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Development of abnormalities at the neuromuscular junction in the SOD1-G93A mouse model of ALS : dysfunction then disruption of postsynaptic structure precede overt motor symptoms

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dc.contributor.authorMcIntosh, Jayne
dc.contributor.authorMekrouda, Imane
dc.contributor.authorDashti, Maryam
dc.contributor.authorGiuraniuc, Claudiu V.
dc.contributor.authorBanks, Robert W.
dc.contributor.authorMiles, Gareth B.
dc.contributor.authorBewick, Guy S.
dc.contributor.institutionUniversity of Aberdeen.Medicine, Medical Sciences & Nutritionen
dc.contributor.institutionUniversity of Aberdeen.Neuroscienceen
dc.contributor.institutionUniversity of Aberdeen.Institute of Medical Sciencesen
dc.contributor.institutionUniversity of Aberdeen.Medical Sciencesen
dc.date.accessioned2023-10-18T14:28:00Z
dc.date.available2023-10-18T14:28:00Z
dc.date.issued2023-05-19
dc.descriptionFunding This project was funded by a PhD studentship to JM from Motor Neurone Disease Scotland, on grant number RGB3753 to GB and GM.en
dc.description.statusPeer revieweden
dc.format.extent16
dc.format.extent6495017
dc.identifier237068001
dc.identifier22af9be0-73d3-43af-80b2-44c4b6662624
dc.identifier37273905
dc.identifier85161088402
dc.identifier.citationMcIntosh, J, Mekrouda, I, Dashti, M, Giuraniuc, C V, Banks, R W, Miles, G B & Bewick, G S 2023, 'Development of abnormalities at the neuromuscular junction in the SOD1-G93A mouse model of ALS : dysfunction then disruption of postsynaptic structure precede overt motor symptoms', Frontiers in Molecular Neuroscience, vol. 16, 1169075. https://doi.org/10.3389/fnmol.2023.1169075en
dc.identifier.doi10.3389/fnmol.2023.1169075
dc.identifier.issn1662-5099
dc.identifier.otherBibtex: 10.3389/fnmol.2023.1169075
dc.identifier.otherBibtex: 10.3389/fnmol.2023.1169075
dc.identifier.otherORCID: /0000-0001-8266-7797/work/145600620
dc.identifier.urihttps://hdl.handle.net/2164/21949
dc.identifier.vol16en
dc.language.isoeng
dc.relation.ispartofFrontiers in Molecular Neuroscienceen
dc.subjectneuromuscular junctionen
dc.subjectmotor neuron diseaseen
dc.subjectneuromuscular transmissionen
dc.subjectSOD1-G93Aen
dc.subjectALSen
dc.subjectacetylcholine receptoren
dc.subjectmouseen
dc.subjectR Medicineen
dc.subjectOtheren
dc.subjectRGB3753en
dc.subject.lccRen
dc.titleDevelopment of abnormalities at the neuromuscular junction in the SOD1-G93A mouse model of ALS : dysfunction then disruption of postsynaptic structure precede overt motor symptomsen
dc.typeJournal articleen

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