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Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 11, 2024
Canonical MAPK signaling in auditory neuropathyYueying Wang, Lusha Huang, Xiaoqing Cen, et al.Molecular Genetics & Genomic Medicine|February 2, 2022
Report of rare and novel mutations in candidate genes in a cohort of hearing-impaired patientsMin Liu, Yue Liang, Bixue Huang, et al.International Journal of Pediatric Otorhinolaryngology|December 31, 2017
Germinal mosaicism of PAX3 mutation caused Waardenburg syndrome type IKaitian Chen, Yuan Zhan, Xuan Wu, et al.International Journal of Pediatric Otorhinolaryngology|October 13, 2016
Compound heterozygous MYO7A mutations segregating Usher syndrome type 2 in a Han familyLing Zong, Kaitian Chen, Xuan Wu, et al.Acta Oto-Laryngologica|May 4, 2019
Different prognoses in patients with profound sudden sensorineural hearing lossFan-Qin Wei, Lanying Wen, Kaitian Chen, et al.American Journal of Otolaryngology|November 27, 2018
Audiological outcomes in sudden sensorineural hearing loss with presumed inner ear hemorrhageKaitian Chen, Lanying Wen, Ling Zong, et al.Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|December 24, 2015
[Clinical research of sudden sensorineural hearing loss due to inner-ear hemorrhage]Xuan Wu, Liang Sun, Kaitian Chen, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 9, 2024
[Late-onset hereditary hearing loss caused by TMPRSS3 compound heterozygous mutations]Yueying Wang, Yue Liang, Bixue Huang, et al.International Journal of Pediatric Otorhinolaryngology|August 22, 2012
Novel heterozygous mutation c.662_663insG compound with IVS7-2A>G mutation in SLC26A4 gene in a Chinese family with Pendred syndromeKaitian Chen, Wei Zhou, Ling Zong, et al.Immunological Investigations|January 21, 2020
MiR-146a Promotes Tolerogenic Properties of Dendritic Cells and through Targeting Notch1 SignalingHaocheng Tang, Yinyan Lai, Jing Zheng, et al.Pageof 4