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Disease Info Card
Hypotrichosis Simplex
Information about Hypotrichosis Simplex: 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 Hypotrichosis Simplex
Most recent studies have shown that Hypotrichosis Simplex shares some biological mechanisms with amyloidosis, androgenetic-alopecia, atrichia, congenital-absence, dermatologic-disorders, dysplasia, exfoliative-dermatitis, hair-diseases, hypotrichosis, ichthyosis-linearis-circumflexa, ichthyosis-vulgaris, loss-of-scalp-hair, pituitary-diseases, pruritus, scoliosis-unspecified, skin-diseases-genetic, tissue-adhesions, wooly-hair.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hypotrichosis Simplex, and have been seen in publications frequently: Anagen, Axis Specification, Cornification, Generation Of Neurons, Hair Cycle, Localization, Telogen, Translation
Quite a number of genes have been found to play important roles in Hypotrichosis Simplex, such as APCDD1, CDSN, GALNT3, GFER, GJA1, HR, LIPC, LIPH, LPA, LPAR4, LPAR5, LPAR6, MTSS1, PANK2, RPL21, SGSH, SPAG9, TEAD1, TGIF1. 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 Hypotrichosis Simplex
This information is being compiled and will come in a future update
| Anagen | Axis Specification | Cornification |
| Generation Of Neurons | Hair Cycle | Localization |
| Telogen | Translation |