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Disease Info Card
Pituitary Gland Hypoplasia
Information about Pituitary Gland Hypoplasia: 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 Pituitary Gland Hypoplasia
Most recent studies have shown that Pituitary Gland Hypoplasia shares some biological mechanisms with congenital-abnormality, congenital-absence, dwarfism, dysplasia, growth-disorders, growth-retardation, hypogonadism, hypopituitarism, hypoplasia, hypothyroidism, isolated-somatotropin-deficiency, neoplasms, optic-nerve-hypoplasia, pituitary-diseases, pituitary-dwarfism, pituitary-neoplasms, septo-optic-dysplasia, shwachman-syndrome, somatotropin-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pituitary Gland Hypoplasia, and have been seen in publications frequently: Aging, Cell Cycle, Cell Death, Cell Growth, Cell Migration, Cell Proliferation, Embryo Implantation, Eye Development, Growth Hormone Secretion, Hormone Secretion, Hypersensitivity, Immune Response, Localization, Menstruation, Mrna Splicing, Pathogenesis, Pigmentation, Progesterone Secretion, Secretion, Translation
Quite a number of genes have been found to play important roles in Pituitary Gland Hypoplasia, such as BRD2, GGH, GH1, GHRH, GHRHR, HESX1, IGF1, IGHD, INS, LHX3, LHX4, PBX1, POMC, POU1F1, PRL, PROP1, SLC20A1, SOX2, SOX3. 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.