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Iscience
|
October 25, 2023
LRRK2 G2019S promotes astrocytic inflammation induced by oligomeric α-synuclein through NF-κB pathway
Kai-Jie He, Jin-Bao Zhang, Jun-Yi Liu, et al.
Scientific Reports
|
May 28, 2020
Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson's disease
Kai Li, Yi-Lun Ge, Chen-Chen Gu, et al.
Translational Neurodegeneration
|
December 7, 2025
LRRK2 G2019S mutation contributes to mitochondrial transfer dysfunction in a Drp1-STX17-dependent manner
Mei Ding, Fen Wang, Lan-Lan Jiang, et al.
Translational Neurodegeneration
|
February 14, 2026
Correction: LRRK2 G2019S mutation contributes to mitochondrial transfer dysfunction in a Drp1-STX17-dependent manner
Mei Ding, Fen Wang, Lan-Lan Jiang, et al.
CNS Neuroscience & Therapeutics
|
October 7, 2024
Lack variation of low slow-wave activity over time in the frontal region in NREM sleep may be associated with dyskinesia in Parkinson's disease
Yi-Ming Wang, Jun-Yi Liu, Fan Gao, et al.
Parkinsonism & Related Disorders
|
June 7, 2023
A systematic analysis of genotype-phenotype associations with PLA2G6
Jian Xue, Dong-Xue Ding, Guang-Yu Xu, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 28, 2025
An Interpretable Machine Learning Model Based on Metabolomics for Predicting Plaque Burden in Cryptogenic Stroke
Zi-Miao Liu, Yin-Yu Zi, Xiao-Yu Cheng, et al.
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Search research articles
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Showing results (41-50 of 47) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 47 results.
Iscience
|
October 25, 2023
LRRK2 G2019S promotes astrocytic inflammation induced by oligomeric α-synuclein through NF-κB pathway
Kai-Jie He, Jin-Bao Zhang, Jun-Yi Liu, et al.
Scientific Reports
|
May 28, 2020
Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson's disease
Kai Li, Yi-Lun Ge, Chen-Chen Gu, et al.
Translational Neurodegeneration
|
December 7, 2025
LRRK2 G2019S mutation contributes to mitochondrial transfer dysfunction in a Drp1-STX17-dependent manner
Mei Ding, Fen Wang, Lan-Lan Jiang, et al.
Translational Neurodegeneration
|
February 14, 2026
Correction: LRRK2 G2019S mutation contributes to mitochondrial transfer dysfunction in a Drp1-STX17-dependent manner
Mei Ding, Fen Wang, Lan-Lan Jiang, et al.
CNS Neuroscience & Therapeutics
|
October 7, 2024
Lack variation of low slow-wave activity over time in the frontal region in NREM sleep may be associated with dyskinesia in Parkinson's disease
Yi-Ming Wang, Jun-Yi Liu, Fan Gao, et al.
Parkinsonism & Related Disorders
|
June 7, 2023
A systematic analysis of genotype-phenotype associations with PLA2G6
Jian Xue, Dong-Xue Ding, Guang-Yu Xu, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 28, 2025
An Interpretable Machine Learning Model Based on Metabolomics for Predicting Plaque Burden in Cryptogenic Stroke
Zi-Miao Liu, Yin-Yu Zi, Xiao-Yu Cheng, et al.
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of 5