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Sen Zhao

Showing results (291-300 of 345) with videos related to

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Current Gene Therapy|September 25, 2019
A Recurrent Rare SOX9 Variant (M469V) is Associated with Congenital Vertebral MalformationsNan Wu, Lianlei Wang, Jianhua Hu, et al.
Orphanet Journal of Rare Diseases|May 23, 2022
Phenotype expansion of variants affecting p38 MAPK signaling in hypospadias patientsDefu Lin, Huakang Du, Sen Zhao, et al.
American Journal of Human Genetics|January 22, 2022
PhenoApt leverages clinical expertise to prioritize candidate genes via machine learningZefu Chen, Yu Zheng, Yongxin Yang, et al.
Human Molecular Genetics|July 18, 2023
COL11A2 as a candidate gene for vertebral malformations and congenital scoliosisDenise Rebello, Elizabeth Wohler, Vida Erfani, et al.
European Journal of Pharmacology|April 6, 2019
Schisandrin B prevents ulcerative colitis and colitis-associated-cancer by activating focal adhesion kinase and influence on gut microbiota in an in vivo and in vitro modelJiani Li, Yuan Lu, Duowei Wang, 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 of Medicine|May 3, 2025
Developing a polygenic risk score for pelvic organ prolapse: a combined risk assessment approach in Chinese womenXi Cheng, Lei Li, Xijuan Lin, et al.
BMC Musculoskeletal Disorders|May 26, 2021
Factors and predictive model associated with perioperative complications after long fusion in the treatment of adult non-degenerative scoliosisNan Wu, Jiashen Shao, Zhen Zhang, 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.
Orphanet Journal of Rare Diseases|October 15, 2020
Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variantsWen Tian, Yingzhao Huang, Liying Sun, et al.
Pageof 35

Showing results (291-300 of 345) with videos related to

Sort By:
Pageof 35
Current Gene Therapy|September 25, 2019
A Recurrent Rare SOX9 Variant (M469V) is Associated with Congenital Vertebral MalformationsNan Wu, Lianlei Wang, Jianhua Hu, et al.
Orphanet Journal of Rare Diseases|May 23, 2022
Phenotype expansion of variants affecting p38 MAPK signaling in hypospadias patientsDefu Lin, Huakang Du, Sen Zhao, et al.
American Journal of Human Genetics|January 22, 2022
PhenoApt leverages clinical expertise to prioritize candidate genes via machine learningZefu Chen, Yu Zheng, Yongxin Yang, et al.
Human Molecular Genetics|July 18, 2023
COL11A2 as a candidate gene for vertebral malformations and congenital scoliosisDenise Rebello, Elizabeth Wohler, Vida Erfani, et al.
European Journal of Pharmacology|April 6, 2019
Schisandrin B prevents ulcerative colitis and colitis-associated-cancer by activating focal adhesion kinase and influence on gut microbiota in an in vivo and in vitro modelJiani Li, Yuan Lu, Duowei Wang, 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 of Medicine|May 3, 2025
Developing a polygenic risk score for pelvic organ prolapse: a combined risk assessment approach in Chinese womenXi Cheng, Lei Li, Xijuan Lin, et al.
BMC Musculoskeletal Disorders|May 26, 2021
Factors and predictive model associated with perioperative complications after long fusion in the treatment of adult non-degenerative scoliosisNan Wu, Jiashen Shao, Zhen Zhang, 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.
Orphanet Journal of Rare Diseases|October 15, 2020
Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variantsWen Tian, Yingzhao Huang, Liying Sun, et al.
Pageof 35