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Mark W Head

Showing results (51-60 of 68) with videos related to

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The Journal of Experimental Medicine|November 17, 2017
Human stem cell-derived astrocytes replicate human prions in a <i>PRNP</i> genotype-dependent mannerZuzana Krejciova, James Alibhai, Chen Zhao, et al.
Transfusion|November 5, 2008
Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob diseaseMichael Jones, Alexander H Peden, Helen Yull, et al.
Brain Pathology (Zurich, Switzerland)|January 5, 2002
Immunohistochemistry for the prion protein: comparison of different monoclonal antibodies in human prion disease subtypesGábor G Kovács, Mark W Head, Ivan Hegyi, et al.
Investigative Ophthalmology & Visual Science|December 31, 2002
Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob diseaseMark W Head, Victoria Northcott, Kathleen Rennison, et al.
Emerging Infectious Diseases|May 19, 2017
Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic PatientsJean Y Douet, Caroline Lacroux, Naima Aron, 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.
The American Journal of Pathology|June 25, 2004
Prion protein accumulation and neuroprotection in hypoxic brain damageNeil F McLennan, Paul M Brennan, Alisdair McNeill, et al.
Acta Neuropathologica|March 4, 2010
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literatureCasper Jansen, Willem Voet, Mark W Head, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 11, 2015
A case of variably protease-sensitive prionopathy treated with doxycyclinHamid Assar, Raffi Topakian, Serge Weis, et al.
Annals of Neurology|June 3, 2004
Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002Mark W Head, Tristan J R Bunn, Matthew T Bishop, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
The Journal of Experimental Medicine|November 17, 2017
Human stem cell-derived astrocytes replicate human prions in a <i>PRNP</i> genotype-dependent mannerZuzana Krejciova, James Alibhai, Chen Zhao, et al.
Transfusion|November 5, 2008
Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob diseaseMichael Jones, Alexander H Peden, Helen Yull, et al.
Brain Pathology (Zurich, Switzerland)|January 5, 2002
Immunohistochemistry for the prion protein: comparison of different monoclonal antibodies in human prion disease subtypesGábor G Kovács, Mark W Head, Ivan Hegyi, et al.
Investigative Ophthalmology & Visual Science|December 31, 2002
Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob diseaseMark W Head, Victoria Northcott, Kathleen Rennison, et al.
Emerging Infectious Diseases|May 19, 2017
Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic PatientsJean Y Douet, Caroline Lacroux, Naima Aron, 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.
The American Journal of Pathology|June 25, 2004
Prion protein accumulation and neuroprotection in hypoxic brain damageNeil F McLennan, Paul M Brennan, Alisdair McNeill, et al.
Acta Neuropathologica|March 4, 2010
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literatureCasper Jansen, Willem Voet, Mark W Head, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 11, 2015
A case of variably protease-sensitive prionopathy treated with doxycyclinHamid Assar, Raffi Topakian, Serge Weis, et al.
Annals of Neurology|June 3, 2004
Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002Mark W Head, Tristan J R Bunn, Matthew T Bishop, et al.
Pageof 7