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Loss of sarcospan exacerbates pathology in mdx mice, but does not affect utrophin amelioration of disease.
Hum Mol Genet. 2021 Apr 26;30(3-4):149-159. doi: 10.1093/hmg/ddaa264.
Hum Mol Genet. 2021.
PMID: 33432327
Free PMC article.
Mouse models of two missense mutations in actin-binding domain 1 of dystrophin associated with Duchenne or Becker muscular dystrophy.
McCourt JL, Talsness DM, Lindsay A, Arpke RW, Chatterton PD, Nelson DM, Chamberlain CM, Olthoff JT, Belanto JJ, McCourt PM, Kyba M, Lowe DA, Ervasti JM.
McCourt JL, et al.
Hum Mol Genet. 2018 Feb 1;27(3):451-462. doi: 10.1093/hmg/ddx414.
Hum Mol Genet. 2018.
PMID: 29194514
Free PMC article.
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Multi-omics analysis of sarcospan overexpression in mdx skeletal muscle reveals compensatory remodeling of cytoskeleton-matrix interactions that promote mechanotransduction pathways.
McCourt JL, Stearns-Reider KM, Mamsa H, Kannan P, Afsharinia MH, Shu C, Gibbs EM, Shin KM, Kurmangaliyev YZ, Schmitt LR, Hansen KC, Crosbie RH.
McCourt JL, et al.
Skelet Muscle. 2023 Jan 6;13(1):1. doi: 10.1186/s13395-022-00311-x.
Skelet Muscle. 2023.
PMID: 36609344
Free PMC article.
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Distinct mechanical properties in homologous spectrin-like repeats of utrophin.
Rajaganapathy S, McCourt JL, Ghosal S, Lindsay A, McCourt PM, Lowe DA, Ervasti JM, Salapaka MV.
Rajaganapathy S, et al. Among authors: mccourt jl.
Sci Rep. 2019 Mar 26;9(1):5210. doi: 10.1038/s41598-019-41569-4.
Sci Rep. 2019.
PMID: 30914715
Free PMC article.
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In vitro stability of therapeutically relevant, internally truncated dystrophins.
McCourt JL, Rhett KK, Jaeger MA, Belanto JJ, Talsness DM, Ervasti JM.
McCourt JL, et al.
Skelet Muscle. 2015 Apr 28;5:13. doi: 10.1186/s13395-015-0040-z. eCollection 2015.
Skelet Muscle. 2015.
PMID: 25954502
Free PMC article.
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Modifications of the computer programme SCOGS.
McBryde WA, McCourt JL.
McBryde WA, et al. Among authors: mccourt jl.
Talanta. 1972 Nov;19(11):1486-7. doi: 10.1016/0039-9140(72)80154-1.
Talanta. 1972.
PMID: 18961212
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