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Disease Info Card
Panhypopituitarism
Information about Panhypopituitarism: 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 Panhypopituitarism
Most recent studies have shown that Panhypopituitarism shares some biological mechanisms with adenoma, adrenal-gland-hypofunction, craniopharyngioma, diabetes-mellitus, dwarfism, headache, hemorrhage, hypoglycemia, hypogonadism, hypopituitarism, hypothyroidism, malignant-neoplasms, neoplasms, pituitary-adenoma, pituitary-diseases, pituitary-neoplasms, sheehan-syndrome, somatotropin-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Panhypopituitarism, and have been seen in publications frequently: Aging, Aldosterone Secretion, Bone Maturation, Circadian Rhythm, Excretion, Fertilization, Glomerular Filtration, Growth Hormone Secretion, Hormone Secretion, Lactation, Localization, Menstruation, Ovulation, Pathogenesis, Prolactin Secretion, Secretion, Spermatogenesis, Testosterone Secretion, Transposition, Vasopressin Secretion
Quite a number of genes have been found to play important roles in Panhypopituitarism, such as AVP, BRD2, CRH, CSF2, GGH, GH1, GHRH, IGF1, IGFBP3, INS, LAMC2, PBX1, PLOD1, POMC, POU1F1, PRL, SLC20A1, SLC25A5, 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.