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 ...

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.

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 ...

Sickle cell anemia, first described in 1910, primarily affects people of African, Mediterranean and Middle Eastern descent.

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.