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Cell Reports|June 21, 2016
Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and HumansYubin Wang, Joshua Hersheson, Dulce Lopez, et al.Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.Neuro-Degenerative Diseases|July 12, 2007
Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutationJanel Johnson, Coro Paisán-Ruíz, Grisel Lopez, et al.Neurobiology of Disease|June 18, 2016
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodiesJoshua T Geiger, Jinhui Ding, Barbara Crain, et al.American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, 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.Human Molecular Genetics|September 24, 2013
Genetic comorbidities in Parkinson's diseaseMike A Nalls, Mohamad Saad, Alastair J Noyce, et al.Proceedings of the National Academy of Sciences of the United States of America|July 27, 2016
Menopause accelerates biological agingMorgan E Levine, Ake T Lu, Brian H Chen, et al.Nature Neuroscience|August 11, 2022
A CRISPRi/a platform in human iPSC-derived microglia uncovers regulators of disease statesNina M Dräger, Sydney M Sattler, Cindy Tzu-Ling Huang, et al.Pageof 48