Controlling the activity of specific genes in the laboratory through the editing of their epigenetic marks is now a reality ...

Sickle cell disease is the most common genetic blood disorder in the world, most prevalent among people of colour. On World Sickle Cell Awareness Day, doctors, patients and grieving families are ...

In the UK, the two most common haemoglobinopathies are sickle cell disease and beta thalassaemia. This article, the first of four in a series on sickle cell disease and beta thalassaemia, outlines ...

Victoria Gray, the first person cured of sickle cell using CRISPR gene editing therapies, spoke in Fargo about her journey and the need to lower the $2M treatment cost.

Sickle Cell Disease Pipeline 2025: Key Developments, Emerging Therapies, and Clinical Trials Detailed Analysis by DelveInsight | Sanofi, Novartis AG, Bluebird Biotech, Pfizer Inc., Aruvant Sciences ...

WATCH: A story of love and sacrifice helps heal a young girl with sickle cell disease Alijiah is 10 years old and got tested to see if he was a match to donate bone marrow to Aliyah.

Robert F. Kennedy Jr. announces sickle-cell treatment program in Charleston while assuring SC Sen. Tim Scott that federal minority health effort will continue.

Sickle cell experts say the future of a critical data collection program is in flux after staff at the CDC's Division of Blood Disorders were placed on administrative leave without a clear future ...

The House unanimously passed bipartisan legislation Wednesday in response to a scandal involving a former Colorado Bureau of Investigation DNA analyst.

Addressing sickle cell disease requires urgent action, starting with improving access to comprehensive care and advocating for affordable or free bone marrow transplants, just like in the UK.

The underutilization of disease-modifying therapy by people with sickle cell disease is “persistent and alarming,” according to an analysis of real-world data.The findings, presented ...

A new discovery offers hope for Huntington’s disease. This discovery provides hope that a DNA repair process may help slow or stop disease progression.