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Jiachen Lin

Showing results (31-40 of 44) with videos related to

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Elife|March 19, 2020
Piezo1/2 mediate mechanotransduction essential for bone formation through concerted activation of NFAT-YAP1-ß-cateninTaifeng Zhou, Bo Gao, Yi Fan, et al.
Angewandte Chemie (International Ed. in English)|August 18, 2022
A Long-Circulating Vector for Aptamers Based upon Polyphosphodiester-Backboned Molecular BrushesYuyan Wang, Dali Wang, Jiachen Lin, 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.
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.
Journal of Human Genetics|January 13, 2022
A genotype-first analysis in a cohort of Mullerian anomalyWeijie Tian, Na Chen, Yang Ye, et al.
Nature Communications|October 28, 2022
Oxygen mediated oxidative couplings of flavones in alkaline waterXin Yang, Sophie Hui Min Lim, Jiachen Lin, et al.
Human Molecular Genetics|October 12, 2018
TBX6 compound inheritance leads to congenital vertebral malformations in humans and miceNan Yang, Nan Wu, Ling Zhang, 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.
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 Medical Genetics|August 19, 2018
Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)Kun Wang, Sen Zhao, Bowen Liu, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Elife|March 19, 2020
Piezo1/2 mediate mechanotransduction essential for bone formation through concerted activation of NFAT-YAP1-ß-cateninTaifeng Zhou, Bo Gao, Yi Fan, et al.
Angewandte Chemie (International Ed. in English)|August 18, 2022
A Long-Circulating Vector for Aptamers Based upon Polyphosphodiester-Backboned Molecular BrushesYuyan Wang, Dali Wang, Jiachen Lin, 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.
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.
Journal of Human Genetics|January 13, 2022
A genotype-first analysis in a cohort of Mullerian anomalyWeijie Tian, Na Chen, Yang Ye, et al.
Nature Communications|October 28, 2022
Oxygen mediated oxidative couplings of flavones in alkaline waterXin Yang, Sophie Hui Min Lim, Jiachen Lin, et al.
Human Molecular Genetics|October 12, 2018
TBX6 compound inheritance leads to congenital vertebral malformations in humans and miceNan Yang, Nan Wu, Ling Zhang, 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.
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 Medical Genetics|August 19, 2018
Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)Kun Wang, Sen Zhao, Bowen Liu, et al.
Pageof 5