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Protein RS1 ( RSC1A1) Downregulates the Exocytotic Pathway of Glucose Transporter SGLT1 at Low Intracellular Glucose via Inhibition of Ornithine Decarboxylase. , Chintalapati C., Mol Pharmacol. November 1, 2016; 90 (5): 508-521.
Phosphorylation of RS1 ( RSC1A1) Steers Inhibition of Different Exocytotic Pathways for Glucose Transporter SGLT1 and Nucleoside Transporter CNT1, and an RS1-Derived Peptide Inhibits Glucose Absorption. , Veyhl-Wichmann M., Mol Pharmacol. January 1, 2016; 89 (1): 118-32.
Distinct action of the α-glucosidase inhibitor miglitol on SGLT3, enteroendocrine cells, and GLP1 secretion. , Lee EY ., J Endocrinol. March 1, 2015; 224 (3): 205-14.
Up-regulation of Na(+)-coupled glucose transporter SGLT1 by caveolin-1. , Elvira B., Biochim Biophys Acta. November 1, 2013; 1828 (11): 2394-8.
SMIT2 mediates all myo-inositol uptake in apical membranes of rat small intestine. , Aouameur R., Am J Physiol Gastrointest Liver Physiol. December 1, 2007; 293 (6): G1300-7.
Tripeptides of RS1 ( RSC1A1) inhibit a monosaccharide-dependent exocytotic pathway of Na+-D-glucose cotransporter SGLT1 with high affinity. , Vernaleken A., J Biol Chem. September 28, 2007; 282 (39): 28501-13.
A glucose sensor hiding in a family of transporters. , Diez-Sampedro A., Proc Natl Acad Sci U S A. September 30, 2003; 100 (20): 11753-8.
Polyphenol-induced inhibition of the response of na(+)/glucose cotransporter expressed in Xenopus oocytes. , Hossain SJ., J Agric Food Chem. August 28, 2002; 50 (18): 5215-9.
Cloning and functional expression of an SGLT-1-like protein from the Xenopus laevis intestine. , Nagata K., Am J Physiol. May 1, 1999; 276 (5): G1251-9.
Regulation of Na+/glucose cotransporters. , Wright EM., J Exp Biol. January 1, 1997; 200 (Pt 2): 287-93.
The high affinity Na+/glucose cotransporter. Re-evaluation of function and distribution of expression. , Lee WS., J Biol Chem. April 22, 1994; 269 (16): 12032-9.
Cloning of a membrane-associated protein which modifies activity and properties of the Na(+)-D-glucose cotransporter. , Veyhl M., J Biol Chem. November 25, 1993; 268 (33): 25041-53.
[30 years' work on congenital glucose and galactose malabsorption: from phenotype to genotype]. , Desjeux JF., Ann Gastroenterol Hepatol (Paris). October 1, 1993; 29 (5): 263-6; discussion 266-8.
[Thirty years of research on congenital glucose and galactose malabsorption: from phenotype to genotype]. , Desjeux JF., Bull Acad Natl Med. January 1, 1993; 177 (1): 125-31; discussion 132-5.
Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter. , Turk E., Nature. March 28, 1991; 350 (6316): 354-6.