The effects of telmisartan on the nuclear factor of activated T lymphocytes signalling pathway in hypertensive patients

por Huang, Sha-Sha, He, Si-Li, Zhang, Yuan-Ming
Publicado 2016

Inhibitory effects of telmisartan on culture and proliferation of and Kv1.3 potassium channel expression in peripheral blood CD4(+) T lymphocytes from Xinjiang Kazakh patients with...

por Huang, Sha-Sha, Zhang, Qiu-Bing, Yuan, Qing-Yan, He, Si-Li, Zhang, Yuan-Ming
Publicado 2016

Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling

por Li, Qi, Zhu, Qing-wen, Yuan, Yong-yi, Huang, Sha-sha, Han, Dong-yi, Huang, De-liang, Dai, Pu
Publicado 2012

Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families

por Su, Yu, Gao, Xue, Huang, Sha-Sha, Mao, Jing-Ning, Huang, Bang-Qing, Zhao, Jian-Dong, Kang, Dong-Yang, Zhang, Xin, Dai, Pu
Publicado 2018

Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation

por Guo, Chang, Huang, Sha-Sha, Yuan, Yong-Yi, Zhou, Ying, Wang, Ning, Kang, Dong-Yang, Yang, Su-Yan, Zhang, Xin, Gao, Xue, Dai, Pu
Publicado 2020

Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss

por Cui, Tian-Yi, Gao, Xue, Huang, Sha-Sha, Sun, Yan-Yan, Zhang, Si-Qi, Jiang, Xin-Xia, Yang, Yan-Zhong, Kang, Dong-Yang, Zhu, Qing-Wen, Yuan, Yong-Yi
Publicado 2020

Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss

por Wang, Wei-Qian, Gao, Xue, Huang, Sha-Sha, Kang, Dong-Yang, Xu, Jin-Cao, Yang, Kun, Han, Ming-Yu, Zhang, Xin, Yang, Su-Yan, Yuan, Yong-Yi, Dai, Pu
Publicado 2022

A gross deletion of the PAX3 gene in a large Chinese family with Waardenburg syndrome type I

por Yang, Shu-Zhi, Hou, Lei, Qi, Xin, Wang, Guo-Jian, Huang, Sha-Sha, Zhang, Shan-Shan, Huang, Bang-Qing, Yang, Ying, Li, Bei-Cheng, Liu, Shuo, Dai, Pu, Su, Yu
Publicado 2023

Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

por Gao, Xue, Huang, Sha-Sha, Yuan, Yong-Yi, Xu, Jin-Cao, Gu, Ping, Bai, Dan, Kang, Dong-Yang, Han, Ming-Yu, Wang, Guo-Jian, Zhang, Mei-Guang, Li, Jia, Dai, Pu
Publicado 2017

Novel Compound Heterozygous TMC1 Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family

por Gao, Xue, Su, Yu, Guan, Li-Ping, Yuan, Yong-Yi, Huang, Sha-Sha, Lu, Yu, Wang, Guo-Jian, Han, Ming-Yu, Yu, Fei, Song, Yue-Shuai, Zhu, Qing-Yan, Wu, Jing, Dai, Pu
Publicado 2013

Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing

por Gao, Xue, Zhu, Qing-yan, Song, Yue-Shuai, Wang, Guo-Jian, Yuan, Yong-Yi, Xin, Feng, Huang, Sha-Sha, Kang, Dong-Yang, Han, Ming-Yu, Guan, Li-ping, Zhang, Jian-guo, Dai, Pu
Publicado 2013

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

por Gao, Xue, Xu, Jin-Cao, Wang, Wei-Qian, Yuan, Yong-Yi, Bai, Dan, Huang, Sha-Sha, Wang, Guo-Jian, Su, Yu, Li, Jia, Kang, Dong-Yang, Zhang, Mei-Guang, Lin, Xi, Dai, Pu
Publicado 2018

Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family

por Gao, Xue, Su, Yu, Chen, Yu-Lan, Han, Ming-Yu, Yuan, Yong-Yi, Xu, Jin-Cao, Xin, Feng, Zhang, Mei-Guang, Huang, Sha-Sha, Wang, Guo-Jian, Kang, Dong-Yang, Guan, Li-Ping, Zhang, Jian-Guo, Dai, Pu
Publicado 2015

Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site v...

por Yang, Jin-Yuan, Wang, Wei-Qian, Han, Ming-Yu, Huang, Sha-Sha, Wang, Guo-Jian, Su, Yu, Xu, Jin-Cao, Fu, Ying, Kang, Dong-Yang, Yang, Kun, Zhang, Xin, Liu, Xing, Gao, Xue, Yuan, Yong-Yi, Dai, Pu
Publicado 2022

A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss

por Su, Yu, Tang, Wen-Xue, Gao, Xue, Yu, Fei, Dai, Zhi-Yao, Zhao, Jian-Dong, Lu, Yu, Ji, Fei, Huang, Sha-Sha, Yuan, Yong-Yi, Han, Ming-Yu, Song, Yue-Shuai, Zhu, Yu-Hua, Kang, Dong-Yang, HAN, Dong-Yi, Dai, Pu
Publicado 2014

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

por Gao, Xue, Yuan, Yong-Yi, Lin, Qiong-Fen, Xu, Jin-Cao, Wang, Wei-Qian, Qiao, Yue-Hua, Kang, Dong-Yang, Bai, Dan, Xin, Feng, Huang, Sha-Sha, Qiu, Shi-Wei, Guan, Li-Ping, Su, Yu, Wang, Guo-Jian, Han, Ming-Yu, Jiang, Yi, Liu, Han-Kui, Dai, Pu
Publicado 2018