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John Collinge

Showing results (261-270 of 295) with videos related to

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Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.
Human Molecular Genetics|March 13, 2010
Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutationsHazel Urwin, Astrid Authier, Jorgen E Nielsen, et al.
Neurobiology of Disease|November 23, 2023
Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6Emma Jones, Elizabeth Hill, Jacqueline Linehan, et al.
Brain : a Journal of Neurology|February 1, 2008
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesJonathan Beck, Jonathan D Rohrer, Tracy Campbell, et al.
Acta Neuropathologica|July 3, 2013
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementiaPietro Fratta, Mark Poulter, Tammaryn Lashley, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
Acta Neuropathologica|December 20, 2019
PrP is a central player in toxicity mediated by soluble aggregates of neurodegeneration-causing proteinsGrant T Corbett, Zemin Wang, Wei Hong, et al.
Human Molecular Genetics|January 18, 2017
Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutationEmma L Clayton, Renzo Mancuso, Troels Tolstrup Nielsen, et al.
JAMA Neurology|February 24, 2016
Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob DiseaseSimon Mead, Matthew Burnell, Jessica Lowe, et al.
Nature Genetics|July 26, 2005
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementiaGaia Skibinski, Nicholas J Parkinson, Jeremy M Brown, et al.
Pageof 30

Showing results (261-270 of 295) with videos related to

Sort By:
Pageof 30
Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.
Human Molecular Genetics|March 13, 2010
Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutationsHazel Urwin, Astrid Authier, Jorgen E Nielsen, et al.
Neurobiology of Disease|November 23, 2023
Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6Emma Jones, Elizabeth Hill, Jacqueline Linehan, et al.
Brain : a Journal of Neurology|February 1, 2008
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesJonathan Beck, Jonathan D Rohrer, Tracy Campbell, et al.
Acta Neuropathologica|July 3, 2013
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementiaPietro Fratta, Mark Poulter, Tammaryn Lashley, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
Acta Neuropathologica|December 20, 2019
PrP is a central player in toxicity mediated by soluble aggregates of neurodegeneration-causing proteinsGrant T Corbett, Zemin Wang, Wei Hong, et al.
Human Molecular Genetics|January 18, 2017
Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutationEmma L Clayton, Renzo Mancuso, Troels Tolstrup Nielsen, et al.
JAMA Neurology|February 24, 2016
Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob DiseaseSimon Mead, Matthew Burnell, Jessica Lowe, et al.
Nature Genetics|July 26, 2005
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementiaGaia Skibinski, Nicholas J Parkinson, Jeremy M Brown, et al.
Pageof 30