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Hemoglobin subunit beta. In human, the HBB gene is located on chromosome 11 at position p15.5. Hemoglobin subunit beta ( beta globin, β-globin, haemoglobin beta, hemoglobin beta) is a globin protein, coded for by the HBB gene, which along with alpha globin ( HBA ), makes up the most common form of haemoglobin in adult humans, hemoglobin A (HbA ...
Napoleon Bonaparte (born Napoleone di Buonaparte; [1] [b] 15 August 1769 – 5 May 1821), later known by his regnal name Napoleon I, was a French emperor and military commander who rose to prominence during the French Revolution and led successful campaigns during the Revolutionary Wars.
The human disease sickle cell anemia is caused by a genetic mutation in the codon for the sixth amino acid of the blood protein beta-hemoglobin.The normal DNA sequence G-A-G codes for the amino acid glutamate, while the mutation changes the middle adenine to a thymine, leading to the sequence G-T-G (G-U-G in the mRNA).
Southeast Asian ovalocytosis. It is hereditary hemolytic anaemia in which the red blood cell is oval-shaped. The primary defect in SAO differs significantly from other forms of elliptocytosis in that it is a defect in the gene coding for a protein that is not directly involved in the cytoskeleton scaffolding of the cell.
Occupation. Member of Provincial Parliament. Andrea Daria Khanjin [1] (born December 27, 1987, in Moscow) [2] is a Canadian politician who was elected to the Legislative Assembly of Ontario since the 2018 general election representing the riding of Barrie-Innisfil. [3] [4] [5] She has been the longest serving Deputy Government House Leader [6 ...
Molar mass. 146 232.04 g·mol −1. Crizanlizumab, sold under the brand name Adakveo among others, is a monoclonal antibody medication that binds to P-selectin. [3] It is a medication used to reduce the frequency of vaso-occlusive crisis in people aged 16 years and older who have sickle cell anemia. [3] [4] [6] It is given by injection into a vein.
Category:People with sickle-cell disease. Category. : People with sickle-cell disease. This is a non-diffusing parent category of Category:Deaths from sickle-cell disease. The contents of that subcategory can also be found within this category, or in diffusing subcategories of it.
Sickle Cell Anemia, a Molecular Disease. " Sickle Cell Anemia, a Molecular Disease " is a 1949 scientific paper by Linus Pauling, Harvey A. Itano, Seymour J. Singer and Ibert C. Wells that established sickle-cell anemia as a genetic disease in which affected individuals have a different form of the metalloprotein hemoglobin in their blood.
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