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Regulation of Urate Homeostasis by Membrane Transporters.
- Published in:
- Gout, Urate, & Crystal Deposition Disease, 2024, v. 2, n. 2, p. 206, doi. 10.3390/gucdd2020016
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- Publication type:
- Article
Single-nephron assessment of urate excretion in patients with IgA nephropathy.
- Published in:
- Clinical Kidney Journal, 2024, v. 17, n. 3, p. 1, doi. 10.1093/ckj/sfae036
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- Publication type:
- Article
Plasma and Urinary Metabolomic Analysis of Gout and Asymptomatic Hyperuricemia and Profiling of Potential Biomarkers: A Pilot Study.
- Published in:
- Biomedicines, 2024, v. 12, n. 2, p. 300, doi. 10.3390/biomedicines12020300
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- Publication type:
- Article
Dysuricemia.
- Published in:
- Biomedicines, 2023, v. 11, n. 12, p. 3169, doi. 10.3390/biomedicines11123169
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- Publication type:
- Article
Exploring the Multifaceted Nexus of Uric Acid and Health: A Review of Recent Studies on Diverse Diseases.
- Published in:
- Biomolecules (2218-273X), 2023, v. 13, n. 10, p. 1519, doi. 10.3390/biom13101519
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- Publication type:
- Article
Possible Use of Non-purine Selective Xanthine Oxidoreductase Inhibitors for Prevention of Exercise-induced Acute Kidney Injury Associated with Renal Hypouricemia.
- Published in:
- Internal Medicine, 2023, v. 62, n. 18, p. 2725, doi. 10.2169/internalmedicine.0678-22
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- Publication type:
- Article
Characterization of Urate Metabolism and Complications of Patients with Renal Hypouricemia.
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- Internal Medicine, 2023, v. 62, n. 13, p. 1915, doi. 10.2169/internalmedicine.0457-22
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- Publication type:
- Article
Vitamin C transporter SVCT1 serves a physiological role as a urate importer: functional analyses and in vivo investigations.
- Published in:
- Pflügers Archiv: European Journal of Physiology, 2023, v. 475, n. 4, p. 489, doi. 10.1007/s00424-023-02792-1
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- Publication type:
- Article
Evaluation of ABCG2-mediated extra-renal urate excretion in hemodialysis patients.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-022-26519-x
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- Publication type:
- Article
Genetic Basis of the Epidemiological Features and Clinical Significance of Renal Hypouricemia.
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- Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071696
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- Publication type:
- Article
Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal Hypouricemia.
- Published in:
- Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071584
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- Publication type:
- Article
A Novel PRPS1 Mutation in a Japanese Patient with CMTX5 .
- Published in:
- Internal Medicine, 2022, v. 61, n. 11, p. 1749, doi. 10.2169/internalmedicine.8029-21
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- Publication type:
- Article
Xanthinuria Type 1 with a Novel Mutation in Xanthine Dehydrogenase and a Normal Endothelial Function.
- Published in:
- Internal Medicine, 2022, v. 61, n. 9, p. 1383, doi. 10.2169/internalmedicine.7897-21
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- Publication type:
- Article
OAT10/SLC22A13 Acts as a Renal Urate Re-Absorber: Clinico-Genetic and Functional Analyses With Pharmacological Impacts.
- Published in:
- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.842717
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- Publication type:
- Article
A meta-analysis of genome-wide association studies using Japanese and Taiwanese has revealed novel loci associated with gout susceptibility.
- Published in:
- Human Cell, 2022, v. 35, n. 2, p. 767, doi. 10.1007/s13577-021-00665-2
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- Publication type:
- Article
Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene.
- Published in:
- Rheumatology, 2022, v. 61, n. 3, p. 1276, doi. 10.1093/rheumatology/keab545
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- Publication type:
- Article
Association of Mutations Identified in Xanthinuria with the Function and Inhibition Mechanism of Xanthine Oxidoreductase.
- Published in:
- Biomedicines, 2021, v. 9, n. 11, p. 1723, doi. 10.3390/biomedicines9111723
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- Publication type:
- Article
Substantial anti-gout effect conferred by common and rare dysfunctional variants of URAT1/SLC22A12.
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- Rheumatology, 2021, v. 60, n. 11, p. 5224, doi. 10.1093/rheumatology/keab327
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- Publication type:
- Article
First clinical practice guideline for renal hypouricaemia: a rare disorder that aided the development of urate-lowering drugs for gout.
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- Rheumatology, 2021, v. 60, n. 9, p. 3961, doi. 10.1093/rheumatology/keab322
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- Publication type:
- Article
Effect of uric acid-lowering therapy on renal function in patients with chronic kidney disease: a systematic review and meta-analysis.
- Published in:
- Renal Replacement Therapy, 2021, v. 7, n. 1, p. 1, doi. 10.1186/s41100-021-00363-7
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- Publication type:
- Article
Association between polymorphism at IGF-1 rs35767 gene locus and long-term decline in renal function: a Japanese retrospective longitudinal cohort study.
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- 2021
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- Publication type:
- journal article
Renaturation of Lyophilized Concanavalin a Treated in Water Content Controlled Hydrated Ionic Liquids.
- Published in:
- Applied Sciences (2076-3417), 2021, v. 11, n. 1, p. 57, doi. 10.3390/app11010057
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- Publication type:
- Article
Dysfunctional ABCG2 gene polymorphisms are associated with serum uric acid levels and all-cause mortality in hemodialysis patients.
- Published in:
- Human Cell, 2020, v. 33, n. 3, p. 559, doi. 10.1007/s13577-020-00342-w
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- Publication type:
- Article
A common variant of LDL receptor related protein 2 (LRP2) gene is associated with gout susceptibility: a meta-analysis in a Japanese population.
- Published in:
- Human Cell, 2020, v. 33, n. 2, p. 303, doi. 10.1007/s13577-019-00318-5
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- Publication type:
- Article
Electrochemical analysis of uric acid excretion to the intestinal lumen: Effect of serum uric acid-lowering drugs and 5/6 nephrectomy on intestinal uric acid levels.
- Published in:
- PLoS ONE, 2019, v. 14, n. 12, p. N.PAG, doi. 10.1371/journal.pone.0226918
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- Publication type:
- Article
Renal stone and chronic kidney failure associated with hypouricemia: Questions.
- Published in:
- 2019
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- Publication type:
- Case Study
Renal stone and chronic kidney failure associated with hypouricemia: Answers.
- Published in:
- Pediatric Nephrology, 2019, v. 34, n. 7, p. 1225, doi. 10.1007/s00467-018-4170-5
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- Publication type:
- Article
Clinical practice guideline for renal hypouricemia (1st edition).
- Published in:
- Human Cell, 2019, v. 32, n. 2, p. 83, doi. 10.1007/s13577-019-00239-3
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- Publication type:
- Article
Diet-induced hyperhomocysteinemia impairs vasodilation in 5/6-nephrectomized rats.
- Published in:
- Amino Acids, 2018, v. 50, n. 10, p. 1485, doi. 10.1007/s00726-018-2626-3
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- Publication type:
- Article
Meta-analysis confirms an association between gout and a common variant of LRRC16A locus.
- Published in:
- Modern Rheumatology, 2017, v. 27, n. 3, p. 553, doi. 10.1080/14397595.2016.1218413
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- Publication type:
- Article
Identification of Febuxostat as a New Strong ABCG2 Inhibitor: Potential Applications and Risks in Clinical Situations.
- Published in:
- Frontiers in Pharmacology, 2016, v. 7, p. 1, doi. 10.3389/fphar.2016.00518
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- Publication type:
- Article
Hyperuricemia in acute gastroenteritis is caused by decreased urate excretion via ABCG2.
- Published in:
- Scientific Reports, 2016, p. 31003, doi. 10.1038/srep31003
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- Publication type:
- Article
Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.
- Published in:
- Clinical & Experimental Nephrology, 2016, v. 20, n. 4, p. 578, doi. 10.1007/s10157-015-1186-z
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- Publication type:
- Article
Rare case of nephrocalcinosis in the distal tubules caused by hereditary renal hypouricaemia 3 months after kidney transplantation.
- Published in:
- Nephrology, 2016, v. 21, p. 67, doi. 10.1111/nep.12774
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- Publication type:
- Article
The effects of URAT1/SLC22A12 nonfunctional variants,R90H and W258X, on serum uric acid levels and gout/hyperuricemia progression.
- Published in:
- Scientific Reports, 2016, p. 20148, doi. 10.1038/srep20148
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- Publication type:
- Article
Apoptosis induced by an uromodulin mutant C112Y and its suppression by topiroxostat.
- Published in:
- Clinical & Experimental Nephrology, 2015, v. 19, n. 4, p. 576, doi. 10.1007/s10157-014-1032-8
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- Publication type:
- Article
NPT1/SLC17A1 Is a Renal Urate Exporter in Humans and Its Common Gain-of-Function Variant Decreases the Risk of Renal Underexcretion Gout.
- Published in:
- Arthritis & Rheumatology, 2015, v. 67, n. 1, p. 281, doi. 10.1002/art.38884
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- Publication type:
- Article
Common variant of ALPK1 is not associated with gout: a replication study.
- Published in:
- Human Cell, 2015, v. 28, n. 1, p. 1, doi. 10.1007/s13577-014-0103-1
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- Publication type:
- Article
Effects of irbesartan on serum uric acid levels in patients with hypertension and diabetes.
- Published in:
- Clinical Pharmacology, 2014, v. 6, p. 79, doi. 10.2147/CPAA.S61462
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- Publication type:
- Article
Paracellular route is the major urate transport pathway across the blood-placental barrier.
- Published in:
- Physiological Reports, 2014, v. 2, n. 5, p. n/a, doi. 10.14814/phy2.12013
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- Publication type:
- Article
Common variants of a urate-associated gene LRP2 are not associated with gout susceptibility.
- Published in:
- Rheumatology International, 2014, v. 34, n. 4, p. 473, doi. 10.1007/s00296-013-2924-8
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- Publication type:
- Article
Ependymal cells of the mouse brain express urate transporter 1 (URAT1).
- Published in:
- Fluids & Barriers of the CNS, 2013, v. 10, n. 1, p. 2, doi. 10.1186/2045-8118-10-31
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- Publication type:
- Article
A common missense variant of monocarboxylate transporter 9 (<i>MCT9/SLC16A9</i>) gene is associated with renal overload gout, but not with all gout susceptibility.
- Published in:
- Human Cell, 2013, v. 26, n. 4, p. 133, doi. 10.1007/s13577-013-0073-8
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- Publication type:
- Article
Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1067, doi. 10.1038/ejhg.2013.3
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- Publication type:
- Article
Common dysfunctional variants in ABCG2 are a major cause of early-onset gout.
- Published in:
- Scientific Reports, 2013, p. 1, doi. 10.1038/srep02014
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- Publication type:
- Article
Mutations Associated with Functional Disorder of Xanthine Oxidoreductase and Hereditary Xanthinuria in Humans.
- Published in:
- International Journal of Molecular Sciences, 2012, v. 13, n. 11, p. 15475, doi. 10.3390/ijms131115475
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- Publication type:
- Article
Altered d-methionine kinetics in rats with renal impairment.
- Published in:
- Amino Acids, 2011, v. 40, n. 4, p. 1205, doi. 10.1007/s00726-010-0746-5
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- Publication type:
- Article
Prenatal Brain Disruption in Molybdenum Cofactor Deficiency.
- Published in:
- Journal of Child Neurology, 2011, v. 26, n. 4, p. 460, doi. 10.1177/0883073810383017
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- Publication type:
- Article
Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency.
- Published in:
- Developmental Medicine & Child Neurology, 2010, v. 52, n. 9, p. 868, doi. 10.1111/j.1469-8749.2010.03724.x
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- Publication type:
- Article
Synthesis of optically active deuterium-labeled homocysteine thiolactone.
- Published in:
- Journal of Labelled Compounds & Radiopharmaceuticals, 2010, v. 53, n. 8, p. 552, doi. 10.1002/jlcr.1782
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- Publication type:
- Article