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Zihui Yan

Showing results (31-40 of 50) with videos related to

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Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|March 29, 2020
Estrogen Receptors (ESRs) Mutations in Adolescent Idiopathic Scoliosis: A Cross-Sectional StudyLianlei Wang, Yuanqiang Zhang, 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.
Molecular Therapy. Nucleic Acids|June 7, 2021
Deciphering the mutational signature of congenital limb malformationsLiying Sun, Yingzhao Huang, Sen Zhao, et al.
Imeta|June 17, 2024
Changes in seminal plasma microecological dynamics and the mechanistic impact of core metabolite hexadecanamide in asthenozoospermia patientsBaoquan Han, Yongyong Wang, Wei Ge, 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.
Journal of Human Genetics|August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)Kun Wang, Sen Zhao, Qianqian Zhang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short statureXin Fan, Sen Zhao, Chenxi Yu, et al.
Journal of Human Genetics|December 13, 2019
Identification of novel FBN1 variations implicated in congenital scoliosisMao Lin, Sen Zhao, Gang Liu, et al.
Cell Research|August 29, 2025
Modeling post-gastrula development via bidirectional pluripotent stem cellsKuisheng Liu, Zihui Yan, Dandan Bai, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|March 29, 2020
Estrogen Receptors (ESRs) Mutations in Adolescent Idiopathic Scoliosis: A Cross-Sectional StudyLianlei Wang, Yuanqiang Zhang, 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.
Molecular Therapy. Nucleic Acids|June 7, 2021
Deciphering the mutational signature of congenital limb malformationsLiying Sun, Yingzhao Huang, Sen Zhao, et al.
Imeta|June 17, 2024
Changes in seminal plasma microecological dynamics and the mechanistic impact of core metabolite hexadecanamide in asthenozoospermia patientsBaoquan Han, Yongyong Wang, Wei Ge, 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.
Journal of Human Genetics|August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)Kun Wang, Sen Zhao, Qianqian Zhang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short statureXin Fan, Sen Zhao, Chenxi Yu, et al.
Journal of Human Genetics|December 13, 2019
Identification of novel FBN1 variations implicated in congenital scoliosisMao Lin, Sen Zhao, Gang Liu, et al.
Cell Research|August 29, 2025
Modeling post-gastrula development via bidirectional pluripotent stem cellsKuisheng Liu, Zihui Yan, Dandan Bai, et al.
Pageof 5