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Biorxiv : the Preprint Server for Biology|January 31, 2024
miRNA family miR-29 inhibits PINK1-PRKN dependent mitophagy via ATG9ABriana N Markham, Chloe Ramnarine, Songeun Kim, et al.
Nature Genetics|December 28, 2023
Multi-ancestry genome-wide association meta-analysis of Parkinson's diseaseJonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, et al.
Medrxiv : the Preprint Server for Health Sciences|November 21, 2023
Investigation of the genetic aetiology of Lewy body diseases with and without dementiaLesley Wu, Raquel Real, Alejandro Martinez, et al.
Neurology|September 16, 2016
A genome-wide association study in multiple system atrophyAnna Sailer, Sonja W Scholz, Michael A Nalls, et al.
Human Molecular Genetics|September 24, 2013
Genetic comorbidities in Parkinson's diseaseMike A Nalls, Mohamad Saad, Alastair J Noyce, et al.
Aging and Disease|December 16, 2025
Phosphorylated Ubiquitin as a Clinical Biomarker for Mitochondrial Damage in Neurodegenerative DiseasesFabienne C Fiesel, Jens O Watzlawik, Michael G Heckman, et al.
Annals of Neurology|April 17, 2008
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's diseaseOwen A Ross, Yih-Ru Wu, Mei-Ching Lee, et al.
JAMA Neurology|March 19, 2019
Association of MAPT Subhaplotypes With Risk of Progressive Supranuclear Palsy and Severity of Tau PathologyMichael G Heckman, Rebecca R Brennan, Catherine Labbé, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 2012
An evaluation of the impact of MAPT, SNCA and APOE on the burden of Alzheimer's and Lewy body pathologyChristian Wider, Owen A Ross, Kenya Nishioka, et al.
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