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Physical Chemistry Chemical Physics : PCCP
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December 23, 2014
Cyano-substituted oligo(p-phenylene vinylene) single-crystal with balanced hole and electron injection and transport for ambipolar field-effect transistors
Jian 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 identified
Zhongyan 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 activation
Yuanyuan 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 infection
Can Yang, Liqun Liu, Ji Liu, et al.
Nature Communications
|
December 12, 2025
Regulating the morphology of two-dimensional perovskite single-crystals via high-throughput experimentations
Jingyan Qi, Wei Meng, Kang An, et al.
Molecular Neurodegeneration
|
July 11, 2015
Mutations in LRRK2 potentiate age-related impairment of autophagic flux
Shamol 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-regulation
Jianjun 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 Scatterplots
Liqun 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 Mutations
Lingjuan Liu, Lu Zhang, Peng Huang, et al.
Epilepsy Research
|
November 13, 2017
Early-onset epileptic encephalopathy with de novo SCN8A mutation
Yangyang Xiao, Jie Xiong, Ding'an Mao, et al.
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of 15
Search research articles
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Showing results (61-70 of 144) with videos related to
Sort By:
Page
of 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 transistors
Jian 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 identified
Zhongyan 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 activation
Yuanyuan 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 infection
Can Yang, Liqun Liu, Ji Liu, et al.
Nature Communications
|
December 12, 2025
Regulating the morphology of two-dimensional perovskite single-crystals via high-throughput experimentations
Jingyan Qi, Wei Meng, Kang An, et al.
Molecular Neurodegeneration
|
July 11, 2015
Mutations in LRRK2 potentiate age-related impairment of autophagic flux
Shamol 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-regulation
Jianjun 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 Scatterplots
Liqun 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 Mutations
Lingjuan Liu, Lu Zhang, Peng Huang, et al.
Epilepsy Research
|
November 13, 2017
Early-onset epileptic encephalopathy with de novo SCN8A mutation
Yangyang Xiao, Jie Xiong, Ding'an Mao, et al.
Page
of 15