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- Table of Contents
Information about Disorders Of Sex Development: 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.
Most recent studies have shown that Disorders Of Sex Development shares some biological mechanisms with adrenal-hyperplasia, ambiguous-genitalia, congenital-abnormality, congenital-adrenal-hyperplasia, cryptorchidism, embryonic-mosaic, feminization, gonadal-dysgenesis, hermaphroditism, hyperplasia, hypospadias, klinefelter-syndrome, neoplasms, pseudohermaphroditism-male, sex-chromosome-aberrations, testicular-feminization, true-hermaphroditism-(disorder), turner-syndrome, virilism.
Among the many pathways, these few ones have gauged particular interests from scientists studying Disorders Of Sex Development, and have been seen in publications frequently: Cell Differentiation, Dosage Compensation, Excretion, Fertilization, Hatching, Localization, Male Sex Determination, Mating, Meiosis, Metaphase, Oogenesis, Ovulation, Pathogenesis, Secretion, Sex Determination, Sex Differentiation, Sperm Competition, Spermatogenesis, Translation, Transport
Quite a number of genes have been found to play important roles in Disorders Of Sex Development, such as AKR1B1, AMH, AR, AREG, BRD2, CYP19A1, FDXR, KDM5D, NR0B1, NR5A1, PLOD1, POMC, SOX9, SRD5A2, SRY, WT1. 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.