FVIII, the blood clotting protein missing in hemophilia A, adopts multiple shapes, making it more likely to be targeted by ...

Genetic testing for hereditary cancer unexpectedly uncovered a case of myelodysplastic syndrome (MDS), highlighting the need ...

Researchers from the Centenary Institute have uncovered a reason why some people with hemophilia A develop resistance to ...

Genentech’s short film draws on the experiences of multiple families caring for children with hemophilia A, seeking to ...

Cell and gene therapies harbor great hopes for biomedicine. They are becoming increasingly important for diseases that are ...

A man’s acquired hemophilia coincided with a rare liver disease, a connection that had not been reported before, per a case ...

Mobile genetic elements such as CAST provide an idea of the coding potential of nature for genome manipulation. It is in the ...

Treatment options for children with hemophilia A have expanded with the FDA approval of Bayer's Jivi antihemophilic factor (recombinant), PEGylated-aucl for the treatment of pediatric patients between ...

Minister emphasizes raising awareness about genetic disorders like thalassemia, sickle cell anemia, and hemophilia for timely ...

Objectives X chromosome has been considered as a risk factor for SLE, which is a prototype of autoimmune diseases with a significant sex difference (female:male ratio is around 9:1). Our study aimed ...

Hemophilia A manifests through several characteristic symptoms that vary in severity depending on Factor VIII levels in the bloodstream. Even with the same genetic alteration, symptom presentation ...