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Disease Info Card
Secondary Polycythemia
Information about Secondary Polycythemia: 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 Secondary Polycythemia
Most recent studies have shown that Secondary Polycythemia shares some biological mechanisms with anemia, anoxia, chronic-obstructive-airway-disease, congenital-heart-defects, erythrocytosis, heart-diseases, hypertensive-disease, hypoxia, leukemia, lung-diseases, lung-diseases-obstructive, myeloproliferative-disease, neoplasms, polycythemia, polycythemia-vera, primary-myelofibrosis, thrombocythemia-essential, thrombocytosis, thrombosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Secondary Polycythemia, and have been seen in publications frequently: Aging, Angiogenesis, Cell Cycle, Cell Proliferation, Coagulation, Diuresis, Excretion, Glomerular Filtration, Hemopoiesis, Hemostasis, Hypersensitivity, Oxygen Transport, Pathogenesis, Platelet Activation, Platelet Aggregation, Response To Hypoxia, Secretion, Transport, Transposition, Vasoconstriction
Quite a number of genes have been found to play important roles in Secondary Polycythemia, such as ACE, ARHGEF7, ASCC1, BCR, CD177, CD40, DBI, EPO, EPOR, EPX, IGF1, IL3, JAK2, MPL, REN, TFF2, TIMP1. 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.