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SiSi Li

Showing results (391-400 of 404) with videos related to

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Scientific Reports|February 10, 2017
Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery DiseaseDan Yin, Duraid Hamied Naji, Yunlong Xia, et al.
Frontiers in Public Health|January 23, 2024
Prevalence of depressive symptoms and correlates among individuals who self-reported SARS-CoV-2 infection after optimizing the COVID-19 response in ChinaLiangjia Wei, Jiao Qin, Zhifeng Lin, et al.
Human Genetics|November 26, 2010
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID populationCong Li, Fan Wang, Yanzong Yang, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 28, 2017
Reduction of NANOG Mediates the Inhibitory Effect of Aspirin on Tumor Growth and Stemness in Colorectal CancerHefei Wang, Bing Liu, Jing Wang, et al.
American Journal of Human Genetics|October 1, 2013
The IL-33-ST2L pathway is associated with coronary artery disease in a Chinese Han populationXin Tu, Shaofang Nie, Yuhua Liao, et al.
Atherosclerosis|October 16, 2013
Meta-analysis identifies robust association between SNP rs17465637 in MIA3 on chromosome 1q41 and coronary artery diseaseXiuchun Li, Yufeng Huang, Dan Yin, et al.
Advanced Materials (Deerfield Beach, Fla.)|December 14, 2020
Strong Ferromagnetism Achieved via Breathing Lattices in Atomically Thin CobaltitesSisi Li, Qinghua Zhang, Shan Lin, et al.
Scientific Reports|February 21, 2018
Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial FibrillationPengxia Wang, Weixi Qin, Pengyun Wang, et al.
Signal Transduction and Targeted Therapy|April 1, 2022
Nuclear Aurora kinase A switches m<sup>6</sup>A reader YTHDC1 to enhance an oncogenic RNA splicing of tumor suppressor RBM4SiSi Li, YangFan Qi, JiaChuan Yu, et al.
Annals of Human Genetics|March 2, 2019
Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillationHongbo Xiong, Qin Yang, Xiaoping Zhang, et al.
Pageof 41

Showing results (391-400 of 404) with videos related to

Sort By:
Pageof 41
Scientific Reports|February 10, 2017
Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery DiseaseDan Yin, Duraid Hamied Naji, Yunlong Xia, et al.
Frontiers in Public Health|January 23, 2024
Prevalence of depressive symptoms and correlates among individuals who self-reported SARS-CoV-2 infection after optimizing the COVID-19 response in ChinaLiangjia Wei, Jiao Qin, Zhifeng Lin, et al.
Human Genetics|November 26, 2010
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID populationCong Li, Fan Wang, Yanzong Yang, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 28, 2017
Reduction of NANOG Mediates the Inhibitory Effect of Aspirin on Tumor Growth and Stemness in Colorectal CancerHefei Wang, Bing Liu, Jing Wang, et al.
American Journal of Human Genetics|October 1, 2013
The IL-33-ST2L pathway is associated with coronary artery disease in a Chinese Han populationXin Tu, Shaofang Nie, Yuhua Liao, et al.
Atherosclerosis|October 16, 2013
Meta-analysis identifies robust association between SNP rs17465637 in MIA3 on chromosome 1q41 and coronary artery diseaseXiuchun Li, Yufeng Huang, Dan Yin, et al.
Advanced Materials (Deerfield Beach, Fla.)|December 14, 2020
Strong Ferromagnetism Achieved via Breathing Lattices in Atomically Thin CobaltitesSisi Li, Qinghua Zhang, Shan Lin, et al.
Scientific Reports|February 21, 2018
Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial FibrillationPengxia Wang, Weixi Qin, Pengyun Wang, et al.
Signal Transduction and Targeted Therapy|April 1, 2022
Nuclear Aurora kinase A switches m<sup>6</sup>A reader YTHDC1 to enhance an oncogenic RNA splicing of tumor suppressor RBM4SiSi Li, YangFan Qi, JiaChuan Yu, et al.
Annals of Human Genetics|March 2, 2019
Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillationHongbo Xiong, Qin Yang, Xiaoping Zhang, et al.
Pageof 41