Ichida K - Search Results

1

Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis.

Stiburkova B, Sebesta I, Ichida K, Nakamura M, Hulkova H, Krylov V, Kryspinova L, Jahnova H. Stiburkova B, et al. Among authors: ichida k. Eur J Hum Genet. 2013 Oct;21(10):1067-73. doi: 10.1038/ejhg.2013.3. Epub 2013 Feb 6. Eur J Hum Genet. 2013. PMID: 23386035 Free PMC article.

2

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. Ichida K, et al. Clin Genet. 2008 Sep;74(3):243-51. doi: 10.1111/j.1399-0004.2008.01021.x. Epub 2008 May 15. Clin Genet. 2008. PMID: 18492088

3

Concentration-dependent inhibitory effect of irbesartan on renal uric acid transporters.

Nakamura M, Anzai N, Jutabha P, Sato H, Sakurai H, Ichida K. Nakamura M, et al. Among authors: ichida k. J Pharmacol Sci. 2010;114(1):115-8. doi: 10.1254/jphs.10064sc. Epub 2010 Aug 21. J Pharmacol Sci. 2010. PMID: 20736511 Free article.

4

Novel homozygous insertion in SLC2A9 gene caused renal hypouricemia.

Stiburkova B, Ichida K, Sebesta I. Stiburkova B, et al. Among authors: ichida k. Mol Genet Metab. 2011 Apr;102(4):430-5. doi: 10.1016/j.ymgme.2010.12.016. Epub 2011 Jan 4. Mol Genet Metab. 2011. PMID: 21256783

5

Diagnostic tests for primary renal hypouricemia.

Sebesta I, Stiburkova B, Bartl J, Ichida K, Hosoyamada M, Taylor J, Marinaki A. Sebesta I, et al. Among authors: ichida k. Nucleosides Nucleotides Nucleic Acids. 2011 Dec;30(12):1112-6. doi: 10.1080/15257770.2011.611483. Nucleosides Nucleotides Nucleic Acids. 2011. PMID: 22132965

6

Identification of a xanthinuria type I case with mutations of xanthine dehydrogenase in an Afghan child.

Nakamura M, Yuichiro Y, Sass JO, Tomohiro M, Schwab KO, Takeshi N, Tatsuo H, Ichida K. Nakamura M, et al. Among authors: ichida k. Clin Chim Acta. 2012 Dec 24;414:158-60. doi: 10.1016/j.cca.2012.08.011. Epub 2012 Aug 17. Clin Chim Acta. 2012. PMID: 22981351

7

Ependymal cells of the mouse brain express urate transporter 1 (URAT1).

Tomioka NH, Nakamura M, Doshi M, Deguchi Y, Ichida K, Morisaki T, Hosoyamada M. Tomioka NH, et al. Among authors: ichida k. Fluids Barriers CNS. 2013 Oct 24;10(1):31. doi: 10.1186/2045-8118-10-31. Fluids Barriers CNS. 2013. PMID: 24156345 Free PMC article.

8

Effects of irbesartan on serum uric acid levels in patients with hypertension and diabetes.

Nakamura M, Sasai N, Hisatome I, Ichida K. Nakamura M, et al. Among authors: ichida k. Clin Pharmacol. 2014 May 3;6:79-86. doi: 10.2147/CPAA.S61462. eCollection 2014. Clin Pharmacol. 2014. PMID: 24833923 Free PMC article.

9

Depletion of Uric Acid Due to SLC22A12 (URAT1) Loss-of-Function Mutation Causes Endothelial Dysfunction in Hypouricemia.

Sugihara S, Hisatome I, Kuwabara M, Niwa K, Maharani N, Kato M, Ogino K, Hamada T, Ninomiya H, Higashi Y, Ichida K, Yamamoto K. Sugihara S, et al. Among authors: ichida k. Circ J. 2015;79(5):1125-32. doi: 10.1253/circj.CJ-14-1267. Epub 2015 Feb 23. Circ J. 2015. PMID: 25739858 Free article.

10

Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease.

Stiburkova B, Stekrova J, Nakamura M, Ichida K. Stiburkova B, et al. Among authors: ichida k. Am J Med Sci. 2015 Oct;350(4):268-71. doi: 10.1097/MAJ.0000000000000550. Am J Med Sci. 2015. PMID: 26418379

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