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- Table of Contents
Information about Supravalvular Aortic Stenosis: 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 Supravalvular Aortic Stenosis shares some biological mechanisms with aortic-coarctation, aortic-diseases, aortic-valve-insufficiency, aortic-valve-stenosis, congenital-heart-defects, congenital-supravalvular-aortic-stenosis, haploinsufficiency, heart-diseases, hypercalcemia, hypertensive-disease, hypertrophic-cardiomyopathy, hypertrophy, hypoplasia, pulmonary-stenosis, pulmonary-valve-stenosis, regurgitation, stenosis, stricture-of-artery, williams-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Supravalvular Aortic Stenosis, and have been seen in publications frequently: Aging, Calcitonin Secretion, Cardiac Conduction, Cell Migration, Cell Proliferation, Cognition, Dehiscence, Dosage Compensation, Elastic Fiber Assembly, Hypersensitivity, Localization, Meiosis, Muscle Cell Proliferation, Neural Crest Cell Migration, Pathogenesis, Reflex, Secretion, Translation, Transposition, Vasoconstriction
Quite a number of genes have been found to play important roles in Supravalvular Aortic Stenosis, such as ACE, AGT, CALCA, CDKN1C, ELN, FBLN5, FBN1, FKBP6, GTF2I, GTF2IRD1, INPP5K, IRF6, LDLR, LIMK1, MB, NANS, NSUN5, PDLIM1, TSPAN31. 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.