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Disease Info Card
Rosselli-gulienetti Syndrome
Information about Rosselli-gulienetti 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 Rosselli-gulienetti Syndrome
Most recent studies have shown that Rosselli-gulienetti Syndrome shares some biological mechanisms with bustos-simosa-pinto-cisternas-syndrome, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, cleft-palate-x-linked, congenital-abnormality, congenital-webbing, dysplasia, ectodermal-dysplasia, hay-wells-syndrome-of-ectodermal-dysplasia, limb-deformities-congenital, malignant-neoplasms, neoplasms, nervousness, pterygium, syndactyly, tissue-adhesions, tooth-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Rosselli-gulienetti Syndrome, and have been seen in publications frequently: Cell Adhesion, Cell-cell Adhesion, Face Development, Localization, Tropism
Quite a number of genes have been found to play important roles in Rosselli-gulienetti Syndrome, such as CADM4, CKAP4, CTNNBL1, FLG, IRF6, MTSS1, NHLH1, PVR, TBX22, TNFRSF14, TNFSF14, TNIP1, TP63, UVRAG. 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.
Pathways Related to Rosselli-gulienetti Syndrome
This information is being compiled and will come in a future update
| Cell Adhesion | Cell cell Adhesion | Face Development |
| Localization | Tropism |