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Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia.
Matsuo H, Chiba T, Nagamori S, Nakayama A, Domoto H, Phetdee K, Wiriyasermkul P, Kikuchi Y, Oda T, Nishiyama J, Nakamura T, Morimoto Y, Kamakura K, Sakurai Y, Nonoyama S, Kanai Y, Shinomiya N. Matsuo H, et al. Am J Hum Genet. 2008 Dec;83(6):744-51. doi: 10.1016/j.ajhg.2008.11.001. Epub 2008 Nov 20. Am J Hum Genet. 2008. PMID: 19026395 Free PMC article.
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: matsuo h. Nature. 2002 May 23;417(6887):447-52. doi: 10.1038/nature742. Epub 2002 Apr 14. Nature. 2002. PMID: 12024214
The role of CD98 in astrocytic neoplasms.
Nawashiro H, Otani N, Shinomiya N, Fukui S, Nomura N, Yano A, Shima K, Matsuo H, Kanai Y. Nawashiro H, et al. Among authors: matsuo h. Hum Cell. 2002 Mar;15(1):25-31. doi: 10.1111/j.1749-0774.2002.tb00096.x. Hum Cell. 2002. PMID: 12126061 Review.
Somatosensory evoked potential in neurosyphilis.
Mochizuki H, Kamakura K, Kanzaki M, Nishii T, Matsuo H, Motoyoshi K. Mochizuki H, et al. Among authors: matsuo h. J Neurol. 2002 Sep;249(9):1220-2. doi: 10.1007/s00415-002-0813-2. J Neurol. 2002. PMID: 12242542
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: matsuo 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
2,266 results