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Liang Fan

Showing results (171-180 of 356) with videos related to

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Foods (Basel, Switzerland)|January 10, 2026
Authenticity Identification and Quantitative Analysis of <i>Dendrobium officinale</i> Based on Near-Infrared Spectroscopy Combined with ChemometricsZhi-Liang Fan, Qian Li, Zhi-Tong Zhang, et al.
Molecular Biology Reports|September 4, 2024
A novel variant (p.A524P) in Spastin is responsible for a Chinese family with hereditary spastic paraplegiaYu-Han Jin, Yang-Ziyu Xiang, Mei-Fang Zhao, et al.
ACS Macro Letters|October 29, 2024
Mechanism of Density Evolution of Polystyrene Adsorbed Layers on the SubstrateLu Bai, Zhenwei Jiang, Liang Fan, et al.
Journal of Cellular and Molecular Medicine|October 28, 2017
Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden deathHao Huang, Ya-Qin Chen, Liang-Liang Fan, et al.
Journal of Experimental & Clinical Cancer Research : CR|July 19, 2018
PBX3/MEK/ERK1/2/LIN28/let-7b positive feedback loop enhances mesenchymal phenotype to promote glioblastoma migration and invasionXiupeng Xu, Zhongyuan Bao, Yinlong Liu, et al.
Clinical Chemistry and Laboratory Medicine|September 13, 2018
A de novo mutation of SMYD1 (p.F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patientLiang-Liang Fan, Dong-Bo Ding, Hao Huang, et al.
The Journal of Surgical Research|July 27, 2020
Shenmai Injection Upregulates Heme Oxygenase-1 to Confer Protection Against Severe Acute PancreatitisFei-Hu Zhang, Yang Liu, Xiao-Bin Dong, et al.
Annals of Clinical and Laboratory Science|December 29, 2019
Whole Exome Sequencing Identified a 13 Base Pair <i>MYH7</i> Deletion-mutation in a Patient with Restrictive Cardiomyopathy and Left Ventricle HypertrophyLiang-Liang Fan, Shuai Guo, Jie-Yuan Jin, et al.
Gene|February 6, 2014
A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosisRong Xiang, Liang-Liang Fan, Hao Huang, et al.
Huan Jing Ke Xue= Huanjing Kexue|January 18, 2013
[Influences of long-term application of organic and inorganic fertilizers on the composition and abundance of nirS-type denitrifiers in black soil]Chang Yin, Fen-Liang Fan, Zhao-Jun Li, et al.
Pageof 36

Showing results (171-180 of 356) with videos related to

Sort By:
Pageof 36
Foods (Basel, Switzerland)|January 10, 2026
Authenticity Identification and Quantitative Analysis of <i>Dendrobium officinale</i> Based on Near-Infrared Spectroscopy Combined with ChemometricsZhi-Liang Fan, Qian Li, Zhi-Tong Zhang, et al.
Molecular Biology Reports|September 4, 2024
A novel variant (p.A524P) in Spastin is responsible for a Chinese family with hereditary spastic paraplegiaYu-Han Jin, Yang-Ziyu Xiang, Mei-Fang Zhao, et al.
ACS Macro Letters|October 29, 2024
Mechanism of Density Evolution of Polystyrene Adsorbed Layers on the SubstrateLu Bai, Zhenwei Jiang, Liang Fan, et al.
Journal of Cellular and Molecular Medicine|October 28, 2017
Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden deathHao Huang, Ya-Qin Chen, Liang-Liang Fan, et al.
Journal of Experimental & Clinical Cancer Research : CR|July 19, 2018
PBX3/MEK/ERK1/2/LIN28/let-7b positive feedback loop enhances mesenchymal phenotype to promote glioblastoma migration and invasionXiupeng Xu, Zhongyuan Bao, Yinlong Liu, et al.
Clinical Chemistry and Laboratory Medicine|September 13, 2018
A de novo mutation of SMYD1 (p.F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patientLiang-Liang Fan, Dong-Bo Ding, Hao Huang, et al.
The Journal of Surgical Research|July 27, 2020
Shenmai Injection Upregulates Heme Oxygenase-1 to Confer Protection Against Severe Acute PancreatitisFei-Hu Zhang, Yang Liu, Xiao-Bin Dong, et al.
Annals of Clinical and Laboratory Science|December 29, 2019
Whole Exome Sequencing Identified a 13 Base Pair <i>MYH7</i> Deletion-mutation in a Patient with Restrictive Cardiomyopathy and Left Ventricle HypertrophyLiang-Liang Fan, Shuai Guo, Jie-Yuan Jin, et al.
Gene|February 6, 2014
A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosisRong Xiang, Liang-Liang Fan, Hao Huang, et al.
Huan Jing Ke Xue= Huanjing Kexue|January 18, 2013
[Influences of long-term application of organic and inorganic fertilizers on the composition and abundance of nirS-type denitrifiers in black soil]Chang Yin, Fen-Liang Fan, Zhao-Jun Li, et al.
Pageof 36