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- Table of Contents
Information about Autoimmune Hemolytic Anemia: 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.
Most recent studies have shown that Autoimmune Hemolytic Anemia shares some biological mechanisms with anemia, anemia-hemolytic, autoimmune-diseases, autoimmune-reaction, autoimmunity, chronic-lymphocytic-leukemia, cold-hemagglutinin-disease, evans-syndrome, hematological-disease, hemolysis-(disorder), hepatitis, immune-hemolytic-anemia, leukemia, lupus-erythematosus-systemic, lymphoid-leukemia, lymphoma, neoplasms, purpura, purpura-thrombocytopenic-idiopathic, thrombocytopenic-purpura.
Among the many pathways, these few ones have gauged particular interests from scientists studying Autoimmune Hemolytic Anemia, and have been seen in publications frequently: Aging, B Cell Activation, Cell Activation, Cell Proliferation, Coagulation, Complement Activation, Cytokine Production, Excretion, Hemopoiesis, Hypersensitivity, Immune Response, Inflammatory Response, Localization, Lymphocyte Activation, Pathogenesis, Phagocytosis, Regeneration, Secretion, Sensitization, Transport
Quite a number of genes have been found to play important roles in Autoimmune Hemolytic Anemia, such as ABO, C3, C4A, CTLA4, EPO, HLA-DQA1, HP, IGHG3, IL10, IL2, KRT20, MS4A1, NOD2, RHCE, RHD, SLC6A3. 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.