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Shinichi Uchida

Showing results (51-60 of 302) with videos related to

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Journal of Agricultural and Food Chemistry|June 27, 2019
Identification of a Novel Peptide from β-Casein That Enhances Spatial and Object Recognition Memory in MiceYasuhisa Ano, Toshiko Kutsukake, Toshinori Sasaki, et al.
Medicine|January 21, 2022
Congenital nephrogenic diabetes insipidus presenting as osmotic demyelination syndrome in infancy: A case reportSatoru Kobayashi, Nana Mizuno, Kyoko Yokoi, et al.
Clinical Kidney Journal|June 9, 2016
A novel heterozygous mutation in the ATP6V0A4 gene encoding the V-ATPase a4 subunit in an adult patient with incomplete distal renal tubular acidosisEri Imai, Shuzo Kaneko, Takayasu Mori, et al.
American Journal of Physiology. Renal Physiology|March 31, 2017
Responses of distal nephron Na<sup>+</sup> transporters to acute volume depletion and hyperkalemiaGustavo Frindt, Lei Yang, Shinichi Uchida, et al.
Clinical Kidney Journal|June 12, 2015
Fibronectin glomerulopathyIkue Ishimoto, Eisei Sohara, Eisaku Ito, et al.
Physical Review Letters|April 12, 2003
Superconductivity of the Sr2Ca12Cu24O41 spin-ladder system: are the superconducting pairing and the spin-gap formation of the same origin?Naoki Fujiwara, Nobuo Môri, Yoshiya Uwatoko, et al.
Molecular and Cellular Biology|August 2, 2005
Impaired urea accumulation in the inner medulla of mice lacking the urea transporter UT-A2Shinichi Uchida, Eisei Sohara, Tatemitsu Rai, et al.
Biochemical and Biophysical Research Communications|July 27, 2017
WNK4 is indispensable for the pathogenesis of pseudohypoaldosteronism type II caused by mutant KLHL3Koichiro Susa, Eisei Sohara, Daiei Takahashi, et al.
Pediatric Nephrology (Berlin, Germany)|May 22, 2013
CUL3 gene analysis enables early intervention for pediatric pseudohypoaldosteronism type II in infancyMadori Osawa, Yumi Ogura, Kiyoshi Isobe, et al.
CEN Case Reports|May 17, 2017
Development of minimal-change glomerular disease and Hashimoto's thyroiditis during the treatment of sarcoidosisFumiaki Ando, Tomokazu Okado, Eisei Sohara, et al.
Pageof 31

Showing results (51-60 of 302) with videos related to

Sort By:
Pageof 31
Journal of Agricultural and Food Chemistry|June 27, 2019
Identification of a Novel Peptide from β-Casein That Enhances Spatial and Object Recognition Memory in MiceYasuhisa Ano, Toshiko Kutsukake, Toshinori Sasaki, et al.
Medicine|January 21, 2022
Congenital nephrogenic diabetes insipidus presenting as osmotic demyelination syndrome in infancy: A case reportSatoru Kobayashi, Nana Mizuno, Kyoko Yokoi, et al.
Clinical Kidney Journal|June 9, 2016
A novel heterozygous mutation in the ATP6V0A4 gene encoding the V-ATPase a4 subunit in an adult patient with incomplete distal renal tubular acidosisEri Imai, Shuzo Kaneko, Takayasu Mori, et al.
American Journal of Physiology. Renal Physiology|March 31, 2017
Responses of distal nephron Na<sup>+</sup> transporters to acute volume depletion and hyperkalemiaGustavo Frindt, Lei Yang, Shinichi Uchida, et al.
Clinical Kidney Journal|June 12, 2015
Fibronectin glomerulopathyIkue Ishimoto, Eisei Sohara, Eisaku Ito, et al.
Physical Review Letters|April 12, 2003
Superconductivity of the Sr2Ca12Cu24O41 spin-ladder system: are the superconducting pairing and the spin-gap formation of the same origin?Naoki Fujiwara, Nobuo Môri, Yoshiya Uwatoko, et al.
Molecular and Cellular Biology|August 2, 2005
Impaired urea accumulation in the inner medulla of mice lacking the urea transporter UT-A2Shinichi Uchida, Eisei Sohara, Tatemitsu Rai, et al.
Biochemical and Biophysical Research Communications|July 27, 2017
WNK4 is indispensable for the pathogenesis of pseudohypoaldosteronism type II caused by mutant KLHL3Koichiro Susa, Eisei Sohara, Daiei Takahashi, et al.
Pediatric Nephrology (Berlin, Germany)|May 22, 2013
CUL3 gene analysis enables early intervention for pediatric pseudohypoaldosteronism type II in infancyMadori Osawa, Yumi Ogura, Kiyoshi Isobe, et al.
CEN Case Reports|May 17, 2017
Development of minimal-change glomerular disease and Hashimoto's thyroiditis during the treatment of sarcoidosisFumiaki Ando, Tomokazu Okado, Eisei Sohara, et al.
Pageof 31