text] [Related]

  • 6. Glycinergic innervation of motoneurons is deficient in amyotrophic lateral sclerosis mice: a quantitative confocal analysis.
    Chang Q, Martin LJ.
    Am J Pathol; 2009 Feb; 174(2):574-85. PubMed ID: 19116365
    [Abstract] [Full Text] [Related]

  • 7. Altered Functionality, Morphology, and Vesicular Glutamate Transporter Expression of Cortical Motor Neurons from a Presymptomatic Mouse Model of Amyotrophic Lateral Sclerosis.
    Saba L, Viscomi MT, Caioli S, Pignataro A, Bisicchia E, Pieri M, Molinari M, Ammassari-Teule M, Zona C.
    Cereb Cortex; 2016 Apr; 26(4):1512-28. PubMed ID: 25596588
    [Abstract] [Full Text] [Related]

  • 8. Differential involvement of vesicular and glial glutamate transporters around spinal α-motoneurons in the pathogenesis of SOD1G93A mouse model of amyotrophic lateral sclerosis.
    Ohgomori T, Yamasaki R, Takeuchi H, Kadomatsu K, Kira JI, Jinno S.
    Neuroscience; 2017 Jul 25; 356():114-124. PubMed ID: 28526579
    [Abstract] [Full Text] [Related]

  • 9. Galectin-1 deficiency improves axonal swelling of motor neurones in SOD1(G93A) transgenic mice.
    Kobayakawa Y, Sakumi K, Kajitani K, Kadoya T, Horie H, Kira J, Nakabeppu Y.
    Neuropathol Appl Neurobiol; 2015 Feb 25; 41(2):227-44. PubMed ID: 24707896
    [Abstract] [Full Text] [Related]

  • 10. Gender-specific perturbations in modulatory inputs to motoneurons in a mouse model of amyotrophic lateral sclerosis.
    Herron LR, Miles GB.
    Neuroscience; 2012 Dec 13; 226():313-23. PubMed ID: 23000617
    [Abstract] [Full Text] [Related]

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  • 12. C-Boutons and Their Influence on Amyotrophic Lateral Sclerosis Disease Progression.
    Wells TL, Myles JR, Akay T.
    J Neurosci; 2021 Sep 22; 41(38):8088-8101. PubMed ID: 34380764
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  • 14. 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]

  • 15. 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 02; 64():48-59. PubMed ID: 24361555
    [Abstract] [Full Text] [Related]

  • 16. Axonal degeneration, distal collateral branching and neuromuscular junction architecture alterations occur prior to symptom onset in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Clark JA, Southam KA, Blizzard CA, King AE, Dickson TC.
    J Chem Neuroanat; 2016 Oct 02; 76(Pt A):35-47. PubMed ID: 27038603
    [Abstract] [Full Text] [Related]

  • 17. The role of mutated SOD1 gene in synaptic stripping and MHC class I expression following nerve axotomy in ALS murine model.
    Kassa RM, Bonafede R, Boschi F, Malatesta M, Mariotti R.
    Eur J Histochem; 2018 May 17; 62(2):2904. PubMed ID: 29943955
    [Abstract] [Full Text] [Related]

  • 18. Downregulation of the potassium chloride cotransporter KCC2 in vulnerable motoneurons in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
    Fuchs A, Ringer C, Bilkei-Gorzo A, Weihe E, Roeper J, Schütz B.
    J Neuropathol Exp Neurol; 2010 Oct 17; 69(10):1057-70. PubMed ID: 20838240
    [Abstract] [Full Text] [Related]

  • 19. A potential role for the p75 low-affinity neurotrophin receptor in spinal motor neuron degeneration in murine and human amyotrophic lateral sclerosis.
    Lowry KS, Murray SS, McLean CA, Talman P, Mathers S, Lopes EC, Cheema SS.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2001 Sep 17; 2(3):127-34. PubMed ID: 11771768
    [Abstract] [Full Text] [Related]

  • 20. GAB(A) receptors present higher affinity and modified subunit composition in spinal motor neurons from a genetic model of amyotrophic lateral sclerosis.
    Carunchio I, Mollinari C, Pieri M, Merlo D, Zona C.
    Eur J Neurosci; 2008 Oct 17; 28(7):1275-85. PubMed ID: 18973555
    [Abstract] [Full Text] [Related]

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