CRISPR-Cas9 is not the first method available to scientists for modifying DNA; it is by far, however, the easiest to use. With CRISPR-Cas9, the crRNA/tracrRNA sequence or an artificial guide RNA ...

Now, using state-of-the-art technology, researchers from Children's Hospital of Philadelphia (CHOP) have identified several specific steps needed for CRISPR to become active and perform its gene ...

Using state-of-the-art technology, researchers have identified several specific steps needed for CRISPR to become active and perform its gene editing function. These preclinical findings could ...

Rotten tomatoes no more: growing sweeter tomatoes is possible by editing just two of the fruit’s genes. Deleting the genes ...

Now, using state-of-the-art technology, researchers from Children's Hospital of Philadelphia (CHOP) have identified several specific steps needed for CRISPR to become active and perform its gene ...

The essence of CRISPR is simple: it’s a way of finding a specific bit of DNA inside a cell. After that, the next step in CRISPR gene editing is usually to alter that piece of DNA. However ...

CRISPR/Cas-initiated HDR in mouse embryos will be used to generate founder animals ... The requested information must be provided to the core and the core must approve the approach prior to proceeding ...

Scientists around the world are already using the powerful new CRISPR technique to treat disease, modify plants and animals, and even create designer babies. Here's everything you need to know.

CRISPR/Cas-initiated HR in mouse embryos will be used to generate founder animals harboring inserted sequence targeted to the ROSA26 locus. The targeting will be done in embryos using microinjection ...