Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|February 23, 2020
[Analysis of genotypes and hearing phenotypes of mutation infants with deafness]Xianlei Wang, Xuelei Zhao, Lihui Huang, et al.
Bioscience Trends|November 27, 2018
Novel compound heterozygous mutations in SLC26A4 gene in a Chinese family with enlarged vestibular aqueductXuelei Zhao, Xiaohua Cheng, Lihui Huang, et al.
Frontiers in Immunology|May 1, 2023
Identification and validation of chemokine system-related genes in idiopathic pulmonary fibrosisTianming Zhao, Xu Wu, Xuelei Zhao, et al.
Journal of Lipid Research|January 10, 2026
COP9 Signalosome is Required for Adipose Tissue Maintenance and Metabolic HealthHongyi Zhou, Shayantani Chakraborty, Xuelei Zhao, et al.
Bioscience Trends|June 28, 2019
Analysis of mutations in the FOXI1 and KCNJ10 genes in infants with a single-allele SLC26A4 mutationXuelei Zhao, Xiaohua Cheng, Lihui Huang, et al.
Bioscience Trends|August 28, 2018
Children with GJB2 gene mutations have various audiological phenotypesXianlei Wang, Lihui Huang, Xuelei Zhao, et al.
Medicine|December 15, 2018
The higher serum endocan levels may be a risk factor for the onset of cardiovascular disease: A meta-analysisTianming Zhao, Yao Kecheng, Xuelei Zhao, et al.
International Journal of Pediatric Otorhinolaryngology|December 18, 2018
Genotyping and audiological characteristics of infants with a single-allele SLC26A4 mutationXuelei Zhao, Lihui Huang, Xueyao Wang, et al.
Bioscience Trends|October 29, 2019
Mutation analysis of the SLC26A4 gene in three Chinese familiesCheng Wen, Shijie Wang, Xuelei Zhao, et al.
Pageof 2