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Disease Info Card
Fetal Alcohol Syndrome
Information about Fetal Alcohol Syndrome: 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 Fetal Alcohol Syndrome
Most recent studies have shown that Fetal Alcohol Syndrome shares some biological mechanisms with attention-deficit-hyperactivity-disorder, brain-injuries, child-behavior-disorders, congenital-abnormality, developmental-disabilities, fetal-growth-retardation, growth-retardation, hypoplasia, impairment-(finding), malnutrition, microcephaly, nervousness, pregnancy-complications, substance-related-disorders, teratogenic-effect.
Among the many pathways, these few ones have gauged particular interests from scientists studying Fetal Alcohol Syndrome, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cell Cycle, Cell Death, Cell Migration, Cell Proliferation, Cognition, Gastrulation, Lactation, Localization, Mating, Myelination, Nervous System Development, Neurogenesis, Neuroprotection, Parturition, Pathogenesis, Secretion, System Development, Transport
Quite a number of genes have been found to play important roles in Fetal Alcohol Syndrome, such as AKR1A1, AVP, BDNF, CA1, CASP3, FANCE, FAS, FASN, GFAP, IGF1, IGF2, IL2, INS, NTF3, PAEP, PFAS, POMC, SS18L1, VIP. 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.