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Frontiers in Genome Editing|October 29, 2021
Efficient Targeted Mutagenesis Mediated by CRISPR-Cas12a Ribonucleoprotein Complexes in MaizeShujie Dong, Yinping Lucy Qin, Christopher A Vakulskas, et al.
Stem Cells Translational Medicine|May 23, 2023
Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell ReplacementJessica A Cooke, Andrew P Voigt, Michael A Collingwood, et al.
Nature|April 9, 2025
Reprogramming site-specific retrotransposon activity to new DNA sitesChristopher W Fell, Lukas Villiger, Justin Lim, et al.
Nature Medicine|January 30, 2019
Identification of preexisting adaptive immunity to Cas9 proteins in humansCarsten T Charlesworth, Priyanka S Deshpande, Daniel P Dever, et al.
Science Translational Medicine|June 17, 2021
Development of β-globin gene correction in human hematopoietic stem cells as a potential durable treatment for sickle cell diseaseAnnalisa Lattanzi, Joab Camarena, Premanjali Lahiri, et al.
Blood Advances|December 14, 2023
Genetically corrected RAG2-SCID human hematopoietic stem cells restore V(D)J-recombinase and rescue lymphoid deficiencyMara Pavel-Dinu, Cameron L Gardner, Yusuke Nakauchi, et al.
Nature Communications|June 24, 2021
AsCas12a ultra nuclease facilitates the rapid generation of therapeutic cell medicinesLiyang Zhang, John A Zuris, Ramya Viswanathan, et al.
Nature Biotechnology|November 24, 2022
Drag-and-drop genome insertion of large sequences without double-strand DNA cleavage using CRISPR-directed integrasesMatthew T N Yarnall, Eleonora I Ioannidi, Cian Schmitt-Ulms, et al.
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