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Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice.
Mol Ther Methods Clin Dev. 2021 Mar 3;21:144-160. doi: 10.1016/j.omtm.2021.02.024. eCollection 2021 Jun 11.
Mol Ther Methods Clin Dev. 2021.
PMID: 33850950
Free PMC article.
Erratum: Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice.
Hamm SE, Fathalikhani DD, Bukovec KE, Addington AK, Zhang H, Perry JB, McMillan RP, Lawlor MW, Prom MJ, Vanden Avond MA, Kumar SN, Coleman KE, Dupont JB, Mack DL, Brown DA, Morris CA, Gonzalez JP, Grange RW.
Hamm SE, et al. Among authors: bukovec ke.
Mol Ther Methods Clin Dev. 2021 Nov 5;23:460. doi: 10.1016/j.omtm.2021.10.005. eCollection 2021 Dec 10.
Mol Ther Methods Clin Dev. 2021.
PMID: 34820472
Free PMC article.
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Laminin-111 protein therapy after disease onset slows muscle disease in a mouse model of laminin-α2 related congenital muscular dystrophy.
Barraza-Flores P, Bukovec KE, Dagda M, Conner BW, Oliveira-Santos A, Grange RW, Burkin DJ.
Barraza-Flores P, et al. Among authors: bukovec ke.
Hum Mol Genet. 2020 Aug 3;29(13):2162-2170. doi: 10.1093/hmg/ddaa104.
Hum Mol Genet. 2020.
PMID: 32472139
Free PMC article.
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A novel ex vivo protocol to mimic human walking gait: implications for Duchenne muscular dystrophy.
Bukovec KE, Hu X, Borkowski M, Jeffery D, Blemker SS, Grange RW.
Bukovec KE, et al.
J Appl Physiol (1985). 2020 Oct 1;129(4):779-791. doi: 10.1152/japplphysiol.00002.2020. Epub 2020 Sep 3.
J Appl Physiol (1985). 2020.
PMID: 32881620
Free PMC article.
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