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Summary Anatomy Item Literature (6354) Expression Attributions Wiki
XB-ANAT-254

Papers associated with oocyte (and slc15a1)

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Thiodipeptides targeting the intestinal oligopeptide transporter as a general approach to improving oral drug delivery., Foley DW., Eur J Med Chem. August 5, 2018; 156 180-189.            


Effect of N-glycosylation on the transport activity of the peptide transporter PEPT1., Stelzl T., Am J Physiol Gastrointest Liver Physiol. January 15, 2016; 310 (2): G128-41.


Human intestine luminal ACE2 and amino acid transporter expression increased by ACE-inhibitors., Vuille-dit-Bille RN., Amino Acids. April 1, 2015; 47 (4): 693-705.


Raltegravir is a substrate for SLC22A6: a putative mechanism for the interaction between raltegravir and tenofovir., Moss DM., Antimicrob Agents Chemother. February 1, 2011; 55 (2): 879-87.


Frog oocytes to unveil the structure and supramolecular organization of human transport proteins., Bergeron MJ., PLoS One. January 1, 2011; 6 (7): e21901.          


Serine side chain-linked peptidomimetic conjugates of cyclic HPMPC and HPMPA: synthesis and interaction with hPEPT1., Peterson LW., Mol Pharm. December 6, 2010; 7 (6): 2349-61.


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.                


Substrate-induced changes in the density of peptide transporter PEPT1 expressed in Xenopus oocytes., Mertl M., Am J Physiol Cell Physiol. November 1, 2008; 295 (5): C1332-43.


Site-directed mutagenesis of Arginine282 suggests how protons and peptides are co-transported by rabbit PepT1., Pieri M., Int J Biochem Cell Biol. January 1, 2008; 40 (4): 721-30.                  


Evidence that the rabbit proton-peptide co-transporter PepT1 is a multimer when expressed in Xenopus laevis oocytes., Panitsas KE., Pflugers Arch. April 1, 2006; 452 (1): 53-63.


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.


A novel inhibitor of the mammalian peptide transporter PEPT1., Knütter I., Biochemistry. April 10, 2001; 40 (14): 4454-8.


Direct evidence for peptide transporter (PepT1)-mediated uptake of a nonpeptide prodrug, valacyclovir., Balimane PV., Biochem Biophys Res Commun. September 18, 1998; 250 (2): 246-51.


Identification of the histidine residues involved in substrate recognition by a rat H+/peptide cotransporter, PEPT1., Terada T., FEBS Lett. September 30, 1996; 394 (2): 196-200.


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.

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