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Disease Info Card
Xyy Karyotype
Information about Xyy Karyotype: 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 Xyy Karyotype
Most recent studies have shown that Xyy Karyotype shares some biological mechanisms with 47-xyy-syndrome, aneuploidy, antisocial-personality-disorder, congenital-abnormality, cytogenetic-abnormality, disorders-of-sex-development, down-syndrome, embryonic-mosaic, gonadal-dysgenesis, hypogonadism, infertility, klinefelter-syndrome, leukemia, male-infertility, mental-disorders, sex-chromosome-aberrations, trisomy, turner-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Xyy Karyotype, and have been seen in publications frequently: Amelogenesis, Brain Development, Chromosome Segregation, Cytokinesis, Development Of Secondary Sexual Characteristics, Fertilization, Fibrinolysis, Interphase, Meiosis, Meiosis I, Meiosis Ii, Metaphase, Pachytene, Pathogenesis, Prolactin Secretion, Prophase, Secretion, Sex Determination, Spermatogenesis
Quite a number of genes have been found to play important roles in Xyy Karyotype, such as AR, BCR, BRD2, FLT3, GH1, IGF1, IGFBP3, IL2, INVS, KDM5D, LHCGR, NPM1, PGD, PHGDH, PLOD1, PRL, SERPINE1, SRY, SYCP3. 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.