Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation

Por Tong, Yi, Sun, Yan-Hong, Zhou, Xiangtian, Zhao, Fuxin, Mao, Yijian, Wei, Qi-ping, Yang, Li, Qu, Jia, Guan, Min-Xin
Publicado em 2010

Leber's Hereditary Optic Neuropathy Affects Only Female Matrilineal Relatives in Two Chinese Families

Por Qu, Jia, Wang, Ying, Tong, Yi, Zhou, Xiangtian, Zhao, Fuxin, Yang, Li, Zhang, Shoukang, Zhang, Juanjuan, West, Constance E., Guan, Min-Xin
Publicado em 2010

Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population

Por Zhao, Fuxin, Bai, Jian, Chen, Wei, Xue, Anquan, Li, Chaohua, Yan, Zhonghui, Chen, Hui, Lu, Fan, Hu, Yongwu, Qu, Jia, Zeng, Changqing, Zhou, Xiangtian
Publicado em 2010

Experimental murine myopia induces collagen type Iα1 (COL1A1) DNA methylation and altered COL1A1 messenger RNA expression in sclera

Por Zhou, Xiangtian, Ji, Fengtao, An, Jianhong, Zhao, Fuxin, Shi, Fanjun, Huang, Furong, Li, Yuan, Jiao, Shiming, Yan, Dongsheng, Chen, Xiaoyan, Chen, JiangFan, Qu, Jia
Publicado em 2012

Very high penetrance and occurrence of Leber’s hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation

Por Zhou, Xiangtian, Zhang, Hongxing, Zhao, Fuxin, Ji, Yanchun, Tong, Yi, Zhang, Juanjuan, Zhang, Yu, Yang, Li, Qian, Yaping, Lu, Fan, Qu, Jia, Guan, Min-Xin
Publicado em 2010

Extremely Low Penetrance of Leber’s Hereditary Optic Neuropathy in 8 Han Chinese Families Carrying the ND4 G11778A Mutation

Por Qu, Jia, Zhou, Xiangtian, Zhang, Juanjuan, Zhao, Fuxin, Sun, Yan-Hong, Tong, Yi, Wei, Qi-Ping, Cai, Wansi, Yang, Li, West, Constance E., Guan, Min-Xin
Publicado em 2009

cAMP Level Modulates Scleral Collagen Remodeling, a Critical Step in the Development of Myopia

Por Tao, Yijin, Pan, Miaozhen, Liu, Shufeng, Fang, Fang, Lu, Runxia, Lu, Chanyi, Zheng, Min, An, Jianhong, Xu, Hongjia, Zhao, Fuxin, Chen, Jiang-fan, Qu, Jia, Zhou, Xiangtian
Publicado em 2013

Leber's Hereditary Optic Neuropathy Is Associated with the T3866C Mutation in Mitochondrial ND1 Gene in Three Han Chinese Families

Por Zhou, Xiangtian, Qian, Yaping, Zhang, Juanjuan, Tong, Yi, Jiang, Pingping, Liang, Min, Dai, Xianning, Zhou, Huihui, Zhao, Fuxin, Ji, Yanchun, Mo, Jun Qin, Qu, Jia, Guan, Min-Xin
Publicado em 2012

Low penetrance of Leber’s hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation

Por Qu, Jia, Zhou, Xiangtian, Zhao, Fuxin, Liu, Xiaoling, Zhang, Minglian, Sun, Yan-Hong, Liang, Min, Yuan, Meixia, Liu, Qi, Tong, Yi, Wei, Qi-Ping, Yang, Li, Guan, Min-Xin
Publicado em 2009

Leber’s hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation

Por Zhao, Fuxin, Guan, Minqiang, Zhou, Xiangtian, Yuan, Meixia, Liang, Ming, Liu, Qi, Liu, Yan, Zhang, Yongmei, Yang, Li, Tong, Yi, Wei, Qi-Ping, Sun, Yan-Hong, Qu, Jia, Guan, Min-Xin
Publicado em 2009

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

Por Lu, Jianxin, Qian, Yaping, Li, Zhiyuan, Yang, Aifen, Zhu, Yi, Li, Ronghua, Yang, Li, Tang, Xiaowen, Chen, Bobei, Ding, Yu, Li, Yongyan, You, Junyan, Zheng, Jing, Tao, Zhihua, Zhao, Fuxin, Wang, Jindan, Sun, Dongmei, Zhao, Jianyue, Meng, Yanzi, Guan, Min-Xin
Publicado em 2009

Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population

Por Shi, Yi, Qu, Jia, Zhang, Dingding, Zhao, Peiquan, Zhang, Qingjiong, Tam, Pancy Oi Sin, Sun, Liangdan, Zuo, Xianbo, Zhou, Xiangtian, Xiao, Xueshan, Hu, Jianbin, Li, Yuanfeng, Cai, Li, Liu, Xiaoqi, Lu, Fang, Liao, Shihuang, Chen, Bin, He, Fei, Gong, Bo, Lin, He, Ma, Shi, Cheng, Jing, Zhang, Jie, Chen, Yiye, Zhao, Fuxin, Yang, Xian, Chen, Yuhong, Yang, Charles, Lam, Dennis Shun Chiu, Li, Xi, Shi, Fanjun, Wu, Zhengzheng, Lin, Ying, Yang, Jiyun, Li, Shiqiang, Ren, Yunqing, Xue, Anquan, Fan, Yingchuan, Li, Dean, Pang, Chi Pui, Zhang, Xuejun, Yang, Zhenglin
Publicado em 2011