Results 1-4 of 4 in Mice, Mutant
  1. the mutation on the NOD background was created using CRISPR/CAS9 whereas the 3 strains where the KO ... used CRISPR to target the Zbtb32 gene for deletion directly in NOD mice and characterized the mutant ... NOD mice, we introduced a targeted deletion using CRISPR/CAS9 techniques. The creation of mutant NOD ...
  2. ... investigated the in vivo function of Fank1. Methods. In this study, we generated Fank1-knockout mice using the CRISPR/Cas9 system. We then investigated the phenotype and in vivo function of Fank1. Testes and epididymis tissues ...
    Date: 1969-12-31T19:00:18-0500
  3. Both targeted traps (tm1a) and null (tm1b and CRISPR induced deletions) alleles are employed ... insertion allele, compared with 20 containing exon deletions (19 tm1b and 1 CRISPR). With either group ...
  4. of the SNARE protein family. Using CRISPR/Cas9 to create a HeLa-VAMP7 knockout cell line together with knockout ... used CRISPR/Cas9 genome editing technology to generate VAMP7 knockout (KO) human HeLa cells and mouse ... editing CRISPR/Cas9 technology to generate VAMP7-knockout (KO) human HeLa cells. This genetically modified ...