Association of POR and PPARα polymorphisms with risk of anti-tuberculosis drug-induced liver injury in Western Chinese Han population

Author:

Zhang Chunying,Jiao Lin,Bai Hao,Zhao Zhenzhen,Hu Xuejiao,Wang Minjin,Wu Tao,Peng Wu,Liu Tangyuheng,Song Jiajia,Zhou Juan,Li Mengjiao,Lyv Mengyuan,Zhang Jingwei,Chen Hao,Chen Jie,Ying BinwuORCID

Funder

National Natural Science Foundation of China

National Science and Technology Major Project of the Ministry of Science and Technology of China

University - City Science and Technology Cooperation Project of Sichuan University & Panzhihua City

Publisher

Elsevier BV

Subject

Infectious Diseases,Microbiology (medical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics,Microbiology

Reference44 articles.

1. Substrate-specific modulation of CYP3A4 activity by genetic variants of cytochrome P450 oxidoreductase;Agrawal;Pharmacogenet. Genomics,2010

2. Association between effectiveness of tuberculosis treatment and cytochrome P-4502E1 polymorphism of the patients;Antonenko;International Journal of Mycobacteriology.,2017

3. Genetic variations associated with anti-tuberculosis drug-induced liver injury;Bao;Current pharmacology reports.,2018

4. Risk factors of isoniazid-induced hepatotoxicity in Tunisian tuberculosis patients;Ben Fredj;Pharmacogenomics J.,2017

5. Influence of various polymorphic variants of cytochrome P450 oxidoreductase (POR) on drug metabolic activity of CYP3A4 and CYP2B6;Chen;PLoS One,2012

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