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Liqun Liu

Showing results (61-70 of 144) with videos related to

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Physical Chemistry Chemical Physics : PCCP|December 23, 2014
Cyano-substituted oligo(p-phenylene vinylene) single-crystal with balanced hole and electron injection and transport for ambipolar field-effect transistorsJian Deng, Jia Tang, Yuanxiang Xu, et al.
Molecular Genetics & Genomic Medicine|July 29, 2021
Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identifiedZhongyan Xiao, Yuan Yang, Hui Huang, et al.
Fish & Shellfish Immunology|July 22, 2019
Black carp PRMT6 inhibits TBK1-IRF3/7 signaling during the antiviral innate immune activationYuanyuan Jiang, Liqun Liu, Shisi Yang, et al.
Developmental and Comparative Immunology|July 2, 2019
Black carp IRF5 interacts with TBK1 to trigger cell death following viral infectionCan Yang, Liqun Liu, Ji Liu, et al.
Nature Communications|December 12, 2025
Regulating the morphology of two-dimensional perovskite single-crystals via high-throughput experimentationsJingyan Qi, Wei Meng, Kang An, et al.
Molecular Neurodegeneration|July 11, 2015
Mutations in LRRK2 potentiate age-related impairment of autophagic fluxShamol Saha, Peter E A Ash, Vivek Gowda, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2002
Role of the short isoform of myosin light chain kinase in the contraction of cultured smooth muscle cells as examined by its down-regulationJianjun Bao, Kazuhiko Oishi, Tomohisa Yamada, et al.
IEEE Transactions on Visualization and Computer Graphics|December 10, 2025
OM4AnI: A Novel Overlap Measure for Anomaly Identification in Multi-Class ScatterplotsLiqun Liu, Leonid Bogachev, Mahdi Rezaei, et al.
Frontiers in Pediatrics|July 14, 2022
Case Report: Aicardi-Goutières Syndrome Type 6 and Dyschromatosis Symmetrica Hereditaria With Congenital Heart Disease and Mitral Valve Calcification - Phenotypic Variants Caused by Adenosine Deaminase Acting on the RNA 1 Gene Homozygous MutationsLingjuan Liu, Lu Zhang, Peng Huang, et al.
Epilepsy Research|November 13, 2017
Early-onset epileptic encephalopathy with de novo SCN8A mutationYangyang Xiao, Jie Xiong, Ding'an Mao, et al.
Pageof 15

Showing results (61-70 of 144) with videos related to

Sort By:
Pageof 15
Physical Chemistry Chemical Physics : PCCP|December 23, 2014
Cyano-substituted oligo(p-phenylene vinylene) single-crystal with balanced hole and electron injection and transport for ambipolar field-effect transistorsJian Deng, Jia Tang, Yuanxiang Xu, et al.
Molecular Genetics & Genomic Medicine|July 29, 2021
Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identifiedZhongyan Xiao, Yuan Yang, Hui Huang, et al.
Fish & Shellfish Immunology|July 22, 2019
Black carp PRMT6 inhibits TBK1-IRF3/7 signaling during the antiviral innate immune activationYuanyuan Jiang, Liqun Liu, Shisi Yang, et al.
Developmental and Comparative Immunology|July 2, 2019
Black carp IRF5 interacts with TBK1 to trigger cell death following viral infectionCan Yang, Liqun Liu, Ji Liu, et al.
Nature Communications|December 12, 2025
Regulating the morphology of two-dimensional perovskite single-crystals via high-throughput experimentationsJingyan Qi, Wei Meng, Kang An, et al.
Molecular Neurodegeneration|July 11, 2015
Mutations in LRRK2 potentiate age-related impairment of autophagic fluxShamol Saha, Peter E A Ash, Vivek Gowda, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2002
Role of the short isoform of myosin light chain kinase in the contraction of cultured smooth muscle cells as examined by its down-regulationJianjun Bao, Kazuhiko Oishi, Tomohisa Yamada, et al.
IEEE Transactions on Visualization and Computer Graphics|December 10, 2025
OM4AnI: A Novel Overlap Measure for Anomaly Identification in Multi-Class ScatterplotsLiqun Liu, Leonid Bogachev, Mahdi Rezaei, et al.
Frontiers in Pediatrics|July 14, 2022
Case Report: Aicardi-Goutières Syndrome Type 6 and Dyschromatosis Symmetrica Hereditaria With Congenital Heart Disease and Mitral Valve Calcification - Phenotypic Variants Caused by Adenosine Deaminase Acting on the RNA 1 Gene Homozygous MutationsLingjuan Liu, Lu Zhang, Peng Huang, et al.
Epilepsy Research|November 13, 2017
Early-onset epileptic encephalopathy with de novo SCN8A mutationYangyang Xiao, Jie Xiong, Ding'an Mao, et al.
Pageof 15