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Analytical Chemistry
|
June 22, 2023
In Situ Fluorescence Imaging Reveals Contribution of Cerebral Hydroxyl Radicals in Hyperhomocysteinemia-Induced Alzheimer-like Dementia
Xilei Xie, Jie Bian, Ye Song, et al.
Journal of Medical Genetics
|
October 27, 2023
Novel <i>TFG</i> mutation causes autosomal-dominant spastic paraplegia and defects in autophagy
Ling Xu, Yaru Wang, Wenqing Wang, et al.
International Journal of Pharmaceutics
|
January 26, 2020
Highly stabilized nanocrystals delivering Ginkgolide B in protecting against the Parkinson's disease
Yao Liu, Wei Liu, Sha Xiong, et al.
Molecular Cancer
|
March 30, 2019
Circular RNA circ-DONSON facilitates gastric cancer growth and invasion via NURF complex dependent activation of transcription factor SOX4
Lixian Ding, Yuying Zhao, Shuwei Dang, et al.
Mitochondrion
|
July 14, 2020
A novel m.11406 T > A mutation in mitochondrial ND4 gene causes MELAS syndrome
Yan Lin, Xuebi Xu, Dandan Zhao, et al.
BMC Neurology
|
July 31, 2025
An auxiliary diagnostic strategy for distinguishing Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy: combining platelet-to-lymphocyte ratio and cerebrospinal fluid interleukin-8 levels
Simin Song, Yunfei Bai, Haoran Mu, et al.
ACS Applied Materials & Interfaces
|
April 8, 2025
Rationally Designing Efficient Biomass Carbon Electrocatalysts for H<sub>2</sub>O<sub>2</sub> Synthesis and Near-Neutral Zn-Air Batteries with Preliminary Machine Learning Guidance
Jiawei He, Zijun Shen, Shengchun Hu, et al.
CNS Neuroscience & Therapeutics
|
May 1, 2021
Juvenile idiopathic inflammatory myopathies with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies in a Chinese cohort
Ying Hou, Kai Shao, Bing Zhao, et al.
Experimental Neurology
|
June 7, 2020
A novel fast-channel myasthenia caused by mutation in β subunit of AChR reveals subunit-specific contribution of the intracellular M1-M2 linker to channel gating
Xin-Ming Shen, Li Di, Shelley Shen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2009
Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations
Bing Wen, Tingjun Dai, Wei Li, et al.
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of 27
Search research articles
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Showing results (181-190 of 264) with videos related to
Sort By:
Page
of 27
Analytical Chemistry
|
June 22, 2023
In Situ Fluorescence Imaging Reveals Contribution of Cerebral Hydroxyl Radicals in Hyperhomocysteinemia-Induced Alzheimer-like Dementia
Xilei Xie, Jie Bian, Ye Song, et al.
Journal of Medical Genetics
|
October 27, 2023
Novel <i>TFG</i> mutation causes autosomal-dominant spastic paraplegia and defects in autophagy
Ling Xu, Yaru Wang, Wenqing Wang, et al.
International Journal of Pharmaceutics
|
January 26, 2020
Highly stabilized nanocrystals delivering Ginkgolide B in protecting against the Parkinson's disease
Yao Liu, Wei Liu, Sha Xiong, et al.
Molecular Cancer
|
March 30, 2019
Circular RNA circ-DONSON facilitates gastric cancer growth and invasion via NURF complex dependent activation of transcription factor SOX4
Lixian Ding, Yuying Zhao, Shuwei Dang, et al.
Mitochondrion
|
July 14, 2020
A novel m.11406 T > A mutation in mitochondrial ND4 gene causes MELAS syndrome
Yan Lin, Xuebi Xu, Dandan Zhao, et al.
BMC Neurology
|
July 31, 2025
An auxiliary diagnostic strategy for distinguishing Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy: combining platelet-to-lymphocyte ratio and cerebrospinal fluid interleukin-8 levels
Simin Song, Yunfei Bai, Haoran Mu, et al.
ACS Applied Materials & Interfaces
|
April 8, 2025
Rationally Designing Efficient Biomass Carbon Electrocatalysts for H<sub>2</sub>O<sub>2</sub> Synthesis and Near-Neutral Zn-Air Batteries with Preliminary Machine Learning Guidance
Jiawei He, Zijun Shen, Shengchun Hu, et al.
CNS Neuroscience & Therapeutics
|
May 1, 2021
Juvenile idiopathic inflammatory myopathies with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies in a Chinese cohort
Ying Hou, Kai Shao, Bing Zhao, et al.
Experimental Neurology
|
June 7, 2020
A novel fast-channel myasthenia caused by mutation in β subunit of AChR reveals subunit-specific contribution of the intracellular M1-M2 linker to channel gating
Xin-Ming Shen, Li Di, Shelley Shen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2009
Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations
Bing Wen, Tingjun Dai, Wei Li, et al.
Page
of 27