Application of Sensory Descriptive Analysis and Consumer Studies to Investigate Traditional and Authentic Foods: A Review

door Yang, Jiyun, Lee, Jeehyun
Gepubliceerd in Foods (2019)

Consumer Perception of Red Wine by the Degree of Familiarity Using Consumer-Based Methodology

door Yang, Jiyun, Lee, Jeehyun
Gepubliceerd in Foods (2021)

The complete mitochondrial genome of Allantus togatus (Panzer, 1801), in view of possible cryptic species

door Yang, Jiyun, Sun, Zemin, Wei, Meicai, Niu, Gengyun
Gepubliceerd in Mitochondrial DNA B Resour (2021)

MicroRNA-126 Inhibits Tumor Cell Growth and Its Expression Level Correlates with Poor Survival in Non-Small Cell Lung Cancer Patients

door Yang, Jiyun, Lan, Haitao, Huang, Xiaobing, Liu, Baoyu, Tong, Yu
Gepubliceerd in 2012

Genetic Variant in Interleukin-18 Is Associated with Idiopathic Recurrent Miscarriage in Chinese Han Population

door Yue, Jun, Tong, Yu, Zhou, Jing, Liu, Qingqing, Yang, Jiyun
Gepubliceerd in Int J Mol Sci (2015)

Genetic variant in IL-33 is associated with idiopathic recurrent miscarriage in Chinese Han population

door Yue, Jun, Tong, Yu, Xie, Lan, Ma, Tao, Yang, Jiyun
Gepubliceerd in Sci Rep (2016)

Two novel likely pathogenic variants of HARS2 identified in a Chinese family with sensorineural hearing loss

door Yu, Jing, Jiang, Wei, Cao, Li, Na, Xiaoxue, Yang, Jiyun
Gepubliceerd in Hereditas (2020)

Identification of two novel PRPF31 mutations in Chinese families with non‐syndromic autosomal dominant retinitis pigmentosa

door Cao, Li, Peng, Chunyan, Yu, Jing, Jiang, Wei, Yang, Jiyun
Gepubliceerd in Mol Genet Genomic Med (2020)

Mutation screening of the USH2A gene in retinitis pigmentosa and USHER patients in a Han Chinese population

door Huang, Lulin, Mao, Yao, Yang, Jiyun, Li, Yuanfeng, Li, Yang, Yang, Zhenglin
Gepubliceerd in Eye (Lond) (2018)

Prenatal diagnosis of familial exudative vitreoretinopathy and Norrie disease

door Liu, Jingjing, Zhu, Jing, Yang, Jiyun, Zhang, Xiang, Zhang, Qi, Zhao, Peiquan
Gepubliceerd in Mol Genet Genomic Med (2018)

Association between TCF7L2 gene polymorphisms and susceptibility to Type 2 Diabetes Mellitus: a large Human Genome Epidemiology (HuGE) review and meta-analysis

door Tong, Yu, Lin, Ying, Zhang, Yuan, Yang, Jiyun, Zhang, Yawei, Liu, Hengchuan, Zhang, Ben
Gepubliceerd in 2009

Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa

door LIU, SANMEI, XIE, LAN, YUE, JUN, MA, TAO, PENG, CHUNYAN, QIU, BIYUAN, YANG, ZHENGLIN, YANG, JIYUN
Gepubliceerd in Int J Mol Med (2016)

Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades

door Xiang, Jiale, Yang, Jiyun, Chen, Lisha, Chen, Qiang, Yang, Haiyan, Sun, Chengcheng, Zhou, Qing, Peng, Zhiyu
Gepubliceerd in Sci Rep (2020)

Author Correction: Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades

door Xiang, Jiale, Yang, Jiyun, Chen, Lisha, Chen, Qiang, Yang, Haiyan, Sun, Chengcheng, Zhou, Qing, Peng, Zhiyu
Gepubliceerd in Sci Rep (2020)

Association Study of Polymorphisms in Selenoprotein Genes and Kashin–Beck Disease and Serum Selenium/Iodine Concentration in a Tibetan Population

door Huang, Lulin, Shi, Yi, Lu, Fang, Zheng, Hong, Liu, Xiaoqi, Gong, Bo, Yang, Jiyun, Lin, Ying, Cheng, Jing, Ma, Shi, Lin, He, Yang, Zhenglin
Gepubliceerd in 2013

Mutation screening in genes known to be responsible for Retinitis Pigmentosa in 98 Small Han Chinese Families

door Huang, Lulin, Zhang, Qi, Huang, Xin, Qu, Chao, Ma, Shi, Mao, Yao, Yang, Jiyun, Li, You, Li, Yuanfeng, Tan, Chang, Zhao, Peiquan, Yang, Zhenglin
Gepubliceerd in Sci Rep (2017)

The essential effector SCRE1 in Ustilaginoidea virens suppresses rice immunity via a small peptide region

door Zhang, Nan, Yang, Jiyun, Fang, Anfei, Wang, Jiyang, Li, Dayong, Li, Yuejiao, Wang, Shanzhi, Cui, Fuhao, Yu, Junjie, Liu, Yongfeng, Peng, You‐Liang, Sun, Wenxian
Gepubliceerd in Mol Plant Pathol (2020)

A novel deleterious mutation in the COMP gene that causes pseudoachondroplasia

door Luo, Huaichao, Yu, Sisi, Lin, Ying, Guo, Qi, Ma, Rongchuan, Ye, Zimeng, Di, Yanan, Li, Ning, Miao, Yuanying, Zhou, Yu, Li, Yuanfeng, Yang, Jiyun, Yang, Zhenglin
Gepubliceerd in Hum Genome Var (2016)

A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16

door Lin, Ying, Liu, Ting, Li, Jing, Yang, Jiyun, Du, Qiong, Wang, Junfang, Yang, Yang, Liu, Xiaoqi, Fan, Yuanfu, Lu, Fang, Chen, Yilian, Pu, Yonghong, Zhang, Kang, He, Xiangge, Yang, Zhenglin
Gepubliceerd in 2008

An association study of SERPING1 gene and age-related macular degeneration in a Han Chinese population

door Lu, Fang, Zhao, Peiquan, Fan, Yinchuan, Tang, Shibo, Hu, Jianbin, Liu, Xiaoqi, Yang, Xian, Chen, Yiye, Li, Tao, Lei, Chuntao, Yang, Jiyun, Lin, Ying, Ma, Shi, Li, Chunyong, Shi, Yi, Yang, Zhenglin
Gepubliceerd in 2010