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Disease Info Card
Genetic Diseases, X-linked
Information about Genetic Diseases, X-linked: 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 Genetic Diseases, X-linked
Most recent studies have shown that Genetic Diseases, X-linked shares some biological mechanisms with agammaglobulinemia, atrophy, autoimmune-reaction, blind-vision, cardiomyopathies, dysplasia, dystrophy, hereditary-diseases, hypoplasia, immunologic-deficiency-syndromes, infective-disorder, intestinal-diseases, muscular-dystrophy, myopathy, polyendocrinopathies-autoimmune, retinitis-pigmentosa, x-linked-agammaglobulinemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Genetic Diseases, X-linked, and have been seen in publications frequently: Amelogenesis, Autophagy, Cell Adhesion, Cell Death, Cell Development, Cell Proliferation, Cognition, Cytokine Production, Excretion, Fertilization, Immune Response, Localization, Methylation, Muscle Atrophy, Pathogenesis, Secretion, Segmentation, Sex Determination, Translation, Transport
Quite a number of genes have been found to play important roles in Genetic Diseases, X-linked, such as AR, BTK, CACNA1F, CD40LG, DMD, ERG, FOXP3, GJB1, IKBKG, KCNH2, L1CAM, MTM1, NR0B1, RPGR, SH2D1A, TAF1, TAZ, TRAPPC2, WAS. 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.