Is CYP2C70 the key to new mouse models to understand bile acids in humans?-Reference-Cited by-同舟云学术

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Is CYP2C70 the key to new mouse models to understand bile acids in humans?

Published:2020-03 Issue:3 Volume:61 Page:269-271
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Guo Grace L.^ORCID,Chiang John Y.L.

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

HHS | NIH | National Institute of Environmental Health Sciences

HHS | NIH | National Institute of General Medical Sciences

VA | Office of Academic Affiliations, Department of Veterans Affairs

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference7 articles.

1. Animal models to study bile acid metabolism;Li;Bioch. Biophys. Acta Mol. Basis Dis,2019

2. Cyp2c70 is responsible for the species difference in bile acid metabolism between mice and humans;Takahashi;J. Lipid Res,2016

3. A human-like bile acid pool induced by deletion of hepatic Cyp2c70 modulates effects of farnesoid x receptor activation in mice;de Boer;J. Lipid Res,2020

4. Regulation of bile acid metabolism in mouse models with hydrophobic bile acid composition;Honda;J. Lipid Res,2020

5. Bile acid induction of cytokine expression by macrophages correlates with repression of hepatic cholesterol 7alpha -hydroxylase;Miyake;J. Biol. Chem,2000

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