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John Collinge

Showing results (211-220 of 295) with videos related to

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Plos Biology|June 10, 2020
Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSSEmmanuel A Asante, Jacqueline M Linehan, Andrew Tomlinson, et al.
Nature|September 11, 2015
Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathyZane Jaunmuktane, Simon Mead, Matthew Ellis, et al.
Open Biology|June 2, 2016
Ex vivo mammalian prions are formed of paired double helical prion protein fibrilsCassandra Terry, Adam Wenborn, Nathalie Gros, et al.
Neuroimage. Clinical|December 13, 2016
Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry studyEnrico De Vita, Gerard R Ridgway, Mark J White, et al.
Nature|September 17, 2015
Erratum: Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathyZane Jaunmuktane, Simon Mead, Matthew Ellis, et al.
The New England Journal of Medicine|November 20, 2009
A novel protective prion protein variant that colocalizes with kuru exposureSimon Mead, Jerome Whitfield, Mark Poulter, et al.
Neurobiology of Aging|September 11, 2017
TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3)Nina Rostgaard, Peter Roos, Esben Budtz-Jørgensen, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2006
Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous miceEmmanuel A Asante, Jacqueline M Linehan, Ian Gowland, et al.
Journal of Alzheimer'S Disease : JAD|July 4, 2025
Inherited prion disease caused by a novel frameshift mutation of <i>PRNP</i> resulting in protein truncation at codon 157Leah Holm-Mercer, Tze How Mok, Danielle Sequeira, et al.
Emerging Infectious Diseases|November 6, 2013
Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion proteinJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Pageof 30

Showing results (211-220 of 295) with videos related to

Sort By:
Pageof 30
Plos Biology|June 10, 2020
Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSSEmmanuel A Asante, Jacqueline M Linehan, Andrew Tomlinson, et al.
Nature|September 11, 2015
Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathyZane Jaunmuktane, Simon Mead, Matthew Ellis, et al.
Open Biology|June 2, 2016
Ex vivo mammalian prions are formed of paired double helical prion protein fibrilsCassandra Terry, Adam Wenborn, Nathalie Gros, et al.
Neuroimage. Clinical|December 13, 2016
Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry studyEnrico De Vita, Gerard R Ridgway, Mark J White, et al.
Nature|September 17, 2015
Erratum: Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathyZane Jaunmuktane, Simon Mead, Matthew Ellis, et al.
The New England Journal of Medicine|November 20, 2009
A novel protective prion protein variant that colocalizes with kuru exposureSimon Mead, Jerome Whitfield, Mark Poulter, et al.
Neurobiology of Aging|September 11, 2017
TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3)Nina Rostgaard, Peter Roos, Esben Budtz-Jørgensen, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2006
Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous miceEmmanuel A Asante, Jacqueline M Linehan, Ian Gowland, et al.
Journal of Alzheimer'S Disease : JAD|July 4, 2025
Inherited prion disease caused by a novel frameshift mutation of <i>PRNP</i> resulting in protein truncation at codon 157Leah Holm-Mercer, Tze How Mok, Danielle Sequeira, et al.
Emerging Infectious Diseases|November 6, 2013
Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion proteinJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Pageof 30