In this study monoclonal cell lines carrying mutations in snoRNA genes (SNORD74, SNORD75, SNORD77, SNORD80) were obtaine...
CRISPR-Cas9 was used to generate HNF1a mutants (+/- and -/-) in human embryonic stem cell lines and used an in vitro dif...
...CRISPR (KO), unedited controls (WT), or cells transfected with GFP instead of CRISPR. Libraries were generated with a 4n...
...CRISPR/Cas9 mediated 1.4kb deletion of the genomic region harboring rs7903146 in the HCT116 cell line followed by global...
...CRISPR genetic screens were started 10 days post transduction. >1000-fold coverage of mutagenized cells (libraries A and...
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 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 ...
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