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Page 1
Gene and Base Editing as a Therapeutic Option for Cystic Fibrosis-Learning from Other Diseases.
Genes (Basel). 2019 May 21;10(5):387. doi: 10.3390/genes10050387.
Genes (Basel). 2019.
PMID: 31117296
Free PMC article.
Review.
Use of adenine base editing and homology-independent targeted integration strategies to correct the cystic fibrosis causing variant, W1282X.
Mention K, Cavusoglu-Doran K, Joynt AT, Santos L, Sanz D, Eastman AC, Merlo C, Langfelder-Schwind E, Scallan MF, Farinha CM, Cutting GR, Sharma N, Harrison PT.
Mention K, et al.
Hum Mol Genet. 2023 Nov 17;32(23):3237-3248. doi: 10.1093/hmg/ddad143.
Hum Mol Genet. 2023.
PMID: 37649273
Free PMC article.
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Comparison of Cas9 and Cas12a CRISPR editing methods to correct the W1282X-CFTR mutation.
Santos L, Mention K, Cavusoglu-Doran K, Sanz DJ, Bacalhau M, Lopes-Pacheco M, Harrison PT, Farinha CM.
Santos L, et al. Among authors: mention k.
J Cyst Fibros. 2022 Jan;21(1):181-187. doi: 10.1016/j.jcf.2021.05.014. Epub 2021 Jun 5.
J Cyst Fibros. 2022.
PMID: 34103250
Free article.
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