An in vivo base editing approach targeting the PRNP gene led to a 52% increase in the lifespan of mouse models inoculated with the most common sporadic and genetic types of human pathogenic prion ...

Gene therapy has been available since 2022 for ... “We would call that the low-to-mild range. By definition, there are people that are higher and lower.” Patients must have serious disease ...

How CRISPR therapy could cure everything from cancer to infertility The imminent approval of the world's first CRISPR treatment for sickle cell disease is just the start: soon this gene-editing ...

Ministry of Finance has issued Notification No. 02/2025–Integrated Tax (Rate) on January 16, 2025, under the Integrated Goods ...

Patients battling cancer and rare diseases are expected to take a sigh of relief as the Government of India has exempted gene ...

"Our study shows that we can deliver genes to renal tubules and podocytes [highly specialized cells] in the kidney, the two important target cell types for gene therapy, and while there is a ...