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- Table of Contents
Information about Leukocyte-adhesion Deficiency 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 Leukocyte-adhesion Deficiency Syndrome shares some biological mechanisms with bacterial-infections, cattle-diseases, chediak-higashi-syndrome, dog-diseases, graft-vs-host-disease, granulomatous-disease-chronic, hemorrhage, hereditary-diseases, immunologic-deficiency-syndromes, infective-disorder, inflammation, inflammatory-response, leukocyte-adhesion-deficiency, leukocyte-adhesion-deficiency-type-1, leukocytosis, mycoses, periodontitis, primary-immune-deficiency-disorder, tissue-adhesions, ulcer.
Among the many pathways, these few ones have gauged particular interests from scientists studying Leukocyte-adhesion Deficiency Syndrome, and have been seen in publications frequently: Cell Adhesion, Cell Migration, Cell Proliferation, Chemotaxis, Diapedesis, Fucosylation, Glycosylation, Immune Response, Inflammatory Response, Insemination, Integrin Activation, Leukocyte Activation, Localization, Pathogenesis, Phagocytosis, Platelet Aggregation, Respiratory Burst, Secretion, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Leukocyte-adhesion Deficiency Syndrome, such as ABL1, ANPEP, CHAF1A, COL17A1, CTLA4, CTR9, DLD, FERMT3, HLA-DQA1, ITGAL, ITGAM, ITGB2, LAD1, LTBR, NOD2, PIK3R4, SELE, SELP. 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.