Histological Assessment of Gene Therapy in the Canine DMD Model
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Publisher
Springer US
Link
https://link.springer.com/content/pdf/10.1007/978-1-0716-2772-3_16
Reference12 articles.
1. Duan D, Goemans N, Takeda S et al (2021) Duchenne muscular dystrophy. Nat Rev Dis Primer 7:13
2. McGreevy JW, Hakim CH, McIntosh MA et al (2015) Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy. Dis Model Mech 8(3):195–213. https://doi.org/10.1242/dmm.018424
3. Wasala NB, Chen SJ, Duan D (2020) Duchenne muscular dystrophy animal models for high-throughput drug discovery and precision medicine. Expert Opin Drug Discov 15:1–14. https://doi.org/10.1080/17460441.2020.1718100
4. Lai Y, Thomas GD, Yue Y et al (2009) Dystrophins carrying spectrin-like repeats 16 and 17 anchor nNOS to the sarcolemma and enhance exercise performance in a mouse model of muscular dystrophy. J Clin Invest 119(3):624–635. https://doi.org/10.1172/JCI36612
5. Lai Y, Zhao J, Yue Y et al (2013) alpha2 and alpha3 helices of dystrophin R16 and R17 frame a microdomain in the alpha1 helix of dystrophin R17 for neuronal NOS binding. Proc Natl Acad Sci U S A 110(2):525–530. https://doi.org/10.1073/pnas.1211431109
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