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Mark W Head

Showing results (21-30 of 68) with videos related to

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Journal of Virology|September 17, 2010
Distinct stability states of disease-associated human prion protein identified by conformation-dependent immunoassayYoung Pyo Choi, Alexander H Peden, Albrecht Gröner, et al.
Lancet (London, England)|August 11, 2004
Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patientAlexander H Peden, Mark W Head, Diane L Ritchie, et al.
Acta Neuropathologica|November 29, 2018
Renewed assessment of the risk of emergent advanced cell therapies to transmit neuroproteinopathiesPaul A De Sousa, Diane Ritchie, Alison Green, et al.
Acta Neuropathologica|November 4, 2010
Variably protease-sensitive prionopathy in a PRNP codon 129 heterozygous UK patient with co-existing tau, α synuclein and Aβ pathologyMark W Head, Suzanne Lowrie, Gurjit Chohan, et al.
The Journal of General Virology|August 7, 2009
Transmissions of variant Creutzfeldt-Jakob disease from brain and lymphoreticular tissue show uniform and conserved bovine spongiform encephalopathy-related phenotypic properties on primary and secondary passage in wild-type miceDiane L Ritchie, Aileen Boyle, Irene McConnell, et al.
Hybridoma (2005)|January 10, 2009
Production and characterization of a panel of monoclonal antibodies against native human cellular prion proteinMichael Jones, Victoria McLoughlin, John G Connolly, et al.
The Journal of General Virology|September 12, 2006
Application of an immunocapillary electrophoresis assay to the detection of abnormal prion protein in brain, spleen and blood specimens from patients with variant Creutzfeldt-Jakob diseasePaula C Lourenco, Mary Jo Schmerr, Ian MacGregor, et al.
The Journal of Biological Chemistry|August 8, 2014
Genotype-dependent molecular evolution of sheep bovine spongiform encephalopathy (BSE) prions in vitro affects their zoonotic potentialZuzana Krejciova, Marcelo A Barria, Michael Jones, et al.
Emerging Infectious Diseases|December 8, 2009
Molecular model of prion transmission to humansMichael Jones, Darren Wight, Rona Barron, et al.
Neuropathology and Applied Neurobiology|December 10, 2014
Pathological and biochemical investigation of a woman diagnosed with genetic Creutzfeldt-Jakob disease shortly after parturitionMark W Head, Helen M Yull, Klara Törö, et al.
Pageof 7

Showing results (21-30 of 68) with videos related to

Sort By:
Pageof 7
Journal of Virology|September 17, 2010
Distinct stability states of disease-associated human prion protein identified by conformation-dependent immunoassayYoung Pyo Choi, Alexander H Peden, Albrecht Gröner, et al.
Lancet (London, England)|August 11, 2004
Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patientAlexander H Peden, Mark W Head, Diane L Ritchie, et al.
Acta Neuropathologica|November 29, 2018
Renewed assessment of the risk of emergent advanced cell therapies to transmit neuroproteinopathiesPaul A De Sousa, Diane Ritchie, Alison Green, et al.
Acta Neuropathologica|November 4, 2010
Variably protease-sensitive prionopathy in a PRNP codon 129 heterozygous UK patient with co-existing tau, α synuclein and Aβ pathologyMark W Head, Suzanne Lowrie, Gurjit Chohan, et al.
The Journal of General Virology|August 7, 2009
Transmissions of variant Creutzfeldt-Jakob disease from brain and lymphoreticular tissue show uniform and conserved bovine spongiform encephalopathy-related phenotypic properties on primary and secondary passage in wild-type miceDiane L Ritchie, Aileen Boyle, Irene McConnell, et al.
Hybridoma (2005)|January 10, 2009
Production and characterization of a panel of monoclonal antibodies against native human cellular prion proteinMichael Jones, Victoria McLoughlin, John G Connolly, et al.
The Journal of General Virology|September 12, 2006
Application of an immunocapillary electrophoresis assay to the detection of abnormal prion protein in brain, spleen and blood specimens from patients with variant Creutzfeldt-Jakob diseasePaula C Lourenco, Mary Jo Schmerr, Ian MacGregor, et al.
The Journal of Biological Chemistry|August 8, 2014
Genotype-dependent molecular evolution of sheep bovine spongiform encephalopathy (BSE) prions in vitro affects their zoonotic potentialZuzana Krejciova, Marcelo A Barria, Michael Jones, et al.
Emerging Infectious Diseases|December 8, 2009
Molecular model of prion transmission to humansMichael Jones, Darren Wight, Rona Barron, et al.
Neuropathology and Applied Neurobiology|December 10, 2014
Pathological and biochemical investigation of a woman diagnosed with genetic Creutzfeldt-Jakob disease shortly after parturitionMark W Head, Helen M Yull, Klara Törö, et al.
Pageof 7