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Disease Info Card
Isolated Somatotropin Deficiency
Information about Isolated Somatotropin Deficiency: 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 Isolated Somatotropin Deficiency
Most recent studies have shown that Isolated Somatotropin Deficiency shares some biological mechanisms with agammaglobulinemia, dwarfism, growth-disorders, growth-retardation, hypoglycemia, hypopituitarism, hypoplasia, idiopathic-growth-hormone-deficiency, immunologic-deficiency-syndromes, panhypopituitarism, pituitary-diseases, pituitary-dwarfism, pituitary-gland-hypoplasia, shwachman-syndrome, somatotropin-deficiency, x-linked-hypogammaglobulinemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Isolated Somatotropin Deficiency, and have been seen in publications frequently: Aging, Bone Maturation, Cell Differentiation, Cell Proliferation, Development Of Secondary Sexual Characteristics, Excretion, Gene Conversion, Glial Cell Proliferation, Growth Hormone Secretion, Hormone Secretion, Immune Response, Long-term Memory, Menarche, Mrna Splicing, Pathogenesis, Reproductive Process, Reverse Transcription, Secondary Growth, Secretion, Secretory Pathway
Quite a number of genes have been found to play important roles in Isolated Somatotropin Deficiency, such as BRD2, BTK, GGH, GH1, GHR, GHRH, GHRHR, HESX1, IGF1, IGFBP3, IGHD, INS, PLOD1, POMC, POU1F1, PRL, PROP1, TNFRSF10C. 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.