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Recently, through combined application with the CRISPR-Cas9-based base editor, this approach allowed us to characterize individual residues critical for the function of DND1 that is an essential gene in PGC development, 22 in which, a CAG promoter showed to have a high mutagenesis efficiency in vivo

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reported that [Ser (2) exendin (1-9)], a GLP-1R agonist, significantly attenuated kainic acid-induced apoptosis in the CA3 region of the hippocampus (117)