...CRISPR/Cas9-derived heterozygous or homozygous R138X lines were differentiated into stem cell-derived islet-like cluster...
...CRISPR/Cas9 genome editing to generate Slc13a5R337* knock-in mice that terminate NaCT translation at the Arg337 codon, w...
...CRISPR-Cas9 or prolyl hydroxylase domain inhibitors to evaluate FAP cell differentiation. TTDN induced significant capil...
...CRISPR spacer matching evidence, suggesting prior exposure to the relevant sequence space. None of the genomes met our p...
...CRISPR, CAR-T cells, and bispecific antibodies, as well as targeted delivery systems to enhance efficacy and reduce toxi...
...CRISPR). Control ( Lmod1 WT ) and VSMC-restricted Lmod1 knockout ( Lmod1 SMKO ) mice were subjected to various atherogen...
...CRISPRi sign-bias-corrected excess than indirect pairs. Gene-level CRISPRi validation on Replogle K562 and the noncancer...
...CRISPR/Cas9 technology was used to knock down the expression of SARM1 and SNPH in mouse 661W retinal ganglion cells, res...
...CRISPR/Cas9 system has been effective in knocking out both the OsHPP04 gene in rice to confer resistance against Meloido...
...CRISPR-Cas9 knockout of SMARCAL1 with wild-type and helicase-dead rescue in A549/H1299 cell lines, and primary human CXC...
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