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Kimiyoshi Ichida

Showing results (51-60 of 154) with videos related to

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Biological & Pharmaceutical Bulletin|January 5, 2019
Urate Transport via Paracellular Route across Epithelial CellsToru Kimura, Ai Tsukada, Toshiyuki Fukutomi, et al.
Journal of Pharmacological Sciences|August 26, 2010
Concentration-dependent inhibitory effect of irbesartan on renal uric acid transportersMakiko Nakamura, Naohiko Anzai, Promsuk Jutabha, et al.
Biomedicines|December 23, 2023
DysuricemiaAkiyoshi Nakayama, Masafumi Kurajoh, Yu Toyoda, et al.
Biomedicines|February 24, 2024
Plasma and Urinary Metabolomic Analysis of Gout and Asymptomatic Hyperuricemia and Profiling of Potential Biomarkers: A Pilot StudyYuki Ohashi, Hiroshi Ooyama, Hideki Makinoshima, et al.
The American Journal of the Medical Sciences|June 26, 2015
Xanthinuria type I with a novel mutation of xanthine dehydrogenaseKen-Ichiro Tanaka, Ippei Kanazawa, Haruka Yamasaki, et al.
Internal Medicine (Tokyo, Japan)|November 22, 2021
A Novel PRPS1 Mutation in a Japanese Patient with CMTX5Shunichi Shirakawa, Tatsufumi Murakami, Akihiro Hashiguchi, et al.
Clinical and Experimental Nephrology|October 27, 2015
Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2Andrea Mancikova, Vladimir Krylov, Olha Hurba, et al.
Nucleosides, Nucleotides & Nucleic Acids|December 3, 2011
Diagnostic tests for primary renal hypouricemiaIvan Sebesta, Blanka Stiburkova, Josef Bartl, et al.
The Journal of Biological Chemistry|July 3, 2024
Significance and amplification methods of the purine salvage pathway in human brain cellsMai Sekine, Megumi Fujiwara, Ken Okamoto, et al.
Molecular Genetics and Metabolism Reports|February 8, 2021
The effect of dietary protein restriction in a case of molybdenum cofactor deficiency with <i>MOCS1</i> mutationYu Abe, Yu Aihara, Wakaba Endo, et al.
Pageof 16

Showing results (51-60 of 154) with videos related to

Sort By:
Pageof 16
Biological & Pharmaceutical Bulletin|January 5, 2019
Urate Transport via Paracellular Route across Epithelial CellsToru Kimura, Ai Tsukada, Toshiyuki Fukutomi, et al.
Journal of Pharmacological Sciences|August 26, 2010
Concentration-dependent inhibitory effect of irbesartan on renal uric acid transportersMakiko Nakamura, Naohiko Anzai, Promsuk Jutabha, et al.
Biomedicines|December 23, 2023
DysuricemiaAkiyoshi Nakayama, Masafumi Kurajoh, Yu Toyoda, et al.
Biomedicines|February 24, 2024
Plasma and Urinary Metabolomic Analysis of Gout and Asymptomatic Hyperuricemia and Profiling of Potential Biomarkers: A Pilot StudyYuki Ohashi, Hiroshi Ooyama, Hideki Makinoshima, et al.
The American Journal of the Medical Sciences|June 26, 2015
Xanthinuria type I with a novel mutation of xanthine dehydrogenaseKen-Ichiro Tanaka, Ippei Kanazawa, Haruka Yamasaki, et al.
Internal Medicine (Tokyo, Japan)|November 22, 2021
A Novel PRPS1 Mutation in a Japanese Patient with CMTX5Shunichi Shirakawa, Tatsufumi Murakami, Akihiro Hashiguchi, et al.
Clinical and Experimental Nephrology|October 27, 2015
Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2Andrea Mancikova, Vladimir Krylov, Olha Hurba, et al.
Nucleosides, Nucleotides & Nucleic Acids|December 3, 2011
Diagnostic tests for primary renal hypouricemiaIvan Sebesta, Blanka Stiburkova, Josef Bartl, et al.
The Journal of Biological Chemistry|July 3, 2024
Significance and amplification methods of the purine salvage pathway in human brain cellsMai Sekine, Megumi Fujiwara, Ken Okamoto, et al.
Molecular Genetics and Metabolism Reports|February 8, 2021
The effect of dietary protein restriction in a case of molybdenum cofactor deficiency with <i>MOCS1</i> mutationYu Abe, Yu Aihara, Wakaba Endo, et al.
Pageof 16