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Andrew B Singleton

Showing results (111-120 of 397) with videos related to

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Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|May 31, 2007
Association of integrin alpha2 gene variants with ischemic strokeMar Matarin, W Mark Brown, John A Hardy, et al.
Aging Cell|January 15, 2013
Towards a gene expression biomarker set for human biological ageAlice C Holly, David Melzer, Luke C Pilling, et al.
Nature Neuroscience|May 25, 2021
Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosisRuilin Tian, Anthony Abarientos, Jason Hong, et al.
Parkinsonism & Related Disorders|May 16, 2019
Genome-wide estimates of heritability and genetic correlations in essential tremorMonica Diez-Fairen, Sara Bandres-Ciga, Gabrielle Houle, et al.
Aging Cell|December 14, 2011
CCAAT-enhancer-binding protein-beta expression in vivo is associated with muscle strengthLorna W Harries, Luke C Pilling, L Dena G Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2010
Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia seriesJoyce van de Leemput, Fabienne Wavrant-De Vrièze, Ian Rafferty, et al.
Neuroscience Letters|May 25, 2005
Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's diseaseJavier Simon-Sanchez, Melissa Hanson, Amanda Singleton, et al.
Nature|October 4, 2014
Another explanation for apparent epistasisAndrew R Wood, Marcus A Tuke, Mike A Nalls, et al.
Journal of Neurology|November 13, 2010
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9pJustin P Pearson, Nigel M Williams, Elisa Majounie, et al.
Journal of Medical Genetics|December 1, 2019
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's diseaseHampton Leonard, Cornelis Blauwendraat, Lynne Krohn, et al.
Pageof 40

Showing results (111-120 of 397) with videos related to

Sort By:
Pageof 40
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|May 31, 2007
Association of integrin alpha2 gene variants with ischemic strokeMar Matarin, W Mark Brown, John A Hardy, et al.
Aging Cell|January 15, 2013
Towards a gene expression biomarker set for human biological ageAlice C Holly, David Melzer, Luke C Pilling, et al.
Nature Neuroscience|May 25, 2021
Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosisRuilin Tian, Anthony Abarientos, Jason Hong, et al.
Parkinsonism & Related Disorders|May 16, 2019
Genome-wide estimates of heritability and genetic correlations in essential tremorMonica Diez-Fairen, Sara Bandres-Ciga, Gabrielle Houle, et al.
Aging Cell|December 14, 2011
CCAAT-enhancer-binding protein-beta expression in vivo is associated with muscle strengthLorna W Harries, Luke C Pilling, L Dena G Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2010
Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia seriesJoyce van de Leemput, Fabienne Wavrant-De Vrièze, Ian Rafferty, et al.
Neuroscience Letters|May 25, 2005
Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's diseaseJavier Simon-Sanchez, Melissa Hanson, Amanda Singleton, et al.
Nature|October 4, 2014
Another explanation for apparent epistasisAndrew R Wood, Marcus A Tuke, Mike A Nalls, et al.
Journal of Neurology|November 13, 2010
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9pJustin P Pearson, Nigel M Williams, Elisa Majounie, et al.
Journal of Medical Genetics|December 1, 2019
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's diseaseHampton Leonard, Cornelis Blauwendraat, Lynne Krohn, et al.
Pageof 40