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2011 1
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Targeted transcriptional modulation with type I CRISPR-Cas systems in human cells.
Pickar-Oliver A, Black JB, Lewis MM, Mutchnick KJ, Klann TS, Gilcrest KA, Sitton MJ, Nelson CE, Barrera A, Bartelt LC, Reddy TE, Beisel CL, Barrangou R, Gersbach CA. Pickar-Oliver A, et al. Nat Biotechnol. 2019 Dec;37(12):1493-1501. doi: 10.1038/s41587-019-0235-7. Epub 2019 Sep 23. Nat Biotechnol. 2019. PMID: 31548729 Free PMC article.
Long-term evaluation of AAV-CRISPR genome editing for Duchenne muscular dystrophy.
Nelson CE, Wu Y, Gemberling MP, Oliver ML, Waller MA, Bohning JD, Robinson-Hamm JN, Bulaklak K, Castellanos Rivera RM, Collier JH, Asokan A, Gersbach CA. Nelson CE, et al. Nat Med. 2019 Mar;25(3):427-432. doi: 10.1038/s41591-019-0344-3. Epub 2019 Feb 18. Nat Med. 2019. PMID: 30778238 Free PMC article.
Genome Engineering for Personalized Arthritis Therapeutics.
Adkar SS, Brunger JM, Willard VP, Wu CL, Gersbach CA, Guilak F. Adkar SS, et al. Trends Mol Med. 2017 Oct;23(10):917-931. doi: 10.1016/j.molmed.2017.08.002. Epub 2017 Sep 5. Trends Mol Med. 2017. PMID: 28887050 Free PMC article. Review.
54 results