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Jean C Manson

Showing results (51-60 of 61) with videos related to

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Neurobiology of Disease|April 20, 2005
Mice devoid of prion protein have cognitive deficits that are rescued by reconstitution of PrP in neuronsJosé R Criado, Manuel Sánchez-Alavez, Bruno Conti, et al.
The Journal of Pathology|February 23, 2011
Human embryonic stem cells rapidly take up and then clear exogenous human and animal prions in vitroZuzana Krejciova, Steve Pells, Enrico Cancellotti, et al.
Scientific Reports|June 28, 2022
Subclinical infection occurs frequently following low dose exposure to prions by blood transfusionM Khalid F Salamat, Paula Stewart, Helen Brown, et al.
Emerging Infectious Diseases|November 25, 2014
Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission propertiesAbigail B Diack, Diane L Ritchie, Alexander H Peden, et al.
Journal of Cell Science|January 5, 2017
Sideroflexin 3 is an α-synuclein-dependent mitochondrial protein that regulates synaptic morphologyInês S Amorim, Laura C Graham, Roderick N Carter, et al.
Emerging Infectious Diseases|September 29, 2012
Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countriesAbigail B Diack, Diane Ritchie, Matthew Bishop, et al.
Plos One|August 23, 2011
All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJDSandra McCutcheon, Anthony Richard Alejo Blanco, E Fiona Houston, et al.
Plos Pathogens|February 18, 2021
Preclinical transmission of prions by blood transfusion is influenced by donor genotype and route of infectionM Khalid F Salamat, A Richard Alejo Blanco, Sandra McCutcheon, et al.
Elife|July 22, 2017
Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1Jamie McQueen, Tomás J Ryan, Sean McKay, et al.
Brain Pathology (Zurich, Switzerland)|February 1, 2012
MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strainFabio Moda, Silvia Suardi, Giuseppe Di Fede, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Neurobiology of Disease|April 20, 2005
Mice devoid of prion protein have cognitive deficits that are rescued by reconstitution of PrP in neuronsJosé R Criado, Manuel Sánchez-Alavez, Bruno Conti, et al.
The Journal of Pathology|February 23, 2011
Human embryonic stem cells rapidly take up and then clear exogenous human and animal prions in vitroZuzana Krejciova, Steve Pells, Enrico Cancellotti, et al.
Scientific Reports|June 28, 2022
Subclinical infection occurs frequently following low dose exposure to prions by blood transfusionM Khalid F Salamat, Paula Stewart, Helen Brown, et al.
Emerging Infectious Diseases|November 25, 2014
Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission propertiesAbigail B Diack, Diane L Ritchie, Alexander H Peden, et al.
Journal of Cell Science|January 5, 2017
Sideroflexin 3 is an α-synuclein-dependent mitochondrial protein that regulates synaptic morphologyInês S Amorim, Laura C Graham, Roderick N Carter, et al.
Emerging Infectious Diseases|September 29, 2012
Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countriesAbigail B Diack, Diane Ritchie, Matthew Bishop, et al.
Plos One|August 23, 2011
All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJDSandra McCutcheon, Anthony Richard Alejo Blanco, E Fiona Houston, et al.
Plos Pathogens|February 18, 2021
Preclinical transmission of prions by blood transfusion is influenced by donor genotype and route of infectionM Khalid F Salamat, A Richard Alejo Blanco, Sandra McCutcheon, et al.
Elife|July 22, 2017
Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1Jamie McQueen, Tomás J Ryan, Sean McKay, et al.
Brain Pathology (Zurich, Switzerland)|February 1, 2012
MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strainFabio Moda, Silvia Suardi, Giuseppe Di Fede, et al.
Pageof 7