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Disease Info Card
Respiratory Distress Syndrome, Newborn
Information about Respiratory Distress Syndrome, Newborn: 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 Respiratory Distress Syndrome, Newborn
Most recent studies have shown that Respiratory Distress Syndrome, Newborn shares some biological mechanisms with asphyxia-neonatorum, bronchopulmonary-dysplasia, chronic-lung-disease, dysplasia, hemorrhage, hyaline-membrane-disease, hypertensive-disease, intraventricular-brain-hemorrhage, lung-diseases, patent-ductus-arteriosus, pneumonia, premature-obstetric-labor, respiratory-distress, respiratory-distress-syndrome-adult, respiratory-failure, systemic-infection.
Among the many pathways, these few ones have gauged particular interests from scientists studying Respiratory Distress Syndrome, Newborn, and have been seen in publications frequently: Blood Coagulation, Cell Differentiation, Coagulation, Complement Activation, Diuresis, Excretion, Fibrinolysis, Glomerular Filtration, Inflammatory Response, Localization, Lung Development, Lung Growth, Parturition, Pathogenesis, Phagocytosis, Reflex, Secretion, Surfactant Homeostasis, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Respiratory Distress Syndrome, Newborn, such as AGA, ALB, CENPJ, GLS2, IL6, INS, PLG, SERPINC1, SFTPB, SFTPC, SFTPD, SLC26A3, TNF, TRH, 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.