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Frog oocytes to unveil the structure and supramolecular organization of human transport proteins. , Bergeron MJ., PLoS One. January 1, 2011; 6 (7): e21901.
The transmembrane tyrosines Y56, Y91 and Y167 play important roles in determining the affinity and transport rate of the rabbit proton-coupled peptide transporter PepT1. , Pieri M., Int J Biochem Cell Biol. November 1, 2009; 41 (11): 2204-13.
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 rapid in vitro screening for delivery of peptide-derived peptidase inhibitors as potential drug candidates via epithelial peptide transporters. , Foltz M., J Pharmacol Exp Ther. August 1, 2004; 310 (2): 695-702.
Site-directed mutation of arginine 282 to glutamate uncouples the movement of peptides and protons by the rabbit proton-peptide cotransporter PepT1. , Meredith D., J Biol Chem. April 16, 2004; 279 (16): 15795-8.
Identification of the histidyl residue obligatory for the catalytic activity of the human H+/peptide cotransporters PEPT1 and PEPT2. , Fei YJ., Biochemistry. January 14, 1997; 36 (2): 452-60.
The peptide-based thrombin inhibitor CRC 220 is a new substrate of the basolateral rat liver organic anion-transporting polypeptide. , Eckhardt U., Hepatology. August 1, 1996; 24 (2): 380-4.
Nonradioactive monitoring of organic and inorganic solute transport into single Xenopus oocytes by capillary zone electrophoresis. , Nussberger S., Biophys J. February 1, 1996; 70 (2): 998-1005.