Prime-Editing of human ACTB in induced pluripotent stem cells to model human ACTB Loss-of-Function diseases and compensatory mechanisms
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Published:2024-03
Issue:
Volume:75
Page:103304
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ISSN:1873-5061
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Container-title:Stem Cell Research
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language:en
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Short-container-title:Stem Cell Research
Author:
Binder Stephanie, Ramachandran Haribaskar, Hildebrandt Barbara, Dobner Jochen, Rossi AndreaORCID
Reference10 articles.
1. Anzalone, A. V., Randolph, P. B., Davis, J. R., Sousa, A. A., Koblan, L. W., Levy, J. M., Chen, P. J., Wilson, C., Newby, G. A., Raguram, A., & Liu, D. R. (2019). Search-and-replace genome editing without double-strand breaks or donor DNA. Nature 2019 576:7785, 576(7785), 149–157. 10.1038/s41586-019-1711-4. 2. ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder;Cuvertino;Am. J. Hum. Genet.,2017 3. Genetic compensation triggered by mutant mRNA degradation;El-Brolosy;Nature,2019 4. CHOPCHOP v3: Expanding the CRISPR web toolbox beyond genome editing;Labun;Nucleic Acids Res.,2019 5. Minimap2: Pairwise alignment for nucleotide sequences;Li;Bioinformatics,2018
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