Search Results - Xin Zhuang
- Showing 1 - 13 results of 13
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Evolutionarily significant A-to-I RNA editing events originated through G-to-A mutations in primates by An, Ni A., Ding, Wanqiu, Yang, Xin-Zhuang, Peng, Jiguang, He, Bin Z., Shen, Qing Sunny, Lu, Fujian, He, Aibin, Zhang, Yong E., Tan, Bertrand Chin-Ming, Chen, Jia-Yu, Li, Chuan-Yun
Published 2019Text -
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RNA Editome in Rhesus Macaque Shaped by Purifying Selection by Chen, Jia-Yu, Peng, Zhiyu, Zhang, Rongli, Yang, Xin-Zhuang, Tan, Bertrand Chin-Ming, Fang, Huaying, Liu, Chu-Jun, Shi, Mingming, Ye, Zhi-Qiang, Zhang, Yong E., Deng, Minghua, Zhang, Xiuqin, Li, Chuan-Yun
Published 2014Text -
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Hydrogen peroxide primes heart regeneration with a derepression mechanism by Han, Peidong, Zhou, Xiao-Hai, Chang, Nannan, Xiao, Cheng-Lu, Yan, Shouyu, Ren, He, Yang, Xin-Zhuang, Zhang, Mei-Ling, Wu, Qing, Tang, Boyang, Diao, Ju-Peng, Zhu, Xiaojun, Zhang, Chuanmao, Li, Chuan-Yun, Cheng, Heping, Xiong, Jing-Wei
Published 2014Text -
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Exome Sequencing Reveals a Novel Variant in NFX1 Causing Intracranial Aneurysm in a Chinese Family by Ding, Xinghuan, Zhao, Sen, Zhang, Qianqian, Yan, Zihui, Wang, Yang, Wu, Yong, Li, Xiaoxin, Liu, Jian, Niu, Yuchen, Zhang, Yisen, Zhang, Mingqi, Wang, Huizi, Zhang, Ying, Chen, Weisheng, Yang, Xin-Zhuang, Liu, Pengfei, Posey, Jennifer E., Lupski, James R., Wu, Zhihong, Yang, Xinjian, Wu, Nan, Wang, Kun
Published 2019Text -
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Mutational landscape and genetic signatures of cell‐free DNA in tumour‐induced osteomalacia by Wu, Nan, Zhang, Zhen, Zhou, Xi, Zhao, Hengqiang, Ming, Yue, Wu, Xue, Zhang, Xian, Yang, Xin‐Zhuang, Zhou, Meng, Bao, Hua, Chen, Weisheng, Wu, Yong, Liu, Sen, Wang, Huizi, Niu, Yuchen, Li, Yalun, Zheng, Yu, Shao, Yang, Gao, Na, Yang, Ying, Liu, Ying, Li, Wenli, Liu, Jia, Zhang, Na, Yang, Xu, Xu, Yuan, Li, Mei, Sun, Yingli, Su, Jianzhong, Zhang, Jianguo, Xia, Weibo, Qiu, Guixing, Liu, Yong, Liu, Jiaqi, Wu, Zhihong
Published 2020Text -
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Cover by Lin, Mao, Liu, Zhenlei, Liu, Gang, Zhao, Sen, Li, Chao, Chen, Weisheng, Coban Akdemir, Zeynep, Lin, Jiachen, Song, Xiaofei, Wang, Shengru, Xu, Qiming, Zhao, Yanxue, Wang, Lianlei, Zhang, Yuanqiang, Yan, Zihui, Liu, Sen, Liu, Jiaqi, Chen, Yixin, Zuo, Yuzhi, Yang, Xu, Sun, Tianshu, Yang, Xin‐Zhuang, Niu, Yuchen, Li, Xiaoxin, You, Wesley, Qiu, Bintao, Ding, Chen, Liu, Pengfei, Zhang, Shuyang, Carvalho, Claudia M. B., Posey, Jennifer E., Qiu, Guixing, Lupski, James R., Wu, Zhihong, Zhang, Jianguo, Wu, Nan
Published 2020Text -
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Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1 by Lin, Mao, Liu, Zhenlei, Liu, Gang, Zhao, Sen, Li, Chao, Chen, Weisheng, Coban Akdemir, Zeynep, Lin, Jiachen, Song, Xiaofei, Wang, Shengru, Xu, Qiming, Zhao, Yanxue, Wang, Lianlei, Zhang, Yuanqiang, Yan, Zihui, Liu, Sen, Liu, Jiaqi, Chen, Yixin, Zuo, Yuzhi, Yang, Xu, Sun, Tianshu, Yang, Xin‐Zhuang, Niu, Yuchen, Li, Xiaoxin, You, Wesley, Qiu, Bintao, Ding, Chen, Liu, Pengfei, Zhang, Shuyang, Carvalho, Claudia M. B., Posey, Jennifer E., Qiu, Guixing, Lupski, James R., Wu, Zhihong, Zhang, Jianguo, Wu, Nan
Published 2019Text
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