Nuclear factor-I and activator protein-2 bind in a mutually exclusive way to overlapping promoter sequences andtrans-activate the human growth hormone gene
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/18/1/57/6139653/18-1-57.pdf
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1. A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD);European Journal of Endocrinology;2016-08
2. Genetic Polymorphisms in the Locus Control Region and Promoter of GH1 Are Related to Serum IGF-I Levels and Height in Patients with Isolated Growth Hormone Deficiency and Healthy Controls;Hormone Research in Paediatrics;2010
3. Characterisation of a functional intronic polymorphism in the human growth hormone (GHI) gene;Human Genomics;2010
4. Expression of the osteonectin gene potentially controlled by multiple Cis- and trans-acting factors in cultured bone cells;Journal of Bone and Mineral Research;2009-12-03
5. A Functional Common Polymorphism in the Vitamin D-Responsive Element of theGH1Promoter Contributes to Isolated Growth Hormone Deficiency;The Journal of Clinical Endocrinology & Metabolism;2008-03-01
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