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

Jiyun Yang

Showing results (31-40 of 103) with videos related to

Pageof 11
Sort By:
Oncology Reports|February 13, 2015
Recombinant nematode anticoagulant protein c2 inhibits cell invasion by decreasing uPA expression in NSCLC cellsYu Tong, Jun Yue, Meng Mao, et al.
Eye (London, England)|June 15, 2018
Mutation screening of the USH2A gene in retinitis pigmentosa and USHER patients in a Han Chinese populationLulin Huang, Yao Mao, Jiyun Yang, et al.
Foods (Basel, Switzerland)|February 25, 2022
Chemical Analysis of Commercial White Wines and Its Relationship with Consumer AcceptabilitySeongju Han, Jiyun Yang, Kapseong Choi, et al.
International Dental Journal|August 5, 2025
A Novel DSPP Mutation in Dentinogenesis Imperfecta Shields Type II: Clinical, Genetic and Stem Cell PerspectivesQianhua Gao, Zhongren Deng, Ling Yang, et al.
Functional & Integrative Genomics|June 5, 2026
Resolving variants of uncertain significance in neurofibromatosis: An integrated approach combining deep learning and minigene assaysFulin Liu, Yuwei Chenzhang, Jianmei Huang, et al.
Pregnancy Hypertension|June 18, 2025
Rosiglitazone as a potential therapeutic drug in early intervention of preeclampsiaFulin Liu, Xiaoxiao Zhang, Thierry Fournier, et al.
Molecular Medicine Reports|September 18, 2018
Huwe1 is a novel mediator of protection of neural progenitor L2.3 cells against oxygen‑glucose deprivation injuryXiaoqin Jiang, Jiyun Yang, Hedong Li, et al.
Frontiers in Neurology|July 29, 2024
Two novel <i>SUCLA2</i> variants cause mitochondrial DNA depletion syndrome, type 5 in two siblingsXiaohuan Zhang, Guo Zhang, Li Cao, et al.
Gene|August 2, 2020
Identification and functional analysis of fourteen NR5A1 variants in patients with the 46 XY disorders of sex developmentXiaoxue Na, Yu Mao, Yunman Tang, et al.
Frontiers in Neurology|February 19, 2024
Clinical, neurophysiological evaluation and genetic features of axonal Charcot-Marie-Tooth disease in a Chinese familyLi Cao, Jie Yang, Xiaohuan Zhang, et al.
Pageof 11

Showing results (31-40 of 103) with videos related to

Sort By:
Pageof 11
Oncology Reports|February 13, 2015
Recombinant nematode anticoagulant protein c2 inhibits cell invasion by decreasing uPA expression in NSCLC cellsYu Tong, Jun Yue, Meng Mao, et al.
Eye (London, England)|June 15, 2018
Mutation screening of the USH2A gene in retinitis pigmentosa and USHER patients in a Han Chinese populationLulin Huang, Yao Mao, Jiyun Yang, et al.
Foods (Basel, Switzerland)|February 25, 2022
Chemical Analysis of Commercial White Wines and Its Relationship with Consumer AcceptabilitySeongju Han, Jiyun Yang, Kapseong Choi, et al.
International Dental Journal|August 5, 2025
A Novel DSPP Mutation in Dentinogenesis Imperfecta Shields Type II: Clinical, Genetic and Stem Cell PerspectivesQianhua Gao, Zhongren Deng, Ling Yang, et al.
Functional & Integrative Genomics|June 5, 2026
Resolving variants of uncertain significance in neurofibromatosis: An integrated approach combining deep learning and minigene assaysFulin Liu, Yuwei Chenzhang, Jianmei Huang, et al.
Pregnancy Hypertension|June 18, 2025
Rosiglitazone as a potential therapeutic drug in early intervention of preeclampsiaFulin Liu, Xiaoxiao Zhang, Thierry Fournier, et al.
Molecular Medicine Reports|September 18, 2018
Huwe1 is a novel mediator of protection of neural progenitor L2.3 cells against oxygen‑glucose deprivation injuryXiaoqin Jiang, Jiyun Yang, Hedong Li, et al.
Frontiers in Neurology|July 29, 2024
Two novel <i>SUCLA2</i> variants cause mitochondrial DNA depletion syndrome, type 5 in two siblingsXiaohuan Zhang, Guo Zhang, Li Cao, et al.
Gene|August 2, 2020
Identification and functional analysis of fourteen NR5A1 variants in patients with the 46 XY disorders of sex developmentXiaoxue Na, Yu Mao, Yunman Tang, et al.
Frontiers in Neurology|February 19, 2024
Clinical, neurophysiological evaluation and genetic features of axonal Charcot-Marie-Tooth disease in a Chinese familyLi Cao, Jie Yang, Xiaohuan Zhang, et al.
Pageof 11