Lessons from new mouse models of glycogen storage disease type 1a in relation to the time course and organ specificity of the disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-014-9761-0
Reference50 articles.
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2. Chatelain F, Pégorier JP, Minassian C et al (1998) Development and regulation of glucose-6-phosphatase gene expression in rat liver, intestine, and kidney: in vivo and in vitro studies in cultured fetal hepatocytes. Diabetes 47:882–889
3. Chou JY, Jun HS, Mansfield BC (2010) Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy. Nat Rev Endocrinol 6:676–688. doi: 10.1038/nrendo.2010.189
4. Clar J, Gri B, Calderaro J et al (2014) Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy. Kidney Int. doi: 10.1038/ki.2014.102
5. Croset M, Rajas F, Zitoun C et al (2001) Rat small intestine is an insulin-sensitive gluconeogenic organ. Diabetes 50:740–746
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