24 results for author:"Ichida K." in Literature citations
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| Increased expression of SLC2A9 decreases urate excretion from the kidney. Kimura T., Amonpatumrat S., Tsukada A., Fukutomi T., Jutabha P., Thammapratip T., Lee E.J., Ichida K., Anzai N., Sakurai H. Nucleosides Nucleotides Nucleic Acids 30:1295-1301(2011) · Mapped (1) |
| ABCG2/BCRP dysfunction as a major cause of gout. Matsuo H., Takada T., Ichida K., Nakamura T., Nakayama A., Suzuki H., Hosoya T., Shinomiya N. Nucleosides Nucleotides Nucleic Acids 30:1117-1128(2011) · Mapped (5) |
| Identification of ABCG2 dysfunction as a major factor contributing to gout. Matsuo H., Takada T., Ichida K., Nakamura T., Nakayama A., Takada Y., Okada C., Sakurai Y., Hosoya T., Kanai Y. et al. Nucleosides Nucleotides Nucleic Acids 30:1098-1104(2011) · Mapped (5) |
| ABCG2 is a high-capacity urate transporter and its genetic impairment increases serum uric acid levels in humans. Nakayama A., Matsuo H., Takada T., Ichida K., Nakamura T., Ikebuchi Y., Ito K., Hosoya T., Kanai Y., Suzuki H. et al. Nucleosides Nucleotides Nucleic Acids 30:1091-1097(2011) · Mapped (5) |
| Two cases of nephrotic syndrome (NS)-induced acute kidney injury (AKI) associated with renal hypouricemia. Takeda Y., Abe A., Nakanishi S., Umezu M., Hirano K., Hayakawa H., Ohno I., Ichida K., Yamaguchi Y., Hosoya T. et al. Clin. Nephrol. 76:78-82(2011) · Mapped (5) |
| Establishment and analysis of SLC22A12 (URAT1) knockout mouse. Hosoyamada M., Takiue Y., Morisaki H., Cheng J., Ikawa M., Okabe M., Morisaki T., Ichida K., Hosoya T., Shibasaki T. Nucleosides Nucleotides Nucleic Acids 29:314-320(2010) · Mapped (1) |
| Common defects of ABCG2, a high-capacity urate exporter, cause gout: a function-based genetic analysis in a Japanese population. Matsuo H., Takada T., Ichida K., Nakamura T., Nakayama A., Ikebuchi Y., Ito K., Kusanagi Y., Chiba T., Tadokoro S. et al. Sci. Transl. Med. 1:5ra11-5ra11(2009) · UniProtKB (1) · Mapped (4) |
| Plasma urate level is directly regulated by a voltage-driven urate efflux transporter URATv1 (SLC2A9) in humans. Anzai N., Ichida K., Jutabha P., Kimura T., Babu E., Jin C.J., Srivastava S., Kitamura K., Hisatome I., Endou H. et al. J. Biol. Chem. 283:26834-26838(2008) · Mapped (6) |
| Uricosuric action of losartan via the inhibition of urate transporter 1 (URAT 1) in hypertensive patients. Hamada T., Ichida K., Hosoyamada M., Mizuta E., Yanagihara K., Sonoyama K., Sugihara S., Igawa O., Hosoya T., Ohtahara A. et al. Am. J. Hypertens. 21:1157-1162(2008) · Mapped (5) |
| Production and characterization of transgenic mice harboring mutant human UMOD gene. Takiue Y., Hosoyamada M., Yokoo T., Kimura M., Ochiai M., Kaneko K., Ichida K., Hosoya T., Shibasaki T. Nucleosides Nucleotides Nucleic Acids 27:596-600(2008) · Mapped (4) |
| Age and origin of the G774A mutation in SLC22A12 causing renal hypouricemia in Japanese. Ichida K., Hosoyamada M., Kamatani N., Kamitsuji S., Hisatome I., Shibasaki T., Hosoya T. Clin. Genet. 74:243-251(2008) · Mapped (5) |
| Plasma adiponectin concentrations and placental adiponectin expression in pre-eclamptic women. Ichida K., Moriyama T., Morita H., Kondo T., Yoshida S., Ohara N., Maruo T. Gynecol. Endocrinol. 23:238-243(2007) · Mapped (3) |
| Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure. Ohtsuka Y., Zaitsu M., Ichida K., Isomura N., Tsuji K., Sato T., Hamasaki Y. Pediatr Int 49:235-237(2007) · Mapped (5) |
| 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. Yamaguchi Y., Matsumura T., Ichida K., Okamoto K., Nishino T. |
| Molybdenum cofactor deficiency: clinical features in a Turkish patient. Per H., Gumus H., Ichida K., Caglayan O., Kumandas S. Brain Dev. 29:365-368(2007) · Mapped (2) |
| Function and localization of urate transporter 1 in mouse kidney. Hosoyamada M., Ichida K., Enomoto A., Hosoya T., Endou H. J. Am. Soc. Nephrol. 15:261-268(2004) · UniProtKB (1) · Mapped (1) |
| Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. Ichida K., Hosoyamada M., Hisatome I., Enomoto A., Hikita M., Endou H., Hosoya T. J. Am. Soc. Nephrol. 15:164-173(2004) · UniProtKB (1) |
| Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria. Gok F., Ichida K., Topaloglu R. Nephrol. Dial. Transplant. 18:2278-2283(2003) · UniProtKB (1) |
| Molecular identification of a renal urate anion exchanger that regulates blood urate levels. Enomoto A., Kimura H., Chairoungdua A., Shigeta Y., Jutabha P., Cha S.H., Hosoyamada M., Takeda M., Sekine T., Igarashi T. et al. |
| Human organic anion transporters and human organic cation transporters mediate renal transport of prostaglandins. Kimura H., Takeda M., Narikawa S., Enomoto A., Ichida K., Endou H. J. Pharmacol. Exp. Ther. 301:293-298(2002) · UniProtKB (1) |
| Mutation of human molybdenum cofactor sulfurase gene is responsible to classical xanthinuria type II. Ichida K., Matsumura T., Sakuma R., Hosoya T., Nishino T. Biochem. Biophys. Res. Commun. 282:1194-1200(2001) · UniProtKB (2) |
| XDH gene mutation is the underlying cause of classical xanthinuria: a second report. Levartovsky D., Lagziel A., Sperling O., Liberman U., Yaron M., Hosoya T., Ichida K., Peretz H. Kidney Int. 57:2215-2220(2000) · UniProtKB (1) |
| Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria. Ichida K., Amaya Y., Kamatani N., Nishino T., Hosoya T., Sakai O. J. Clin. Invest. 99:2391-2397(1997) · UniProtKB (1) · Mapped (3) |
| Cloning of the cDNA encoding human xanthine dehydrogenase (oxidase): structural analysis of the protein and chromosomal location of the gene. Ichida K., Amaya Y., Noda K., Minoshima S., Hosoya T., Sakai O., Shimizu N., Nishino T. Gene 133:279-284(1993) · UniProtKB (1) |