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Pengfei Lin

Showing results (21-30 of 235) with videos related to

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Frontiers in Nutrition|June 30, 2025
Association analysis between nutritional factors within the genome and the risk of osteoarthritisLiangming Kang, Guihua Wu, Pengfei Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 1, 2022
[Analysis of clinical features and genetic variants in three Chinese pedigrees affected with Limb girdle muscular dystrophy type 2I]Guangyu Wang, Ling Xu, Dandan Zhao, et al.
Scientific Reports|August 1, 2020
Lagrangian eddy kinetic energy of ocean mesoscale eddies and its application to the Northwestern PacificMengrong Ding, Pengfei Lin, Hailong Liu, et al.
Journal of Human Genetics|June 28, 2026
Activation of cryptic donor splice site due to an exonic MYPN variant in congenital myopathyGuangyu Wang, Guiguan Yang, Yaru Wang, et al.
European Journal of Human Genetics : EJHG|December 16, 2022
Somatic and germinal mosaicism in a Han Chinese family with laminopathiesGuangyu Wang, Ying Hou, Xiaoqing Lv, et al.
Journal of Human Genetics|July 5, 2023
Aberrant mRNA processing caused by splicing mutations in TTN-related neuromuscular disordersGuangyu Wang, Wenjing Wu, Xiaoqing Lv, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 9, 2023
Exon Skipping Caused by Noncanonical Splicing Mutation in PRDX3-Related Spinocerebellar AtaxiaGuangyu Wang, Bin Wang, Qingtao Qin, et al.
Frontiers in Microbiology|November 20, 2018
Preparation, Antidermatophyte Activity, and Mechanism of Methylphloroglucinol DerivativesLianbao Ye, Pengfei Lin, Wenjun Du, et al.
Frontiers in Cell and Developmental Biology|April 4, 2022
<i>Tcap</i> Deficiency in Zebrafish Leads to ROS Production and Mitophagy, and Idebenone Improves its PhenotypesXiaoqing Lv, Rui Zhang, Ling Xu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 30, 2012
Novel PANK2 gene mutations in two Chinese siblings with atypical pantothenate kinase-associated neurodegenerationJingli Shan, Bing Wen, Jun Zhu, et al.
Pageof 24

Showing results (21-30 of 235) with videos related to

Sort By:
Pageof 24
Frontiers in Nutrition|June 30, 2025
Association analysis between nutritional factors within the genome and the risk of osteoarthritisLiangming Kang, Guihua Wu, Pengfei Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 1, 2022
[Analysis of clinical features and genetic variants in three Chinese pedigrees affected with Limb girdle muscular dystrophy type 2I]Guangyu Wang, Ling Xu, Dandan Zhao, et al.
Scientific Reports|August 1, 2020
Lagrangian eddy kinetic energy of ocean mesoscale eddies and its application to the Northwestern PacificMengrong Ding, Pengfei Lin, Hailong Liu, et al.
Journal of Human Genetics|June 28, 2026
Activation of cryptic donor splice site due to an exonic MYPN variant in congenital myopathyGuangyu Wang, Guiguan Yang, Yaru Wang, et al.
European Journal of Human Genetics : EJHG|December 16, 2022
Somatic and germinal mosaicism in a Han Chinese family with laminopathiesGuangyu Wang, Ying Hou, Xiaoqing Lv, et al.
Journal of Human Genetics|July 5, 2023
Aberrant mRNA processing caused by splicing mutations in TTN-related neuromuscular disordersGuangyu Wang, Wenjing Wu, Xiaoqing Lv, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 9, 2023
Exon Skipping Caused by Noncanonical Splicing Mutation in PRDX3-Related Spinocerebellar AtaxiaGuangyu Wang, Bin Wang, Qingtao Qin, et al.
Frontiers in Microbiology|November 20, 2018
Preparation, Antidermatophyte Activity, and Mechanism of Methylphloroglucinol DerivativesLianbao Ye, Pengfei Lin, Wenjun Du, et al.
Frontiers in Cell and Developmental Biology|April 4, 2022
<i>Tcap</i> Deficiency in Zebrafish Leads to ROS Production and Mitophagy, and Idebenone Improves its PhenotypesXiaoqing Lv, Rui Zhang, Ling Xu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 30, 2012
Novel PANK2 gene mutations in two Chinese siblings with atypical pantothenate kinase-associated neurodegenerationJingli Shan, Bing Wen, Jun Zhu, et al.
Pageof 24