Search Results - Ting Bai
- Showing 1 - 14 results of 14
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Early Feeding Behaviors and Breastfeeding Outcomes After Cesarean Section by Feng Zhang, Jing Cheng, Shuhan Yan, Hua Wu, Ting Bai
Published 2019Artigo -
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Noninvasive Prenatal Testing for Wilson Disease by Use of Circulating Single-Molecule Amplification and Resequencing Technology (cSMART) by Weigang Lv, Xianda Wei, Ruolan Guo, Qin Liu, Zheng Yu, Jiazhen Chang, Ting Bai, Haoxian Li, Jianguang Zhang, Zhuo Song, David S. Cram, Desheng Liang, Lingqian Wu
Published 2014Artigo -
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Clinical application of noninvasive prenatal screening for sex chromosome aneuploidies in 50,301 pregnancies: initial experience in a Chinese hospital by Cechuan Deng, Qian Zhu, Sha Liu, Jianlong Liu, Ting Bai, Xiaosha Jing, Tianyu Xia, Yunyun Liu, Jing Cheng, Zhunduo Li, Xiangjin Wei, Lingling Xing, Yuan Luo, Hongqian Liu
Published 2019Artigo -
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Sleep Deprivation Induces Dry Eye Through Inhibition of PPARα Expression in Corneal Epithelium by Liying Tang, Xue Wang, Jieli Wu, San Ming Li, Zhaoqiang Zhang, San‐Gang Wu, Ting Su, Zhirong Lin, Xueting Chen, Xu‐Lin Liao, Ting Bai, Yan Qiu, Peter S. Reinach, Wei Li, Yongxiong Chen, Zuguo Liu
Published 2018Artigo -
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Endothelial POFUT1 controls injury-induced liver fibrosis by repressing fibrinogen synthesis by Shan He, Yuru Luo, Wangge Ma, X Y Wang, Chengrong Yan, Wenyang Hao, Fang Yuan, Hongyu Su, Baochang Lai, Junhui Liu, Ying Xiong, Ting Bai, Xiaoyong Ren, Enqi Liu, Hua Han, Yue Wu, Zuyi Yuan, Yidong Wang
Published 2024Artigo -
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Phenotype‐to‐genotype approach reveals head‐circumference‐associated genes in an autism spectrum disorder cohort by Huidan Wu, Honghui Li, Ting Bai, Lin Han, Jianjun Ou, Guanglei Xun, Yu Zhang, Yazhe Wang, Guiqin Duan, Ningxia Zhao, Biyuan Chen, Xiaogang Du, Meiling Yao, Xiaobing Zou, Jingping Zhao, Zhengmao Hu, Evan E. Eichler, Hui Guo, Kun Xia
Published 2019Artigo -
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A NeuroD1 AAV-Based Gene Therapy for Functional Brain Repair after Ischemic Injury through In Vivo Astrocyte-to-Neuron Conversion by Yu‐Chen Chen, Ningxin Ma, Zi-Fei Pei, Zheng Wu, Fabricio H Do Monte, Susan H. Keefe, Emma Yellin, Miranda S. Chen, Jiu-Chao Yin, Grace Lee, Angélica Minier-Toribio, Yi Hu, Yu-Ting Bai, Kathryn Lee, Gregory J. Quirk, Gong Chen
Published 2019Artigo -
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ADAM9 promotes lung cancer progression through vascular remodeling by VEGFA, ANGPT2, and PLAT by Chen-Yuan Lin, Chia-Fong Cho, Shih-Ting Bai, Jing-Pei Liu, Ting-Ting Kuo, Li‐Ju Wang, Yu-Sen Lin, Ching‐Chan Lin, Liang‐Chuan Lai, Tzu‐Pin Lu, Chih-Ying Hsieh, Chin-Nan Chu, Da-Chuan Cheng, Yuh‐Pyng Sher
Published 2017Artigo -
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Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort by Hui Guo, Peng Yu, Zhengmao Hu, Ying Li, Guanglei Xun, Jianjun Ou, Liangdan Sun, Zhimin Xiong, Yanling Liu, Tianyun Wang, Jingjing Chen, Lu Xia, Ting Bai, Yidong Shen, Qi Tian, Yiqiao Hu, Lu Shen, Rongjuan Zhao, Xuejun Zhang, Fengyu Zhang, Jingping Zhao, Xiaobing Zou, Kun Xia
Published 2017Artigo -
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De novo genic mutations among a Chinese autism spectrum disorder cohort by Tianyun Wang, Hui Guo, Bo Xiong, Holly A.F. Stessman, Huidan Wu, Bradley P. Coe, Tychele N. Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema, Laura Vives, Lu Xia, Meina Tang, Jianjun Ou, Biyuan Chen, Yidong Shen, Guanglei Xun, Long Min, Janice Lin, Zev Kronenberg, Yu Peng, Ting Bai, Honghui Li, Xiaoyan Ke, Zhengmao Hu, Jingping Zhao, Xiaobing Zou, Kun Xia, Evan E. Eichler
Published 2016Artigo -
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Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model by Hui Guo, Tianyun Wang, Huidan Wu, Long Min, Bradley P. Coe, Honghui Li, Guanglei Xun, Jianjun Ou, Biyuan Chen, Guiqin Duan, Ting Bai, Ningxia Zhao, Yidong Shen, Yun Li, Yazhe Wang, Yu Zhang, Carl Baker, Yanling Liu, Nan Pang, Li’an Huang, Lin Han, Xiangbin Jia, Cenying Liu, Hailun Ni, Xinyi Yang, Lu Xia, Jingjing Chen, Lu Shen, Ying Li, Rongjuan Zhao, Wenjing Zhao, Jing Peng, Qian Pan, Zhigao Long, Wei Su, Jieqiong Tan, Xiaogang Du, Xiaoyan Ke, Meiling Yao, Zhengmao Hu, Xiaobing Zou, Jingping Zhao, Raphael Bernier, Evan E. Eichler, Kun Xia
Published 2018Artigo -
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Disruptive variants of <i>CSDE1</i> associate with autism and interfere with neuronal development and synaptic transmission by Hui Guo, Ying Li, Lu Shen, Tianyun Wang, Xiangbin Jia, Lijuan Liu, Tao Xu, Mengzhu Ou, Kendra Hoekzema, Huidan Wu, Madelyn A. Gillentine, Cenying Liu, Hailun Ni, Pengwei Peng, Rongjuan Zhao, Yu Zhang, Chanika Phornphutkul, Alexander P.A. Stegmann, Carlos E. Prada, Robert J. Hopkin, Joseph T.C. Shieh, Kirsty McWalter, Kristin G. Monaghan, Peter M. van Hasselt, Koen L.I. van Gassen, Ting Bai, Long Min, Lin Han, Yingting Quan, Meilin Chen, Yaowen Zhang, Kuokuo Li, Qiumeng Zhang, Jieqiong Tan, Tengfei Zhu, Yaning Liu, Nan Pang, Jing Peng, Daryl A. Scott, Seema R. Lalani, Mahshid S. Azamian, Grazia M.S. Mancini, Darius J. Adams, Malin Kvarnung, Anna Lindstrand, Ann Nordgren, Jonathan Pevsner, Ikeoluwa Osei‐Owusu, Corrado Romano, Giuseppe Calabrese, Ornella Galesi, Jozef Gécz, Eric Haan, Judith D. Ranells, Melissa Racobaldo, Magnus Nordenskjöld, Suneeta Madan‐Khetarpal, Jessica Sebastian, Susie Ball, Xiaobing Zou, Jingping Zhao, Zhengmao Hu, Fan Xia, Pengfei Liu, Jill A. Rosenfeld, Bert B.A. de Vries, Raphael Bernier, Qing Xu, Honghui Li, Wei Xie, Robert B. Hufnagel, Evan E. Eichler, Kun Xia
Published 2019Artigo
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