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SaveShare Save Share Save Share Save Share Save Advances in meniscus tissue engineering: Towards bridging the gaps from bench to bedside
Bian, Yixin; Cai, Xuejie; Zhou, Runze; Lv, Zehui; Xu, Yiming; Wang, Yingjie; Wang, Han; Zhu, Wei; Sun, Hanyang; Zhao, Xiuli; Feng, Bin; Weng, Xisheng Share Save Share Save CRISPR/Cas9 correction of a dominant cis-double-variant in COL1A1 isolated from a patient with osteogenesis imperfecta increases the osteogenic capacity of induced pluripotent stem cellsCao, Yixuan; Li, Lulu; Ren, Xiuzhi; Mao, Bin; Yang, Yujiao; Mi, Huan; Guan, Yun; Li, Shan; Zhou, Siji; Guan, Xin; Yang, Tao; Zhao, Xiuli Share Save Share Save Share Save Exome sequencing reveals genetic architecture in patients with isolated or syndromic short statureFan, Xin; Zhao, Sen; Yu, Chenxi; Wu, Di; Yan, Zihui; Fan, Lijun; Song, Yanning; Wang, Yi; Li, Chuan; Ming, Yue; Gui, Baoheng; Niu, Yuchen; Li, Xiaoxin; Yang, Xinzhuang; Luo, Shiyu; Zhang, Qiang; Zhao, Xiuli; Pan, Hui; Li, Mei; Xia, Weibo; Qiu, Guixing; Liu, Pengfei; Zhang, Shuyang; Zhang, Jianguo; Wu, Zhihong; Lupski, James R.; Posey, Jennifer E.; Chen, Shaoke; Gong, Chunxiu; Wu, Nan Share Save Share Save TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage modelLiu, Jiaqi; Wu, Nan; Yang, Nan; Takeda, Kazuki; Chen, Weisheng; Li, Weiyu; Du, Renqian; Sen Liu; Zhou, Yangzhong; Zhang, Ling; Liu, Zhenlei; Zuo, Yuzhi; Zhao, Sen; Blank, Robert; Pehlivan, Davut; Dong, Shuangshuang; Zhang, Jianguo; Shen, Jianxiong; Si, Nuo; Wang, Yipeng; Liu, Gang; Li, Shugang; Zhao, Yanxue; Zhao, Hong; Chen, Yixin; Zhao, Yu; Song, Xiaofei; Hu, Jianhua; Lin, Mao; Tian, Ye; Yuan, Bo; Yu, Keyi; Niu, Yuchen; Yu, Bin; Li, Xiaoxin; Chen, Jia; Yan, Zihui; Zhu, Qiankun; Meng, Xiaolu; Chen, Xiaoli; Su, Jianzhong; Zhao, Xiuli; Wang, Xiaoyue; Ming, Yue; Li, Xiao; Raggio, Cathleen L.; Zhang, Baozhong; Weng, Xisheng; Zhang, Shuyang; Zhang, Xue; Watanabe, Kota; Matsumoto, Morio; Jin, Li; Shen, Yiping; Sobreira, Nara L.; Posey, Jennifer E.; Giampietro, Philip F.; Valle, David; Liu, Pengfei; Wu, Zhihong; Ikegawa, Shiro; Lupski, James R.; Zhang, Feng; Qiu, Guixing; Kawakami, Noriaki; Kotani, Toshiaki; Sudo, Hideki; Yonezawa, Ikuho; Uno, Koki; Taneichi, Hiroshi; Watanabe, Kei; Minami, Shohei; Shigematsu, Hideki; Sugawara, Ryo; Taniguchi, Yuki; Ootomo, Nao Share Save Share Save Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfectaLi, Lulu; Mao, Bin; Li, Shan; Xiao, Jifang; Wang, Han; Zhang, Jing; Ren, Xiuzhi; Wang, Yanzhou; Wu, Yiyang; Cao, Yixuan; Lu, Chaoxia; Gao, Jinsong; You, Yi; Zhao, Feiyue; Geng, Xingzhu; Xiao, Yaxiong; Jiang, Chendan; Ye, Yuqian; Yang, Tao; Zhao, Xiuli; Zhang, Xue Share Save Novel mutations in BMP1 induce a rare type of osteogenesis imperfectaXu, Xiao-jie; Lv, Fang; Song, Yu-wen; Li, Lu-jiao; Asan; Wei, Xiu-xiu; Zhao, Xiu-li; Jiang, Yan; Wang, Ou; Xing, Xiao-ping; Xia, Wei-bo; Li, Mei Share Save Share Save The adenosine deaminase acting on RNA 1 p150 isoform is involved in the pathogenesis of dyschromatosis symmetrica hereditariaZhang, J. Y.; Chen, X. D.; Zhang, Z.; Wang, H. L.; Guo, L.; Liu, Y.; Zhao, X. Z.; Cao, W.; Xing, Q. H.; Shao, F. M. Share Save Share Save Mutations of the EPHA2 Receptor Tyrosine Kinase Gene Cause Autosomal Dominant Congenital CataractZhang, Tianxiao; Hua, Rui; Xiao, Wei; Burdon, Kathryn P.; Bhattacharya, Shomi S.; Craig, Jamie E.; Shang, Dandan; Zhao, Xiuli; Mackey, David A.; Moore, Anthony T.; Luo, Yang; Zhang, Jinsong; Zhang, Xue Share Save 
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