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Disease Info Card
Congenital Atresia Of Pulmonary Valve
Information about Congenital Atresia Of Pulmonary Valve: 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 Congenital Atresia Of Pulmonary Valve
Most recent studies have shown that Congenital Atresia Of Pulmonary Valve shares some biological mechanisms with atresia, common-ventricle-disorder, congenital-heart-defects, congenital-heart-disease, double-outlet-right-ventricle, heart-diseases, heart-septal-defects, hypoplasia, patent-ductus-arteriosus, pulmonary-stenosis, pulmonary-valve-stenosis, regurgitation, stenosis, tetralogy-of-fallot, transposition-of-great-vessels, tricuspid-atresia, truncus-arteriosus-persistent, ventricular-septal-defects.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Atresia Of Pulmonary Valve, and have been seen in publications frequently: Aging, Angiogenesis, Artery Development, Cell Migration, Coagulation, Dehiscence, Heart Growth, Hemostasis, Lung Development, Neural Crest Cell Development, Neural Crest Cell Migration, Nodal Signaling Pathway, Ossification, Pathogenesis, Reflex, Segmentation, Transport, Transposition, Tube Fusion, Wound Healing
Quite a number of genes have been found to play important roles in Congenital Atresia Of Pulmonary Valve, such as AMY2A, BCHE, BLOC1S6, BTN1A1, CELA3B, CPB1, ENOPH1, EPB42, FEZF2, GDF1, PRH1, PVR, SERPINB2, SERPINE1, SLC4A7, SS18L1, TBX1. 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.