This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Van Der Woude Syndrome
Information about Van Der Woude 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 Van Der Woude Syndrome
Most recent studies have shown that Van Der Woude Syndrome shares some biological mechanisms with bilateral-cleft-lip, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, congenital-abnormality, congenital-lip-pits, craniofacial-abnormalities, cytogenetic-abnormality, developmental-absence-of-tooth, hypodontia, lip-diseases, multiple-pterygium-syndrome, oral-fistula, pathologic-fistula, popliteal-pterygium-syndrome, pterygium, salivary-gland-diseases, tissue-adhesions.
Among the many pathways, these few ones have gauged particular interests from scientists studying Van Der Woude Syndrome, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cell Cycle, Cell Death, Cell Migration, Dehiscence, Dna Replication, Excretion, Fertilization, Gastrulation, Localization, Metaphase, Mitosis, Pathogenesis, Programmed Cell Death, Secretion, Wound Healing
Quite a number of genes have been found to play important roles in Van Der Woude Syndrome, such as CALML3, CNTN2, COTL1, CP, CSRP3, CXCR1, CXCR2, ESR1, F13A1, INPP5K, IRF6, KCTD11, NHLH1, RARA, REN, SFN, SMG1, STS, TNIP1. 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.