Browsing by Author Wang, Wenwen
Showing results 1 to 4 of 4
Issue Date | Title | Author(s) |
2019 | Congenital nephrotic syndrome associated with 22q11.2 duplication syndrome in a Chinese family and functional analysis of the intronic NPHS1 c. 3286+5G > A mutation | Li, Liangliang; Yi, Zhi; Xi, Hongmin; Ma, Lili; Shao, Hui; Wang, Wenwen; Pan, Hong; Li, Miaomiao; Jiang, Hong |
14-Feb-2024 | Deep whole-genome analysis of 494 hepatocellular carcinomas | Chen, Lei; Zhang, Chong; Xue, Ruidong; Liu, Mo; Bai, Jian; Bao, Jinxia; Wang, Yin; Jiang, Nanhai; Li, Zhixuan; Wang, Wenwen; Wang, Ruiru; Zheng, Bo; Yang, Airong; Hu, Ji; Liu, Ke; Shen, Siyun; Zhang, Yangqianwen; Bai, Mixue; Wang, Yan; Zhu, Yanjing; Yang, Shuai; Gao, Qiang; Gu, Jin; Gao, Dong; Wang, Xin Wei; Nakagawa, Hidewaki; Zhang, Ning; Wu, Lin; Rozen, Steven G.; Bai, Fan; Wang, Hongyang |
2011 | Hydrological effects of sustainable drainage systems in an urbanizing area | Qin, Huapeng; Wang, Wenwen; Zhao, Zhijie; Khu, Soon Thiam |
Jun-2020 | Methylation of PLK1 by SET7/9 ensures accurate kinetochore-microtubule dynamics | Yu, Ruoying; Wu, Huihui; Ismail, Hazrat; Du, Shihao; Cao, Jun; Wang, Jianyu; Ward, Tarsha; Yang, Fengrui; Gui, Ping; Ali, Mahboob; Chu, Lingluo; Mo, Fei; Wang, Qi; Chu, Youjun; Zang, Jianye; Zhao, Yun; Ye, Mingliang; Fang, Guowei; Chen, Peng R.; Dou, Zhen; Gao, Xinjiao; Wang, Wenwen; Liu, Xing; Yao, Xuebiao |