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Description
Evidence for the essential role of IGF-1 signaling in normal regulation of growth comes from individuals with Laron dwarfism, a condition caused by deletion or mutation of the GH receptor that results in congenital IGF-1 deficiency [17]
B Katzung, Vanderah TW (Editors)

For the Duo-72 duodenum cultures, improvements in response to scTS2/16 were measured both on BME (amplification 2.4-fold) and collagen (amplification 2.4-fold)

doi: 10.1016/j.neulet.2008.09.058

doi:10.1016/j.cell.2008.09.002