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Disease Info Card
Oral Leukokeratoses
Information about Oral Leukokeratoses: 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 Oral Leukokeratoses
Most recent studies have shown that Oral Leukokeratoses shares some biological mechanisms with dermatologic-disorders, dystrophia-unguium, dystrophy, ectodermal-dysplasia, follicular-hyperkeratosis, hoarseness, hyperkeratosis, hypertrophy, keratosis, keratosis-follicularis, leukokeratosis, leukokeratosis-hereditary-mucosal, melanocytic-nevus, nails-malformed, natal-teeth, pachyonychia-congenita, palmoplantar-keratosis, thickened-nails.
Among the many pathways, these few ones have gauged particular interests from scientists studying Oral Leukokeratoses, and have been seen in publications frequently: Pigmentation
Quite a number of genes have been found to play important roles in Oral Leukokeratoses, such as DES, ENPP1, GDI1, GJB2, KCNG1, KLKB1, KRT13, KRT16, KRT17, KRT4, KRT6A, KRT6B, MTSS1, PKD1, PTEN, RHBDF2, TPD52. 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 Oral Leukokeratoses
This information is being compiled and will come in a future update
| Pigmentation |