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John Collinge

Showing results (181-190 of 295) with videos related to

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Journal of Molecular Biology|April 5, 2025
Corrigendum to "Prion Propagation is Dependent on Key Amino Acids in Charge Cluster 2 within the Prion Protein" [J. Mol. Biol. 435(4) (2023) 167925]Savroop Bhamra, Parineeta Arora, Szymon W Manka, et al.
Human Mutation|June 29, 2010
PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion UnitJon A Beck, Mark Poulter, Tracy A Campbell, et al.
Neurobiology of Aging|January 4, 2011
Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK seriesDaniel McNaughton, William Knight, Rita Guerreiro, et al.
Annals of Clinical and Translational Neurology|May 23, 2015
The cognitive profile of prion disease: a prospective clinical and imaging studyDiana Caine, Renata J Tinelli, Harpreet Hyare, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion diseaseSebastian Brandner, Jerome Whitfield, Ken Boone, et al.
Plos Pathogens|October 3, 2013
Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion proteinEmmanuel A Asante, Jacqueline M Linehan, Michelle Smidak, et al.
Science (New York, N.Y.)|April 12, 2003
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemicsSimon Mead, Michael P H Stumpf, Jerome Whitfield, et al.
Brain : a Journal of Neurology|April 7, 2006
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion proteinJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
The Journal of General Virology|February 17, 2009
Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteinsEmmanuel A Asante, Ian Gowland, Andrew Grimshaw, et al.
Journal of Molecular Biology|February 14, 2006
Elongated oligomers assemble into mammalian PrP amyloid fibrilsM Howard Tattum, Sara Cohen-Krausz, Kanjana Thumanu, et al.
Pageof 30

Showing results (181-190 of 295) with videos related to

Sort By:
Pageof 30
Journal of Molecular Biology|April 5, 2025
Corrigendum to "Prion Propagation is Dependent on Key Amino Acids in Charge Cluster 2 within the Prion Protein" [J. Mol. Biol. 435(4) (2023) 167925]Savroop Bhamra, Parineeta Arora, Szymon W Manka, et al.
Human Mutation|June 29, 2010
PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion UnitJon A Beck, Mark Poulter, Tracy A Campbell, et al.
Neurobiology of Aging|January 4, 2011
Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK seriesDaniel McNaughton, William Knight, Rita Guerreiro, et al.
Annals of Clinical and Translational Neurology|May 23, 2015
The cognitive profile of prion disease: a prospective clinical and imaging studyDiana Caine, Renata J Tinelli, Harpreet Hyare, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion diseaseSebastian Brandner, Jerome Whitfield, Ken Boone, et al.
Plos Pathogens|October 3, 2013
Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion proteinEmmanuel A Asante, Jacqueline M Linehan, Michelle Smidak, et al.
Science (New York, N.Y.)|April 12, 2003
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemicsSimon Mead, Michael P H Stumpf, Jerome Whitfield, et al.
Brain : a Journal of Neurology|April 7, 2006
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion proteinJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
The Journal of General Virology|February 17, 2009
Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteinsEmmanuel A Asante, Ian Gowland, Andrew Grimshaw, et al.
Journal of Molecular Biology|February 14, 2006
Elongated oligomers assemble into mammalian PrP amyloid fibrilsM Howard Tattum, Sara Cohen-Krausz, Kanjana Thumanu, et al.
Pageof 30