At present, the idea of genome modification has revolutionized the modern therapeutic
research era. Genome modification studies have traveled a long way from gene …

Clustered regularly interspaced short palindromic repeat (CRISPR) and their associated
protein (Cas-9) is the most effective, efficient, and accurate method of genome editing tool in …

The CRISPR-Cas9 (clustered regularly interspaced short palindromic repeats with CRISPR-
associated protein 9) system is a genome editing system that is easy to design, highly …

Gene editing technology has completely transformed the life sciences and medical
treatment, because it makes precise and stable genetic alterations to genomic sequences …

Drug discovery is a complex enterprise bringing together a variety of skills and techniques.
Oncology drug discovery has taken advantage of cancer genetics to identify drug molecules …

We are advancing a novel strategy for the treatment of solid tumors by employing CRISPR-
directed gene editing to reduce levels of standard of care required to halt or reverse the …

Abstract CRISPR (Clustered Regularly Interspaced Short Palindromic Repeat) is one of the
hallmark of biological tools, contemplated as a valid and hopeful alternatives to genome …

With the expansion of the microbiology field of research, a new genome editing tool arises
from the biology of bacteria that holds the promise of achieving precise modifications in the …

The CRISPR/Cas9 system is an RNA-based adaptive immune system in bacteria and
archaea. Various studies have shown that it is possible to target a wide range of human …

CRISPR-Cas9, which is characterized by simplicity, effectiveness and direct targeting, can
be used to treat some incurable genetic diseases by editing DNA sequence. In recent years …