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Inhibition of FLT1 ameliorates muscular dystrophy phenotype by increased vasculature in a mouse model of Duchenne muscular dystrophy.
PLoS Genet. 2019 Dec 26;15(12):e1008468. doi: 10.1371/journal.pgen.1008468. eCollection 2019 Dec.
PLoS Genet. 2019.
PMID: 31877123
Free PMC article.
Vascular-targeted therapies for Duchenne muscular dystrophy.
Ennen JP, Verma M, Asakura A.
Ennen JP, et al.
Skelet Muscle. 2013 Apr 23;3(1):9. doi: 10.1186/2044-5040-3-9.
Skelet Muscle. 2013.
PMID: 23618411
Free PMC article.
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