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Shinichi Uchida

Showing results (201-210 of 288) with videos related to

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Journal of the American Society of Nephrology : JASN|September 4, 2010
SPAK-knockout mice manifest Gitelman syndrome and impaired vasoconstrictionSung-Sen Yang, Yi-Fen Lo, Chin-Chen Wu, et al.
Journal of the American Society of Nephrology : JASN|November 8, 2014
Discovery of Novel SPAK Inhibitors That Block WNK Kinase Signaling to Cation Chloride TransportersEriko Kikuchi, Takayasu Mori, Moko Zeniya, et al.
Internal Medicine (Tokyo, Japan)|October 8, 2025
Delayed Therapeutic Response to Oral Corticosteroids and Rituximab Leading to Dialysis Independence in a Patient with Treatment-resistant C3 GlomerulonephritisYuki Nakao, Junko Kunieda, Towako Taguchi, et al.
Kidney Diseases (Basel, Switzerland)|June 15, 2022
Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney DiseaseRyohei Miyamoto, Akinari Sekine, Takuya Fujimaru, et al.
Hypertension (Dallas, Tex. : 1979)|October 11, 2023
National Trends in Mortality and Urgent Dialysis after Acute Hypertension in Japan From 2010 Through 2019Hisazumi Matsuki, Taku Genma, Shintaro Mandai, et al.
International Journal of Surgery (London, England)|August 9, 2022
Nationwide mortality associated with perioperative acute dialysis requirement in major surgeriesYuta Nakano, Shintaro Mandai, Taku Genma, et al.
CEN Case Reports|July 11, 2018
Ruptured infected aneurysm of the thoracic aorta associated with tunneled dialysis catheter-related methicillin-resistant Staphylococcus aureus bacteremia in a hemodialysis patientFumiko Katsuragawa, Kiyotaka Nagahama, Shotaro Naito, et al.
Cell Metabolism|May 10, 2007
Molecular pathogenesis of pseudohypoaldosteronism type II: generation and analysis of a Wnk4(D561A/+) knockin mouse modelSung-Sen Yang, Tetsuji Morimoto, Tatemitsu Rai, et al.
Internal Medicine (Tokyo, Japan)|April 5, 2021
A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like PhenotypeYuji Oe, Eikan Mishima, Takayasu Mori, et al.
JCI Insight|September 9, 2021
Impairment in renal medulla development underlies salt wasting in Clc-k2 channel deficiencyMeng-Hsuan Lin, Jen-Chi Chen, Xuejiao Tian, et al.
Pageof 29

Showing results (201-210 of 288) with videos related to

Sort By:
Pageof 29
Journal of the American Society of Nephrology : JASN|September 4, 2010
SPAK-knockout mice manifest Gitelman syndrome and impaired vasoconstrictionSung-Sen Yang, Yi-Fen Lo, Chin-Chen Wu, et al.
Journal of the American Society of Nephrology : JASN|November 8, 2014
Discovery of Novel SPAK Inhibitors That Block WNK Kinase Signaling to Cation Chloride TransportersEriko Kikuchi, Takayasu Mori, Moko Zeniya, et al.
Internal Medicine (Tokyo, Japan)|October 8, 2025
Delayed Therapeutic Response to Oral Corticosteroids and Rituximab Leading to Dialysis Independence in a Patient with Treatment-resistant C3 GlomerulonephritisYuki Nakao, Junko Kunieda, Towako Taguchi, et al.
Kidney Diseases (Basel, Switzerland)|June 15, 2022
Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney DiseaseRyohei Miyamoto, Akinari Sekine, Takuya Fujimaru, et al.
Hypertension (Dallas, Tex. : 1979)|October 11, 2023
National Trends in Mortality and Urgent Dialysis after Acute Hypertension in Japan From 2010 Through 2019Hisazumi Matsuki, Taku Genma, Shintaro Mandai, et al.
International Journal of Surgery (London, England)|August 9, 2022
Nationwide mortality associated with perioperative acute dialysis requirement in major surgeriesYuta Nakano, Shintaro Mandai, Taku Genma, et al.
CEN Case Reports|July 11, 2018
Ruptured infected aneurysm of the thoracic aorta associated with tunneled dialysis catheter-related methicillin-resistant Staphylococcus aureus bacteremia in a hemodialysis patientFumiko Katsuragawa, Kiyotaka Nagahama, Shotaro Naito, et al.
Cell Metabolism|May 10, 2007
Molecular pathogenesis of pseudohypoaldosteronism type II: generation and analysis of a Wnk4(D561A/+) knockin mouse modelSung-Sen Yang, Tetsuji Morimoto, Tatemitsu Rai, et al.
Internal Medicine (Tokyo, Japan)|April 5, 2021
A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like PhenotypeYuji Oe, Eikan Mishima, Takayasu Mori, et al.
JCI Insight|September 9, 2021
Impairment in renal medulla development underlies salt wasting in Clc-k2 channel deficiencyMeng-Hsuan Lin, Jen-Chi Chen, Xuejiao Tian, et al.
Pageof 29