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Disease Info Card
Choanal Atresia
Information about Choanal Atresia: 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 Choanal Atresia
Most recent studies have shown that Choanal Atresia shares some biological mechanisms with airway-obstruction, atresia, charge-syndrome, cleft-lip, cleft-palate, complete-hearing-loss, congenital-abnormality, congenital-heart-defects, congenital-ocular-coloboma-(disorder), developmental-disabilities, esophageal-atresia, growth-disorders, heart-diseases, hypoplasia, nasopharyngeal-diseases, nose-deformities-acquired, respiratory-distress, stenosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Choanal Atresia, and have been seen in publications frequently: Coagulation, Ear Morphogenesis, Feeding Behavior, Fertilization, Fibroblast Proliferation, Glucose Homeostasis, Hemostasis, Inner Ear Development, Limb Development, Localization, Lymphangiogenesis, Myelination, Ossification, Palate Development, Pathogenesis, Reflex, Secretion, Thyroid Gland Development, Transport, Transposition
Quite a number of genes have been found to play important roles in Choanal Atresia, such as ABCB6, BMP4, C2, CENPJ, CHD7, CSF2, CYP51A1, EFTUD2, FBN1, FGFR2, FGFR3, FOXE1, GLYAT, IL13, LAMC2, SHH, SS18L1, SUB1. 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.