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Shinichi Uchida

Showing results (161-170 of 288) with videos related to

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Bone|November 22, 2023
Effect of osteosarcopenia on longitudinal mortality risk and chronic kidney disease progression in older adultsYuta Nakano, Shintaro Mandai, Shotaro Naito, et al.
Internal Medicine (Tokyo, Japan)|November 3, 2016
Acquired Gitelman Syndrome in an Anti-SSA Antibody-positive Patient with a SLC12A3 Heterozygous MutationTakeshi Kusuda, Tadashi Hosoya, Takayasu Mori, et al.
Bioscience Reports|March 25, 2014
WNK4 is the major WNK positively regulating NCC in the mouse kidneyDaiei Takahashi, Takayasu Mori, Naohiro Nomura, et al.
Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy|April 22, 2021
Adjustment by hematocrit level in calculation of removal rate in therapeutic apheresisTakatoshi Sakurasawa, Atsushi Ohkubo, Yuki Hoshikawa, et al.
Journal of Nephrology|November 27, 2024
Nationwide mortality following acute type B aortic dissection and the survival advantage of obesity among dialysis patients in JapanYuta Nakano, Shintaro Mandai, Yutaro Mori, et al.
Molecular Pharmacology|March 9, 2023
In Vitro Pharmacological Profile of KW-6356, a Novel Adenosine A<sub>2A</sub> Receptor Antagonist/Inverse AgonistYutaro Ohno, Michihiko Suzuki, Hidetsugu Asada, et al.
CEN Case Reports|October 7, 2021
Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitusKenichiro Iio, Takayasu Mori, Saki Bessho, et al.
Plos One|November 30, 2018
Short-term prognosis of emergently hospitalized dialysis-independent chronic kidney disease patients: A nationwide retrospective cohort study in JapanHiroaki Kikuchi, Eiichiro Kanda, Takayasu Mori, et al.
Plos One|September 17, 2013
SPAK deficiency corrects pseudohypoaldosteronism II caused by WNK4 mutationPei-Yi Chu, Chih-Jen Cheng, Yi-Chang Wu, et al.
Nephrology (Carlton, Vic.)|July 4, 2020
Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 geneKiyoshi Nakano, Yasuo Kubota, Takayuki Mori, et al.
Pageof 29

Showing results (161-170 of 288) with videos related to

Sort By:
Pageof 29
Bone|November 22, 2023
Effect of osteosarcopenia on longitudinal mortality risk and chronic kidney disease progression in older adultsYuta Nakano, Shintaro Mandai, Shotaro Naito, et al.
Internal Medicine (Tokyo, Japan)|November 3, 2016
Acquired Gitelman Syndrome in an Anti-SSA Antibody-positive Patient with a SLC12A3 Heterozygous MutationTakeshi Kusuda, Tadashi Hosoya, Takayasu Mori, et al.
Bioscience Reports|March 25, 2014
WNK4 is the major WNK positively regulating NCC in the mouse kidneyDaiei Takahashi, Takayasu Mori, Naohiro Nomura, et al.
Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy|April 22, 2021
Adjustment by hematocrit level in calculation of removal rate in therapeutic apheresisTakatoshi Sakurasawa, Atsushi Ohkubo, Yuki Hoshikawa, et al.
Journal of Nephrology|November 27, 2024
Nationwide mortality following acute type B aortic dissection and the survival advantage of obesity among dialysis patients in JapanYuta Nakano, Shintaro Mandai, Yutaro Mori, et al.
Molecular Pharmacology|March 9, 2023
In Vitro Pharmacological Profile of KW-6356, a Novel Adenosine A<sub>2A</sub> Receptor Antagonist/Inverse AgonistYutaro Ohno, Michihiko Suzuki, Hidetsugu Asada, et al.
CEN Case Reports|October 7, 2021
Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitusKenichiro Iio, Takayasu Mori, Saki Bessho, et al.
Plos One|November 30, 2018
Short-term prognosis of emergently hospitalized dialysis-independent chronic kidney disease patients: A nationwide retrospective cohort study in JapanHiroaki Kikuchi, Eiichiro Kanda, Takayasu Mori, et al.
Plos One|September 17, 2013
SPAK deficiency corrects pseudohypoaldosteronism II caused by WNK4 mutationPei-Yi Chu, Chih-Jen Cheng, Yi-Chang Wu, et al.
Nephrology (Carlton, Vic.)|July 4, 2020
Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 geneKiyoshi Nakano, Yasuo Kubota, Takayuki Mori, et al.
Pageof 29