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Andrew Singleton

Showing results (71-80 of 286) with videos related to

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Mechanisms of Ageing and Development|January 28, 2014
Splicing factor 3B1 hypomethylation is associated with altered SF3B1 transcript expression in older humansAlice C Holly, Luke C Pilling, Dena Hernandez, et al.
Frontiers in Neurology|April 12, 2021
Clinical Variability of <i>SYNJ1</i>-Associated Early-Onset ParkinsonismSuzanne Lesage, Graziella Mangone, Christelle Tesson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2004
A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletionOkan Dogu, Janel Johnson, Dena Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 9, 2005
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohortJose Miguel Bras, Rita Joao Guerreiro, Maria Helena Ribeiro, et al.
Lancet (London, England)|October 12, 2025
Parkinson's disease: emerging opportunities through global collaborationAndrew Singleton, Cornelis Blauwendraat, Huw R Morris, et al.
BMC Neurology|January 24, 2008
Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2Jose Bras, Rita Guerreiro, Maria Ribeiro, et al.
Mechanisms of Ageing and Development|July 21, 2012
Advancing age is associated with gene expression changes resembling mTOR inhibition: evidence from two human populationsLorna W Harries, Alexander D Fellows, Luke C Pilling, et al.
Alcoholism, Clinical and Experimental Research|March 22, 2007
Linkage disequilibrium and association analysis of alpha-synuclein and alcohol and drug dependence in two American Indian populationsJordi Clarimon, Rebecca R Gray, Lindsey N Williams, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|December 28, 2018
Anticholinergic Drug Induced Cognitive and Physical Impairment: Results from the InCHIANTI StudyLana Sargent, Mike Nalls, Elaine J Amella, et al.
Human Mutation|November 13, 2007
Genomewide SNP assay reveals mutations underlying Parkinson diseaseJavier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, et al.
Pageof 29

Showing results (71-80 of 286) with videos related to

Sort By:
Pageof 29
Mechanisms of Ageing and Development|January 28, 2014
Splicing factor 3B1 hypomethylation is associated with altered SF3B1 transcript expression in older humansAlice C Holly, Luke C Pilling, Dena Hernandez, et al.
Frontiers in Neurology|April 12, 2021
Clinical Variability of <i>SYNJ1</i>-Associated Early-Onset ParkinsonismSuzanne Lesage, Graziella Mangone, Christelle Tesson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2004
A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletionOkan Dogu, Janel Johnson, Dena Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 9, 2005
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohortJose Miguel Bras, Rita Joao Guerreiro, Maria Helena Ribeiro, et al.
Lancet (London, England)|October 12, 2025
Parkinson's disease: emerging opportunities through global collaborationAndrew Singleton, Cornelis Blauwendraat, Huw R Morris, et al.
BMC Neurology|January 24, 2008
Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2Jose Bras, Rita Guerreiro, Maria Ribeiro, et al.
Mechanisms of Ageing and Development|July 21, 2012
Advancing age is associated with gene expression changes resembling mTOR inhibition: evidence from two human populationsLorna W Harries, Alexander D Fellows, Luke C Pilling, et al.
Alcoholism, Clinical and Experimental Research|March 22, 2007
Linkage disequilibrium and association analysis of alpha-synuclein and alcohol and drug dependence in two American Indian populationsJordi Clarimon, Rebecca R Gray, Lindsey N Williams, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|December 28, 2018
Anticholinergic Drug Induced Cognitive and Physical Impairment: Results from the InCHIANTI StudyLana Sargent, Mike Nalls, Elaine J Amella, et al.
Human Mutation|November 13, 2007
Genomewide SNP assay reveals mutations underlying Parkinson diseaseJavier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, et al.
Pageof 29