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Disease Info Card
Laron Syndrome
Information about Laron Syndrome: 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 Laron Syndrome
Most recent studies have shown that Laron Syndrome shares some biological mechanisms with acromegaly, diabetes-mellitus, diabetes-mellitus-non-insulin-dependent, dwarfism, growth-disorders, growth-retardation, hereditary-diseases, hypoglycemia, insulin-resistance, malignant-neoplasms, malnutrition, obesity, osteoporosis, pituitary-diseases, pituitary-dwarfism, shwachman-syndrome, somatotropin-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Laron Syndrome, and have been seen in publications frequently: Adiponectin Secretion, Aging, Anagen, Bone Maturation, Brain Development, Cell Adhesion, Cell Growth, Cell Proliferation, Excretion, Glucose Homeostasis, Localization, Menarche, Mrna Splicing, Ovulation, Pathogenesis, Primary Growth, Secretion, Signal Transmission, Translation, Transport
Quite a number of genes have been found to play important roles in Laron Syndrome, such as BLVRB, GGH, GH1, GHR, GHRH, IGF1, IGF2, IGFBP3, IGHD, INS, JAK2, LIAS, PRL, RANGAP1, SLC17A5, STAT5A, STAT5B. 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.