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John Collinge

Showing results (171-180 of 295) with videos related to

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Acta Neuropathologica Communications|November 21, 2013
Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseasesLilla Reiniger, Ilaria Mirabile, Ana Lukic, et al.
Lancet (London, England)|December 13, 2006
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case reportStephen J Wroe, Suvankar Pal, Durrenajaf Siddique, et al.
The Journal of Biological Chemistry|May 5, 2004
The residue 129 polymorphism in human prion protein does not confer susceptibility to Creutzfeldt-Jakob disease by altering the structure or global stability of PrPCLaszlo L P Hosszu, Graham S Jackson, Clare R Trevitt, et al.
Biochemistry|August 20, 2010
The H187R mutation of the human prion protein induces conversion of recombinant prion protein to the PrP(Sc)-like formLaszlo L P Hosszu, M Howard Tattum, Samantha Jones, et al.
Nature Communications|March 6, 2014
mGlu5 receptors and cellular prion protein mediate amyloid-β-facilitated synaptic long-term depression in vivoNeng-Wei Hu, Andrew J Nicoll, Dainan Zhang, et al.
Dementia and Geriatric Cognitive Disorders Extra|September 11, 2012
Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1Christopher Carswell, Michael Rañopa, Suvankar Pal, et al.
Journal of Molecular Biology|December 19, 2022
Prion Propagation is Dependent on Key Amino Acids in Charge Cluster 2 within the Prion ProteinSavroop Bhamra, Parineeta Arora, Szymon W Manka, et al.
Brain Research|December 30, 2018
PrP-grafted antibodies bind certain amyloid β-protein aggregates, but do not prevent toxicityDavid Mengel, Wei Hong, Grant T Corbett, et al.
Open Biology|November 17, 2017
Soluble Aβ aggregates can inhibit prion propagationClaire J Sarell, Emma Quarterman, Daniel C-M Yip, et al.
Dementia and Geriatric Cognitive Disorders|June 5, 2004
Frontotemporal dementia linked to chromosome 3Jerry Brown, Susanne Gydesen, Peter Johannsen, et al.
Pageof 30

Showing results (171-180 of 295) with videos related to

Sort By:
Pageof 30
Acta Neuropathologica Communications|November 21, 2013
Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseasesLilla Reiniger, Ilaria Mirabile, Ana Lukic, et al.
Lancet (London, England)|December 13, 2006
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case reportStephen J Wroe, Suvankar Pal, Durrenajaf Siddique, et al.
The Journal of Biological Chemistry|May 5, 2004
The residue 129 polymorphism in human prion protein does not confer susceptibility to Creutzfeldt-Jakob disease by altering the structure or global stability of PrPCLaszlo L P Hosszu, Graham S Jackson, Clare R Trevitt, et al.
Biochemistry|August 20, 2010
The H187R mutation of the human prion protein induces conversion of recombinant prion protein to the PrP(Sc)-like formLaszlo L P Hosszu, M Howard Tattum, Samantha Jones, et al.
Nature Communications|March 6, 2014
mGlu5 receptors and cellular prion protein mediate amyloid-β-facilitated synaptic long-term depression in vivoNeng-Wei Hu, Andrew J Nicoll, Dainan Zhang, et al.
Dementia and Geriatric Cognitive Disorders Extra|September 11, 2012
Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1Christopher Carswell, Michael Rañopa, Suvankar Pal, et al.
Journal of Molecular Biology|December 19, 2022
Prion Propagation is Dependent on Key Amino Acids in Charge Cluster 2 within the Prion ProteinSavroop Bhamra, Parineeta Arora, Szymon W Manka, et al.
Brain Research|December 30, 2018
PrP-grafted antibodies bind certain amyloid β-protein aggregates, but do not prevent toxicityDavid Mengel, Wei Hong, Grant T Corbett, et al.
Open Biology|November 17, 2017
Soluble Aβ aggregates can inhibit prion propagationClaire J Sarell, Emma Quarterman, Daniel C-M Yip, et al.
Dementia and Geriatric Cognitive Disorders|June 5, 2004
Frontotemporal dementia linked to chromosome 3Jerry Brown, Susanne Gydesen, Peter Johannsen, et al.
Pageof 30