Impact of quercetin-induced changes in drug-metabolizing enzyme and transporter expression on the pharmacokinetics of cyclosporine in rats

by Liu, Yani, Luo, Xiaomei, Yang, Chunxiao, Yang, Tingyu, Zhou, Jiali, Shi, Shaojun
Published 2016

Association of RAC1 Gene Polymorphisms with Primary End-Stage Renal Disease in Chinese Renal Recipients

by Liu, Yani, Zhou, Jiali, Luo, Xiaomei, Yang, Chunxiao, Zhang, Yu, Shi, Shaojun
Published 2016

The therapeutic effect of bevacizumab on plaque neovascularization in a rabbit model of atherosclerosis during contrast-enhanced ultrasonography

by Li, Yang, Zhu, Ying, Deng, Youbin, Liu, Yani, Mao, Yuhang, Wang, Junli, Sun, Jie
Published 2016

Novel and Recurrent MYO7A Mutations in Usher Syndrome Type 1 and Type 2

by Rong, Weining, Chen, Xue, Zhao, Kanxing, Liu, Yani, Liu, Xiaoxing, Ha, Shaoping, Liu, Wenzhou, Kang, Xiaoli, Sheng, Xunlun, Zhao, Chen
Published 2014

Association of insulin-like growth factor-1 polymorphisms with high myopia in the Chinese population

by Zhuang, Wenjuan, Yang, Peizeng, Li, Zili, Sheng, Xunlun, Zhao, Jingjing, Li, Shanshan, Yang, Xueqiu, Xiang, Wei, Rong, Weining, Liu, Yani, Zhang, Fangxia
Published 2012

Redox-Dependent Modulation of T-Type Ca2+ Channels in Sensory Neurons Contributes to Acute Anti-Nociceptive Effect of Substance P

by Huang, Dongyang, Huang, Sha, Gao, Haixia, Liu, Yani, Qi, Jinlong, Chen, Pingping, Wang, Caixue, Scragg, Jason L., Vakurov, Alexander, Peers, Chris, Du, Xiaona, Zhang, Hailin, Gamper, Nikita
Published 2016

Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia

by Sheng, Xunlun, Chen, Xue, Lei, Bo, Chen, Rui, Wang, Hui, Zhang, Fangxia, Rong, Weining, Ha, Ruoshui, Liu, Yani, Zhao, Feng, Yang, Peizeng, Zhao, Chen
Published 2015

Targeted Next-Generation Sequencing Reveals Novel USH2A Mutations Associated with Diverse Disease Phenotypes: Implications for Clinical and Molecular Diagnosis

by Chen, Xue, Sheng, Xunlun, Liu, Xiaoxing, Li, Huiping, Liu, Yani, Rong, Weining, Ha, Shaoping, Liu, Wenzhou, Kang, Xiaoli, Zhao, Kanxing, Zhao, Chen
Published 2014

Targeted Next-generation Sequencing Reveals Novel EYS Mutations in Chinese Families with Autosomal Recessive Retinitis Pigmentosa

by Chen, Xue, Liu, Xiaoxing, Sheng, Xunlun, Gao, Xiang, Zhang, Xiumei, Li, Zili, Li, Huiping, Liu, Yani, Rong, Weining, Zhao, Kanxing, Zhao, Chen
Published 2015

Next-generation Sequencing Extends the Phenotypic Spectrum for LCA5 Mutations: Novel LCA5 Mutations in Cone Dystrophy

by Chen, Xue, Sheng, Xunlun, Sun, Xiantao, Zhang, Yuxin, Jiang, Chao, Li, Huiping, Ding, Sijia, Liu, Yani, Liu, Wenzhou, Li, Zili, Zhao, Chen
Published 2016

CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability

by Minegishi, Yuriko, Sheng, XunLun, Yoshitake, Kazutoshi, Sergeev, Yuri, Iejima, Daisuke, Shibagaki, Yoshio, Monma, Norikazu, Ikeo, Kazuho, Furuno, Masaaki, Zhuang, Wenjun, Liu, Yani, Rong, Weining, Hattori, Seisuke, Iwata, Takeshi
Published 2016