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- Table of Contents
Information about Wiskott-aldrich Syndrome: 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 Wiskott-aldrich Syndrome shares some biological mechanisms with agammaglobulinemia, agammaglobulinemia, anemia, ataxia-telangiectasia, autoimmune-diseases, autoimmune-diseases, autoimmune-reaction, autoimmune-reaction, autoimmunity, autoimmunity, cell-invasion, congenital-combined-immunodeficiency, congenital-combined-immunodeficiency, eczema, eczema, graft-vs-host-disease, graft-vs-host-disease, granulomatous-disease-chronic, hemorrhage, hemorrhage, hereditary-diseases, immunologic-deficiency-syndromes, immunologic-deficiency-syndromes, infective-disorder, infective-disorder, leukemia, leukemia, lymphoma, lymphoma, malignant-neoplasms, malignant-neoplasms, neoplasms, neoplasms, primary-immune-deficiency-disorder, primary-immune-deficiency-disorder, severe-combined-immunodeficiency, severe-combined-immunodeficiency, tissue-adhesions, tissue-adhesions, wiskott-aldrich-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Wiskott-aldrich Syndrome, and have been seen in publications frequently: Actin Nucleation, Actin Nucleation, Cell Activation, Cell Activation, Cell Adhesion, Cell Adhesion, Cell Migration, Cell Migration, Cell Motility, Cell Motility, Cell Proliferation, Cell Proliferation, Chemotaxis, Chemotaxis, Cytokine Production, Cytokine Production, Cytokinesis, Endocytosis, Endocytosis, Hypersensitivity, Immune Response, Immune Response, Localization, Localization, Locomotion, Methylation, Pathogenesis, Pathogenesis, Phagocytosis, Phagocytosis, Platelet Aggregation, Rna Interference, Rna Interference, Secretion, Secretion, T Cell Activation, T Cell Activation, Translation, Transport, Transport
Quite a number of genes have been found to play important roles in Wiskott-aldrich Syndrome, such as ACTR2, ACTR2, ACTR3, ACTR3, AICDA, AICDA, AKT1, AKT1, ANGPTL2, ANGPTL2, CD4, CDC42, CDC42, CTLA4, CTLA4, HLA-DQA1, HLA-DQA1, IL2, IL2, NCK1, NOD2, NOD2, RPS4X, RPS4X, SPN, SPN, SRC, SRC, WAS, WAS, WASF1, WASF1, WASF2, WASF2, WASL, WASL, WIPF1, WIPF1. 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.