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Acta Epileptologica
|
September 12, 2025
Correction: SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy
Wenwei Liu, Kai Gao, Xilong Du, et al.
Journal of Virology
|
August 7, 2015
Structural and Functional Diversity of Nairovirus-Encoded Nucleoproteins
Wenming Wang, Xiang Liu, Xu Wang, et al.
Gene
|
March 25, 2019
Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation
Jinliang Li, Kai Gao, Huifang Yan, et al.
Science China. Life Sciences
|
May 2, 2023
Superresolution live-cell imaging reveals that the localization of TMEM106B to filopodia in oligodendrocytes is compromised by the hypomyelination-related D252N mutation
Shijia Xing, Xiaolu Zheng, Huifang Yan, et al.
Scientific Reports
|
November 21, 2025
Spatial lipidomics reveals altered lipid profiles in TMEM63A mutant rats with hypomyelination
Junyu Wang, Liang Wang, Yu Zhang, et al.
Inflammation
|
July 24, 2019
Pseudoginsenoside-F11 Attenuates Lipopolysaccharide-Induced Acute Lung Injury by Suppressing Neutrophil Infiltration and Accelerating Neutrophil Clearance
Pengwei Wang, Ying Hou, Wen Zhang, et al.
Scientific Reports
|
June 4, 2016
CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens
Binbin Wang, Taoyun Ji, Xueya Zhou, et al.
Advanced Materials (Deerfield Beach, Fla.)
|
April 22, 2025
Superhigh Magnetostriction in Non-Equilibrium Grown Fe-Ga Single-Crystals by Rapid-Directional-Solidification
Yichen Xu, Yuye Wu, Yunquan Li, et al.
ACS Applied Bio Materials
|
January 15, 2022
Recent Advances in Synthesis, Optical Properties, and Biomedical Applications of Carbon Dots
Sadat Anwar, Haizhen Ding, Mingsheng Xu, et al.
Orphanet Journal of Rare Diseases
|
March 29, 2022
Genotype-phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus-merzbacher disease
Ruoyu Duan, Haoran Ji, Huifang Yan, et al.
Page
of 18
Search research articles
Search
Showing results (121-130 of 175) with videos related to
Sort By:
Page
of 18
Acta Epileptologica
|
September 12, 2025
Correction: SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy
Wenwei Liu, Kai Gao, Xilong Du, et al.
Journal of Virology
|
August 7, 2015
Structural and Functional Diversity of Nairovirus-Encoded Nucleoproteins
Wenming Wang, Xiang Liu, Xu Wang, et al.
Gene
|
March 25, 2019
Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation
Jinliang Li, Kai Gao, Huifang Yan, et al.
Science China. Life Sciences
|
May 2, 2023
Superresolution live-cell imaging reveals that the localization of TMEM106B to filopodia in oligodendrocytes is compromised by the hypomyelination-related D252N mutation
Shijia Xing, Xiaolu Zheng, Huifang Yan, et al.
Scientific Reports
|
November 21, 2025
Spatial lipidomics reveals altered lipid profiles in TMEM63A mutant rats with hypomyelination
Junyu Wang, Liang Wang, Yu Zhang, et al.
Inflammation
|
July 24, 2019
Pseudoginsenoside-F11 Attenuates Lipopolysaccharide-Induced Acute Lung Injury by Suppressing Neutrophil Infiltration and Accelerating Neutrophil Clearance
Pengwei Wang, Ying Hou, Wen Zhang, et al.
Scientific Reports
|
June 4, 2016
CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens
Binbin Wang, Taoyun Ji, Xueya Zhou, et al.
Advanced Materials (Deerfield Beach, Fla.)
|
April 22, 2025
Superhigh Magnetostriction in Non-Equilibrium Grown Fe-Ga Single-Crystals by Rapid-Directional-Solidification
Yichen Xu, Yuye Wu, Yunquan Li, et al.
ACS Applied Bio Materials
|
January 15, 2022
Recent Advances in Synthesis, Optical Properties, and Biomedical Applications of Carbon Dots
Sadat Anwar, Haizhen Ding, Mingsheng Xu, et al.
Orphanet Journal of Rare Diseases
|
March 29, 2022
Genotype-phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus-merzbacher disease
Ruoyu Duan, Haoran Ji, Huifang Yan, et al.
Page
of 18