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Dongyi Han

Showing results (91-100 of 141) with videos related to

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Journal of Environmental Sciences (China)|December 29, 2025
Enhancement of synergistic co-removal for zinc and cefazolin by a novel bio-adsorbent: Batch experiments and DFT calculationsRongping Chen, Wenjie Xu, Bingcai Cai, et al.
Plos One|August 8, 2015
Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, ChinaYi Jiang, Shasha Huang, Tao Deng, et al.
Journal of Translational Medicine|October 4, 2011
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueductShasha Huang, Dongyi Han, Yongyi Yuan, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype]Guojian Wang, Yongyi Yuan, Rong Li, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 23, 2022
Surgical management of endolymphatic sac tumor: classification, outcomes and strategy. A single institution's experienceNan Wu, Xiaoyan Ma, Weidong Shen, et al.
Acta Oto-Laryngologica|December 6, 2016
Identification of KCNQ1 compound heterozygous mutations in three Chinese families with Jervell and Lange-Nielsen SyndromeCuicui Wang, Yu Lu, Jing Cheng, et al.
American Journal of Human Genetics|December 19, 2003
Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese familyHui Zhao, Ronghua Li, Qiuju Wang, et al.
Biochemical and Biophysical Research Communications|August 1, 2006
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese familiesPu Dai, Yongyi Yuan, Deliang Huang, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|July 15, 2006
[Surgical approach and materials in reparation of cerebrospinal rhinorrhea (54 cases reports)]Yungao Zhang, Rongguang Wang, Wenming Wu, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|January 4, 2011
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing lossJianzhong Li, Jing Cheng, Yanping Lu, et al.
Pageof 15

Showing results (91-100 of 141) with videos related to

Sort By:
Pageof 15
Journal of Environmental Sciences (China)|December 29, 2025
Enhancement of synergistic co-removal for zinc and cefazolin by a novel bio-adsorbent: Batch experiments and DFT calculationsRongping Chen, Wenjie Xu, Bingcai Cai, et al.
Plos One|August 8, 2015
Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, ChinaYi Jiang, Shasha Huang, Tao Deng, et al.
Journal of Translational Medicine|October 4, 2011
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueductShasha Huang, Dongyi Han, Yongyi Yuan, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype]Guojian Wang, Yongyi Yuan, Rong Li, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 23, 2022
Surgical management of endolymphatic sac tumor: classification, outcomes and strategy. A single institution's experienceNan Wu, Xiaoyan Ma, Weidong Shen, et al.
Acta Oto-Laryngologica|December 6, 2016
Identification of KCNQ1 compound heterozygous mutations in three Chinese families with Jervell and Lange-Nielsen SyndromeCuicui Wang, Yu Lu, Jing Cheng, et al.
American Journal of Human Genetics|December 19, 2003
Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese familyHui Zhao, Ronghua Li, Qiuju Wang, et al.
Biochemical and Biophysical Research Communications|August 1, 2006
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese familiesPu Dai, Yongyi Yuan, Deliang Huang, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|July 15, 2006
[Surgical approach and materials in reparation of cerebrospinal rhinorrhea (54 cases reports)]Yungao Zhang, Rongguang Wang, Wenming Wu, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|January 4, 2011
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing lossJianzhong Li, Jing Cheng, Yanping Lu, et al.
Pageof 15