Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family

Por Qi, Yu-He, Gao, Feng-Juan, Hu, Fang-Yuan, Zhang, Sheng-Hai, Chen, Jun-Yi, Huang, Wan-Jing, Tian, Guo-Hong, Wang, Min, Gan, De-Kang, Wu, Ji-Hong, Xu, Ge-Zhi
Publicado no Front Genet (2017)

Targeted next-generation sequencing analysis identifies novel mutations in families with severe familial exudative vitreoretinopathy

Por Huang, Xiao-Yan, Zhuang, Hong, Wu, Ji-Hong, Li, Jian-Kang, Hu, Fang-Yuan, Zheng, Yu, Tellier, Laurent Christian Asker M., Zhang, Sheng-Hai, Gao, Feng-Juan, Zhang, Jian-Guo, Xu, Ge-Zhi
Publicado no Mol Vis (2017)

Genetic association of FOXO1A and FOXO3A with longevity trait in Han Chinese populations

Por Li, Yang, Wang, Wen-Jing, Cao, Huiqing, Lu, Jiehua, Wu, Chong, Hu, Fang-Yuan, Guo, Jian, Zhao, Ling, Yang, Fan, Zhang, Yi-Xin, Li, Wei, Zheng, Gu-Yan, Cui, Hanbin, Chen, Xiaomin, Zhu, Zhiming, He, Hongbo, Dong, Birong, Mo, Xianming, Zeng, Yi, Tian, Xiao-Li
Publicado em 2009

NEXN inhibits GATA4 and leads to atrial septal defects in mice and humans

Por Yang, Fan, Zhou, Lei, Wang, Qiguang, You, Xin, Li, Ying, Zhao, Yong, Han, Xiaonan, Chang, Zai, He, Xin, Cheng, Chunyan, Wu, Chong, Wang, Wen-Jing, Hu, Fang-Yuan, Zhao, Ting, Li, Yang, Zhao, Ming, Zheng, Gu-Yan, Dong, Jie, Fan, Chun, Yang, Juxian, Meng, Xianmin, Zhang, Youyi, Zhu, Xianyang, Xiong, Jingwei, Tian, Xiao-Li, Cao, Huiqing
Publicado no Cardiovasc Res (2014)