Swedish scientists have reconstructed the face of a 400-year-old woman buried with a padlock on her foot and an iron sickle ...

Hemoglobin is made up of four proteins organized around the iron-carrying heme group. These proteins are called globins, and each hemoglobin molecule has two alpha and two beta-globins.

Feb. 25, 2025 — A bone marrow transplant process is safe and curative for adults with sickle cell disease, according to results of a trial completed at about 20 cancer ... Brains of People With ...

Can we predict that natural selection will weed out genetic disease over time? Sickle-cell trait haplotype distribution shows the genetic advantages of this mutation. In the deoxygenated ...

Doctors noticed that patients who had sickle cell anemia, a serious hereditary blood disease, were more likely to survive malaria, a disease which kills some 1.2 million people every year.

Hydroxyurea Significantly Reduces Infections in Children With Sickle Cell Anemia Jan. 29 ... 2022 — Two proteins ensure that cells can take up iron when needed. If both control proteins are ...

Today, CASGEVY is approved for use in patients with sickle cell disease in the United States and multiple countries in Europe and the Middle East. “It’s an amazing gift to have been able to ...

Sickle cell disease is a genetic blood disorder ... reduces oxidative damage to red blood cells; and improves iron absorption, which can be beneficial in individuals with SCD-related anemia.