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Disease Info Card
Ichthyosis Linearis Circumflexa
Information about Ichthyosis Linearis Circumflexa: 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 Ichthyosis Linearis Circumflexa
Most recent studies have shown that Ichthyosis Linearis Circumflexa shares some biological mechanisms with atopic-reaction, bamboo-hair, congenital-ichthyosis, congenital-nonbullous-ichthyosiform-erythroderma, dermatitis, dermatitis-atopic, dermatologic-disorders, ectodermal-dysplasia, exfoliative-dermatitis, failure-to-thrive, hair-diseases, ichthyoses, ichthyosiform-erythroderma-congenital, ichthyosis-vulgaris, infective-disorder, psoriasis, scalp-dermatoses, skin-diseases-genetic.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ichthyosis Linearis Circumflexa, and have been seen in publications frequently: Anagen, Brain Development, Catagen, Cell Cycle, Corneocyte Desquamation, Cornification, Diuresis, Excretion, Hypersensitivity, Keratinization, Keratinocyte Differentiation, Lipid Storage, Localization, Pathogenesis, Proteolysis, Secretion, Skin Development, Translation, Transport, Virulence
Quite a number of genes have been found to play important roles in Ichthyosis Linearis Circumflexa, such as CDSN, DSC1, DSC3, DSG1, ERMAP, FLG, FURIN, GNL3, KLK4, KLK5, KLK6, KLK7, KRAS, SPINK5, TGM1, TSLP. 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.