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A Single CRISPR-Cas9 Deletion Strategy that Targets the Majority of DMD Patients Restores Dystrophin Function in hiPSC-Derived Muscle Cells.
Young CS, Hicks MR, Ermolova NV, Nakano H, Jan M, Younesi S, Karumbayaram S, Kumagai-Cresse C, Wang D, Zack JA, Kohn DB, Nakano A, Nelson SF, Miceli MC, Spencer MJ, Pyle AD. Young CS, et al. Among authors: pyle ad. Cell Stem Cell. 2016 Apr 7;18(4):533-40. doi: 10.1016/j.stem.2016.01.021. Epub 2016 Feb 11. Cell Stem Cell. 2016. PMID: 26877224 Free PMC article.
In Vivo Human Somitogenesis Guides Somite Development from hPSCs.
Xi H, Fujiwara W, Gonzalez K, Jan M, Liebscher S, Van Handel B, Schenke-Layland K, Pyle AD. Xi H, et al. Among authors: pyle ad. Cell Rep. 2017 Feb 7;18(6):1573-1585. doi: 10.1016/j.celrep.2017.01.040. Cell Rep. 2017. PMID: 28178531 Free PMC article.
CRISPR for Neuromuscular Disorders: Gene Editing and Beyond.
Young CS, Pyle AD, Spencer MJ. Young CS, et al. Among authors: pyle ad. Physiology (Bethesda). 2019 Sep 1;34(5):341-353. doi: 10.1152/physiol.00012.2019. Physiology (Bethesda). 2019. PMID: 31389773 Free PMC article. Review.
Beyond the genome: RNA control of stem cells.
Xi H, Pyle A. Xi H, et al. Science. 2019 Nov 8;366(6466):684-685. doi: 10.1126/science.aaz4859. Science. 2019. PMID: 31699921 Free PMC article. No abstract available.
62 results