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Liang Fan

Showing results (201-210 of 356) with videos related to

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Disease Markers|February 13, 2023
Silencing <i>MYOT</i> Expression May Inhibit Autophagy in Human Skeletal Muscle CellsZhao-Jing Lin, Jun-Mei Xu, He-Yu Ji, et al.
Clinical Genetics|August 23, 2021
A novel POF1B variant in a Chinese patient is associated with premature ovarian failureZhuang-Zhuang Yuan, Chen-Yu Wang, Jie-Yuan Jin, et al.
Microbial Drug Resistance (Larchmont, N.Y.)|November 15, 2013
Prevalence and molecular characterization of fluoroquinolone resistance in Escherichia coli isolates from dairy cattle with endometritis in ChinaHong-Xia Zhao, Jun-Li Zhao, Jian-Zhong Shen, et al.
Annals of Medicine|October 25, 2025
Anterior quadratus lumborum block at the lateral supra-arcuate ligament versus thoracic paravertebral block for postoperative analgesia after laparoscopic nephrectomy: a randomized non-inferiority trialChun-Ying Zheng, Shu-Qin He, Peng Ye, et al.
Frontiers in Aging Neuroscience|July 16, 2021
Case Report: A Homozygous Mutation (p.Y62X) of <i>Phospholipase D3</i> May Lead to a New Leukoencephalopathy SyndromeYi-Hui Liu, Hai-Feng Zhang, Jie-Yuan Jin, et al.
Huan Jing Ke Xue= Huanjing Kexue|January 22, 2011
[Effects of different long-term fertilizations on community properties and functions of methanotrophs in dark brown soil]Qian-Bao Yang, Fen-Liang Fan, Wan-Xiong Wang, et al.
Medcomm|March 17, 2023
Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK-IDH2 pathwayHao Huang, Shuai Guo, Ya-Qin Chen, et al.
Medicine|November 15, 2025
A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case reportGao-Hui Cao, Ai-Qian Zhang, Yi Dong, et al.
Digestive Diseases (Basel, Switzerland)|October 14, 2025
Gut Microbiota and Chemotherapy-Induced Gastrointestinal Toxicity: Mechanisms and Intervention StrategiesWei Peng, Xinxin Fan, Hongrui Shi, et al.
Frontiers in Genetics|May 14, 2023
Case report: A novel mutation of RecQ-like helicase 5 in a Chinese family with early myocardial infarction, coronary artery disease, and stroke hemiplegiaYi Tang, Qian Wang, Wei-Kai Zhang, et al.
Pageof 36

Showing results (201-210 of 356) with videos related to

Sort By:
Pageof 36
Disease Markers|February 13, 2023
Silencing <i>MYOT</i> Expression May Inhibit Autophagy in Human Skeletal Muscle CellsZhao-Jing Lin, Jun-Mei Xu, He-Yu Ji, et al.
Clinical Genetics|August 23, 2021
A novel POF1B variant in a Chinese patient is associated with premature ovarian failureZhuang-Zhuang Yuan, Chen-Yu Wang, Jie-Yuan Jin, et al.
Microbial Drug Resistance (Larchmont, N.Y.)|November 15, 2013
Prevalence and molecular characterization of fluoroquinolone resistance in Escherichia coli isolates from dairy cattle with endometritis in ChinaHong-Xia Zhao, Jun-Li Zhao, Jian-Zhong Shen, et al.
Annals of Medicine|October 25, 2025
Anterior quadratus lumborum block at the lateral supra-arcuate ligament versus thoracic paravertebral block for postoperative analgesia after laparoscopic nephrectomy: a randomized non-inferiority trialChun-Ying Zheng, Shu-Qin He, Peng Ye, et al.
Frontiers in Aging Neuroscience|July 16, 2021
Case Report: A Homozygous Mutation (p.Y62X) of <i>Phospholipase D3</i> May Lead to a New Leukoencephalopathy SyndromeYi-Hui Liu, Hai-Feng Zhang, Jie-Yuan Jin, et al.
Huan Jing Ke Xue= Huanjing Kexue|January 22, 2011
[Effects of different long-term fertilizations on community properties and functions of methanotrophs in dark brown soil]Qian-Bao Yang, Fen-Liang Fan, Wan-Xiong Wang, et al.
Medcomm|March 17, 2023
Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK-IDH2 pathwayHao Huang, Shuai Guo, Ya-Qin Chen, et al.
Medicine|November 15, 2025
A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case reportGao-Hui Cao, Ai-Qian Zhang, Yi Dong, et al.
Digestive Diseases (Basel, Switzerland)|October 14, 2025
Gut Microbiota and Chemotherapy-Induced Gastrointestinal Toxicity: Mechanisms and Intervention StrategiesWei Peng, Xinxin Fan, Hongrui Shi, et al.
Frontiers in Genetics|May 14, 2023
Case report: A novel mutation of RecQ-like helicase 5 in a Chinese family with early myocardial infarction, coronary artery disease, and stroke hemiplegiaYi Tang, Qian Wang, Wei-Kai Zhang, et al.
Pageof 36