Online Health Information Seeking Behavior: A Systematic Review

por Jia, Xiaoyun, Pang, Yan, Liu, Liangni Sally
Publicado 2021

Understanding consumers’ continuance intention to watch streams: A value-based continuance intention model

por Jia, Xiaoyun, Pang, Yan, Huang, Bingqi, Hou, Feng
Publicado 2023

Distribution and risk factor analysis for Clostridium difficile‐associated diarrhea among hospitalized children over one year of age

por Zhao, Chunna, Guo, Shu, Jia, Xiaoyun, Xu, Xiwei
Publicado 2019

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 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 2016

Genome-wide characterization and expression analysis of GRAS gene family in pepper (Capsicum annuum L.)

por Liu, Baoling, Sun, Yan, Xue, Jinai, Jia, Xiaoyun, Li, Runzhi
Publicado 2018

Spectrum, frequency, and genotype–phenotype of mutations in SPATA7

por Xiao, Xueshan, Sun, Wenmin, Li, Shiqiang, Jia, Xiaoyun, Zhang, Qingjiong
Publicado 2019

Non-Pharmaceutical Interventions against COVID-19 Causing a Lower Trend in Age of LHON Onset

por Zheng, Yuxi, Jia, Xiaoyun, Li, Shiqiang, Xiao, Xueshan, Zhang, Qingjiong, Wang, Panfeng
Publicado 2023

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 2008

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 2010

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 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 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 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 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 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 2017

GPR143 mutations in Chinese patients with ocular albinism type 1

por Jia, Xiuhua, Yuan, Jin, Jia, Xiaoyun, Ling, Shiqi, Li, Shiqiang, Guo, Xiangming
Publicado 2017

Novel mutations of FRMD7 in Chinese patients with congenital motor nystagmus

por Jia, Xiuhua, Zhu, Xiang, Li, Qigen, Jia, Xiaoyun, Li, Shiqiang, Guo, Xiangming
Publicado 2017

Stearoyl-ACP Δ(9) Desaturase 6 and 8 (GhA-SAD6 and GhD-SAD8) Are Responsible for Biosynthesis of Palmitoleic Acid Specifically in Developing Endosperm of Upland Cotton Seeds

por Liu, Baoling, Sun, Yan, Xue, Jinai, Mao, Xue, Jia, Xiaoyun, Li, Runzhi
Publicado 2019

Overexpression of Sweet Potato Carotenoid Cleavage Dioxygenase 4 (IbCCD4) Decreased Salt Tolerance in Arabidopsis thaliana

por Zhang, Jie, He, Liheng, Dong, Jingjing, Zhao, Cailiang, Tang, Ruimin, Jia, Xiaoyun
Publicado 2022