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John Collinge

Showing results (51-60 of 295) with videos related to

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Nature|January 5, 2017
Structural variation in amyloid-β fibrils from Alzheimer's disease clinical subtypesWei Qiang, Wai-Ming Yau, Jun-Xia Lu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 11, 2008
Alterations in Ca2+-buffering in prion-null mice: association with reduced afterhyperpolarizations in CA1 hippocampal neuronsAndrew D Powell, Emil C Toescu, John Collinge, et al.
European Journal of Human Genetics : EJHG|June 26, 2022
Estimation of the number of inherited prion disease mutation carriers in the UKRosie Corbie, Tracy Campbell, Lee Darwent, et al.
Transfusion|February 26, 2010
Discrimination between prion-infected and normal blood samples by protein misfolding cyclic amplificationM Howard Tattum, Samantha Jones, Suvankar Pal, et al.
Neurogenetics|October 2, 2009
A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouseSarah E Lloyd, Emma G Maytham, Julia Grizenkova, et al.
Neurology|April 8, 2015
MRI detection of prion protein plaques in variant Creutzfeldt-Jakob diseaseHarpreet Hyare, Po-Wah So, Sebastian Brandner, et al.
Science (New York, N.Y.)|November 1, 2003
Depleting neuronal PrP in prion infection prevents disease and reverses spongiosisGiovanna Mallucci, Andrew Dickinson, Jacqueline Linehan, et al.
Biological Psychiatry|May 13, 2018
Reply to: Intrinsic Toxicity of Antibodies to the Globular Domain of the Prion ProteinSilvia A Purro, Simon Mead, Azadeh Khalili-Shirazi, et al.
Nature|February 26, 2011
Prion propagation and toxicity in vivo occur in two distinct mechanistic phasesMalin K Sandberg, Huda Al-Doujaily, Bernadette Sharps, et al.
Scientific Reports|December 4, 2015
Preclinical detection of infectivity and disease-specific PrP in blood throughout the incubation period of prion diseaseElizabeth B Sawyer, Julie Ann Edgeworth, Claire Thomas, et al.
Pageof 30

Showing results (51-60 of 295) with videos related to

Sort By:
Pageof 30
Nature|January 5, 2017
Structural variation in amyloid-β fibrils from Alzheimer's disease clinical subtypesWei Qiang, Wai-Ming Yau, Jun-Xia Lu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 11, 2008
Alterations in Ca2+-buffering in prion-null mice: association with reduced afterhyperpolarizations in CA1 hippocampal neuronsAndrew D Powell, Emil C Toescu, John Collinge, et al.
European Journal of Human Genetics : EJHG|June 26, 2022
Estimation of the number of inherited prion disease mutation carriers in the UKRosie Corbie, Tracy Campbell, Lee Darwent, et al.
Transfusion|February 26, 2010
Discrimination between prion-infected and normal blood samples by protein misfolding cyclic amplificationM Howard Tattum, Samantha Jones, Suvankar Pal, et al.
Neurogenetics|October 2, 2009
A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouseSarah E Lloyd, Emma G Maytham, Julia Grizenkova, et al.
Neurology|April 8, 2015
MRI detection of prion protein plaques in variant Creutzfeldt-Jakob diseaseHarpreet Hyare, Po-Wah So, Sebastian Brandner, et al.
Science (New York, N.Y.)|November 1, 2003
Depleting neuronal PrP in prion infection prevents disease and reverses spongiosisGiovanna Mallucci, Andrew Dickinson, Jacqueline Linehan, et al.
Biological Psychiatry|May 13, 2018
Reply to: Intrinsic Toxicity of Antibodies to the Globular Domain of the Prion ProteinSilvia A Purro, Simon Mead, Azadeh Khalili-Shirazi, et al.
Nature|February 26, 2011
Prion propagation and toxicity in vivo occur in two distinct mechanistic phasesMalin K Sandberg, Huda Al-Doujaily, Bernadette Sharps, et al.
Scientific Reports|December 4, 2015
Preclinical detection of infectivity and disease-specific PrP in blood throughout the incubation period of prion diseaseElizabeth B Sawyer, Julie Ann Edgeworth, Claire Thomas, et al.
Pageof 30