This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Cockayne-touraine Disease
Information about Cockayne-touraine Disease: 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 Cockayne-touraine Disease
Most recent studies have shown that Cockayne-touraine Disease shares some biological mechanisms with bulla, cicatrix, cytogenetic-abnormality, de-novo-mutation, dermatologic-disorders, dystrophia-unguium, dystrophy, epidermolysis-bullosa, epidermolysis-bullosa-dystrophica, hallopeau-siemens-disease, leg-dermatoses, milium-cyst, mucinous-adenocarcinoma, nail-diseases, pretibial-epidermolysis-bullosa, pruritus, skin-diseases-genetic.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cockayne-touraine Disease, and have been seen in publications frequently: Cell Adhesion, Mrna Splicing, Pathogenesis, Phagocytosis, Secretion, Transport
Quite a number of genes have been found to play important roles in Cockayne-touraine Disease, such as ABCB6, ARL2BP, BSND, COL7A1, GALNS, PLOD1, RNF103, TXNDC15. 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 Cockayne-touraine Disease
This information is being compiled and will come in a future update
| Cell Adhesion | Mrna Splicing | Pathogenesis |
| Phagocytosis | Secretion | Transport |