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Updated: Sep 20, 2026

Comparative Analysis of Human Growth Hormone in Serum Using SPRi, Nano-SPRi and ELISA Assays
Published on: January 7, 2016
Analysis of the human growth hormone receptor and IGF-I coding sequences in children with growth disorders
Aleksandra Obrepalska-Steplowska1, Andrzej Kedzia, Anna Goździcka-Józefiak
1Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland. alexandr@amu.edu.pl
Abstract:
Analysis of GHR and IGF-I coding sequences in 47 children with normal serum levels of GH, low IGF-I and growth disorders generally did not show mutation in the genes studied. Only one boy had a mutation located in the fifth exon of the GHR gene (C-->T in codon 88). This suggests that the growth disorders in this group of children might be due to a defect in a DNA region regulating expression of the GHR and IGF1 genes or genes involved in their regulation.
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