Sickle cell disease (SCD) and beta thalassaemia belong to a group of inherited conditions known as haemoglobinopathies, where the haemoglobin in red blood cells (RBCs) is affected by a genetic ...

A 69-year-old woman was referred to the retina service for abnormal posterior segment findings.The patient’s medical history ...

Discover a revolutionary gene therapy method using CRISPR to reactivate dormant genes, offering hope for sickle cell and beta-thalassemia patients.

Faulty hemoglobin The new strategy offers hope for patients with sickle cell disease and beta-thalassemia. In these genetic blood diseases, the adult globin gene is broken. This causes the protein ...

A high-level overview of Taysha Gene Therapies, Inc. (TSHA) stock. View (TSHA) real-time stock price, chart, news, analysis, analyst reviews and more.

Transcription of Wnt target genes is regulated by nuclear β-catenin. How does β-catenin interact with chromatin to regulate Wnt target gene transcription?

Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structural alterations were studied to identify the alpha-globin gene mutations present in the population of ...

Tocopheryl acetate is a form of vitamin E that’s often found in skin care products and dietary supplements. Learn about its potential benefits and risks.

However, if alpha-emitting materials are taken into the body by breathing, eating, or drinking, they can expose internal tissues directly and may, therefore, cause biological damage. Beta radiation ...

Sickle cell anemia is a blood disorder that affects people who have a defect in the beta globin gene. As a result, the hemoglobin molecule (which carries oxygen in red blood cells) is shaped ...