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Disease Info Card
Congenital Hypoplasia
Information about Congenital Hypoplasia: 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 Hypoplasia
Most recent studies have shown that Congenital Hypoplasia shares some biological mechanisms with atresia, atrophy, cleft-lip, cleft-palate, congenital-abnormality, congenital-absence, congenital-heart-defects, dysplasia, facial-asymmetry, fetal-growth-retardation, hernia, hypertensive-disease, hypoplasia, infective-disorder, malnutrition, malocclusion, neoplasms, nervousness, stenosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Hypoplasia, and have been seen in publications frequently: Aging, Cell Death, Cell Proliferation, Immune Response, Innervation, Lactation, Localization, Lung Development, Lung Growth, Mastication, Ossification, Parturition, Pathogenesis, Reflex, Regeneration, Secretion, Spermatogenesis, Translation, Transport, Transposition
Quite a number of genes have been found to play important roles in Congenital Hypoplasia, such as ANGPT1, ANGPT2, AR, BRD2, CAT, FUT3, GGH, GH1, GJB2, HNF1B, HPS4, IGF1, INS, PLOD1, SHH, SLC17A5, SLC25A5, SS18L1. 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.