Modeling Congenital Hyperinsulinism with ABCC8-Deficient Human Embryonic Stem Cells Generated by CRISPR/Cas9
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-03349-w.pdf
Reference53 articles.
1. Rahman, S. A., Nessa, A. & Hussain, K. Molecular mechanisms of congenital hyperinsulinism. Journal of molecular endocrinology 54, R119–129, doi: 10.1530/JME-15-0016 (2015).
2. Senniappan, S., Arya, V. B. & Hussain, K. The molecular mechanisms, diagnosis and management of congenital hyperinsulinism. Indian journal of endocrinology and metabolism 17, 19–30, doi: 10.4103/2230-8210.107822 (2013).
3. Fournet, J. C. & Junien, C. The genetics of neonatal hyperinsulinism. Hormone research 59 Suppl 1, 30–34, doi:67842 (2003).
4. Nessa, A., Rahman, S. A. & Hussain, K. Hyperinsulinemic Hypoglycemia - The Molecular Mechanisms. Frontiers in endocrinology 7, 29, doi: 10.3389/fendo.2016.00029 (2016).
5. Kapoor, R. R. et al. Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism. European journal of endocrinology 168, 557–564, doi: 10.1530/EJE-12-0673 (2013).
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