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Manu Sharma

Showing results (271-280 of 325) with videos related to

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Biological Psychiatry|March 24, 2020
Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk LociOlav B Smeland, Alexey Shadrin, Shahram Bahrami, et al.
Molecular Psychiatry|July 8, 2021
PIAS2-mediated blockade of IFN-β signaling: a basis for sporadic Parkinson disease dementiaJoana Magalhaes, Emilie Tresse, Patrick Ejlerskov, et al.
Biorxiv : the Preprint Server for Biology|September 25, 2023
Human iPSC 4R tauopathy model uncovers modifiers of tau propagationCeleste Parra Bravo, Alice Maria Giani, Jesus Madero Perez, et al.
Gut|May 20, 2016
Sex-specific effects of TLR9 promoter variants on spontaneous clearance of HCV infectionJanett Fischer, Alexander N R Weber, Stephan Böhm, et al.
JAMA Neurology|April 10, 2018
Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia SpectrumCeleste M Karch, Natalie Wen, Chun C Fan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 29, 2009
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative studyEvangelos Evangelou, Demetrius M Maraganore, Grazia Annesi, et al.
Neurobiology of Aging|November 8, 2016
Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian populationAnamika Giri, Kin Y Mok, Iris Jansen, et al.
Brain : a Journal of Neurology|October 21, 2017
Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's diseaseJulia C Fitzgerald, Alexander Zimprich, Daniel A Carvajal Berrio, et al.
Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Plos One|August 23, 2013
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locusDaniah Trabzuni, Mina Ryten, Warren Emmett, et al.
Pageof 33

Showing results (271-280 of 325) with videos related to

Sort By:
Pageof 33
Biological Psychiatry|March 24, 2020
Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk LociOlav B Smeland, Alexey Shadrin, Shahram Bahrami, et al.
Molecular Psychiatry|July 8, 2021
PIAS2-mediated blockade of IFN-β signaling: a basis for sporadic Parkinson disease dementiaJoana Magalhaes, Emilie Tresse, Patrick Ejlerskov, et al.
Biorxiv : the Preprint Server for Biology|September 25, 2023
Human iPSC 4R tauopathy model uncovers modifiers of tau propagationCeleste Parra Bravo, Alice Maria Giani, Jesus Madero Perez, et al.
Gut|May 20, 2016
Sex-specific effects of TLR9 promoter variants on spontaneous clearance of HCV infectionJanett Fischer, Alexander N R Weber, Stephan Böhm, et al.
JAMA Neurology|April 10, 2018
Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia SpectrumCeleste M Karch, Natalie Wen, Chun C Fan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 29, 2009
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative studyEvangelos Evangelou, Demetrius M Maraganore, Grazia Annesi, et al.
Neurobiology of Aging|November 8, 2016
Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian populationAnamika Giri, Kin Y Mok, Iris Jansen, et al.
Brain : a Journal of Neurology|October 21, 2017
Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's diseaseJulia C Fitzgerald, Alexander Zimprich, Daniel A Carvajal Berrio, et al.
Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Plos One|August 23, 2013
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locusDaniah Trabzuni, Mina Ryten, Warren Emmett, et al.
Pageof 33