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Disease Info Card
Transitory Tachypnea Of Newborn
Information about Transitory Tachypnea Of 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 Transitory Tachypnea Of Newborn
Most recent studies have shown that Transitory Tachypnea Of Newborn shares some biological mechanisms with asphyxia, asphyxia-neonatorum, diabetes-mellitus, dysplasia, hyaline-membrane-disease, hypertensive-disease, lung-diseases, meconium-aspiration-syndrome, pneumonia, pulmonary-edema, pulmonary-hypertension, respiration-disorders, respiratory-distress, respiratory-distress-syndrome-newborn, tachypnea.
Among the many pathways, these few ones have gauged particular interests from scientists studying Transitory Tachypnea Of Newborn, and have been seen in publications frequently: Excretion, Fertilization, Ion Transport, Pathogenesis, Secretion, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Transitory Tachypnea Of Newborn, such as AGA, AVP, CENPJ, CRP, CS, CSRP1, EDN1, GLS2, IL6, INS, KCNJ11, MAS1, MUC1, NPPA, RNASE3, SFTPB, TTN. 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.
Pathways Related to Transitory Tachypnea Of Newborn
This information is being compiled and will come in a future update
| Excretion | Fertilization | Ion Transport |
| Pathogenesis | Secretion | Transport |
| Vasoconstriction |