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Hisamitsu Hayashi

Showing results (51-60 of 68) with videos related to

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Pediatrics International : Official Journal of the Japan Pediatric Society|February 5, 2016
Effects of 4-phenylbutyrate therapy in a preterm infant with cholestasis and liver fibrosisShogo Ito, Hisamitsu Hayashi, Tokio Sugiura, et al.
The Journal of Pediatrics|February 18, 2014
Improved liver function and relieved pruritus after 4-phenylbutyrate therapy in a patient with progressive familial intrahepatic cholestasis type 2Sotaro Naoi, Hisamitsu Hayashi, Takeshi Inoue, et al.
Nihon Jibiinkoka Gakkai Kaiho|July 17, 2018
[Eight Cases of Small Cell Neuroendocrine Carcinoma of the Head and Neck]Takanori Wakaoka, Keisuke Mizuta, Hirofumi Shibata, et al.
Hepatology (Baltimore, Md.)|January 21, 2012
AP2 adaptor complex mediates bile salt export pump internalization and modulates its hepatocanalicular expression and transport functionHisamitsu Hayashi, Kaori Inamura, Kensuke Aida, et al.
The Journal of Biological Chemistry|March 14, 2012
Sorting nexin 27 interacts with multidrug resistance-associated protein 4 (MRP4) and mediates internalization of MRP4Hisamitsu Hayashi, Sotaro Naoi, Takayuki Nakagawa, et al.
Molecular Genetics and Metabolism|March 2, 2021
A randomized trial to examine the impact of food on pharmacokinetics of 4-phenylbutyrate and change in amino acid availability after a single oral administration of sodium 4-phenylbutyrarte in healthy volunteersShuhei Osaka, Satoshi Nakano, Tadahaya Mizuno, et al.
Orphanet Journal of Rare Diseases|July 16, 2014
Intractable itch relieved by 4-phenylbutyrate therapy in patients with progressive familial intrahepatic cholestasis type 1Yasuhiro Hasegawa, Hisamitsu Hayashi, Sotaro Naoi, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|February 20, 2020
Proposal of a liver histology-based scoring system for bile salt export pump deficiencyYoh Zen, Hiroki Kondou, Atsuko Nakazawa, et al.
Orphanet Journal of Rare Diseases|February 10, 2024
Clinical symptoms, biochemistry, and liver histology during the native liver period of progressive familial intrahepatic cholestasis type 2Hiroki Kondou, Satoshi Nakano, Tadahaya Mizuno, et al.
Molecular Genetics and Metabolism|October 6, 2023
Dried blood spot-based newborn screening for bile acid synthesis disorders, Zellweger spectrum disorder, and Niemann-Pick type C1 by detection of bile acid metabolitesYamato Muto, Mitsuyoshi Suzuki, Hajime Takei, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Pediatrics International : Official Journal of the Japan Pediatric Society|February 5, 2016
Effects of 4-phenylbutyrate therapy in a preterm infant with cholestasis and liver fibrosisShogo Ito, Hisamitsu Hayashi, Tokio Sugiura, et al.
The Journal of Pediatrics|February 18, 2014
Improved liver function and relieved pruritus after 4-phenylbutyrate therapy in a patient with progressive familial intrahepatic cholestasis type 2Sotaro Naoi, Hisamitsu Hayashi, Takeshi Inoue, et al.
Nihon Jibiinkoka Gakkai Kaiho|July 17, 2018
[Eight Cases of Small Cell Neuroendocrine Carcinoma of the Head and Neck]Takanori Wakaoka, Keisuke Mizuta, Hirofumi Shibata, et al.
Hepatology (Baltimore, Md.)|January 21, 2012
AP2 adaptor complex mediates bile salt export pump internalization and modulates its hepatocanalicular expression and transport functionHisamitsu Hayashi, Kaori Inamura, Kensuke Aida, et al.
The Journal of Biological Chemistry|March 14, 2012
Sorting nexin 27 interacts with multidrug resistance-associated protein 4 (MRP4) and mediates internalization of MRP4Hisamitsu Hayashi, Sotaro Naoi, Takayuki Nakagawa, et al.
Molecular Genetics and Metabolism|March 2, 2021
A randomized trial to examine the impact of food on pharmacokinetics of 4-phenylbutyrate and change in amino acid availability after a single oral administration of sodium 4-phenylbutyrarte in healthy volunteersShuhei Osaka, Satoshi Nakano, Tadahaya Mizuno, et al.
Orphanet Journal of Rare Diseases|July 16, 2014
Intractable itch relieved by 4-phenylbutyrate therapy in patients with progressive familial intrahepatic cholestasis type 1Yasuhiro Hasegawa, Hisamitsu Hayashi, Sotaro Naoi, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|February 20, 2020
Proposal of a liver histology-based scoring system for bile salt export pump deficiencyYoh Zen, Hiroki Kondou, Atsuko Nakazawa, et al.
Orphanet Journal of Rare Diseases|February 10, 2024
Clinical symptoms, biochemistry, and liver histology during the native liver period of progressive familial intrahepatic cholestasis type 2Hiroki Kondou, Satoshi Nakano, Tadahaya Mizuno, et al.
Molecular Genetics and Metabolism|October 6, 2023
Dried blood spot-based newborn screening for bile acid synthesis disorders, Zellweger spectrum disorder, and Niemann-Pick type C1 by detection of bile acid metabolitesYamato Muto, Mitsuyoshi Suzuki, Hajime Takei, et al.
Pageof 7