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

Yuchen Niu

Showing results (31-40 of 59) with videos related to

Pageof 6
Sort By:
Frontiers in Bioengineering and Biotechnology|January 11, 2020
Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic ScoliosisGang Liu, Lianlei Wang, Xinyu Wang, et al.
BMC Musculoskeletal Disorders|April 13, 2020
The mutational burden and oligogenic inheritance in Klippel-Feil syndromeZiquan Li, Sen Zhao, Siyi Cai, et al.
Gene|December 21, 2018
Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han populationGang Liu, Sen Liu, Xiaoxin Li, et al.
Human Genetics|September 13, 2022
Dissection of mendelian predisposition and complex genetic architecture of craniovertebral junction malformationZhenlei Liu, Huakang Du, Hengqiang Zhao, et al.
Orphanet Journal of Rare Diseases|September 16, 2020
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosisZefu Chen, Zihui Yan, Chenxi Yu, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosisLianlei Wang, Zhaoyang Liu, Sen Zhao, et al.
Frontiers in Genetics|April 1, 2022
Identification of Novel <i>FBN2</i> Variants in a Cohort of Congenital Contractural ArachnodactylyLiying Sun, Yingzhao Huang, Sen Zhao, et al.
Journal of Human Genetics|January 13, 2022
A genotype-first analysis in a cohort of Mullerian anomalyWeijie Tian, Na Chen, Yang Ye, et al.
Journal of Neurointerventional Surgery|August 12, 2019
Exome sequencing reveals a novel variant in <i>NFX1</i> causing intracranial aneurysm in a Chinese familyXinghuan Ding, Sen Zhao, Qianqian Zhang, et al.
Nano Letters|May 18, 2026
Chiral Molecular Intercalation Enables Light-Controlled 2D Multiferroic HeterostructuresZhongxuan Wang, Yong Hu, Zhenyao Fang, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Frontiers in Bioengineering and Biotechnology|January 11, 2020
Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic ScoliosisGang Liu, Lianlei Wang, Xinyu Wang, et al.
BMC Musculoskeletal Disorders|April 13, 2020
The mutational burden and oligogenic inheritance in Klippel-Feil syndromeZiquan Li, Sen Zhao, Siyi Cai, et al.
Gene|December 21, 2018
Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han populationGang Liu, Sen Liu, Xiaoxin Li, et al.
Human Genetics|September 13, 2022
Dissection of mendelian predisposition and complex genetic architecture of craniovertebral junction malformationZhenlei Liu, Huakang Du, Hengqiang Zhao, et al.
Orphanet Journal of Rare Diseases|September 16, 2020
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosisZefu Chen, Zihui Yan, Chenxi Yu, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosisLianlei Wang, Zhaoyang Liu, Sen Zhao, et al.
Frontiers in Genetics|April 1, 2022
Identification of Novel <i>FBN2</i> Variants in a Cohort of Congenital Contractural ArachnodactylyLiying Sun, Yingzhao Huang, Sen Zhao, et al.
Journal of Human Genetics|January 13, 2022
A genotype-first analysis in a cohort of Mullerian anomalyWeijie Tian, Na Chen, Yang Ye, et al.
Journal of Neurointerventional Surgery|August 12, 2019
Exome sequencing reveals a novel variant in <i>NFX1</i> causing intracranial aneurysm in a Chinese familyXinghuan Ding, Sen Zhao, Qianqian Zhang, et al.
Nano Letters|May 18, 2026
Chiral Molecular Intercalation Enables Light-Controlled 2D Multiferroic HeterostructuresZhongxuan Wang, Yong Hu, Zhenyao Fang, et al.
Pageof 6