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Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia.
Wakida N, Tuyen DG, Adachi M, Miyoshi T, Nonoguchi H, Oka T, Ueda O, Tazawa M, Kurihara S, Yoneta Y, Shimada H, Oda T, Kikuchi Y, Matsuo H, Hosoyamada M, Endou H, Otagiri M, Tomita K, Kitamura K. Wakida N, et al. Among authors: endou h. J Clin Endocrinol Metab. 2005 Apr;90(4):2169-74. doi: 10.1210/jc.2004-1111. Epub 2005 Jan 5. J Clin Endocrinol Metab. 2005. PMID: 15634722
Molecular identification of a renal urate anion exchanger that regulates blood urate levels.
Enomoto A, Kimura H, Chairoungdua A, Shigeta Y, Jutabha P, Cha SH, Hosoyamada M, Takeda M, Sekine T, Igarashi T, Matsuo H, Kikuchi Y, Oda T, Ichida K, Hosoya T, Shimokata K, Niwa T, Kanai Y, Endou H. Enomoto A, et al. Among authors: endou h. Nature. 2002 May 23;417(6887):447-52. doi: 10.1038/nature742. Epub 2002 Apr 14. Nature. 2002. PMID: 12024214
Human sodium phosphate transporter 4 (hNPT4/SLC17A3) as a common renal secretory pathway for drugs and urate.
Jutabha P, Anzai N, Kitamura K, Taniguchi A, Kaneko S, Yan K, Yamada H, Shimada H, Kimura T, Katada T, Fukutomi T, Tomita K, Urano W, Yamanaka H, Seki G, Fujita T, Moriyama Y, Yamada A, Uchida S, Wempe MF, Endou H, Sakurai H. Jutabha P, et al. Among authors: endou h. J Biol Chem. 2010 Nov 5;285(45):35123-32. doi: 10.1074/jbc.M110.121301. Epub 2010 Sep 1. J Biol Chem. 2010. PMID: 20810651 Free PMC article.
411 results