Gene therapies to treat rheumatoid arthritis have evolved slowly, but one is ready to move into human trials and an ...

Racial disparities in mortality are increasing. This article explores how the production of DNA-edited ethnically diverse ...

Nice It works by editing the faulty gene in a patient’s own stem cells. Cells are taken from a patient to a laboratory where the Crispr technology is used. The edited cells are then infused back ...

Treatment for sickle cell disease, the most common inherited blood disorder in Kenya, has been approved for use in England for older children and adults with a severe form of the disease.The treatment ...

A mouse with two dads — or a bi-paternal mouse — has made it to adulthood. Several mice, in fact. As detailed in a study published in the journal Cell Stem Cell, scientists achieved this feat of ...

Stem cell engineering and CRISPR were used to create mice with two male parents. Could we use this technique on humans?

The concept of biological reproduction between same-sex individuals in mammals has always been deemed impossible. However, ...

Fate Therapeutics uses iPSC and gene editing to offer scalable off-the-shelf therapies. Read more to see why I rate FATE ...

With the addition of Casgevy, Children’s Hospital Los Angeles now offers two gene therapies for sickle cell, the first being Lyfgenia.

A gene-editing therapy for sickle cell disease, with a price tag of £1.65m, is to be offered to patients on the NHS in ...

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 ...