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Dongyi Han

Showing results (61-70 of 141) with videos related to

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Chinese Medical Journal|April 10, 2002
Deletions are easy detectable in cochlear mitochondrial DNA of Cu/Zn superoxide dismutase gene knockout miceXinxin Zhang, Dongyi Han, Dalian Ding, et al.
Chinese Medical Journal|November 2, 2002
Cochlear mitochondrial DNA3867bp deletion in aged miceXinxin Zhang, Dongyi Han, Dalian Ding, et al.
Acta Oto-Laryngologica|January 15, 2025
Metabolome modification and underlying biomarker of noise-induced hearing loss Guinea pig cochlear fluidGuowei Qi, Jinge Tang, Handai Qin, et al.
Acta Oto-Laryngologica|April 10, 2004
Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusisPu Dai, Weiyan Yang, Sichang Jiang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 9, 2012
[Clinical and genetic analysis of a patient with Treacher Collins syndrome in TCOF1 gene]Hongbo Li, Xu Zhang, Zhenyue Li, et al.
Acta Oto-Laryngologica|December 27, 2019
Clinical characteristics of petrosal cholesteatoma and value of MRI-DWI in the diagnosisWenjing Zuo, Fangyuan Wang, Shiming Yang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|July 27, 2007
[Molecular etiology of 573 patients with nonsyndromic hearing loss in 5 provinces of northwest region of China]Qingwen Zhu, Xin Liu, Dongyi Han, et al.
American Journal of Medical Genetics. Part A|October 17, 2008
A de novo GJB2 (connexin 26) mutation, R75W, in a Chinese pedigree with hearing loss and palmoplantar keratodermaYongyi Yuan, Deliang Huang, Fei Yu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 14, 2013
[Clinical characteristics and surgical management of extensive cholesteatoma of external auditory canal]Huibing Wang, Fei Yu, Xizheng Shan, et al.
Experimental and Therapeutic Medicine|September 7, 2018
Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndromeZhiqiang Yan, Yu Lu, Yanfei Wang, et al.
Pageof 15

Showing results (61-70 of 141) with videos related to

Sort By:
Pageof 15
Chinese Medical Journal|April 10, 2002
Deletions are easy detectable in cochlear mitochondrial DNA of Cu/Zn superoxide dismutase gene knockout miceXinxin Zhang, Dongyi Han, Dalian Ding, et al.
Chinese Medical Journal|November 2, 2002
Cochlear mitochondrial DNA3867bp deletion in aged miceXinxin Zhang, Dongyi Han, Dalian Ding, et al.
Acta Oto-Laryngologica|January 15, 2025
Metabolome modification and underlying biomarker of noise-induced hearing loss Guinea pig cochlear fluidGuowei Qi, Jinge Tang, Handai Qin, et al.
Acta Oto-Laryngologica|April 10, 2004
Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusisPu Dai, Weiyan Yang, Sichang Jiang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 9, 2012
[Clinical and genetic analysis of a patient with Treacher Collins syndrome in TCOF1 gene]Hongbo Li, Xu Zhang, Zhenyue Li, et al.
Acta Oto-Laryngologica|December 27, 2019
Clinical characteristics of petrosal cholesteatoma and value of MRI-DWI in the diagnosisWenjing Zuo, Fangyuan Wang, Shiming Yang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|July 27, 2007
[Molecular etiology of 573 patients with nonsyndromic hearing loss in 5 provinces of northwest region of China]Qingwen Zhu, Xin Liu, Dongyi Han, et al.
American Journal of Medical Genetics. Part A|October 17, 2008
A de novo GJB2 (connexin 26) mutation, R75W, in a Chinese pedigree with hearing loss and palmoplantar keratodermaYongyi Yuan, Deliang Huang, Fei Yu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 14, 2013
[Clinical characteristics and surgical management of extensive cholesteatoma of external auditory canal]Huibing Wang, Fei Yu, Xizheng Shan, et al.
Experimental and Therapeutic Medicine|September 7, 2018
Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndromeZhiqiang Yan, Yu Lu, Yanfei Wang, et al.
Pageof 15