Single-cell RNA sequencing of neural stem cells derived from human trisomic iPSCs reveals the abnormalities during neural differentiation of Down syndrome by Jia-jun Qiu, Yan-na Liu, Hao Wei, Fanyi Zeng, Fanyi Zeng, Fanyi Zeng, Jing-bin Yan, Jing-bin Yan

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RNA editing regulates lncRNA splicing in human early embryo development. by Jiajun Qiu, Xiao Ma, Fanyi Zeng, Jingbin Yan

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The Study of Alternative Splicing Events in Human Induced Pluripotent Stem Cells From a Down's Syndrome Patient by Yunjie Wang, Yunjie Wang, Zexu Li, Zexu Li, Guanheng Yang, Guanheng Yang, Linlin Cai, Linlin Cai, Fan Yang, Fan Yang, Yaqiong Zhang, Yaqiong Zhang, Yitao Zeng, Yitao Zeng, Qingwen Ma, Qingwen Ma, Fanyi Zeng, Fanyi Zeng, Fanyi Zeng

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Activation of proHGF by St14 induces mouse embryonic stem cell differentiation by Xiaoshuang Yan, Yan Xue, Yiye Zhou, Yan Cheng, Shang Yin, Qingwen Ma, Fanyi Zeng

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Feasibility study of Syngo iFlow in predicting hemodynamic improvement post-endovascular procedure in peripheral artery disease by Ming Tang, Fanyi Zeng, Xindong Chang, Mingfei He, Qingqing Fang, Lele Xue, Xinyi Luo, Shiwu Yin

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Identification of Cellular Compositions in Different Microenvironments and Their Potential Impacts on Hematopoietic Stem Cells HSCs Using Single-Cell RNA Sequencing with Systematic... by Yanan Chi, Guanheng Yang, Chuanliang Guo, Shaoqing Zhang, Lei Hong, Huixiang Tang, Xiao Sang, Jie Wang, Ji Ma, Yan Xue, Fanyi Zeng

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Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the <i>ZC4H2</i> Gene by Jing-Jing Sun, Qin Cai, Miao Xu, Yan-Na Liu, Wan-Rui Li, Juan Li, Li Ma, Cheng Cai, Xiao-Hui Gong, Yi-Tao Zeng, Zhao-Rui Ren, Fanyi Zeng

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Clinical Study of 8 Cases of CHD2 Gene Mutation–Related Neurological Diseases and Their Mechanisms by Xiaona Luo, Xiaoang Sun, Yilin Wang, Longlong Lin, Fang Yuan, Simei Wang, Wenjing Zhang, Xiaobing Ji, Meiyan Liu, Shengnan Wu, Xiaoping Lan, Jie Zhang, Jingbin Yan, Fanyi Zeng, Yucai Chen, Yucai Chen

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Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndro... by Yilin Wang, Fang Yuan, Anqi Wang, Chao Wang, Longlong Lin, Simei Wang, Chunmei Wang, Xiaona Luo, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Xiaomin Sun, Jiaming Xi, Jingbin Yan, Fanyi Zeng, Yucai Chen

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Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.... by Xiaona Luo, Yilin Wang, Fang Yuan, Longlong Lin, Anqi Wang, Chao Wang, Miao Guo, Simei Wang, Chunmei Wang, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Zhiping Liu, Wuhen Xu, Jingbin Yan, Fanyi Zeng, Yucai Chen

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Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan–Herndon–Dudley syndrome by Anqi Wang, Jiaming Xi, Fang Yuan, Yilin Wang, Simei Wang, Chunmei Wang, Chao Wang, Longlong Lin, Xiaona Luo, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Xiaomin Sun, Jie Yang, Jingbin Yan, Fanyi Zeng, Yucai Chen

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Segawa syndrome caused by TH gene mutation and its mechanism by Yilin Wang, Chunmei Wang, Meiyan Liu, Wuhen Xu, Simei Wang, Fang Yuan, Xiaona Luo, Quanmei Xu, Rongrong Yin, Anqi Wang, Miao Guo, Longlong Lin, Chao Wang, Hongyi Cheng, Zhiping Liu, Yuanfeng Zhang, Fanyi Zeng, Jingbin Yan, Yucai Chen

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Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene by Xiaona Luo, Chunmei Wang, Longlong Lin, Fang Yuan, Simei Wang, Yilin Wang, Anqi Wang, Chao Wang, Shengnan Wu, Xiaoping Lan, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Jiaming Xi, Jie Zhang, Xiaomin Sun, Jingbin Yan, Fanyi Zeng, Yucai Chen, Yucai Chen

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