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Plos One
|
May 15, 2020
Myotonia congenita and periodic hypokalemia paralysis in a consanguineous marriage pedigree: Coexistence of a novel CLCN1 mutation and an SCN4A mutation
Chenyu Zhao, DongFang Tang, Hui Huang, et al.
Scientific Reports
|
August 31, 2017
Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis
Hui Huang, Yongjun Wang, Yong Cao, et al.
BMC Neurology
|
October 15, 2025
Clinical and radiological characteristics of adult-onset X-linked adrenoleukodystrophy: a Chinese cohort study and review of the literature
Han Xiao, Hui Huang, Ying Chen, et al.
Plos One
|
July 12, 2013
Novel ATPase Cu(2+) transporting beta polypeptide mutations in Chinese families with Wilson's disease
Shaojuan Gu, Huarong Yang, Yong Qi, et al.
Frontiers in Pharmacology
|
December 8, 2017
Electrophysiological and Pharmacological Analyses of Na<sub>v</sub>1.9 Voltage-Gated Sodium Channel by Establishing a Heterologous Expression System
Xi Zhou, Zhen Xiao, Yan Xu, et al.
European Journal of Mass Spectrometry (Chichester, England)
|
August 8, 2009
Analysis of global DNA methylation levels in human blood using high-performance liquid chromatography/tandem electrospray ionization mass spectrometry
Huimin Ma, Wenbing Zhang, Junjie Hu, et al.
Pain
|
July 30, 2021
Protein arginine methyltransferase 7 modulates neuronal excitability by interacting with NaV1.9
Tingbin Ma, Lulu Li, Rui Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 4, 2019
O-GlcNAcylation of core components of the translation initiation machinery regulates protein synthesis
Xuexia Li, Qiang Zhu, Xiaoliu Shi, et al.
Nature Metabolism
|
January 2, 2025
A feeding-induced myokine modulates glucose homeostasis
Xiaoliu Shi, Xiao Hu, Xinlei Fang, et al.
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of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
Plos One
|
May 15, 2020
Myotonia congenita and periodic hypokalemia paralysis in a consanguineous marriage pedigree: Coexistence of a novel CLCN1 mutation and an SCN4A mutation
Chenyu Zhao, DongFang Tang, Hui Huang, et al.
Scientific Reports
|
August 31, 2017
Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis
Hui Huang, Yongjun Wang, Yong Cao, et al.
BMC Neurology
|
October 15, 2025
Clinical and radiological characteristics of adult-onset X-linked adrenoleukodystrophy: a Chinese cohort study and review of the literature
Han Xiao, Hui Huang, Ying Chen, et al.
Plos One
|
July 12, 2013
Novel ATPase Cu(2+) transporting beta polypeptide mutations in Chinese families with Wilson's disease
Shaojuan Gu, Huarong Yang, Yong Qi, et al.
Frontiers in Pharmacology
|
December 8, 2017
Electrophysiological and Pharmacological Analyses of Na<sub>v</sub>1.9 Voltage-Gated Sodium Channel by Establishing a Heterologous Expression System
Xi Zhou, Zhen Xiao, Yan Xu, et al.
European Journal of Mass Spectrometry (Chichester, England)
|
August 8, 2009
Analysis of global DNA methylation levels in human blood using high-performance liquid chromatography/tandem electrospray ionization mass spectrometry
Huimin Ma, Wenbing Zhang, Junjie Hu, et al.
Pain
|
July 30, 2021
Protein arginine methyltransferase 7 modulates neuronal excitability by interacting with NaV1.9
Tingbin Ma, Lulu Li, Rui Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 4, 2019
O-GlcNAcylation of core components of the translation initiation machinery regulates protein synthesis
Xuexia Li, Qiang Zhu, Xiaoliu Shi, et al.
Nature Metabolism
|
January 2, 2025
A feeding-induced myokine modulates glucose homeostasis
Xiaoliu Shi, Xiao Hu, Xinlei Fang, et al.
Page
of 5