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John Collinge

Showing results (91-100 of 295) with videos related to

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BMC Neurology|December 11, 2012
MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob diseaseChristopher Carswell, Andrew Thompson, Ana Lukic, et al.
Immunology|May 9, 2008
The cellular prion protein is preferentially expressed by CD4+ CD25+ Foxp3+ regulatory T cellsJeremy D Isaacs, Oliver A Garden, Gurman Kaur, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Review. The origin of the prion agent of kuru: molecular and biological strain typingJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Annals of Neurology|September 14, 2006
Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromesJonathan D Rohrer, Simon Mead, Rohani Omar, et al.
The American Journal of Psychiatry|March 4, 2014
Behavioral and psychiatric symptoms in prion diseaseAndrew Thompson, Angus MacKay, Peter Rudge, et al.
Brain Communications|September 21, 2020
Enteral feeding is associated with longer survival in the advanced stages of prion diseaseKirsty McNiven, Akin Nihat, Tze How Mok, et al.
Nature Chemical Biology|January 16, 2023
A structural basis for prion strain diversitySzymon W Manka, Adam Wenborn, Jemma Betts, et al.
The Journal of General Virology|August 16, 2005
PrP glycoforms are associated in a strain-specific ratio in native PrPScAzadeh Khalili-Shirazi, Linda Summers, Jacqueline Linehan, et al.
Human Mutation|June 14, 2008
Successful amplification of degraded DNA for use with high-throughput SNP genotyping platformsSimon Mead, Mark Poulter, John Beck, et al.
Brain : a Journal of Neurology|June 25, 2003
Regional heterogeneity of cellular prion protein isoforms in the mouse brainVincent Beringue, Gary Mallinson, Maria Kaisar, et al.
Pageof 30

Showing results (91-100 of 295) with videos related to

Sort By:
Pageof 30
BMC Neurology|December 11, 2012
MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob diseaseChristopher Carswell, Andrew Thompson, Ana Lukic, et al.
Immunology|May 9, 2008
The cellular prion protein is preferentially expressed by CD4+ CD25+ Foxp3+ regulatory T cellsJeremy D Isaacs, Oliver A Garden, Gurman Kaur, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Review. The origin of the prion agent of kuru: molecular and biological strain typingJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Annals of Neurology|September 14, 2006
Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromesJonathan D Rohrer, Simon Mead, Rohani Omar, et al.
The American Journal of Psychiatry|March 4, 2014
Behavioral and psychiatric symptoms in prion diseaseAndrew Thompson, Angus MacKay, Peter Rudge, et al.
Brain Communications|September 21, 2020
Enteral feeding is associated with longer survival in the advanced stages of prion diseaseKirsty McNiven, Akin Nihat, Tze How Mok, et al.
Nature Chemical Biology|January 16, 2023
A structural basis for prion strain diversitySzymon W Manka, Adam Wenborn, Jemma Betts, et al.
The Journal of General Virology|August 16, 2005
PrP glycoforms are associated in a strain-specific ratio in native PrPScAzadeh Khalili-Shirazi, Linda Summers, Jacqueline Linehan, et al.
Human Mutation|June 14, 2008
Successful amplification of degraded DNA for use with high-throughput SNP genotyping platformsSimon Mead, Mark Poulter, John Beck, et al.
Brain : a Journal of Neurology|June 25, 2003
Regional heterogeneity of cellular prion protein isoforms in the mouse brainVincent Beringue, Gary Mallinson, Maria Kaisar, et al.
Pageof 30