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Dongyang Kang

Showing results (11-20 of 54) with videos related to

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Plos One|March 2, 2016
Spatial Variations in Vitreous Oxygen ConsumptionKarthik Murali, Dongyang Kang, Hossein Nazari, et al.
International Journal of Pediatric Otorhinolaryngology|August 27, 2011
De novo dominant mutation of GJB2 in two Chinese families with nonsyndromic hearing lossShasha Huang, Yongyi Yuan, Jun Liu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|September 25, 2014
[Assessment of the curative effective of cochlear implantation in childer with GJB2-associated NSSNHL]Chaochan Cai, Shasha Huang, Xue Gao, et al.
Plos One|November 7, 2013
Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type IIShuzhi Yang, Pu Dai, Xin Liu, et al.
Plos One|November 6, 2014
KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjectsJiandong Zhao, Yongyi Yuan, Shasha Huang, et al.
Heliyon|March 19, 2024
Mitochondrial tRNA<sup>Ser(UCN)</sup> mutations associated non-syndromic sensorineural hearing loss in Chinese familiesDejun Zhang, Jie Wu, Yongyi Yuan, et al.
Ebiomedicine|July 2, 2019
A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disabilityWeihao Zhao, Xue Gao, Shiwei Qiu, et al.
International Journal of Pediatric Otorhinolaryngology|May 12, 2015
Rapid identification of aminoglycoside-induced deafness gene mutations using multiplex real-time polymerase chain reactionShasha Huang, Guangxin Xiang, Dongyang Kang, et al.
BMC Genetics|February 19, 2014
Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutationYuhua Zhu, Shasha Huang, Dongyang Kang, 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.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Plos One|March 2, 2016
Spatial Variations in Vitreous Oxygen ConsumptionKarthik Murali, Dongyang Kang, Hossein Nazari, et al.
International Journal of Pediatric Otorhinolaryngology|August 27, 2011
De novo dominant mutation of GJB2 in two Chinese families with nonsyndromic hearing lossShasha Huang, Yongyi Yuan, Jun Liu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|September 25, 2014
[Assessment of the curative effective of cochlear implantation in childer with GJB2-associated NSSNHL]Chaochan Cai, Shasha Huang, Xue Gao, et al.
Plos One|November 7, 2013
Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type IIShuzhi Yang, Pu Dai, Xin Liu, et al.
Plos One|November 6, 2014
KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjectsJiandong Zhao, Yongyi Yuan, Shasha Huang, et al.
Heliyon|March 19, 2024
Mitochondrial tRNA<sup>Ser(UCN)</sup> mutations associated non-syndromic sensorineural hearing loss in Chinese familiesDejun Zhang, Jie Wu, Yongyi Yuan, et al.
Ebiomedicine|July 2, 2019
A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disabilityWeihao Zhao, Xue Gao, Shiwei Qiu, et al.
International Journal of Pediatric Otorhinolaryngology|May 12, 2015
Rapid identification of aminoglycoside-induced deafness gene mutations using multiplex real-time polymerase chain reactionShasha Huang, Guangxin Xiang, Dongyang Kang, et al.
BMC Genetics|February 19, 2014
Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutationYuhua Zhu, Shasha Huang, Dongyang Kang, 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.
Pageof 6