埃替拉韦 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "埃替拉韦" in Chinese language version.

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Shimura K, Kodama E, Sakagami Y, et al. Broad Anti-Retroviral Activity and Resistance Profile of a Novel Human Immunodeficiency Virus Integrase Inhibitor, Elvitegravir (JTK-303/GS-9137). J Virol. 2007, 82 (2): 764–74. PMC 2224569 . PMID 17977962. doi:10.1128/JVI.01534-07.
Sax, P. E.; Dejesus, E.; Mills, A.; Zolopa, A.; Cohen, C.; Wohl, D.; Gallant, J. E.; Liu, H. C.; Zhong, L.; Yale, K.; White, K.; Kearney, B. P.; Szwarcberg, J.; Quirk, E.; Cheng, A. K.; Gs-Us-236-0102 Study, T. Co-formulated elvitegravir, cobicistat, emtricitabine, and tenofovir versus co-formulated efavirenz, emtricitabine, and tenofovir for initial treatment of HIV-1 infection: A randomised, double-blind, phase 3 trial, analysis of results after 48 weeks. The Lancet. 2012, 379 (9835): 2439–2448. PMID 22748591. S2CID 24183976. doi:10.1016/S0140-6736(12)60917-9.
Zhang, D; Chando, T. J.; Everett, D. W.; Patten, C. J.; Dehal, S. S.; Humphreys, W. G. In vitro inhibition of UDP glucuronosyltransferases by atazanavir and other HIV protease inhibitors and the relationship of this property to in vivo bilirubin glucuronidation. Drug Metabolism and Disposition. 2005, 33 (11): 1729–39. PMID 16118329. S2CID 1964934. doi:10.1124/dmd.105.005447.

Press Announcements - FDA approves new treatment for HIV. www.fda.gov. [2016-01-10]. （原始内容存档于2018-01-25）（英语）.

Shimura K, Kodama E, Sakagami Y, et al. Broad Anti-Retroviral Activity and Resistance Profile of a Novel Human Immunodeficiency Virus Integrase Inhibitor, Elvitegravir (JTK-303/GS-9137). J Virol. 2007, 82 (2): 764–74. PMC 2224569 . PMID 17977962. doi:10.1128/JVI.01534-07.
Stellbrink HJ. Antiviral drugs in the treatment of AIDS: what is in the pipeline ?. Eur. J. Med. Res. 2007, 12 (9): 483–95. PMID 17933730.
Sax, P. E.; Dejesus, E.; Mills, A.; Zolopa, A.; Cohen, C.; Wohl, D.; Gallant, J. E.; Liu, H. C.; Zhong, L.; Yale, K.; White, K.; Kearney, B. P.; Szwarcberg, J.; Quirk, E.; Cheng, A. K.; Gs-Us-236-0102 Study, T. Co-formulated elvitegravir, cobicistat, emtricitabine, and tenofovir versus co-formulated efavirenz, emtricitabine, and tenofovir for initial treatment of HIV-1 infection: A randomised, double-blind, phase 3 trial, analysis of results after 48 weeks. The Lancet. 2012, 379 (9835): 2439–2448. PMID 22748591. S2CID 24183976. doi:10.1016/S0140-6736(12)60917-9.
Zhang, D; Chando, T. J.; Everett, D. W.; Patten, C. J.; Dehal, S. S.; Humphreys, W. G. In vitro inhibition of UDP glucuronosyltransferases by atazanavir and other HIV protease inhibitors and the relationship of this property to in vivo bilirubin glucuronidation. Drug Metabolism and Disposition. 2005, 33 (11): 1729–39. PMID 16118329. S2CID 1964934. doi:10.1124/dmd.105.005447.

"Vitekta Package Insert" （页面存档备份，存于互联网档案馆） Foster City, CA: Gilead Sciences, Inc.; 2014. Accessed November 1, 2014

Sax, P. E.; Dejesus, E.; Mills, A.; Zolopa, A.; Cohen, C.; Wohl, D.; Gallant, J. E.; Liu, H. C.; Zhong, L.; Yale, K.; White, K.; Kearney, B. P.; Szwarcberg, J.; Quirk, E.; Cheng, A. K.; Gs-Us-236-0102 Study, T. Co-formulated elvitegravir, cobicistat, emtricitabine, and tenofovir versus co-formulated efavirenz, emtricitabine, and tenofovir for initial treatment of HIV-1 infection: A randomised, double-blind, phase 3 trial, analysis of results after 48 weeks. The Lancet. 2012, 379 (9835): 2439–2448. PMID 22748591. S2CID 24183976. doi:10.1016/S0140-6736(12)60917-9.
Zhang, D; Chando, T. J.; Everett, D. W.; Patten, C. J.; Dehal, S. S.; Humphreys, W. G. In vitro inhibition of UDP glucuronosyltransferases by atazanavir and other HIV protease inhibitors and the relationship of this property to in vivo bilirubin glucuronidation. Drug Metabolism and Disposition. 2005, 33 (11): 1729–39. PMID 16118329. S2CID 1964934. doi:10.1124/dmd.105.005447.