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Disease Info Card
Vacterl Association
Information about Vacterl Association: 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 Vacterl Association
Most recent studies have shown that Vacterl Association shares some biological mechanisms with anemia, anus-imperforate, atresia, congenital-abnormality, congenital-absence, congenital-heart-defects, dysplasia, esophageal-atresia, fanconi-anemia, gastroesophageal-reflux-disease, heart-septal-defects, hypoplasia, limb-defect, limb-deformities-congenital, multiple-congenital-anomalies, pathologic-fistula, stenosis, tetralogy-of-fallot, tracheoesophageal-fistula.
Among the many pathways, these few ones have gauged particular interests from scientists studying Vacterl Association, and have been seen in publications frequently: Cardiac Conduction, Cell Adhesion, Cell Death, Cell Motility, Centromere Separation, Chromosome Breakage, Cognition, Foregut Morphogenesis, Gastrulation, Hypersensitivity, Intraflagellar Transport, Localization, Mating, Pathogenesis, Pigmentation, Reflex, Segmentation, Transport, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Vacterl Association, such as CRAT, ELSPBP1, FANCC, FGF10, FOXC2, FOXF1, FUT1, GLI1, GLI2, GLI3, HOXA3, HOXA5, HOXB3, HOXC4, LPP, SHH, SLC7A5, TEF, 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.