Receptor-mediated selective impairment of insulin-like growth factor-1 activity in congenital disorders of glycosylation patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://www.nature.com/articles/pr201696.pdf
Reference24 articles.
1. Jaeken J, Matthijs G. Congenital disorders of glycosylation: a rapidly expanding disease family. Annu Rev Genomics Hum Genet 2007;8:261–78.
2. Jaeken J. Congenital disorders of glycosylation. Ann N Y Acad Sci 2010;1214:190–8.
3. Woods AG, Woods CW, Snow TM. Congenital disorders of glycosylation. Adv Neonatal Care 2012;12:90–5.
4. Jaeken J. Congenital disorders of glycosylation (CDG): it’s (nearly) all in it! J Inherit Metab Dis 2011;34:853–8.
5. Makhseed N, Dhaunsi G, Jaeken J. Distinct features of congenital disorder of glycosylation type IIx in Kuwait: a case report. J Child Neurol 2012;27:222–4.
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Defective IGF-1 prohormone N-glycosylation and reduced IGF-1 receptor signaling activation in congenital disorders of glycosylation;Cellular and Molecular Life Sciences;2022-02-24
2. Receptor-mediated attenuation of insulin-like growth factor-1 activity by galactose-1-phosphate in neonate skin fibroblast cultures: Galactosemia pathogenesis;Advances in Clinical and Experimental Medicine;2020-04-30
3. Mosaicism of the UDP-Galactose transporter SLC35A2 in a female causing a congenital disorder of glycosylation: a case report;BMC Medical Genetics;2018-06-15
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