CRISPR/Cas9 genome editing is a promising therapeutic technique, which makes precise
and rapid gene editing technology possible on account of its high sensitivity and efficiency …

CRISPR/Cas9 genome editing platforms are widely applied as powerful tools in basic
research and potential therapeutics for genome regulation. The appropriate alternative of …

The CRISPR-Cas9 technology has changed the landscape of genome editing and has
demonstrated extraordinary potential for treating otherwise incurable diseases. Engineering …

CRISPR/Cas9 is an effective gene editing tool with broad applications for the prevention or
treatment of numerous diseases. It depends on CRISPR (clustered regularly interspaced …

Background The clustered regularly interspaced short palindromic repeats (CRISPR) and
Cas9 protein system is a revolutionary tool for gene therapy. Despite promising reports of …

CRISPR/dCas9 systems can precisely control endogenous gene expression without
interrupting host genomic sequence and have provided a novel and feasible strategy for the …

CRISPR/Cas systems (clustered regularly interspaced short palindromic repeats) have
emerged as powerful tools to manipulate the genome for both research and therapeutic …

Abstract CRISPR/Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats) is
today one of the most reliable method for gene-editing, supporting previous gene therapies …

The CRISPR–Cas9 system is widely used for target-specific genome engineering. CRISPR–
Cas12a (Cpf1) is one of the CRISPR effectors that controls target genes by recognizing …

The RNA-guided endonuclease Cas9 (CRISPR-Cas9) genome editing system has been
widely used for biomedical research and holds great potential for therapeutic applications in …