Bile acid conjugation deficiency causes hypercholanemia, hyperphagia, islet dysfunction, and gut dysbiosis in mice-Reference-Cited by-同舟云学术

Bile acid conjugation deficiency causes hypercholanemia, hyperphagia, islet dysfunction, and gut dysbiosis in mice

Published:2022-07-22 Issue:10 Volume:6 Page:2765-2780
ISSN:2471-254X
Container-title:Hepatology Communications
language:en
Short-container-title:Hepatology Communications

Author:

Alrehaili Bandar D.¹²³,Lee Mikang¹,Takahashi Shogo⁴,Novak Robert⁵,Rimal Bipin⁶,Boehme Shannon¹,Trammell Samuel A. J.⁷,Grevengoed Trisha J.⁷,Kumar Devendra⁸,Alnouti Yazen⁸,Chiti Katya⁹,Wang Xinwen⁹,Patterson Andrew D.⁶^ORCID,Chiang John Y. L.¹^ORCID,Gonzalez Frank J.⁴^ORCID,Lee Yoon‐Kwang¹²^ORCID

Affiliation:

1. Department of Integrative Medical Sciences Northeast Ohio Medical University Rootstown Ohio USA

2. Graduate Program of Biomedical Sciences Kent State University Kent Ohio USA

3. Department of Pharmacology and Toxicology Pharmacy College Taibah University Medina Saudi Arabia

4. Laboratory of Metabolism Center for Cancer Research National Cancer Institute NIH Bethesda Maryland USA

5. Department of Pathology College of Medicine Northeast Ohio Medical University Rootstown Ohio USA

6. Department of Molecular Toxicology The Pennsylvania State University University Park Pennsylvania USA

7. Department of Biomedical Sciences Faculty of Health and Medical Sciences University of Copenhagen Copenhagen Denmark

8. Department of Pharmaceutical Sciences University of Nebraska Medical Center Omaha NA USA

9. Department of Pharmaceutical Sciences College of Pharmacy Northeast Ohio Medical University Rootstown Ohio USA

Funder

Foundation for the National Institutes of Health

Novo Nordisk Fonden

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hep4.2041

Reference35 articles.

1. Bile acids: regulation of synthesis

2. Levels of 7α-hydroxy-4-cholesten-3-one in plasma reflect rates of bile acid synthesis in man

3. Participation of Two Members of the Very Long-chain Acyl-CoA Synthetase Family in Bile Acid Synthesis and Recycling

4. The Sister of P-glycoprotein Represents the Canalicular Bile Salt Export Pump of Mammalian Liver

5. Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT

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