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Qianhao Zhao

Showing results (1-10 of 36) with videos related to

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Frontiers in Surgery|January 26, 2023
Case Report: A report on the countermeasures after the rupture of the scalp venous indwelling needle catheter in 12 casesHaiyan Zhong, Mengze Wang, Yang Gui, et al.
Cerebrovascular Diseases (Basel, Switzerland)|October 30, 2025
Moyamoya Disease: Epidemiology, Clinical Characteristics, Diagnosis, Physiopathology, and TreatmentZeyuan Liu, Yonggang Wang, Chunli Li, et al.
Journal of Forensic Sciences|November 20, 2018
HCN4 Gene Variations in Sudden Unexplained Nocturnal Death Syndrome in the Southern Han Chinese PopulationQiuping Wu, Qianhao Zhao, Kun Yin, et al.
APL Photonics|September 20, 2024
Deep-ultraviolet Fourier ptychography (DUV-FP) for label-free biochemical imaging via feature-domain optimizationQianhao Zhao, Ruihai Wang, Shuhe Zhang, et al.
Optics Letters|November 15, 2021
Geometric optimization method for a polarization state generator of a Mueller matrix microscopeQianhao Zhao, Tongyu Huang, Zheng Hu, et al.
Journal of Medical Genetics|July 3, 2023
Mutation in mitral valve prolapse susceptible gene <i>DCHS1</i> causes familial mitral annular disjunctionNan Zhou, Qianhao Zhao, Rui Li, et al.
Medicine|January 3, 2023
Exosomes: A new option for osteoporosis treatmentGuijiang Huang, Qianhao Zhao, Wenhu Li, et al.
Forensic Science International|July 30, 2013
Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han populationChao Liu, Qianhao Zhao, Terry Su, et al.
Molecular Genetics & Genomic Medicine|October 3, 2023
RAF1 mutation leading to hypertrophic cardiomyopathy in a Chinese family with a history of sudden cardiac death: A diagnostic insight into Noonan syndromeJingjing Zheng, Longyun Peng, Ruofei Cheng, et al.
Scientific Reports|July 1, 2025
Identification of pyroptosis related genes and subtypes in atherosclerosis using multiomic and single cell analysisKaisheng Jiang, Yang He, Bingjie Hu, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Frontiers in Surgery|January 26, 2023
Case Report: A report on the countermeasures after the rupture of the scalp venous indwelling needle catheter in 12 casesHaiyan Zhong, Mengze Wang, Yang Gui, et al.
Cerebrovascular Diseases (Basel, Switzerland)|October 30, 2025
Moyamoya Disease: Epidemiology, Clinical Characteristics, Diagnosis, Physiopathology, and TreatmentZeyuan Liu, Yonggang Wang, Chunli Li, et al.
Journal of Forensic Sciences|November 20, 2018
HCN4 Gene Variations in Sudden Unexplained Nocturnal Death Syndrome in the Southern Han Chinese PopulationQiuping Wu, Qianhao Zhao, Kun Yin, et al.
APL Photonics|September 20, 2024
Deep-ultraviolet Fourier ptychography (DUV-FP) for label-free biochemical imaging via feature-domain optimizationQianhao Zhao, Ruihai Wang, Shuhe Zhang, et al.
Optics Letters|November 15, 2021
Geometric optimization method for a polarization state generator of a Mueller matrix microscopeQianhao Zhao, Tongyu Huang, Zheng Hu, et al.
Journal of Medical Genetics|July 3, 2023
Mutation in mitral valve prolapse susceptible gene <i>DCHS1</i> causes familial mitral annular disjunctionNan Zhou, Qianhao Zhao, Rui Li, et al.
Medicine|January 3, 2023
Exosomes: A new option for osteoporosis treatmentGuijiang Huang, Qianhao Zhao, Wenhu Li, et al.
Forensic Science International|July 30, 2013
Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han populationChao Liu, Qianhao Zhao, Terry Su, et al.
Molecular Genetics & Genomic Medicine|October 3, 2023
RAF1 mutation leading to hypertrophic cardiomyopathy in a Chinese family with a history of sudden cardiac death: A diagnostic insight into Noonan syndromeJingjing Zheng, Longyun Peng, Ruofei Cheng, et al.
Scientific Reports|July 1, 2025
Identification of pyroptosis related genes and subtypes in atherosclerosis using multiomic and single cell analysisKaisheng Jiang, Yang He, Bingjie Hu, et al.
Pageof 4