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Disease Info Card
Hypopituitarism
Information about Hypopituitarism: 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 Hypopituitarism
Most recent studies have shown that Hypopituitarism shares some biological mechanisms with acromegaly, adenoma, adrenal-gland-hypofunction, craniopharyngioma, cushing-syndrome, diabetes-mellitus, dwarfism, headache, hypoglycemia, hypogonadism, hypothyroidism, neoplasms, panhypopituitarism, pituitary-adenoma, pituitary-diseases, pituitary-neoplasms, sheehan-syndrome, somatotropin-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hypopituitarism, and have been seen in publications frequently: Aging, Bone Resorption, Cell Proliferation, Circadian Rhythm, Coagulation, Cortisol Secretion, Excretion, Glucose Homeostasis, Gonadotropin Secretion, Growth Hormone Secretion, Hormone Secretion, Lactation, Localization, Menopause, Menstruation, Ovulation, Pathogenesis, Prolactin Secretion, Secretion, Spermatogenesis
Quite a number of genes have been found to play important roles in Hypopituitarism, such as AVP, BRD2, CRH, GCG, GGH, GH1, GHRH, IGF1, IGFBP3, INS, PBX1, PLOD1, POMC, POU1F1, PRL, PROP1, SST, TRH. 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.