Scientists at the San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Milan, have found that gene editing using ...

Researchers have identified an early postnatal window that allows gene transfer to circulating blood stem cells, advancing ...

New gene therapy improves the life of 18-year-old with Sickle Cell Disease which affects 5,000 New Jersey residents living ...

KJ Muldoon, a 10-month-old baby, was diagnosed with the genetic disease carbamoyl-phosphate synthetase 1 deficiency after he ...

Discover how gene editing and lab-grown meat are revolutionising healthcare and food in 2025, offering personalised ...

With gene therapy offering new hope for thalassemia, experts urge Indian govt to invest in early diagnosis, genetic testing, ...

Cell and gene therapy (C&GT) is set to revolutionise treatment of complex diseases, offering new possibilities for patients.

Thalassemia, a group of inherited blood disorders characterized by reduced or abnormal hemoglobin production, continues to ...

In medical breakthrough, a baby diagnosed with rare genetic disorder is thriving after customized CRISPR gene editing therapy ...

China announced Wednesday that four children with thalassemia, a severe genetic blood disorder usually diagnosed in toddlers, have been cured using a domestically developed DNA base editing therapy ..

A personalized gene editing ... The first CRISPR-based therapy, Casgevy (exagamglogene autotemcel), was approved in December 2023 to treat patients with sickle cell disease and in January 2024 to ...