One year after receiving CRISPR gene editing therapy at CHOP, a Delaware County baby is thriving, and doctors want to expand ...
"Gene editing takes centre stage in FDA’s new rare disease approval pathway" was originally created and published by ...
Engineers at the University of Pennsylvania and Rice University have refined a technology for editing individual genetic ...
The framework, first introduced by FDA Commissioner Marty Makary and Center for Biologics Evaluation and Research head Vinay ...
FDA Commissioner Marty Makary says the agency wants to remove barriers for patients suffering from rare genetic conditions.
Researchers have found that a new base-editing gene therapy can help treat a rare neurodevelopmental disorder called Snijders Blok–Campeau syndrome caused by mutations in the CHD3 gene. A specialized ...
Vector-borne diseases (VBDs) represent a critical challenge in infectious disease control due to their complex transmission dynamics, diverse vector ...
Scientists have long sought to understand why some plants are fragrant powerhouses while others remain subtle. Now, a ...
Humans have been shaping life for thousands of years through farming, breeding, and selective cultivation. But with modern tools like CRISPR, we can now directly edit DNA itself—rewriting the very ...
Gene-editing approaches being developed by two companies show hints that switching off certain genes could dramatically ...
A team of scientists has developed a cutting-edge CRISPR system that can not only combat antibiotic resistance but actively reverse it. This breakthrough could change the course of modern medicine, ...
A woman in her late 20s presented with a 5-year history of progressive fatigue and generalised weakness. Examination revealed signs of premature ageing, anaemia, neuropathy and hepatosplenomegaly.