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Disease Info Card
Monster (disorder)
Information about Monster (disorder): 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 Monster (disorder)
Most recent studies have shown that Monster (disorder) shares some biological mechanisms with abnormality-severe-teratoid, acardiac-monster, anencephaly, carcinoma, congenital-abnormality, congenital-heart-defects, cutaneous-fibrous-histiocytoma, diabetes-mellitus, diabetes-mellitus-non-insulin-dependent, diseases-in-twins, double-monster, histiocytoma-benign-fibrous, malignant-paraganglionic-neoplasm, multiple-pregnancy, neoplasms, skin-neoplasms, teratoma, twins-conjoined.
Among the many pathways, these few ones have gauged particular interests from scientists studying Monster (disorder), and have been seen in publications frequently: Anaphylaxis, Brain Development, Cell Adhesion, Cell Cycle, Cell Division, Cell Proliferation, Exocytosis, Gastric Acid Secretion, Gastric Emptying, Glucagon Secretion, Glucose Homeostasis, Insulin Secretion, Mating, Meiosis, Pathogenesis, Response To Nutrient, Secretion, Sensory Processing, Spermatogenesis
Quite a number of genes have been found to play important roles in Monster (disorder), such as AFP, CD34, DES, DPP4, F13A1, GCG, GHRH, GIP, GLP1R, GNAI2, GPI, INS, KNG1, PLA2G1B, PLB1, SCT, VIP. 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.