Gap junctions amplify TRPV4 activation-initiated cell injury via modification of intracellular Ca(2+) and Ca(2+)-dependent regulation of TXNIP

por Zhang, Xiling, Mao, Zhimin, Huang, Yanru, Zhang, Zhen, Yao, Jian
Publicado 2020

The role of DNA methylation in syndromic and non-syndromic congenital heart disease

por Cao, Jiali, Wu, Qichang, Huang, Yanru, Wang, Lingye, Su, Zhiying, Ye, Huiming
Publicado 2021

Connexin43 Is Required for the Effective Activation of Spleen Cells and Immunoglobulin Production

por Huang, Yanru, Mao, Zhimin, Zhang, Xiling, Yang, Xiawen, Sawada, Norifumi, Takeda, Masayuki, Yao, Jian
Publicado 2019

Prevalence and genotype distribution of HPV infection among women in Xiamen, China

por Shen, Ye, Huang, Yanru, Wang, Wenbo, Zhang, Jian, Chen, Xiaolu, Zhang, Lutan, Huang, Xiaomei, Ge, Yunsheng
Publicado 2023

Hydrogen Sulfide Mediates Tumor Cell Resistance to Thioredoxin Inhibitor

por Mao, Zhimin, Yang, Xiawen, Mizutani, Sayumi, Huang, Yanru, Zhang, Zhen, Shinmori, Hideyuki, Gao, Kun, Yao, Jian
Publicado 2020

Reductively modified albumin attenuates DSS-Induced mouse colitis through rebalancing systemic redox state

por Yang, Xiawen, Mao, Zhimin, Huang, Yanru, Yan, Haizhao, Yan, Qiaojing, Hong, Jingru, Fan, Jianglin, Yao, Jian
Publicado 2021

Clinical Utility of the Prenatal BACs-on-Beads™ Assay in Invasive Prenatal Diagnosis

por Jiang, Yu, Wu, Lili, Ge, Yunshen, Zhang, Jian, Huang, Yanru, Wu, Qichang, Zhang, Yanhong, Zhou, Yulin
Publicado 2022

Effects of replacing hybrid giant napier with sugarcane bagasse and fermented sugarcane bagasse on growth performance, nutrient digestibility, rumen fermentation characteristics, a...

por Jin, Yadong, Huang, Yanru, Luo, Haocen, Wang, Langzhou, Chen, Binlong, Zhang, Yi, Deng, Kaimei, Zhao, Ningbo, Lai, Anqiang
Publicado 2023

Glutathione inhibits antibody and complement-mediated immunologic cell injury via multiple mechanisms

por Zhang, Zhen, Zhang, Xiling, Fang, Xin, Niimi, Manabu, Huang, Yanru, Piao, Honglan, Gao, Shan, Fan, Jianglin, Yao, Jian
Publicado 2017

Identification of pathogenic mutations in 6 Chinese families with multiple exostoses by whole-exome sequencing and multiplex ligation-dependent probe amplification: Case series

por Long, Xigui, Li, Zhuo, Huang, Yanru, Zhang, Li, Lv, Weigang, Teng, Yanling, Linpeng, Siyuan, Liang, Desheng, Wu, Lingqian
Publicado 2019

Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 cases

por Ge, Yunsheng, Li, Jia, Zhuang, Jianlong, Zhang, Jian, Huang, Yanru, Tan, Meihua, Li, Wei, Chen, Jiayan, Zhou, Yulin
Publicado 2021

Mutations in FIGLA Associated With Premature Ovarian Insufficiency in a Chinese Population

por Mei, Libin, Huang, Yanru, Wu, Xiaoling, He, Huang, Ye, Ronghui, Ma, Jinxiu, He, XueMei, Shi, Yuhua, Li, Ping
Publicado 2021

Corrigendum: Mutations in FIGLA associated with premature ovarian insufficiency in a Chinese population

por Mei, Libin, Huang, Yanru, Wu, Xiaoling, He, Huang, Ye, Ronghui, Ma, Jinxiu, He, XueMei, Shi, Yuhua, Li, Ping
Publicado 2022

Migration risk of fall armyworm (Spodoptera frugiperda) from North Africa to Southern Europe

por Wang, Jing, Huang, Yanru, Huang, Linsheng, Dong, Yingying, Huang, Wenjiang, Ma, Huiqin, Zhang, Hansu, Zhang, Xueyan, Chen, Xinyu, Xu, Yunlei
Publicado 2023

Overwintering Distribution of Fall Armyworm (Spodoptera frugiperda) in Yunnan, China, and Influencing Environmental Factors

por Huang, Yanru, Dong, Yingying, Huang, Wenjiang, Ren, Binyuan, Deng, Qiaoyu, Shi, Yue, Bai, Jie, Ren, Yu, Geng, Yun, Ma, Huiqin
Publicado 2020

A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy

por Huang, Yanru, Mei, Libin, Wang, Yangdan, Ye, Huiming, Ma, Xiaomin, Zhang, Jian, Cai, Meijiao, Li, Ping, Ge, Yunsheng, Zhou, Yulin
Publicado 2021

APC/C (Cdh1p) and Slx5p/Slx8p ubiquitin ligases confer resistance to aminoglycoside hygromycin B in Saccharomyces cerevisiae

por Doss, Ellen M., Tragesser-Tiña, Mary E., Huang, Yanru, Smaldino, Philip J., True, Jason D., Kalinski, Ashley L., Rubenstein, Eric M.
Publicado 2022

Three novel mutations of STK11 gene in Chinese patients with Peutz–Jeghers syndrome

por Tan, Hu, Mei, Libin, Huang, Yanru, Yang, Pu, Li, Haoxian, Peng, Ying, Chen, Chen, Wei, Xianda, Pan, Qian, Liang, Desheng, Wu, Lingqian
Publicado 2016

Carbenoxolone inhibits TRPV4 channel‐initiated oxidative urothelial injury and ameliorates cyclophosphamide‐induced bladder dysfunction

por Zhang, Xiling, Gao, Shan, Tanaka, Masayoshi, Zhang, Zhen, Huang, Yanru, Mitsui, Takahiko, Kamiyama, Manabu, Koizumi, Schuichi, Fan, Jianglin, Takeda, Masayuki, Yao, Jian
Publicado 2017

Identification of a novel MIP frameshift mutation associated with congenital cataract in a Chinese family by whole-exome sequencing and functional analysis

por Long, Xigui, Huang, Yanru, Tan, Hu, Li, Zhuo, Zhang, Rui, Linpeng, Siyuan, Lv, Weigang, Cao, Yingxi, Li, Haoxian, Liang, Desheng, Wu, Lingqian
Publicado 2018