Rezultati - 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 od 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
Izdano 2019Text -
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RNA Editome in Rhesus Macaque Shaped by Purifying Selection od 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
Izdano 2014Text -
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Hydrogen peroxide primes heart regeneration with a derepression mechanism od 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
Izdano 2014Text -
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Exome Sequencing Reveals a Novel Variant in NFX1 Causing Intracranial Aneurysm in a Chinese Family od 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
Izdano 2019Text -
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Mutational landscape and genetic signatures of cell‐free DNA in tumour‐induced osteomalacia od 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
Izdano 2020Text -
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Cover od 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
Izdano 2020Text -
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Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1 od 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
Izdano 2019Text
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