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Journal Abstract Search

287 related items for PubMed ID: 29773756

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  • 2. 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; 76(Pt A):35-47. PubMed ID: 27038603
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  • 4. Properties of Glial Cell at the Neuromuscular Junction Are Incompatible with Synaptic Repair in the SOD1G37R ALS Mouse Model.
    Martineau É, Arbour D, Vallée J, Robitaille R.
    J Neurosci; 2020 Sep 30; 40(40):7759-7777. PubMed ID: 32859714
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  • 5. Expression of a Mutant SEMA3A Protein with Diminished Signalling Capacity Does Not Alter ALS-Related Motor Decline, or Confer Changes in NMJ Plasticity after BotoxA-Induced Paralysis of Male Gastrocnemic Muscle.
    Moloney EB, Hobo B, De Winter F, Verhaagen J.
    PLoS One; 2017 Sep 30; 12(1):e0170314. PubMed ID: 28103314
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  • 6. Micro-RNAs secreted through astrocyte-derived extracellular vesicles cause neuronal network degeneration in C9orf72 ALS.
    Varcianna A, Myszczynska MA, Castelli LM, O'Neill B, Kim Y, Talbot J, Nyberg S, Nyamali I, Heath PR, Stopford MJ, Hautbergue GM, Ferraiuolo L.
    EBioMedicine; 2019 Feb 30; 40():626-635. PubMed ID: 30711519
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  • 7. Muscle Fibers Secrete FGFBP1 to Slow Degeneration of Neuromuscular Synapses during Aging and Progression of ALS.
    Taetzsch T, Tenga MJ, Valdez G.
    J Neurosci; 2017 Jan 04; 37(1):70-82. PubMed ID: 28053031
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  • 8. Looking for answers far away from the soma-the (un)known axonal functions of TDP-43, and their contribution to early NMJ disruption in ALS.
    Ionescu A, Altman T, Perlson E.
    Mol Neurodegener; 2023 May 31; 18(1):35. PubMed ID: 37259156
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  • 16. Expression of the axon-guidance protein receptor Neuropilin 1 is increased in the spinal cord and decreased in muscle of a mouse model of amyotrophic lateral sclerosis.
    Körner S, Thau-Habermann N, Kefalakes E, Bursch F, Petri S.
    Eur J Neurosci; 2019 Jun 31; 49(11):1529-1543. PubMed ID: 30589468
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  • 19. Human superoxide dismutase 1 overexpression in motor neurons of Caenorhabditis elegans causes axon guidance defect and neurodegeneration.
    Li J, Li T, Zhang X, Tang Y, Yang J, Le W.
    Neurobiol Aging; 2014 Apr 31; 35(4):837-46. PubMed ID: 24126158
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