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Summary Anatomy Item Literature (3130) Expression Attributions Wiki
XB-ANAT-821

Papers associated with kidney (and slc22a6)

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Eggshell Membrane Ameliorates Hyperuricemia by Increasing Urate Excretion in Potassium Oxonate-Injected Rats., Sung YY., Nutrients. September 23, 2021; 13 (10):


Genetic and Physiological Effects of Insulin on Human Urate Homeostasis., Mandal AK., Front Physiol. January 1, 2021; 12 713710.              


Dual actions on gout flare and acute kidney injury along with enhanced renal transporter activities by Yokuininto, a Kampo medicine., Lee SH., BMC Complement Altern Med. March 12, 2019; 19 (1): 57.        


Organic anion transporters, OAT1 and OAT3, are crucial biopterin transporters involved in bodily distribution of tetrahydrobiopterin and exclusion of its excess., Ohashi A., Mol Cell Biochem. November 1, 2017; 435 (1-2): 97-108.        


Transport of 3-fluoro-L-α-methyl-tyrosine (FAMT) by organic ion transporters explains renal background in [(18)F]FAMT positron emission tomography., Wei L., J Pharmacol Sci. February 1, 2016; 130 (2): 101-9.


Nonclassical MHC-Restricted Invariant Vα6 T Cells Are Critical for Efficient Early Innate Antiviral Immunity in the Amphibian Xenopus laevis., Edholm ES., J Immunol. July 15, 2015; 195 (2): 576-86.


Transporters involved in renal excretion of N-carbamoylglutamate, an orphan drug to treat inborn n-acetylglutamate synthase deficiency., Schwob E., Am J Physiol Renal Physiol. December 15, 2014; 307 (12): F1373-9.


Species differences of organic anion transporters involved in the renal uptake of 4-amino-3-chlorophenyl hydrogen sulfate, a metabolite of resatorvid, between rats and dogs., Takeuchi T., Biopharm Drug Dispos. May 1, 2013; 34 (4): 236-46.


Caffeic acid inhibits organic anion transporters OAT1 and OAT3 in rat kidney., Uwai Y., Drug Metabol Drug Interact. January 1, 2013; 28 (4): 247-50.


Interaction and transport of kynurenic acid via human organic anion transporters hOAT1 and hOAT3., Uwai Y., Pharmacol Res. February 1, 2012; 65 (2): 254-60.


Linkage of organic anion transporter-1 to metabolic pathways through integrated "omics"-driven network and functional analysis., Ahn SY., J Biol Chem. September 9, 2011; 286 (36): 31522-31.


Untargeted metabolomics identifies enterobiome metabolites and putative uremic toxins as substrates of organic anion transporter 1 (Oat1)., Wikoff WR., J Proteome Res. June 3, 2011; 10 (6): 2842-51.


The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps., Drews C., BMC Dev Biol. January 31, 2011; 11 5.              


Analysis of three-dimensional systems for developing and mature kidneys clarifies the role of OAT1 and OAT3 in antiviral handling., Nagle MA., J Biol Chem. January 7, 2011; 286 (1): 243-51.


Human sodium phosphate transporter 4 (hNPT4/SLC17A3) as a common renal secretory pathway for drugs and urate., Jutabha P., J Biol Chem. November 5, 2010; 285 (45): 35123-32.


Interaction of organic cations with organic anion transporters., Ahn SY., J Biol Chem. November 6, 2009; 284 (45): 31422-30.


Molecular evidence for an involvement of organic anion transporters (OATs) in aristolochic acid nephropathy., Bakhiya N., Toxicology. October 1, 2009; 264 (1-2): 74-9.


Organic anion transporters OAT1 and OAT4 mediate the high affinity transport of glutarate derivatives accumulating in patients with glutaric acidurias., Hagos Y., Pflugers Arch. October 1, 2008; 457 (1): 223-31.


Multi-level analysis of organic anion transporters 1, 3, and 6 reveals major differences in structural determinants of antiviral discrimination., Truong DM., J Biol Chem. March 28, 2008; 283 (13): 8654-63.


Involvement of uric acid transporters in alteration of serum uric acid level by angiotensin II receptor blockers., Sato M., Pharm Res. March 1, 2008; 25 (3): 639-46.


Involvement of rat and human organic anion transporter 3 in the renal tubular secretion of topotecan [(S)-9-dimethylaminomethyl-10-hydroxy-camptothecin hydrochloride]., Matsumoto S., J Pharmacol Exp Ther. September 1, 2007; 322 (3): 1246-52.


The contribution of organic anion transporters OAT1 and OAT3 to the renal uptake of rosuvastatin., Windass AS., J Pharmacol Exp Ther. September 1, 2007; 322 (3): 1221-7.


Drug and toxicant handling by the OAT organic anion transporters in the kidney and other tissues., Nigam SK., Nat Clin Pract Nephrol. August 1, 2007; 3 (8): 443-8.


Co-localization and interaction of organic anion transporter 1 with caveolin-2 in rat kidney., Kwak JO., Exp Mol Med. June 30, 2005; 37 (3): 204-12.


Identification and functional assessment of the novel murine organic anion transporter Oat5 (Slc22a19) expressed in kidney., Youngblood GL., Am J Physiol Renal Physiol. August 1, 2004; 287 (2): F236-44.


Stoichiometry of organic anion/dicarboxylate exchange in membrane vesicles from rat renal cortex and hOAT1-expressing cells., Aslamkhan A., Am J Physiol Renal Physiol. October 1, 2003; 285 (4): F775-83.


Human renal organic anion transporter 1-dependent uptake and toxicity of mercuric-thiol conjugates in Madin-Darby canine kidney cells., Aslamkhan AG., Mol Pharmacol. March 1, 2003; 63 (3): 590-6.


Rat renal organic anion transporter rOAT1 mediates transport of urinary-excreted cephalosporins, but not of biliary-excreted cefoperazone., Uwai Y., Drug Metab Pharmacokinet. January 1, 2002; 17 (2): 125-9.


Mercapturic acids (N-acetylcysteine S-conjugates) as endogenous substrates for the renal organic anion transporter-1., Pombrio JM., Mol Pharmacol. November 1, 2001; 60 (5): 1091-9.


Isolation of a family of organic anion transporters from human liver and kidney., Sun W., Biochem Biophys Res Commun. May 4, 2001; 283 (2): 417-22.


Interaction and transport of thiazide diuretics, loop diuretics, and acetazolamide via rat renal organic anion transporter rOAT1., Uwai Y., J Pharmacol Exp Ther. October 1, 2000; 295 (1): 261-5.


Cloning and functional characterization of the bile acid-sensitive methotrexate carrier from rat liver cells., Honscha W., Hepatology. June 1, 2000; 31 (6): 1296-304.


Developmentally regulated expression of organic ion transporters NKT (OAT1), OCT1, NLT (OAT2), and Roct., Pavlova A., Am J Physiol Renal Physiol. April 1, 2000; 278 (4): F635-43.


The interaction and transport of beta-lactam antibiotics with the cloned rat renal organic anion transporter 1., Jariyawat S., J Pharmacol Exp Ther. August 1, 1999; 290 (2): 672-7.


Transport of ochratoxin A by renal multispecific organic anion transporter 1., Tsuda M., J Pharmacol Exp Ther. June 1, 1999; 289 (3): 1301-5.


Molecular cloning and characterization of a new multispecific organic anion transporter from rat brain., Kusuhara H., J Biol Chem. May 7, 1999; 274 (19): 13675-80.


Molecular cloning and characterization of two novel human renal organic anion transporters (hOAT1 and hOAT3)., Race JE., Biochem Biophys Res Commun. February 16, 1999; 255 (2): 508-14.


Functional characterization of the rat multispecific organic anion transporter OAT1 mediating basolateral uptake of anionic drugs in the kidney., Uwai Y., FEBS Lett. November 6, 1998; 438 (3): 321-4.


Cloning and functional characterization of a potential-sensitive, polyspecific organic cation transporter (OCT3) most abundantly expressed in placenta., Kekuda R., J Biol Chem. June 26, 1998; 273 (26): 15971-9.


Identification of multispecific organic anion transporter 2 expressed predominantly in the liver., Sekine T., FEBS Lett. June 12, 1998; 429 (2): 179-82.


Expression cloning and characterization of ROAT1. The basolateral organic anion transporter in rat kidney., Sweet DH., J Biol Chem. November 28, 1997; 272 (48): 30088-95.


Expression cloning and characterization of a renal organic anion transporter from winter flounder., Wolff NA., FEBS Lett. November 17, 1997; 417 (3): 287-91.


Expression cloning and characterization of a novel multispecific organic anion transporter., Sekine T., J Biol Chem. July 25, 1997; 272 (30): 18526-9.


Molecular cloning and characterization of NKT, a gene product related to the organic cation transporter family that is almost exclusively expressed in the kidney., Lopez-Nieto CE., J Biol Chem. March 7, 1997; 272 (10): 6471-8.

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