List/Grid Mouse

Researchers cured mice of a rare liver disorder caused by a single genetic mutation using CRISPR-cas9

Using a new gene-editing system based on bacterial proteins, MIT researchers have cured mice of a rare liver disorder caused by a single genetic mutation. 

Dual sgRNAs facilitate CRISPR/Cas9 mediated mouse genome targeting

The bacterial CRISPR/Cas9 system has been shown recently to be a versatile RNA-guided mammalian genome modification system. One-step generation of mouse genome targeting has been achieved ...

Researchers developed a method to create a comprehensive library of mutations across all genes in the mouse genome.

Researchers have developed a method to create a comprehensive library of mutations across all genes in the mouse genome.
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