The Why Files on MSN4h
The Genetic Arms Race | How CRISPR and AI Destroy the WorldHow CRISPR and AI Destroy the World Imagine a world where the genetic code is as easy to edit as a simple copy-and-paste.
Experts hailed exciting news for some people with sickle cell disease in England as the health watchdog decided to grant ...
News Medical on MSN6h
Researchers create random versions of human genomes to study diseaseThe most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more resilient to significant structural changes than was previously thought.
1don MSN
Australian cancer researchers are the first to establish a next-generation gene-editing tool for modeling and interrogating ...
A GROUNDBREAKING genetic treatment with the potential to cure sickle cell disease will be rolled out on the NHS. The one-off ...
Vertex Pharmaceuticals (VRTX) stock gains as England opts to reimburse its CRSPR (CRSP)-partnered gene therapy Casgevy to ...
It’s a new way to create “bi-paternal” mice that can survive to adulthood—but human applications are still a long way off.
ZME Science on MSN1d
Scientists Create Mice with Two Fathers in a Genetic Breakthrough That Could Save Endangered SpeciesResearchers use CRISPR to overcome seemingly insurmontable reproductive barriers — but that doesn't mean this could work for ...
A £1.65 million treatment has been approved for use for some NHS patients, offering some with an inherited blood disorder ...
The UK’s Medicines and Healthcare Regulatory Agency (MHRA) approved Casgevy for sickle cell disease in 2023, followed by ...
NHS officials estimate that around 50 people a year will receive treatment now that it has been approved for use for certain ...
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