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Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|March 19, 2013
Determination of 3β-hydroxy-Δ5-bile acids and related compounds in biological fluids of patients with cholestasis by liquid chromatography-tandem mass spectrometryTsuyoshi Murai, Kana Oda, Terutake Toyo, et al.
Journal of Lipid Research|September 11, 2022
Characterization of long-chain fatty acid-linked bile acids: a major conjugation form of 3β-hydroxy bile acids in fecesHajime Takei, Seiko Narushima, Mitsuyoshi Suzuki, et al.
Steroids|February 22, 2002
A highly specific heterologous enzyme immunoassay for 5 alpha-androstane-3 alpha, 17 beta-diol 17-glucuronide (androstanediol-17G) and developmental patterns of urinary androstanediol-17G excretionsToshikazu Onishi, Hajime Takei, Akira Kambegawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 14, 2009
Diagnostic determination system for high-risk screening for inborn errors of bile acid metabolism based on an analysis of urinary bile acids using gas chromatography-mass spectrometry: results for 10 years in JapanHiroshi Nittono, Hajime Takei, Atsushi Unno, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 19, 2015
Profile of bile acids in fetal gallbladder and meconium using liquid chromatography-tandem mass spectrometryNakayuki Naritaka, Mitsuyoshi Suzuki, Hiroaki Sato, et al.
Biomedicine Hub|January 30, 2020
Bifidobacterium Supplementation of Colostrum and Breast Milk Enhances Weight Gain and Metabolic Responses Associated with Microbiota Establishment in Very-Preterm InfantsTatsuo Oshiro, Satoru Nagata, Chongxin Wang, et al.
Hepatology Communications|April 16, 2021
Rotor Syndrome: Glucuronidated Bile Acidemia From Defective Reuptake by HepatocytesAkihiko Kimura, Tatehiro Kagawa, Hajime Takei, et al.
Molecular Genetics and Metabolism Reports|December 9, 2024
Efficacy and safety of switching therapy from chenodeoxycholic acid to cholic acid in Japanese patients with bile acid synthesis disordersMitsuyoshi Suzuki, Hajime Takei, Hiromi Suzuki, et al.
JPGN Reports|November 30, 2023
Healthy Patients With AKR1D1 Mutation Not Requiring Primary Bile Acid Therapy: A Case SeriesAkihiko Kimura, Jun Mori, Anh-Hoa Nguyen Pham, et al.
Frontiers in Pediatrics|April 22, 2024
Navigating cholestasis: identifying inborn errors of bile acid metabolism for precision diagnosisHiroshi Nittono, Mitsuyoshi Suzuki, Hiromi Suzuki, et al.
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