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

por Yang, Jiyun, Lee, Jeehyun
Publicado en Foods (2019)

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

por Yang, Jiyun, Lee, Jeehyun
Publicado en Foods (2021)

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

por Yang, Jiyun, Sun, Zemin, Wei, Meicai, Niu, Gengyun
Publicado en 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

por Yang, Jiyun, Lan, Haitao, Huang, Xiaobing, Liu, Baoyu, Tong, Yu
Publicado 2012

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

por Yue, Jun, Tong, Yu, Zhou, Jing, Liu, Qingqing, Yang, Jiyun
Publicado en Int J Mol Sci (2015)

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

por Yue, Jun, Tong, Yu, Xie, Lan, Ma, Tao, Yang, Jiyun
Publicado en Sci Rep (2016)

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

por Yu, Jing, Jiang, Wei, Cao, Li, Na, Xiaoxue, Yang, Jiyun
Publicado en Hereditas (2020)

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

por Cao, Li, Peng, Chunyan, Yu, Jing, Jiang, Wei, Yang, Jiyun
Publicado en Mol Genet Genomic Med (2020)

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

por Huang, Lulin, Mao, Yao, Yang, Jiyun, Li, Yuanfeng, Li, Yang, Yang, Zhenglin
Publicado en Eye (Lond) (2018)

Prenatal diagnosis of familial exudative vitreoretinopathy and Norrie disease

por Liu, Jingjing, Zhu, Jing, Yang, Jiyun, Zhang, Xiang, Zhang, Qi, Zhao, Peiquan
Publicado en 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

por Tong, Yu, Lin, Ying, Zhang, Yuan, Yang, Jiyun, Zhang, Yawei, Liu, Hengchuan, Zhang, Ben
Publicado 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

por LIU, SANMEI, XIE, LAN, YUE, JUN, MA, TAO, PENG, CHUNYAN, QIU, BIYUAN, YANG, ZHENGLIN, YANG, JIYUN
Publicado en Int J Mol Med (2016)

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

por Xiang, Jiale, Yang, Jiyun, Chen, Lisha, Chen, Qiang, Yang, Haiyan, Sun, Chengcheng, Zhou, Qing, Peng, Zhiyu
Publicado en Sci Rep (2020)

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

por Xiang, Jiale, Yang, Jiyun, Chen, Lisha, Chen, Qiang, Yang, Haiyan, Sun, Chengcheng, Zhou, Qing, Peng, Zhiyu
Publicado en Sci Rep (2020)

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

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

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

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

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

por 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
Publicado en Mol Plant Pathol (2020)

A novel deleterious mutation in the COMP gene that causes pseudoachondroplasia

por 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
Publicado en Hum Genome Var (2016)

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

por 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
Publicado 2008

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

por 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
Publicado 2010