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Lambert-Eaton myasthenic syndrome: mouse passive-transfer model illuminates disease pathology and facilitates testing therapeutic leads.
Ann N Y Acad Sci. 2018 Jan;1412(1):73-81. doi: 10.1111/nyas.13512. Epub 2017 Nov 10.
Ann N Y Acad Sci. 2018.
PMID: 29125190
Free PMC article.
Review.
In Search of a Cure: The Development of Therapeutics to Alter the Progression of Spinal Muscular Atrophy.
Ojala KS, Reedich EJ, DiDonato CJ, Meriney SD.
Ojala KS, et al.
Brain Sci. 2021 Feb 5;11(2):194. doi: 10.3390/brainsci11020194.
Brain Sci. 2021.
PMID: 33562482
Free PMC article.
Review.
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Potentiation of neuromuscular transmission by a small molecule calcium channel gating modifier improves motor function in a severe spinal muscular atrophy mouse model.
Ojala KS, Kaufhold CJ, Davey MR, Yang D, Liang M, Wipf P, Badawi Y, Meriney SD.
Ojala KS, et al.
Hum Mol Genet. 2023 May 18;32(11):1901-1911. doi: 10.1093/hmg/ddad019.
Hum Mol Genet. 2023.
PMID: 36757138
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A high-affinity, partial antagonist effect of 3,4-diaminopyridine mediates action potential broadening and enhancement of transmitter release at NMJs.
Ojala KS, Ginebaugh SP, Wu M, Miller EW, Ortiz G, Covarrubias M, Meriney SD.
Ojala KS, et al.
J Biol Chem. 2021 Jan-Jun;296:100302. doi: 10.1016/j.jbc.2021.100302. Epub 2021 Jan 17.
J Biol Chem. 2021.
PMID: 33465376
Free PMC article.
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