Hosoyamada M - Search Results

1

Clinical practice guideline for renal hypouricemia (1st edition).

Nakayama A, Matsuo H, Ohtahara A, Ogino K, Hakoda M, Hamada T, Hosoyamada M, Yamaguchi S, Hisatome I, Ichida K, Shinomiya N. Nakayama A, et al. Among authors: hosoyamada m. Hum Cell. 2019 Apr;32(2):83-87. doi: 10.1007/s13577-019-00239-3. Epub 2019 Feb 19. Hum Cell. 2019. PMID: 30783949 Free PMC article. Review.

2

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: hosoyamada m. Nature. 2002 May 23;417(6887):447-52. doi: 10.1038/nature742. Epub 2002 Apr 14. Nature. 2002. PMID: 12024214

3

Urate transport via human PAH transporter hOAT1 and its gene structure.

Ichida K, Hosoyamada M, Kimura H, Takeda M, Utsunomiya Y, Hosoya T, Endou H. Ichida K, et al. Among authors: hosoyamada m. Kidney Int. 2003 Jan;63(1):143-55. doi: 10.1046/j.1523-1755.2003.00710.x. Kidney Int. 2003. PMID: 12472777 Free article.

4

[Molecular mechanism for urinary excretion of hypoxanthine and xanthine].

Hosoyamada M, Ichida K. Hosoyamada M, et al. Nihon Rinsho. 2003 Jan;61 Suppl 1:450-4. Nihon Rinsho. 2003. PMID: 12629764 Review. Japanese. No abstract available.

5

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. Ichida K, et al. Among authors: hosoyamada m. J Am Soc Nephrol. 2004 Jan;15(1):164-73. doi: 10.1097/01.asn.0000105320.04395.d0. J Am Soc Nephrol. 2004. PMID: 14694169

6

Function and localization of urate transporter 1 in mouse kidney.

Hosoyamada M, Ichida K, Enomoto A, Hosoya T, Endou H. Hosoyamada M, et al. J Am Soc Nephrol. 2004 Feb;15(2):261-8. doi: 10.1097/01.asn.0000107560.80107.19. J Am Soc Nephrol. 2004. PMID: 14747372

7

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: hosoyamada m. 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

8

[Molecular mechanism in biological transport in the kidney: Urate transporter URAT1].

Hosoyamada M, Shibasaki T, Ichida K. Hosoyamada M, et al. Nihon Rinsho. 2006 Feb;64 Suppl 2:176-9. Nihon Rinsho. 2006. PMID: 16523883 Review. Japanese. No abstract available.

9

[Hyperuricemic nephropathy: Pathogenesis, pathophysiology, and therapy].

Ichida K, Hosoya T, Hosoyamada M. Ichida K, et al. Among authors: hosoyamada m. Nihon Rinsho. 2006 Feb;64 Suppl 2:438-41. Nihon Rinsho. 2006. PMID: 16523929 Review. Japanese. No abstract available.

10

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. Among authors: hosoyamada m. 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

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