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Disease Info Card
Bronchopulmonary Dysplasia
Information about Bronchopulmonary Dysplasia: 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 Bronchopulmonary Dysplasia
Most recent studies have shown that Bronchopulmonary Dysplasia shares some biological mechanisms with borderline-personality-disorder, chronic-lung-disease, dysplasia, enterocolitis, enterocolitis-necrotizing, hemorrhage, infant-very-low-birth-weight, inflammation, intraventricular-brain-hemorrhage, lung-diseases, lung-injury, patent-ductus-arteriosus, pneumonia, premature-birth, respiratory-distress, respiratory-distress-syndrome-newborn, retinal-diseases, retinopathy-of-prematurity.
Among the many pathways, these few ones have gauged particular interests from scientists studying Bronchopulmonary Dysplasia, and have been seen in publications frequently: Angiogenesis, Cell Adhesion, Cell Cycle, Cell Death, Cell Growth, Cell Proliferation, Coagulation, Diuresis, Excretion, Fibrinolysis, Inflammatory Response, Localization, Lung Development, Lung Growth, Lung Morphogenesis, Pathogenesis, Regeneration, Secretion, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Bronchopulmonary Dysplasia, such as AGA, CAT, CCL2, CENPJ, ELN, EPO, ERMAP, GLS2, GRP, IL10, IL6, OPN1LW, SCGB1A1, SFTPB, SFTPC, SLC26A3, TNF, VEGFA. 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.