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Disease Info Card
Anemia, Sickle Cell
Information about Anemia, Sickle Cell: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Anemia, Sickle Cell
Most recent studies have shown that Anemia, Sickle Cell shares some biological mechanisms with acute-chest-syndrome, alpha-thalassemia, anemia, anemia-hemolytic, beta-thalassemia, cerebrovascular-accident, hemoglobin-sc-disease, hemoglobinopathies, hemolysis-(disorder), hemorrhage, hypertensive-disease, infarction, infective-disorder, malaria, osteomyelitis, pain, pregnancy-complications-hematologic, sickle-cell-trait, thalassemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Anemia, Sickle Cell, and have been seen in publications frequently: Aging, Cell Adhesion, Coagulation, Excretion, Glomerular Filtration, Hemostasis, Immune Response, Inflammatory Response, Methylation, Oxygen Transport, Pathogenesis, Phagocytosis, Platelet Activation, Platelet Aggregation, Response To Hydroxyurea, Secretion, Translation, Transport, Vasoconstriction, Vasodilation
Quite a number of genes have been found to play important roles in Anemia, Sickle Cell, such as ALB, ATP6V0A2, CEL, EPO, ERMAP, G6PD, GPHA2, HBA1, HBB, HBG2, SCD, SGCA, TEAD1, TF, TNF, UBL4A. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.