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Qianjun Zhang

Showing results (31-40 of 74) with videos related to

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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 13, 2017
[Analysis of FOXL2 gene mutations in 5 families affected with blepharophimosis, ptosis and epicanthus inversus syndrome]Xiaowen Yang, Wen Li, Juan Du, et al.
Scientific Reports|March 26, 2014
Strongly enhanced current densities in Sr0.6K0.4Fe2As2 + Sn superconducting tapesHe Lin, Chao Yao, Xianping Zhang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 2, 2021
Novel variants of the PCCB gene in Chinese patients with propionic acidemiaXiaoxuan Yang, Dongyan Li, Chaofeng Tu, et al.
BMC Pediatrics|April 14, 2023
Diagnostic consistency between admission and discharge of pediatric cases in a tertiary teaching hospital in ChinaDangui Zhang, Baoxin Yan, Siqi He, et al.
Beilstein Journal of Organic Chemistry|December 27, 2021
Synthesis of a novel aminobenzene-containing hemicucurbituril and its fluorescence spectral properties with ionsQingkai Zeng, Qiumeng Long, Jihong Lu, et al.
Journal of the American Chemical Society|December 23, 2025
Spin Polarization by Magnetic Proximity Enhances Electron Transport in CatalystsBingcheng Li, Rubo Fang, Ranran Hou, et al.
Blood|February 29, 2012
Blood T-cell receptor diversity decreases during the course of HIV infection, but the potential for a diverse repertoire persistsPaul D Baum, Jennifer J Young, Diane Schmidt, et al.
Developmental Biology|March 5, 2023
C9orf131 and C10orf120 are not essential for male fertility in humans or miceJiaxin He, Lilan Su, Weili Wang, et al.
Journal of Human Genetics|January 9, 2019
A rare deep intronic mutation of PKHD1 gene, c.8798-459 C > A, causes autosomal recessive polycystic kidney disease by pseudoexon activationJing Chen, Na Ma, Xiaomeng Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 11, 2021
[Analysis and prenatal diagnosis of FMR1 gene mutations among patients with unexplained mental retardation]Shikun Luo, Wenbin He, Yi Liao, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 13, 2017
[Analysis of FOXL2 gene mutations in 5 families affected with blepharophimosis, ptosis and epicanthus inversus syndrome]Xiaowen Yang, Wen Li, Juan Du, et al.
Scientific Reports|March 26, 2014
Strongly enhanced current densities in Sr0.6K0.4Fe2As2 + Sn superconducting tapesHe Lin, Chao Yao, Xianping Zhang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 2, 2021
Novel variants of the PCCB gene in Chinese patients with propionic acidemiaXiaoxuan Yang, Dongyan Li, Chaofeng Tu, et al.
BMC Pediatrics|April 14, 2023
Diagnostic consistency between admission and discharge of pediatric cases in a tertiary teaching hospital in ChinaDangui Zhang, Baoxin Yan, Siqi He, et al.
Beilstein Journal of Organic Chemistry|December 27, 2021
Synthesis of a novel aminobenzene-containing hemicucurbituril and its fluorescence spectral properties with ionsQingkai Zeng, Qiumeng Long, Jihong Lu, et al.
Journal of the American Chemical Society|December 23, 2025
Spin Polarization by Magnetic Proximity Enhances Electron Transport in CatalystsBingcheng Li, Rubo Fang, Ranran Hou, et al.
Blood|February 29, 2012
Blood T-cell receptor diversity decreases during the course of HIV infection, but the potential for a diverse repertoire persistsPaul D Baum, Jennifer J Young, Diane Schmidt, et al.
Developmental Biology|March 5, 2023
C9orf131 and C10orf120 are not essential for male fertility in humans or miceJiaxin He, Lilan Su, Weili Wang, et al.
Journal of Human Genetics|January 9, 2019
A rare deep intronic mutation of PKHD1 gene, c.8798-459 C > A, causes autosomal recessive polycystic kidney disease by pseudoexon activationJing Chen, Na Ma, Xiaomeng Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 11, 2021
[Analysis and prenatal diagnosis of FMR1 gene mutations among patients with unexplained mental retardation]Shikun Luo, Wenbin He, Yi Liao, et al.
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