Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Mei Ouyang

Showing results (41-50 of 43) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 43 results.
Journal of Diabetes Investigation|May 21, 2026
Taiwanese consensus statement on the use of diabetes-specific formula: Scientific evidenceChih-Hsun Chu, Hui-Yu Peng, Chun-Chuan Lee, et al.
Human Genetics|December 4, 2008
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Xue-Zhong Liu, Yongyi Yuan, Denise Yan, et al.
Human Molecular Genetics|April 30, 2003
Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossXue Zhong Liu, Xiao Mei Ouyang, Xia Juan Xia, et al.
Pageof 5

Showing results (41-50 of 43) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 43 results.
Journal of Diabetes Investigation|May 21, 2026
Taiwanese consensus statement on the use of diabetes-specific formula: Scientific evidenceChih-Hsun Chu, Hui-Yu Peng, Chun-Chuan Lee, et al.
Human Genetics|December 4, 2008
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Xue-Zhong Liu, Yongyi Yuan, Denise Yan, et al.
Human Molecular Genetics|April 30, 2003
Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossXue Zhong Liu, Xiao Mei Ouyang, Xia Juan Xia, et al.
Pageof 5