Hajime Takei

Tokyo, Japan

Last Updated: 09/26/2026

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Found 51 publications

Baat-Deficient Mice Recapitulate Elevated 7α-Hydroxy-3-Oxo-4-Cholestenoic Acid Observed in a Japanese Patient With BAAT Deficiency.

Baat-Deficient Mice Recapitulate Elevated 7α-Hydroxy-3-Oxo-4-Cholestenoic Acid Observed in a Japanese Patient With BAAT Deficiency.

Journal: Journal of inherited metabolic disease

Published: January 19, 2026

Postoperative gut dysbiosis in biliary atresia patients treated by portoenterostomy or liver transplantation.

Postoperative gut dysbiosis in biliary atresia patients treated by portoenterostomy or liver transplantation.

Journal: Pediatric surgery international

Published: October 31, 2025

A Comprehensive Analysis of Serum and Urine Bile Acid Profiles in Chronic Kidney Disease: An Exploratory Study of Clinical Associations.

A Comprehensive Analysis of Serum and Urine Bile Acid Profiles in Chronic Kidney Disease: An Exploratory Study of Clinical Associations.

Journal: Nephrology (Carlton, Vic.)

Published: May 26, 2025

Liver specific transgenic expression of CYP7B1 attenuates early western diet-induced MASLD progression.

Liver specific transgenic expression of CYP7B1 attenuates early western diet-induced MASLD progression.

Journal: Journal of lipid research

Published: November 03, 2024

Fecal fatty acid-linked bile acid profiles in pediatric patients with ulcerative colitis.

Fecal fatty acid-linked bile acid profiles in pediatric patients with ulcerative colitis.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: October 08, 2024

Versatile application of fast green FCF as a visible cholangiogram in adult mice to medium-sized mammals.

Versatile application of fast green FCF as a visible cholangiogram in adult mice to medium-sized mammals.

Journal: Scientific reports

Published: July 30, 2024

Efficacy and safety of switching therapy from chenodeoxycholic acid to cholic acid in Japanese patients with bile acid synthesis disorders.

Efficacy and safety of switching therapy from chenodeoxycholic acid to cholic acid in Japanese patients with bile acid synthesis disorders.

Journal: Molecular genetics and metabolism reports

Published: May 18, 2024

Navigating cholestasis: identifying inborn errors of bile acid metabolism for precision diagnosis.

Navigating cholestasis: identifying inborn errors of bile acid metabolism for precision diagnosis.

Journal: Frontiers in pediatrics

Published: February 14, 2024

Bile acid profiles in adult patients with biliary atresia who achieve native liver survival after portoenterostomy.

Bile acid profiles in adult patients with biliary atresia who achieve native liver survival after portoenterostomy.

Journal: Scientific reports

Published: November 01, 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 metabolites.

Dried blood spot-based newborn screening for bile acid synthesis disorders, Zellweger spectrum disorder, and Niemann-Pick type C1 by detection of bile acid metabolites.

Journal: Molecular genetics and metabolism

Published: August 05, 2023

Rapid in vivo evaluation system for cholestasis-related genes in mice with humanized bile acid profiles.

Rapid in vivo evaluation system for cholestasis-related genes in mice with humanized bile acid profiles.

Journal: Hepatology communications

Published: July 24, 2023

Healthy Patients With AKR1D1 Mutation Not Requiring Primary Bile Acid Therapy: A Case Series.

Healthy Patients With AKR1D1 Mutation Not Requiring Primary Bile Acid Therapy: A Case Series.

Journal: JPGN reports

Published: May 14, 2023

Showing 1-12 of 51

Last Updated: 09/26/2026