A non-canonical pathway regulates ER stress signaling and blocks ER stress-induced apoptosis and heart failure

por Yao, Yufeng, Lu, Qiulun, Hu, Zhenkun, Yu, Yubin, Chen, Qiuyun, Wang, Qing K.
Publicado 2017

Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa

por Huang, Yukan, Zhang, Jing, Li, Chang, Yang, Guohua, Liu, Mugen, Wang, Qing K, Tang, Zhaohui
Publicado 2010

Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population

por Chen, Shanshan, Wang, Chuchu, Wang, Xiaojing, Xu, Chengqi, Wu, Manman, Wang, Pengxia, Tu, Xin, Wang, Qing K
Publicado 2015

Cardiac sodium channel regulator MOG1 regulates cardiac morphogenesis and rhythm

por Zhou, Juan, Wang, Longfei, Zuo, Mengxia, Wang, Xiaojing, Ahmed, Abu Shufian Ishtiaq, Chen, Qiuyun, Wang, Qing K.
Publicado 2016

Lack of association between the APLNR variant rs9943582 with ischemic stroke in the Chinese Han GeneID population

por Wang, Pengyun, Wang, Chuchu, Li, Sisi, Wang, Binbin, Xiong, Liang, Tu, Xin, Wang, Qing K., Xu, Cheng-Qi
Publicado 2017

AGGF1 therapy inhibits thoracic aortic aneurysms by enhancing integrin α7-mediated inhibition of TGF-β1 maturation and ERK1/2 signaling

por Da, Xingwen, Li, Ziyan, Huang, Xiaofan, He, Zuhan, Yu, Yubing, Tian, Tongtong, Xu, Chengqi, Yao, Yufeng, Wang, Qing K.
Publicado 2023

A novel FBN2 mutation cosegregates with congenital contractural arachnodactyly in a five‐generation Chinese family

por Zhou, Shiyuan, Wang, Fengyu, Dou, Yongheng, Zhou, Jiping, Hao, Gefang, Xu, Chengqi, Wang, Qing K., Wang, Haili, Wang, Pengyun
Publicado 2018

Protein therapy of skeletal muscle atrophy and mechanism by angiogenic factor AGGF1

por He, Zuhan, Song, Qixue, Yu, Yubing, Liu, Feng, Zhao, Jinyan, Un, Waikeong, Da, Xingwen, Xu, Chengqi, Yao, Yufeng, Wang, Qing K.
Publicado 2023

A novel DSPP mutation is associated with type II dentinogenesis Imperfecta in a chinese family

por Zhang, Xianqin, Chen, Lanying, Liu, Jingyu, Zhao, Zhen, Qu, Erjun, Wang, Xiaotao, Chang, Wei, Xu, Chengqi, Wang, Qing K, Liu, Mugen
Publicado 2007

Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations

por Zhang, Xianqin, Chen, Shenghan, Zhang, Li, Liu, Mugen, Redfearn, Sharon, Bryant, Randall M, Oberti, Carlos, Vincent, G Michael, Wang, Qing K
Publicado 2008

Cloning and Functional Characterization of Novel Variants and Tissue-Specific Expression of Alternative Amino and Carboxyl Termini of Products of Slc4a10

por Liu, Ying, Wang, Deng-Ke, Jiang, De-Zhi, Qin, Xue, Xie, Zhang-Dong, Wang, Qing K., Liu, Mugen, Chen, Li-Ming
Publicado 2013

Up-regulation of miR-95-3p in hepatocellular carcinoma promotes tumorigenesis by targeting p21 expression

por Ye, Jian, Yao, Yufeng, Song, Qixue, Li, Sisi, Hu, Zhenkun, Yu, Yubing, Hu, Changqing, Da, Xingwen, Li, Hui, Chen, Qiuyun, Wang, Qing K.
Publicado 2016

Angiogenic factor AGGF1 blocks neointimal formation after vascular injury via interaction with integrin α7 on vascular smooth muscle cells

por Yu, Yubing, Li, Yong, Peng, Huixin, Song, Qixue, Da, Xingwen, Li, Hui, He, Zuhan, Ren, Xiang, Xu, Chengqi, Yao, Yufeng, Wang, Qing K.
Publicado 2022

Discovery of time-delayed gene regulatory networks based on temporal gene expression profiling

por Li, Xia, Rao, Shaoqi, Jiang, Wei, Li, Chuanxing, Xiao, Yun, Guo, Zheng, Zhang, Qingpu, Wang, Lihong, Du, Lei, Li, Jing, Li, Li, Zhang, Tianwen, Wang, Qing K
Publicado 2006

Genome-Wide Linkage Scan Identifies Two Novel Genetic Loci for Coronary Artery Disease: In GeneQuest Families

por Gao, Hanxiang, Li, Lin, Rao, Shaoqi, Shen, Gongqing, Xi, Quansheng, Chen, Shenghan, Zhang, Zheng, Wang, Kai, Ellis, Stephen G., Chen, Qiuyun, Topol, Eric J., Wang, Qing K.
Publicado 2014

Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease

por Guo, Yang, Wang, Fan, Li, Lin, Gao, Hanxiang, Arckacki, Stephen, Wang, Isabel Z., Barnard, John, Ellis, Stephen, Hubbard, Carlos, Topol, Eric J., Chen, Qiuyun, Wang, Qing K.
Publicado 2017

Integrative Analysis of miRNA and mRNA Expression Profiles Associated With Human Atrial Aging

por Yao, Yan, Jiang, Chenxi, Wang, Fan, Yan, Han, Long, Deyong, Zhao, Jinghua, Wang, Jiangang, Zhang, Chunxiao, Li, Yang, Tian, Xiaoli, Wang, Qing K., Wu, Gang, Zhang, Zhihui
Publicado 2019

Genetic Variants at Newly Identified Lipid Loci Are Associated with Coronary Heart Disease in a Chinese Han Population

por Zhou, Li, Ding, Hu, Zhang, Xiaomin, He, Meian, Huang, Suli, Xu, Yujun, Shi, Ying, Cui, Guanglin, Cheng, Longxian, Wang, Qing K., Hu, Frank B., Wang, Daowen, Wu, Tangchun
Publicado 2011

Functional rare variant in a C/EBP beta binding site in NINJ2 gene increases the risk of coronary artery disease

por Wang, Pengyun, Wang, Yifan, Peng, Huixin, Wang, Jingjing, Zheng, Qian, Wang, Pengxia, Wang, Jing, Zhang, Hongfu, Huang, Yufeng, Xiong, Liang, Zhang, Rongfeng, Xia, Yunlong, Wang, Qing K., Xu, Chengqi
Publicado 2021

Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population

por Wang, Pengyun, Xu, Chengqi, Wang, Chuchu, Wu, Yanxia, Wang, Dan, Chen, Shanshan, Zhao, Yuanyuan, Wang, Xiaojing, Li, Sisi, Yang, Qin, Zeng, Qiutang, Tu, Xin, Liao, Yuhua, Wang, Qing K., Cheng, Xiang
Publicado 2015