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- Table of Contents
Information about Acth-secreting Pituitary Adenoma: 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 Acth-secreting Pituitary Adenoma shares some biological mechanisms with acromegaly, acth-syndrome-ectopic, adenoma, carcinoma, cell-transformation-neoplastic, cushing-syndrome, diabetes-mellitus, growth-hormone-secreting-pituitary-adenoma, hyperplasia, hypertensive-disease, hypopituitarism, nelson-syndrome, neoplasm-metastasis, neoplasm-recurrence-local, neoplasms, pituitary-adenoma, pituitary-dependent-cushings-disease, pituitary-diseases, pituitary-neoplasms, prolactinoma.
Among the many pathways, these few ones have gauged particular interests from scientists studying Acth-secreting Pituitary Adenoma, and have been seen in publications frequently: Angiogenesis, Cell Cycle, Cell Differentiation, Cell Growth, Cell Proliferation, Circadian Rhythm, Cortisol Secretion, Dna Repair, Excretion, Hormone Secretion, Localization, Methylation, Muscle Atrophy, Pathogenesis, Pigmentation, Prolactin Secretion, Proteolysis, S Phase, Secretion
Quite a number of genes have been found to play important roles in Acth-secreting Pituitary Adenoma, such as AVP, BRD2, CDKN2A, CRH, GGH, GH1, GHRH, IGF1, NR3C1, PBX1, PLOD1, POMC, PPARG, PRL, SST, SSTR5, TBX19, TP53. 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.