Thyroid hormone receptor beta mutations alter photoreceptor development and function in Danio rerio (zebrafish) von Deveau, Ciana, Jiao, Xiaodong, Suzuki, Sachihiro C., Krishnakumar, Asha, Yoshimatsu, Takeshi, Hejtmancik, J. Fielding, Nelson, Ralph F.

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Differences in practice and preferences associated with truth-telling to cancer patients von Wu, Jing, Wang, Yan, Jiao, Xiaodong, Wang, Jingting, Ye, Xuchun, Wang, Bei

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Modeling, Synchronization, and FPGA Implementation of Hamiltonian Conservative Hyperchaos von Chen, Zengqiang, Du, Shengzhi, Jiao, Xiaodong, Dong, Enzeng, Qi, Guoyuan

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Dynamic modelling and chaos control for a thin plate oscillator using Bubnov–Galerkin integral method von Jiao, Xiaodong, Wang, Xinyu, Tao, Jin, Sun, Hao, Sun, Qinglin, Chen, Zengqiang

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Tofacitinib for the treatment of immune-related adverse events in cancer immunotherapy: a multi-center observational study von Liu, Qing, Liu, Mengling, Zou, Zhiguo, Lin, Jinyi, Zhang, Ningping, Zhao, Lin, Zhou, Jiahua, Zhou, Haojie, Zhou, Xin, Jiao, Xiaodong, Yu, Yiyi, Liu, Tianshu

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ADAM-17 is a poor prognostic indicator for patients with hilar cholangiocarcinoma and is regulated by FoxM1 von Jiao, Xiaodong, Yu, Wenlong, Qian, Jianxin, Chen, Ying, Wei, Peilian, Fang, Wenzheng, Yu, Guanzhen

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Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis von Li, Lin, Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Wang, Panfeng, Guo, Xiangming, Jiao, Xiaodong, Zhang, Qingjiong, Hejtmancik, J Fielding

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Memristor hyperchaos in a generalized Kolmogorov-type system with extreme multistability von Jiao, Xiaodong, Yuan, Mingfeng, Tao, Jin, Sun, Hao, Sun, Qinglin, Chen, Zengqiang

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CDKN2B polymorphism is associated with primary open-angle glaucoma (POAG) in the Afro-Caribbean population of Barbados, West Indies von Cao, Dan, Jiao, Xiaodong, Liu, Xing, Hennis, Anselm, Leske, M Cristina, Nemesure, Barbara, Hejtmancik, J Fielding

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Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts von JIANJUN CHEN, ZHIWEI MA, AMER RIAZUDDIN, S, FIELDING HEJTMANCIK, J, XIAODONG JIAO, FARISS, Robert, LEE KANTOROW, Wanda, KANTOROW, Marc, PRAS, Eran, FRYDMAN, Moshe, PRAS, Elon, RIAZUDDIN, Sheikh

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A novel mutation of the RPGR gene in a Chinese X-linked retinitis pigmentosa family and possible involvement of X-chromosome inactivation von Wang, Yun, Lu, Lan, Zhang, Daren, Tan, Yueqiu, Li, Danli, He, Fen, Jiao, Xiaodong, Yang, Ming, Hejtmancik, J. Fielding, Liu, Xuyang

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A Bietti Crystalline Dystrophy Mouse Model Shows Increased Sensitivity to Light-Induced Injury von Ma, Zhiwei, Jiao, Xiaodong, Agbaga, Martin-Paul, Anderson, Robert E., Qian, Haohua, Li, Qian, Dong, Lijin, Hejtmancik, J. Fielding

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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma von Rauf, Bushra, Khan, Shahid Y., Jiao, Xiaodong, Irum, Bushra, Ashfaq, Ramla, Zehra, Mubashra, Khan, Asma A., Naeem, Muhammad Asif, Shahzad, Mohsin, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer

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Aged Nrf2-Null Mice Develop All Major Types of Age-Related Cataracts von Rowan, Sheldon, Jiang, Shuhong, Francisco, Sarah G., Pomatto, Laura C. D., Ma, Zhiwei, Jiao, Xiaodong, Campos, Maria M., Aryal, Sandeep, Patel, Shaili D., Mahaling, Binapani, Riazuddin, S. Amer, Duh, Elia J., Lachke, Salil A., Hejtmancik, J. Fielding, de Cabo, Rafael, FitzGerald, Paul G., Taylor, Allen

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Changes in DNA methylation hallmark alterations in chromatin accessibility and gene expression for eye lens differentiation von Disatham, Joshua, Brennan, Lisa, Jiao, Xiaodong, Ma, Zhiwei, Hejtmancik, J Fielding, Kantorow, Marc

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Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family von Jiao, Xiaodong, Khan, Shahid Y, Kaul, Haiba, Butt, Tariq, Naeem, Muhammad Asif, Riazuddin, Sheikh, Hejtmancik, J Fielding, Riazuddin, S Amer

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Kinematic Modes Identification and Its Intelligent Control of Micro-Nano Particle Manipulated by Acoustic Signal von Jiao, Xiaodong, Tao, Jin, Sun, Hao, Sun, Qinglin

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Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa von Li, Lin, Jiao, Xiaodong, D'Atri, Ilaria, Ono, Fumihito, Nelson, Ralph, Chan, Chi-Chao, Nakaya, Naoki, Ma, Zhiwei, Ma, Yan, Cai, Xiaoying, Zhang, Longhua, Lin, Siying, Hameed, Abdul, Chioza, Barry A, Hardy, Holly, Arno, Gavin, Hull, Sarah, Khan, Muhammad Imran, Fasham, James, Harlalka, Gaurav V, Michaelides, Michel, Moore, Anthony T, Coban Akdemir, Zeynep Hande, Jhangiani, Shalini, Lupski, James R, Cremers, Frans P M, Qamar, Raheel, Salman, Ahmed, Chilton, John, Self, Jay, Ayyagari, Radha, Kabir, Firoz, Naeem, Muhammad Asif, Ali, Muhammad, Akram, Javed, Sieving, Paul A, Riazuddin, Sheikh, Baple, Emma L, Riazuddin, S Amer, Crosby, Andrew H, Hejtmancik, J Fielding

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Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts von Jiao, Xiaodong, Khan, Shahid Y, Irum, Bushra, Khan, Arif O, Wang, Qiwei, Kabir, Firoz, Khan, Asma A, Husnain, Tayyab, Akram, Javed, Riazuddin, Sheikh, Hejtmancik, J Fielding, Riazuddin, S Amer

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Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families von Li, Lin, Chen, Yabin, Jiao, Xiaodong, Jin, Chongfei, Jiang, Dan, Tanwar, Mukesh, Ma, Zhiwei, Huang, Li, Ma, Xiaoyin, Sun, Wenmin, Chen, Jianjun, Ma, Yan, M'hamdi, Oussama, Govindarajan, Gowthaman, Cabrera, Patricia E, Li, Jiali, Gupta, Nikhil, Naeem, Muhammad Asif, Khan, Shaheen N, Riazuddin, Sheikh, Akram, Javed, Ayyagari, Radha, Sieving, Paul A, Riazuddin, S Amer, Hejtmancik, J Fielding

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