MicroRNA-184 promotes differentiation of the retinal pigment epithelium by targeting the AKT2/mTOR signaling pathway

Por Jiang, Chao, Qin, Bing, Liu, Guohua, Sun, Xiantao, Shi, Houxia, Ding, Sijia, Liu, Yuan, Zhu, Meidong, Chen, Xue, Zhao, Chen
Publicado no Oncotarget (2016)

Maternal germline mosaicism of kinesin family member 21A (KIF21A) mutation causes complex phenotypes in a Chinese family with congenital fibrosis of the extraocular muscles

Por Liu, Gang, Chen, Xue, Sun, Xiantao, Liu, Hu, Zhao, Kanxing, Chang, Qinglin, Pan, Xinyuan, Wang, Xiuying, Yuan, Songtao, Liu, Qinghuai, Zhao, Chen
Publicado em 2014

Next-generation Sequencing Extends the Phenotypic Spectrum for LCA5 Mutations: Novel LCA5 Mutations in Cone Dystrophy

Por Chen, Xue, Sheng, Xunlun, Sun, Xiantao, Zhang, Yuxin, Jiang, Chao, Li, Huiping, Ding, Sijia, Liu, Yani, Liu, Wenzhou, Li, Zili, Zhao, Chen
Publicado no Sci Rep (2016)

Pre-operative to post-operative serum carcinoembryonic antigen ratio is a prognostic indicator in colorectal cancer

Por Sun, Zhenqiang, Wang, Fuqi, Zhou, Quanbo, Yang, Shuaixi, Sun, Xiantao, Wang, Guixian, Li, Zhen, Zhang, Zhiyong, Song, Junmin, Liu, Jinbo, Yuan, Weitang
Publicado no Oncotarget (2017)

LncRNA ZNF503-AS1 promotes RPE differentiation by downregulating ZNF503 expression

Por Chen, Xue, Jiang, Chao, Qin, Bing, Liu, Guohua, Ji, Jiangdong, Sun, Xiantao, Xu, Min, Ding, Sijia, Zhu, Meidong, Huang, Guofu, Yan, Biao, Zhao, Chen
Publicado no Cell Death Dis (2017)

A large family with inherited optic disc anomalies: a correlation between a new genetic locus and complex ocular phenotypes

Por Wang, Decai, Pan, Xinyuan, Ji, Jiangdong, Gu, Shun, Sun, Xiantao, Jiang, Chao, Xia, Weiyi, Qiu, Zhihua, Kang, Xiaoli, Ding, Sijia, Liu, Qinghuai, Chen, Xue, Lu, Fang, Zhao, Chen
Publicado no Sci Rep (2017)

GUCA1A mutation causes maculopathy in a five-generation family with a wide spectrum of severity

Por Chen, Xue, Sheng, Xunlun, Zhuang, Wenjuan, Sun, Xiantao, Liu, Guohua, Shi, Xun, Huang, Guofu, Mei, Yan, Li, Yingjie, Pan, Xinyuan, Liu, Yani, Li, Zili, Zhao, Qingshun, Yan, Biao, Zhao, Chen
Publicado no Genet Med (2017)