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Dongyang Kang

Showing results (1-10 of 54) with videos related to

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Nutrients|October 16, 2025
Muscle Strength, Lipid Metabolism and Hepatic Steatosis Are Improved with Ursolic Acid Treatment in High-Fat Diet-Induced Obese MiceDongyang Kang, Li Cao
Medicine|September 8, 2023
Intervention study of tai chi training on the intestinal flora of college student basketball playersDongyang Kang, Xiaorong Wang, Jiahong Wang
Langmuir : the ACS Journal of Surfaces and Colloids|August 20, 2009
Fabrication of necklace-like structures via electrospinningYu Jin, Dayong Yang, Dongyang Kang, et al.
Molecular Genetics & Genomic Medicine|October 12, 2020
A follow-up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF geneShuzhi Yang, Cuicui Wang, Chengyong Zhou, et al.
BMC Medical Genomics|May 25, 2022
Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutationPing Gu, Guojian Wang, Xue Gao, et al.
Biomed Research International|February 25, 2020
Prelingual Sensorineural Hearing Loss Caused by a Novel <i>GJB2</i> Dominant Mutation in a Chinese FamilyShasha Huang, Xue Gao, Yufeng Wang, 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.
BMC Medical Genomics|March 29, 2022
Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patientsYing Fu, Shasha Huang, Xue Gao, et al.
Acta Oto-Laryngologica|November 8, 2014
Mutations in the mitochondrial 12S rRNA gene in elderly Chinese peopleYuhua Zhu, Jiandong Zhao, Bo Feng, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Nutrients|October 16, 2025
Muscle Strength, Lipid Metabolism and Hepatic Steatosis Are Improved with Ursolic Acid Treatment in High-Fat Diet-Induced Obese MiceDongyang Kang, Li Cao
Medicine|September 8, 2023
Intervention study of tai chi training on the intestinal flora of college student basketball playersDongyang Kang, Xiaorong Wang, Jiahong Wang
Langmuir : the ACS Journal of Surfaces and Colloids|August 20, 2009
Fabrication of necklace-like structures via electrospinningYu Jin, Dayong Yang, Dongyang Kang, et al.
Molecular Genetics & Genomic Medicine|October 12, 2020
A follow-up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF geneShuzhi Yang, Cuicui Wang, Chengyong Zhou, et al.
BMC Medical Genomics|May 25, 2022
Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutationPing Gu, Guojian Wang, Xue Gao, et al.
Biomed Research International|February 25, 2020
Prelingual Sensorineural Hearing Loss Caused by a Novel <i>GJB2</i> Dominant Mutation in a Chinese FamilyShasha Huang, Xue Gao, Yufeng Wang, 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.
BMC Medical Genomics|March 29, 2022
Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patientsYing Fu, Shasha Huang, Xue Gao, et al.
Acta Oto-Laryngologica|November 8, 2014
Mutations in the mitochondrial 12S rRNA gene in elderly Chinese peopleYuhua Zhu, Jiandong Zhao, Bo Feng, et al.
Pageof 6