CRISPR/Cas9-mediated base editing allows to interchange purine bases or pyrimidine bases independent of homology directe...
...CRISPR/Cas9 method. Here we studied differential gene expression from wild type and RNH1 knock out K562 cells by RNA-Seq...
...CRISPR/Cas9 scarring, and single-cell transcriptomics to analyze state and lineage relationships in iPSC-derived systems...
...CRISPR/Cas9 scarring, and single-cell transcriptomics to analyze state and lineage relationships in iPSC-derived systems...
...CRISPR/Cas9 to introduce the P95H mutation to SRSF2 in K562 leukemia cells, generating an isogenic model so that splicin...
...CRISPR strategy. Allele-specific of Sox2 transcripts in heterozygous enhancer-deletion clones showed that the enhancer a...
...CRISPR/Cas9 or lentivirus vector system. Each engineered gene and engineered methods are described as a single alphabet ...
...CRISPR interference (CRISPRi) has been used in human cells lines, however the rules for designing effective guide RNAs (...
...CRISPR/Cas9 to integrate an A>G mutation in the SF3B1 consensus coding sequence to change the 700th codon from lysine to...
...CRISPR-Cas9 corrected isogenic control iPSC (SOD1 E100E) were used as control. Survival analysis indicated that at 44 da...
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