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Disease Info Card
Precocious Pubarche
Information about Precocious Pubarche: 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 Precocious Pubarche
Most recent studies have shown that Precocious Pubarche shares some biological mechanisms with 3-beta-hydroxysteroid-dehydrogenase-deficiency, acne, adrenal-hyperplasia, cardiovascular-diseases, chronic-active-hepatitis, congenital-adrenal-hyperplasia, diabetes-mellitus, dyslipidemias, hyperinsulinism, hyperplasia, insulin-resistance, insulin-sensitivity, obesity, polycystic-ovary-syndrome, precocious-puberty, virilism.
Among the many pathways, these few ones have gauged particular interests from scientists studying Precocious Pubarche, and have been seen in publications frequently: Androgen Secretion, Bone Maturation, Development Of Secondary Sexual Characteristics, Developmental Maturation, Dna Methylation, Excretion, Gonadotropin Secretion, Hypersensitivity, Insulin Secretion, Limb Development, Menarche, Methylation, Ovulation, Pathogenesis, Response To Metformin, Secretion, Sensitization, Thelarche, Tooth Eruption, Transport
Quite a number of genes have been found to play important roles in Precocious Pubarche, such as ADIPOQ, AR, BLOC1S6, BRD2, CYP21A2, HSD3B1, HSD3B2, IGF1, IGFBP1, IGFBP3, INS, LEP, NR3C1, PLOD1, POMC, PPA1, PPY, SHBG, SULT2A1. 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.