Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

John Collinge

Showing results (61-70 of 295) with videos related to

Pageof 30
Sort By:
Journal of Cell Science|July 2, 2013
Alternative fates of newly formed PrPSc upon prion conversion on the plasma membraneRob Goold, Chris McKinnon, Samira Rabbanian, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 11, 2009
Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfacesJulie Ann Edgeworth, Graham S Jackson, Anthony R Clarke, et al.
The Biochemical Journal|September 15, 2005
Recombinant prion protein does not possess SOD-1 activitySamantha Jones, Mark Batchelor, Daljit Bhelt, et al.
Journal of Neuropathology and Experimental Neurology|November 7, 2006
The human prion protein residue 129 polymorphism lies within a cluster of epitopes for T cell recognitionJeremy D Isaacs, Rebecca J Ingram, John Collinge, et al.
Brain : a Journal of Neurology|April 12, 2021
Cognitive decline heralds onset of symptomatic inherited prion diseaseJoseph Mole, Simon Mead, Peter Rudge, et al.
Acta Neuropathologica|May 18, 2010
Tau, prions and Aβ: the triad of neurodegenerationLilla Reiniger, Ana Lukic, Jacqueline Linehan, et al.
Plos One|January 6, 2018
The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical featureDiana Caine, Akin Nihat, Philippa Crabb, et al.
BMC Neurology|June 29, 2021
Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob diseaseAhamad Hassan, Tracy Campbell, Lee Darwent, et al.
Neuroscience Letters|April 15, 2004
Pathogenic human prion protein rescues PrP null phenotype in transgenic miceEmmanuel A Asante, Yuan-Gen Li, Ian Gowland, et al.
Scientific Reports|May 18, 2022
Prion protein gene mutation detection using long-read Nanopore sequencingFrançois Kroll, Athanasios Dimitriadis, Tracy Campbell, et al.
Pageof 30

Showing results (61-70 of 295) with videos related to

Sort By:
Pageof 30
Journal of Cell Science|July 2, 2013
Alternative fates of newly formed PrPSc upon prion conversion on the plasma membraneRob Goold, Chris McKinnon, Samira Rabbanian, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 11, 2009
Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfacesJulie Ann Edgeworth, Graham S Jackson, Anthony R Clarke, et al.
The Biochemical Journal|September 15, 2005
Recombinant prion protein does not possess SOD-1 activitySamantha Jones, Mark Batchelor, Daljit Bhelt, et al.
Journal of Neuropathology and Experimental Neurology|November 7, 2006
The human prion protein residue 129 polymorphism lies within a cluster of epitopes for T cell recognitionJeremy D Isaacs, Rebecca J Ingram, John Collinge, et al.
Brain : a Journal of Neurology|April 12, 2021
Cognitive decline heralds onset of symptomatic inherited prion diseaseJoseph Mole, Simon Mead, Peter Rudge, et al.
Acta Neuropathologica|May 18, 2010
Tau, prions and Aβ: the triad of neurodegenerationLilla Reiniger, Ana Lukic, Jacqueline Linehan, et al.
Plos One|January 6, 2018
The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical featureDiana Caine, Akin Nihat, Philippa Crabb, et al.
BMC Neurology|June 29, 2021
Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob diseaseAhamad Hassan, Tracy Campbell, Lee Darwent, et al.
Neuroscience Letters|April 15, 2004
Pathogenic human prion protein rescues PrP null phenotype in transgenic miceEmmanuel A Asante, Yuan-Gen Li, Ian Gowland, et al.
Scientific Reports|May 18, 2022
Prion protein gene mutation detection using long-read Nanopore sequencingFrançois Kroll, Athanasios Dimitriadis, Tracy Campbell, et al.
Pageof 30