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Disease Info Card
Embryopathies
Information about Embryopathies: 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 Embryopathies
Most recent studies have shown that Embryopathies shares some biological mechanisms with congenital-abnormality, congenital-heart-defects, diabetes-mellitus, diabetes-mellitus-experimental, fetal-alcohol-syndrome, fetal-diseases, fetal-warfarin-syndrome, growth-retardation, hyperglycemia, hypoplasia, pregnancy-complications, pregnancy-complications-cardiovascular, pregnancy-complications-infectious, pregnancy-in-diabetics, rubella, teratogenic-effect.
Among the many pathways, these few ones have gauged particular interests from scientists studying Embryopathies, and have been seen in publications frequently: Angiogenesis, Anterior Neuropore Closure, Brain Development, Cell Death, Cell Migration, Cell Proliferation, Coagulation, Embryo Development, Endocytosis, Fertilization, Localization, Mating, Neural Crest Cell Migration, Neural Tube Closure, Neuropore Closure, Pathogenesis, Programmed Cell Death, Secretion, Transport, Tube Closure
Quite a number of genes have been found to play important roles in Embryopathies, such as BAX, BGLAP, CAT, DBT, IGF1, INS, MAPK1, MAPK3, MAPK8, NOS2, PAH, PAX3, PRRT2, SOD1, SS18L1, ST3GAL4, 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.