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Disease Info Card
Williams Syndrome
Information about Williams 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 Williams Syndrome
Most recent studies have shown that Williams Syndrome shares some biological mechanisms with anxiety-disorders, aortic-valve-stenosis, autistic-disorder, cognition-disorders, congenital-heart-defects, developmental-disabilities, down-syndrome, fragile-x-syndrome, haploinsufficiency, hereditary-diseases, hypercalcemia, hypertensive-disease, impairment-(finding), malnutrition, prader-willi-syndrome, stenosis, stricture-of-artery, supravalvular-aortic-stenosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Williams Syndrome, and have been seen in publications frequently: Aging, Atp-dependent Chromatin Remodeling, Brain Development, Chromatin Remodeling, Cognition, Developmental Process, Dna Repair, Hypersensitivity, Interphase, Localization, Long-term Memory, Meiosis, Metaphase, Pathogenesis, Reflex, Segmentation, Short-term Memory, Social Behavior, Translation, Transposition
Quite a number of genes have been found to play important roles in Williams Syndrome, such as BAZ1A, BAZ1B, CALCA, CDKN1C, CLIP2, DHDDS, DHPS, ELN, FBN1, GTF2I, GTF2IRD1, LIMK1, MLXIPL, NCF1, PDLIM1, PDLIM5, PRPH2, SMARCA5, STX1A. 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.