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- Table of Contents
Information about Partial Deletion Of Y: 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 Partial Deletion Of Y shares some biological mechanisms with aneuploidy, azoospermia, chromosomal-translocation, congenital-abnormality, congenital-absence-of-germinal-epithelium-of-testes, cryptorchidism, cystic-fibrosis, cytogenetic-abnormality, embryonic-mosaic, fibrosis, growth-arrest, infertility, klinefelter-syndrome, male-infertility, oligospermia, sex-chromosome-aberrations, sex-chromosome-disorders-of-sex-development, steroid-sulfatase-deficiency-disease, varicocele.
Among the many pathways, these few ones have gauged particular interests from scientists studying Partial Deletion Of Y, and have been seen in publications frequently: Carpel Development, Cell Cycle, Cell Development, Cell Differentiation, Chromosome Separation, Developmental Process, Embryo Implantation, Fertilization, Germ Cell Development, Insemination, Localization, Male Meiosis, Mating, Meiosis, Pathogenesis, Prophase, Sex Determination, Sperm Motility, Spermatogenesis, Translation
Quite a number of genes have been found to play important roles in Partial Deletion Of Y, such as AGRP, AKR1B1, AR, AREG, ART2B, BRD2, CFTR, DAZ1, DDX3Y, FDXR, MTHFR, OAT, PLOD1, PRL, RBMY1A1, SRY, STS, USP9Y, ZFY. 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.