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Yuchen Niu

Showing results (21-30 of 59) with videos related to

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Molecular Therapy. Nucleic Acids|March 15, 2021
Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosisGang Liu, Hengqiang Zhao, Zihui Yan, et al.
Gene|December 27, 2021
Aberrant interaction between mutated ADAMTSL2 and LTBP4 is associated with adolescent idiopathic scoliosisBowen Liu, Sen Zhao, Lian Liu, et al.
Frontiers in Cell and Developmental Biology|April 5, 2021
Variants Affecting the C-Terminal of CSF1R Cause Congenital Vertebral Malformation Through a Gain-of-Function MechanismBowen Liu, Sen Zhao, Zihui Yan, et al.
Journal of Cellular and Molecular Medicine|January 25, 2018
Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han populationGang Liu, Sen Liu, Mao Lin, et al.
Genes|October 23, 2021
Disruptive <i>NADSYN1</i> Variants Implicated in Congenital Vertebral MalformationsJiachen Lin, Lina Zhao, Sen Zhao, et al.
Oncology Reports|March 1, 2019
Genome‑wide DNA methylation profile of thymomas and potential epigenetic regulation of thymoma subtypesYalan Bi, Yunxiao Meng, Yuchen Niu, et al.
BMC Medical Genetics|May 29, 2020
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasiaJiashen Shao, Sen Zhao, Zihui Yan, et al.
Neurology|March 1, 2022
Exome-wide Analysis of De Novo and Rare Genetic Variants in Patients With Brain Arteriovenous MalformationKun Wang, Sen Zhao, Zhixin Xie, et al.
Molecular Genetics & Genomic Medicine|August 21, 2020
Mutational burden and potential oligogenic model of TBX6-mediated genes in congenital scoliosisYang Yang, Sen Zhao, Yuanqiang Zhang, et al.
Genes|November 27, 2021
The Mutational Landscape of <i>PTK7</i> in Congenital Scoliosis and Adolescent Idiopathic ScoliosisZhe Su, Yang Yang, Shengru Wang, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
Molecular Therapy. Nucleic Acids|March 15, 2021
Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosisGang Liu, Hengqiang Zhao, Zihui Yan, et al.
Gene|December 27, 2021
Aberrant interaction between mutated ADAMTSL2 and LTBP4 is associated with adolescent idiopathic scoliosisBowen Liu, Sen Zhao, Lian Liu, et al.
Frontiers in Cell and Developmental Biology|April 5, 2021
Variants Affecting the C-Terminal of CSF1R Cause Congenital Vertebral Malformation Through a Gain-of-Function MechanismBowen Liu, Sen Zhao, Zihui Yan, et al.
Journal of Cellular and Molecular Medicine|January 25, 2018
Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han populationGang Liu, Sen Liu, Mao Lin, et al.
Genes|October 23, 2021
Disruptive <i>NADSYN1</i> Variants Implicated in Congenital Vertebral MalformationsJiachen Lin, Lina Zhao, Sen Zhao, et al.
Oncology Reports|March 1, 2019
Genome‑wide DNA methylation profile of thymomas and potential epigenetic regulation of thymoma subtypesYalan Bi, Yunxiao Meng, Yuchen Niu, et al.
BMC Medical Genetics|May 29, 2020
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasiaJiashen Shao, Sen Zhao, Zihui Yan, et al.
Neurology|March 1, 2022
Exome-wide Analysis of De Novo and Rare Genetic Variants in Patients With Brain Arteriovenous MalformationKun Wang, Sen Zhao, Zhixin Xie, et al.
Molecular Genetics & Genomic Medicine|August 21, 2020
Mutational burden and potential oligogenic model of TBX6-mediated genes in congenital scoliosisYang Yang, Sen Zhao, Yuanqiang Zhang, et al.
Genes|November 27, 2021
The Mutational Landscape of <i>PTK7</i> in Congenital Scoliosis and Adolescent Idiopathic ScoliosisZhe Su, Yang Yang, Shengru Wang, et al.
Pageof 6