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Disease Info Card
Turner Syndrome
Information about Turner Syndrome: 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 Turner Syndrome
Most recent studies have shown that Turner Syndrome shares some biological mechanisms with amenorrhea, congenital-abnormality, cytogenetic-abnormality, disorders-of-sex-development, down-syndrome, dwarfism, embryonic-mosaic, female-infertility, gonadal-dysgenesis, growth-disorders, infertility, klinefelter-syndrome, malignant-neoplasms, monosomy, neoplasms, noonan-syndrome, ovarian-failure-premature, premature-menopause, sex-chromosome-aberrations, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Turner Syndrome, and have been seen in publications frequently: Aging, Cognition, Excretion, Fertilization, Growth Hormone Secretion, Hormone Secretion, Interphase, Localization, Meiosis, Menarche, Menopause, Menstruation, Metaphase, Methylation, Ovulation, Pathogenesis, Secretion, Sex Determination, Sex Differentiation, Transposition
Quite a number of genes have been found to play important roles in Turner Syndrome, such as AR, BRD2, CACNA1C, DIAPH2, DMD, FMR1, FSHR, GGH, GH1, IGF1, IGFBP3, INS, PLOD1, RANGAP1, SHOX, SLC17A5, SRY, TBXAS1, TYMS. 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.