17 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Molecular mechanisms of organic cation transport in OCT2-expressing Xenopus oocytes.
Kyoto University Hospital
Cepharanthin, a multidrug resistant modifier, is a substrate for P-glycoprotein.
Kyoto University Hospital
Multispecific substrate recognition of kidney-specific organic anion transporters OAT-K1 and OAT-K2.
Kyoto University Hospital
Trans-stimulation effects of folic acid derivatives on methotrexate transport by rat renal organic anion transporter, OAT-K1.
Kyoto University Hospital
Interaction and transport of thiazide diuretics, loop diuretics, and acetazolamide via rat renal organic anion transporter rOAT1.
Kyoto University Hospital
Interaction between methotrexate and nonsteroidal anti-inflammatory drugs in organic anion transporter.
Kyoto University Hospital
Inhibitory effect of anti-diabetic agents on rat organic anion transporter rOAT1.
Kyoto University Hospital
Distinct characteristics of organic cation transporters, OCT1 and OCT2, in the basolateral membrane of renal tubules.
Kyoto University Hospital
Functional characteristics and membrane localization of rat multispecific organic cation transporters, OCT1 and OCT2, mediating tubular secretion of cationic drugs.
Kyoto University Hospital
Different transport properties between famotidine and cimetidine by human renal organic ion transporters (SLC22A).
Kyoto University Hospital
Interactions of nonsteroidal anti-inflammatory drugs with rat renal organic anion transporter, OAT-K1.
Kyoto University Hospital
Recognition of L-amino acid ester compounds by rat peptide transporters PEPT1 and PEPT2.
Kyoto University Hospital
Effects of glibenclamide on glycylsarcosine transport by the rat peptide transporters PEPT1 and PEPT2.
Kyoto University Hospital
Rat renal organic anion transporter rOAT1 mediates transport of urinary-excreted cephalosporins, but not of biliary-excreted cefoperazone.
Kyoto University Hospital
Structural requirements for determining the substrate affinity of peptide transporters PEPT1 and PEPT2.
Kyoto University Hospital
Inhibitory effect of novel oral hypoglycemic agent nateglinide (AY4166) on peptide transporters PEPT1 and PEPT2.
Kyoto University Hospital