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Linqi Chen

Showing results (1-10 of 68) with videos related to

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The Journal of Chemical Physics|July 21, 2025
In operando optical characterization of organic mixed ionic-electronic conductors for unraveling charge transport and doping dynamics-A perspectiveLinqi Chen, Yingying Ma, Peijun Guo
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 20, 2023
[Genetic analysis of a child with Meier-Gorlin syndrome due to a variant of ORC6 gene]Lili Wang, Fengyun Wang, Xiaoyan Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 14, 2018
[Advance in clinical research on Antley-Bixler syndrome]Min Xie, Hongying Wang, Linqi Chen, et al.
Frontiers in Pediatrics|July 11, 2022
ARID2, a Rare Cause of Coffin-Siris Syndrome: A Clinical Description of Two CasesXiaoyan Wang, Haiying Wu, Hui Sun, et al.
Diabetes Research and Clinical Practice|October 15, 2016
The efficacy and safety of DPP4 inhibitors in patients with type 1 diabetes: A systematic review and meta-analysisHeming Guo, Chen Fang, Yun Huang, et al.
Diabetes Research and Clinical Practice|June 9, 2015
A novel nonsense mutation of the HNF1α in maturity-onset diabetes of the young type 3 in Asian populationChen Fang, Jian Huang, Yun Huang, et al.
International Journal of Biological Sciences|August 23, 2021
URI1 suppresses irradiation-induced reactive oxygen species (ROS) by activating autophagy in hepatocellular carcinoma cellsYue Xu, Yuan Ji, Xiang Li, et al.
Journal of Pediatric and Adolescent Gynecology|February 6, 2017
Serum Anti-Müllerian Hormone and Inhibin B as Potential Markers for Progressive Central Precocious Puberty in GirlsTing Chen, Haiying Wu, Rongrong Xie, et al.
European Journal of Medical Genetics|April 14, 2018
An atypical phenotype of a patient with infantile spinal muscular atrophy with respiratory distress type 1 (SMARD 1)Shuiyan Wu, Ting Chen, Ying Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 12, 2020
[Genetic analysis of three children with disorders of sex development caused by structural rearrangements of Y chromosome]Hongying Wang, Linqi Chen, Yuanyuan Chen, et al.
Pageof 7

Showing results (1-10 of 68) with videos related to

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Pageof 7
The Journal of Chemical Physics|July 21, 2025
In operando optical characterization of organic mixed ionic-electronic conductors for unraveling charge transport and doping dynamics-A perspectiveLinqi Chen, Yingying Ma, Peijun Guo
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 20, 2023
[Genetic analysis of a child with Meier-Gorlin syndrome due to a variant of ORC6 gene]Lili Wang, Fengyun Wang, Xiaoyan Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 14, 2018
[Advance in clinical research on Antley-Bixler syndrome]Min Xie, Hongying Wang, Linqi Chen, et al.
Frontiers in Pediatrics|July 11, 2022
ARID2, a Rare Cause of Coffin-Siris Syndrome: A Clinical Description of Two CasesXiaoyan Wang, Haiying Wu, Hui Sun, et al.
Diabetes Research and Clinical Practice|October 15, 2016
The efficacy and safety of DPP4 inhibitors in patients with type 1 diabetes: A systematic review and meta-analysisHeming Guo, Chen Fang, Yun Huang, et al.
Diabetes Research and Clinical Practice|June 9, 2015
A novel nonsense mutation of the HNF1α in maturity-onset diabetes of the young type 3 in Asian populationChen Fang, Jian Huang, Yun Huang, et al.
International Journal of Biological Sciences|August 23, 2021
URI1 suppresses irradiation-induced reactive oxygen species (ROS) by activating autophagy in hepatocellular carcinoma cellsYue Xu, Yuan Ji, Xiang Li, et al.
Journal of Pediatric and Adolescent Gynecology|February 6, 2017
Serum Anti-Müllerian Hormone and Inhibin B as Potential Markers for Progressive Central Precocious Puberty in GirlsTing Chen, Haiying Wu, Rongrong Xie, et al.
European Journal of Medical Genetics|April 14, 2018
An atypical phenotype of a patient with infantile spinal muscular atrophy with respiratory distress type 1 (SMARD 1)Shuiyan Wu, Ting Chen, Ying Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 12, 2020
[Genetic analysis of three children with disorders of sex development caused by structural rearrangements of Y chromosome]Hongying Wang, Linqi Chen, Yuanyuan Chen, et al.
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