A Wheat (Triticum aestivum) Protein Phosphatase 2A Catalytic Subunit Gene Provides Enhanced Drought Tolerance in Tobacco

Por Xu, Chongyi, Jing, Ruilian, Mao, Xinguo, Jia, Xiaoyun, Chang, Xiaoping
Publicado em 2007

Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis

Por Li, Jie, Jia, Xiaoyun, Li, Shiqiang, Fang, Shaohua, Guo, Xiangming
Publicado em 2014

X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia

Por Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Guo, Xiangming, Zhang, Qingjiong
Publicado no Mol Vis (2016)

microRNAs responsive to ozone-induced oxidative stress in Arabidopsis thaliana

Por Iyer, Niranjani J., Jia, Xiaoyun, Sunkar, Ramanjulu, Tang, Guiliang, Mahalingam, Ramamurthy
Publicado em 2012

Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism

Por Fang, Shaohua, Guo, Xiangming, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Zhang, Qingjiong
Publicado em 2008

A novel mutation of PAX6 in Chinese patients with new clinical features of Peters’ anomaly

Por Jia, Xiuhua, Guo, Xiangming, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Zhang, Qingjiong
Publicado em 2010

Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese

Por Ji, Yanli, Jia, Xiaoyun, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2010

A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese family

Por Xiao, Xueshan, Guo, Xiangming, Jia, Xiaoyun, Li, Shiqiang, Wang, Panfeng, Zhang, Qingjiong
Publicado em 2011

Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients

Por Zhang, A-Mei, Jia, Xiaoyun, Guo, Xiangming, Zhang, Qingjiong, Yao, Yong-Gang
Publicado em 2012

Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy

Por Bi, Rui, Zhang, A-Mei, Jia, Xiaoyun, Zhang, Qingjiong, Yao, Yong-Gang
Publicado em 2012

Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel Analysis

Por Xin, Wei, Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Guo, Xiangming, Zhang, Qingjiong
Publicado no PLoS One (2015)

Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy

Por Li, Yadi, Li, Jie, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Guo, Xiangming
Publicado no PLoS One (2017)

Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy

Por Chen, Yabin, Jia, Xiaoyun, Wang, Panfeng, Xiao, Xueshan, Li, Shiqiang, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2013

Novel RS1 mutations associated with X-linked juvenile retinoschisis

Por YI, JUNHUI, LI, SHIQIANG, JIA, XIAOYUN, XIAO, XUESHAN, WANG, PANFENG, GUO, XIANGMING, ZHANG, QINGJIONG
Publicado em 2012

Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma

Por Zhang, Xiaohui, Li, Shiqiang, Xiao, Xueshan, Jia, Xiaoyun, Wang, Panfeng, Shen, Huangxuan, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2009

Mitochondrial DNA Sequence Variation and Haplogroup Distribution in Chinese Patients with LHON and m.14484T>C

Por Yu, Dandan, Jia, Xiaoyun, Zhang, A-Mei, Li, Shiqiang, Zou, Yang, Zhang, Qingjiong, Yao, Yong-Gang
Publicado em 2010

Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies

Por Wang, Qin, Gao, Yang, Wang, Panfeng, Li, Shiqiang, Jia, Xiaoyun, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2011

Effective Small RNA Destruction by the Expression of a Short Tandem Target Mimic in Arabidopsis([C])([W])

Por Yan, Jun, Gu, Yiyou, Jia, Xiaoyun, Kang, Wenjun, Pan, Shangjin, Tang, Xiaoqing, Chen, Xuemei, Tang, Guiliang
Publicado em 2012

Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia

Por Li, Jiali, Gao, Bei, Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Sun, Wenmin, Guo, Xiangming, Zhang, Qingjiong
Publicado no Mol Vis (2016)

Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma

Por Yang, Mei, Guo, Xiangming, Liu, Xing, Shen, Huangxuan, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Fang, Shaohua, Zhang, Qingjiong
Publicado em 2009