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FGFR2 mutation in a Chinese family with unusual Crouzon syndrome.
Li ZL, Chen X, Zhuang WJ, Zhao W, Liu YN, Zhang FX, Ha RS, Wu JH, Zhao C, Sheng XL. Li ZL, et al. Among authors: zhang fx. Int J Ophthalmol. 2016 Oct 18;9(10):1403-1408. doi: 10.18240/ijo.2016.10.06. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27803855 Free PMC article.
CEP78 is mutated in a distinct type of Usher syndrome.
Fu Q, Xu M, Chen X, Sheng X, Yuan Z, Liu Y, Li H, Sun Z, Li H, Yang L, Wang K, Zhang F, Li Y, Zhao C, Sui R, Chen R. Fu Q, et al. J Med Genet. 2017 Mar;54(3):190-195. doi: 10.1136/jmedgenet-2016-104166. Epub 2016 Sep 14. J Med Genet. 2017. PMID: 27627988 Free PMC article.
Chemical profiling of Zhi-Ke-Bao pills and its potential mechanism against cough by ultra-high performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry and network pharmacology.
Chen DJ, Liu CJ, Chen ZH, Li JJ, Shi W, Zhang QM, Yang X, Chen JX, Zhang FX. Chen DJ, et al. Among authors: zhang fx. J Pharm Biomed Anal. 2024 May 24;247:116257. doi: 10.1016/j.jpba.2024.116257. Online ahead of print. J Pharm Biomed Anal. 2024. PMID: 38815520
344 results