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

Sen Zhao

Showing results (311-320 of 346) with videos related to

Pageof 35
Sort By:
Journal of Medical Genetics|November 13, 2025
Genetic and embryonic transcriptome analyses reveal the molecular and developmental basis of Mayer-Rokitansky-Küster-Hauser syndromeNa Chen, Xi Cheng, Sen Zhao, et al.
American Journal of Medical Genetics. Part A|May 6, 2020
KIAA1217: A novel candidate gene associated with isolated and syndromic vertebral malformationsNoura Al Dhaheri, Nan Wu, Sen Zhao, et al.
Viruses|December 31, 2025
Phylogeographic and Host Interface Analyses Reveal the Evolutionary Dynamics of SAT3 Foot-And-Mouth Disease VirusShuang Zhang, Jianing Lv, Yao Lin, et al.
Plant Communications|December 5, 2025
Prefoldins 3 promotes the turnover of WRKY70 and FHY3 to modulate UV-B-induced hypocotyl growth inhibition in Arabidopsis thalianaYan Song, Meng Liu, Xue-Meng Gao, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2025
Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosisLianlei Wang, Zhaoyang Liu, Sen Zhao, et al.
Pharmacological Research|April 17, 2023
Proinflammatory activation of microglia in the cerebellum hyperexcites Purkinje cells to trigger ataxiaShu-Tao Xie, Wen-Chu Fan, Xian-Sen Zhao, et al.
Molecular Cancer|February 20, 2021
Genome-wide cell-free DNA methylation analyses improve accuracy of non-invasive diagnostic imaging for early-stage breast cancerJiaqi Liu, Hengqiang Zhao, Yukuan Huang, et al.
Human Molecular Genetics|October 12, 2018
TBX6 compound inheritance leads to congenital vertebral malformations in humans and miceNan Yang, Nan Wu, Ling Zhang, et al.
Nature Communications|February 6, 2024
Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spineSen Zhao, Hengqiang Zhao, Lina Zhao, et al.
Frontiers in Cell and Developmental Biology|May 3, 2021
Heterozygous Recurrent Mutations Inducing Dysfunction of <i>ROR2</i> Gene in Patients With Short StatureBaoheng Gui, Chenxi Yu, Xiaoxin Li, et al.
Pageof 35

Showing results (311-320 of 346) with videos related to

Sort By:
Pageof 35
Journal of Medical Genetics|November 13, 2025
Genetic and embryonic transcriptome analyses reveal the molecular and developmental basis of Mayer-Rokitansky-Küster-Hauser syndromeNa Chen, Xi Cheng, Sen Zhao, et al.
American Journal of Medical Genetics. Part A|May 6, 2020
KIAA1217: A novel candidate gene associated with isolated and syndromic vertebral malformationsNoura Al Dhaheri, Nan Wu, Sen Zhao, et al.
Viruses|December 31, 2025
Phylogeographic and Host Interface Analyses Reveal the Evolutionary Dynamics of SAT3 Foot-And-Mouth Disease VirusShuang Zhang, Jianing Lv, Yao Lin, et al.
Plant Communications|December 5, 2025
Prefoldins 3 promotes the turnover of WRKY70 and FHY3 to modulate UV-B-induced hypocotyl growth inhibition in Arabidopsis thalianaYan Song, Meng Liu, Xue-Meng Gao, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2025
Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosisLianlei Wang, Zhaoyang Liu, Sen Zhao, et al.
Pharmacological Research|April 17, 2023
Proinflammatory activation of microglia in the cerebellum hyperexcites Purkinje cells to trigger ataxiaShu-Tao Xie, Wen-Chu Fan, Xian-Sen Zhao, et al.
Molecular Cancer|February 20, 2021
Genome-wide cell-free DNA methylation analyses improve accuracy of non-invasive diagnostic imaging for early-stage breast cancerJiaqi Liu, Hengqiang Zhao, Yukuan Huang, et al.
Human Molecular Genetics|October 12, 2018
TBX6 compound inheritance leads to congenital vertebral malformations in humans and miceNan Yang, Nan Wu, Ling Zhang, et al.
Nature Communications|February 6, 2024
Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spineSen Zhao, Hengqiang Zhao, Lina Zhao, et al.
Frontiers in Cell and Developmental Biology|May 3, 2021
Heterozygous Recurrent Mutations Inducing Dysfunction of <i>ROR2</i> Gene in Patients With Short StatureBaoheng Gui, Chenxi Yu, Xiaoxin Li, et al.
Pageof 35