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Medrxiv : the Preprint Server for Health Sciences|October 1, 2025
Validation of a Mitochondrial Polygenic Score for Parkinson's DiseaseJoshua Chin Ern Ooi, Yi Wen Tay, Ai Huey Tan, et al.
Human Mutation|February 27, 2010
Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter studyEng-King Tan, Rong Peng, Yik-Ying Teo, et al.
International Journal of Molecular Sciences|June 13, 2025
Low Efficiency of Homology-Independent Targeted Integration for CRISPR/Cas9 Correction in the Vicinity of the <i>SLC26A4</i> c.919-2A>G VariantChang-Han Ho, Cheng-Yu Tsai, Chi-Chieh Chang, et al.
Elife|May 22, 2024
Revealing intact neuronal circuitry in centimeter-sized formalin-fixed paraffin-embedded brainYa-Hui Lin, Li-Wen Wang, Yen-Hui Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 17, 2021
Mild Chronic Colitis Triggers Parkinsonism in LRRK2 Mutant Mice Through Activating TNF-α PathwayChin-Hsien Lin, Han-Yi Lin, En-Pong Ho, et al.
Journal of Alzheimer'S Disease Reports|December 6, 2021
Assessment of High Risk for Alzheimer's Disease Using Plasma Biomarkers in Subjects with Normal Cognition in Taiwan: A Preliminary StudyChaur-Jong Hu, Ming-Jang Chiu, Ming-Chyi Pai, et al.
Stem Cell Research & Therapy|September 23, 2021
In vitro genome editing rescues parkinsonism phenotypes in induced pluripotent stem cells-derived dopaminergic neurons carrying LRRK2 p.G2019S mutationKuo-Hsuan Chang, Cheng-Yen Huang, Chih-Hsin Ou-Yang, et al.
Cell Reports|September 22, 2021
UQCRC1 engages cytochrome c for neuronal apoptotic cell deathYu-Chien Hung, Kuan-Lin Huang, Po-Lin Chen, et al.
Journal of Movement Disorders|June 13, 2023
Nine Hereditary Movement Disorders First Described in Asia: Their History and EvolutionPriya Jagota, Yoshikazu Ugawa, Zakiyah Aldaajani, et al.
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