| CRISPR Medicine | This is an overview of our interviews
New research on molecular genetic control of insect vectors of viral diseases led to the development of a CRISPR-based precision-guided sterile insect...
Epigenome editing with CRISPR is one of the new kids on the block. Dr. Nikolajs Zeps, adjunct professor at Monash University and partner at Chrysalis...
Last year, the CasĪ¦ family of CRISPR endonucleases (also know as Cas12j) was discovered as a highly compact CRISPR system in ancient giant phages. At...
Poseida Therapeutics' unique approach to gene editing and delivery addresses some of the major obstacles faced within cell and gene therapy...
To make CRISPR medicines available for patients with genetic diseases, size matters. In a seminal article published today in Molecular Cell,...
New research on X-linked Agammaglobulinemia has led to the development of a potential gene therapy cure for this disease - or as Dr David Gray...
In a recent landmark paper, Dr Bo Wang and his colleagues at Kyoto University used CRISPR to generate triple-knockout, hypoimmunogenic T cells from...
Chinese researchers have invented a novel system, AdBlue, to construct adenovirus vectors for CRISPR-Cas9 mediated gene editing. The novel system is...
