This gene encodes a member of the type I cytokine receptor family, which is a transmembrane receptor for growth hormone. Binding of growth hormone to the receptor leads to receptor dimerization and the activation of an intra- and intercellular signal transduction pathway leading to growth. Mutations in this gene have been associated with Laron syndrome, also known as the growth hormone insensitivity syndrome (GHIS), a disorder characterized by short stature. In humans and rabbits, but not rodents, growth hormone binding protein (GHBP) is generated by proteolytic cleavage of the extracellular ligand-binding domain from the mature growth hormone receptor protein. Multiple alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jun 2011].
Latest Publications for our Growth Hormone Receptor ELISA试剂盒
Ugarte, Irarrazabal, Oh, Dettmar, Ceballos, Rojo, Ibacache, Suazo, Lozano, Delgado, Cavada, Azocar, Delucchi, Cano: "Impaired phosphorylation of JAK2-STAT5b signaling in fibroblasts from uremic children." in: Pediatric nephrology (Berlin, Germany), Vol. 31, Issue 6, pp. 965-74, (2017) (PubMed).
Ayd?n, Demirkol, Ba?, Türko?lu, Kumral, Karaböcüo?lu, C?tak, Darendeliler: "Evaluation of endocrine function in children admitted to pediatric intensive care unit." in: Pediatrics international : official journal of the Japan Pediatric Society, Vol. 56, Issue 3, pp. 349-53, (2014) (PubMed).