Works by Ichida, Kimiyoshi
Results: 76
First verification of human small intestinal uric acid secretion and effect of ABCG2 polymorphisms.
- Published in:
- 2025
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- Publication type:
- Letter
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
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
Pseudogenization of the Slc23a4 gene is necessary for the survival of Xdh-deficient mice.
- Published in:
- Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-87751-9
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- Publication type:
- Article
Exploring the Multifaceted Nexus of Uric Acid and Health: A Review of Recent Studies on Diverse Diseases.
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- Biomolecules (2218-273X), 2023, v. 13, n. 10, p. 1519, doi. 10.3390/biom13101519
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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.
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- Nephrology, 2016, v. 21, p. 67, doi. 10.1111/nep.12774
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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
Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency.
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- 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
Annual change in eGFR in renal hypouricemia: a retrospective pilot study.
- Published in:
- Clinical & Experimental Nephrology, 2025, v. 29, n. 2, p. 173, doi. 10.1007/s10157-024-02558-8
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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.
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- Renal Replacement Therapy, 2021, v. 7, n. 1, p. 1, doi. 10.1186/s41100-021-00363-7
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- Publication type:
- Article
Uricosuric Action of Losartan via the Inhibition of Urate Transporter 1 (URAT1) in Hypertensive Patients.
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- American Journal of Hypertension, 2008, v. 21, n. 10, p. 1157, doi. 10.1038/ajh.2008.245
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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.
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- Biomedicines, 2024, v. 12, n. 2, p. 300, doi. 10.3390/biomedicines12020300
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- Publication type:
- Article
Dysuricemia.
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- Biomedicines, 2023, v. 11, n. 12, p. 3169, doi. 10.3390/biomedicines11123169
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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
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
Paracellular route is the major urate transport pathway across the blood-placental barrier.
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- Physiological Reports, 2014, v. 2, n. 5, p. n/a, doi. 10.14814/phy2.12013
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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
Possible Use of Non-purine Selective Xanthine Oxidoreductase Inhibitors for Prevention of Exercise-induced Acute Kidney Injury Associated with Renal Hypouricemia.
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- 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
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.
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- Internal Medicine, 2022, v. 61, n. 9, p. 1383, doi. 10.2169/internalmedicine.7897-21
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- Publication type:
- Article
Urate transport via human PAH transporter hOAT1 and its gene structure.
- Published in:
- Kidney International, 2003, v. 63, n. 1, p. 143, doi. 10.1046/j.1523-1755.2003.00710.x
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- Publication type:
- Article
XDH gene mutation is the underlying cause of classical xanthinuria: A second report.
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- Kidney International, 2000, v. 57, n. 6, p. 2215, doi. 10.1046/j.1523-1755.2000.00082.x
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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.
- Published in:
- 2021
- By:
- Publication type:
- journal article
A case of renal hypouricemia due to T217M mutation in SLC22A12 incidentally associated with IgA nephropathy.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
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
Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure.
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- Pediatrics International, 2007, v. 49, n. 2, p. 235, doi. 10.1111/j.1442-200X.2007.02337.x
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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
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
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
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
Common variants of a urate-associated gene LRP2 are not associated with gout susceptibility.
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- Rheumatology International, 2014, v. 34, n. 4, p. 473, doi. 10.1007/s00296-013-2924-8
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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.
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- 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
Human Xanthine Oxidase Changes its Substrate Specificity to Aldehyde Oxidase Type upon Mutation of Amino Acid Residues in the Active Site: Roles of Active Site Residues in Binding and Activation of Purine Substrate.
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- Journal of Biochemistry, 2007, v. 141, n. 4, p. 513, doi. 10.1093/jb/mvm053
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- Publication type:
- Article
Synthesis of optically active deuterium-labeled homocysteine thiolactone.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2010, v. 53, n. 8, p. 552, doi. 10.1002/jlcr.1782
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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
Successful living-related kidney transplantation in hereditary renal hypouricaemia.
- Published in:
- Nephrology Dialysis Transplantation, 2006, v. 21, n. 7, p. 2041, doi. 10.1093/ndt/gfk103
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- Publication type:
- Article
Modified forearm ischemic test in hypouricemic patients.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2020, v. 39, n. 10-12, p. 1432, doi. 10.1080/15257770.2020.1750636
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- Publication type:
- Article
Xanthine oxidoreductase knockout mice with high HPRT activity were not rescued by NAD<sup>+</sup> replenishment.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2020, v. 39, n. 10-12, p. 1465, doi. 10.1080/15257770.2020.1725044
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- Publication type:
- Article
Expression of a human NPT1/SLC17A1 missense variant which increases urate export.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2016, v. 35, n. 10-12, p. 536, doi. 10.1080/15257770.2016.1149192
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- Publication type:
- Article
ABCG2 Dysfunction Increases the Risk of Renal Overload Hyperuricemia.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2014, v. 33, n. 4-6, p. 266, doi. 10.1080/15257770.2013.866679
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- Publication type:
- Article
Hypoxanthine Guanine Phosphoribosyltransferase (HPRT) Deficiencies: HPRT1 Mutations in New Japanese Families and PRPP Concentration.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2014, v. 33, n. 4-6, p. 218, doi. 10.1080/15257770.2013.865743
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- Publication type:
- Article
ABCG2 Dysfunction Increases Serum Uric Acid by Decreased Intestinal Urate Excretion.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2014, v. 33, n. 4-6, p. 275, doi. 10.1080/15257770.2013.854902
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- Publication type:
- Article
Gout and Hyperuricemia in Japan: Perspectives for International Research on Purines and Pyrimidines in Man.
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- Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1001, doi. 10.1080/15257770.2011.633955
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- Publication type:
- Article
ABCG2/BCRP Dysfunction as a Major Cause of Gout.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1117, doi. 10.1080/15257770.2011.633954
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- Publication type:
- Article
ABCG2 is a High-Capacity Urate Transporter and its Genetic Impairment Increases Serum Uric Acid Levels in Humans.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1091, doi. 10.1080/15257770.2011.633953
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- Publication type:
- Article
Increased Expression of SLC2A9 Decreases Urate Excretion From the Kidney.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1295, doi. 10.1080/15257770.2011.628354
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- Publication type:
- Article
Diagnostic Tests for Primary Renal Hypouricemia.
- Published in:
- Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1112, doi. 10.1080/15257770.2011.611483
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- Publication type:
- Article