It’s a new way to create “bi-paternal” mice that can survive to adulthood—but human applications are still a long way off.
Experts hailed exciting news for some people with sickle cell disease in England as the health watchdog decided to grant ...
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ZME Science on MSNScientists 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 ...
Grafting patches of lab-grown muscle to the surface of the heart could offer a lifeline for people waiting for a transplant.
Around 1,700 people could be eligible for the one-time treatment, which is seen as a less risky alternative to a donor stem ...
A cutting-edge gene therapy has been approved for NHS use for some patients with severe sickle cell disease. Casgevy, also ...
People in England to benefit from groundbreaking one-off gene therapy for severe sickle cell disease approved by NICE ...
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Pharmaceutical Technology on MSNNHS England to offer Casgevy for sickle cell disease patientsThe UK’s Medicines and Healthcare Regulatory Agency (MHRA) approved Casgevy for sickle cell disease in 2023, followed by ...
One sickle cell patient told ITV News the new gene therapy being rolled out for use on the NHS means they "finally have something to look towards". | ITV National News ...
Base editing utilizes enzymes to modify single amino acids at the most foundational unit of DNA, called a base.
A GROUNDBREAKING genetic treatment with the potential to cure sickle cell disease will be rolled out on the NHS. The one-off ...
The Exa-cel gene therapy treatment is at the forefront of medical technology. It takes the person’s DNA and “edits” out the faulty sickle gene. It’s expensive, too. According to the manufacturer, ...
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