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Disease Info Card
Infant, Very Low Birth Weight
Information about Infant, Very Low Birth Weight: 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 Infant, Very Low Birth Weight
Most recent studies have shown that Infant, Very Low Birth Weight shares some biological mechanisms with bronchopulmonary-dysplasia, cerebral-palsy, chronic-lung-disease, developmental-disabilities, dysplasia, enterocolitis, enterocolitis-necrotizing, hemorrhage, infective-disorder, intraventricular-brain-hemorrhage, lung-diseases, patent-ductus-arteriosus, premature-birth, respiratory-distress, respiratory-distress-syndrome-newborn, retinal-diseases, retinopathy-of-prematurity, systemic-infection.
Among the many pathways, these few ones have gauged particular interests from scientists studying Infant, Very Low Birth Weight, and have been seen in publications frequently: Bone Mineralization, Bone Resorption, Brain Development, Coagulation, Cognition, Diuresis, Excretion, Fertilization, Glomerular Filtration, Immune Response, Inflammatory Response, Lactation, Lung Development, Lung Growth, Myelination, Pathogenesis, Regionalization, Secretion, Transport, Visual Perception
Quite a number of genes have been found to play important roles in Infant, Very Low Birth Weight, such as AGA, CENPJ, CRP, EPO, ERMAP, GLS2, IGF1, IL6, INS, NDUFB6, OPN1LW, P4HB, PADI1, PDIA2, RANGAP1, SLC17A5, SLC26A3, TNF. 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.