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- Table of Contents
Information about Sex Chromosome Disorders: 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 Sex Chromosome Disorders shares some biological mechanisms with ambiguous-genitalia, aneuploidy, azoospermia, chromosomal-translocation, congenital-abnormality, cytogenetic-abnormality, disorders-of-sex-development, down-syndrome, embryonic-mosaic, gonadal-dysgenesis, hypogonadism, infertility, klinefelter-syndrome, male-infertility, muscle-hypotonia, sex-chromosome-aberrations, trisomy, turner-syndrome, xx-male.
Among the many pathways, these few ones have gauged particular interests from scientists studying Sex Chromosome Disorders, and have been seen in publications frequently: Aging, Cell Adhesion, Cytokinesis, Development Of Secondary Sexual Characteristics, Dosage Compensation, Fertilization, Gene Conversion, Gene Silencing, Interphase, Localization, Meiosis Ii, Ovulation, Pathogenesis, Reverse Transcription, Sex Determination, Sex Differentiation, Spermatogenesis, Testosterone Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Sex Chromosome Disorders, such as AR, ARX, BRD2, CDKL5, CHP1, COL18A1, DCTN3, DLG3, FDXR, LHCGR, MECP2, OXSM, PGD, PHF6, PHGDH, PLOD1, RPGR, SRY, STS, UBA2. 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.