Uchida S - Search Results

1

Transplantation of a kidney with a heterozygous mutation in the SLC22A12 (URAT1) gene causing renal hypouricemia: a case report.

Tsuji K, Kitamura M, Muta K, Mochizuki Y, Mori T, Sohara E, Uchida S, Sakai H, Mukae H, Nishino T. Tsuji K, et al. Among authors: uchida s. BMC Nephrol. 2020 Jul 16;21(1):282. doi: 10.1186/s12882-020-01940-4. BMC Nephrol. 2020. PMID: 32677916 Free PMC article.

2

Kelch-like 3/Cullin 3 ubiquitin ligase complex and WNK signaling in salt-sensitive hypertension and electrolyte disorder.

Sohara E, Uchida S. Sohara E, et al. Among authors: uchida s. Nephrol Dial Transplant. 2016 Sep;31(9):1417-24. doi: 10.1093/ndt/gfv259. Epub 2015 Jul 6. Nephrol Dial Transplant. 2016. PMID: 26152401 Review.

3

Comprehensive genetic testing approach for major inherited kidney diseases, using next-generation sequencing with a custom panel.

Mori T, Hosomichi K, Chiga M, Mandai S, Nakaoka H, Sohara E, Okado T, Rai T, Sasaki S, Inoue I, Uchida S. Mori T, et al. Among authors: uchida s. Clin Exp Nephrol. 2017 Feb;21(1):63-75. doi: 10.1007/s10157-016-1252-1. Epub 2016 Feb 26. Clin Exp Nephrol. 2017. PMID: 26920127

4

Genotype-Clinical Correlations in Polycystic Kidney Disease with No Apparent Family History.

Sekine A, Fujimaru T, Hoshino J, Suwabe T, Oguro M, Mizuno H, Kawada M, Sumida K, Hiramatsu R, Hasegawa E, Yamanouchi M, Hayami N, Mandai S, Chiga M, Kikuchi H, Ando F, Mori T, Sohara E, Uchida S, Sawa N, Takaichi K, Ubara Y. Sekine A, et al. Among authors: uchida s. Am J Nephrol. 2019;49(3):233-240. doi: 10.1159/000497444. Epub 2019 Feb 28. Am J Nephrol. 2019. PMID: 30820006

5

Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation.

Tanaka T, Oki E, Mori T, Tsuruga K, Sohara E, Uchida S, Tanaka H. Tanaka T, et al. Among authors: uchida s. Nephrology (Carlton). 2019 Apr;24(4):489-490. doi: 10.1111/nep.13391. Nephrology (Carlton). 2019. PMID: 30919533 No abstract available.

6

Bartter syndrome representing digenic-based salt-losing tubulopathies presumably accelerated by renal insufficiency.

Umene R, Kitamura M, Arai H, Matsumura K, Ishimaru Y, Maeda K, Uramatsu T, Obata Y, Mori T, Sohara E, Uchida S, Nishino T. Umene R, et al. Among authors: uchida s. CEN Case Rep. 2020 Nov;9(4):375-379. doi: 10.1007/s13730-020-00489-3. Epub 2020 Jun 6. CEN Case Rep. 2020. PMID: 32506365 Free PMC article.

7

Genetics May Predict Effectiveness of Tolvaptan in Autosomal Dominant Polycystic Kidney Disease.

Sekine A, Hoshino J, Fujimaru T, Suwabe T, Mizuno H, Kawada M, Hiramatsu R, Hasegawa E, Yamanouchi M, Hayami N, Mandai S, Chiga M, Kikuchi H, Ando F, Mori T, Sohara E, Uchida S, Sawa N, Takaichi K, Ubara Y. Sekine A, et al. Among authors: uchida s. Am J Nephrol. 2020;51(9):745-751. doi: 10.1159/000509817. Epub 2020 Aug 12. Am J Nephrol. 2020. PMID: 32784291 Free article.

8

Effect of heterozygous deletion of WNK1 on the WNK-OSR1/ SPAK-NCC/NKCC1/NKCC2 signal cascade in the kidney and blood vessels.

Susa K, Kita S, Iwamoto T, Yang SS, Lin SH, Ohta A, Sohara E, Rai T, Sasaki S, Alessi DR, Uchida S. Susa K, et al. Among authors: uchida s. Clin Exp Nephrol. 2012 Aug;16(4):530-8. doi: 10.1007/s10157-012-0590-x. Clin Exp Nephrol. 2012. PMID: 22294159

9

Generation of Hypertension-Associated STK39 Polymorphism Knockin Cell Lines With the Clustered Regularly Interspaced Short Palindromic Repeats/Cas9 System.

Mandai S, Mori T, Sohara E, Rai T, Uchida S. Mandai S, et al. Among authors: uchida s. Hypertension. 2015 Dec;66(6):1199-206. doi: 10.1161/HYPERTENSIONAHA.115.05872. Epub 2015 Sep 28. Hypertension. 2015. PMID: 26416847

10

Inherited, not acquired, Gitelman syndrome in a patient with Sjögren's syndrome: importance of genetic testing to distinguish the two forms.

Mishima E, Mori T, Sohara E, Uchida S, Abe T, Ito S. Mishima E, et al. Among authors: uchida s. CEN Case Rep. 2017 Nov;6(2):180-184. doi: 10.1007/s13730-017-0271-4. Epub 2017 Aug 17. CEN Case Rep. 2017. PMID: 28819721 Free PMC article.

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