Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner von Krejciova, Zuzana, Alibhai, James, Zhao, Chen, Krencik, Robert, Rzechorzek, Nina M, Ullian, Erik M, Manson, Jean, Ironside, James W, Head, Mark W, Chandran, Siddharthan

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Susceptibility of Human Prion Protein to Conversion by Chronic Wasting Disease Prions von Barria, Marcelo A, Libori, Adriana, Mitchell, Gordon, Head, Mark W

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Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease von McGuire, Lynne I., Peden, Alexander H., Orrú, Christina D., Wilham, Jason M., Appleford, Nigel E., Mallinson, Gary, Andrews, Mary, Head, Mark W., Caughey, Byron, Will, Robert G., Knight, Richard S. G., Green, Alison J. E.

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Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient von Peden, Alexander H, Head, Mark W, Diane, L Ritchie, Jeanne, E Bell, James, W Ironside

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Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients von Douet, Jean Y, Lacroux, Caroline, Aron, Naima, Head, Mark W, Lugan, Séverine, Tillier, Cécile, Huor, Alvina, Cassard, Hervé, Arnold, Mark, Beringue, Vincent, Ironside, James W, Andréoletti, Olivier

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Human prion diseases: Molecular, cellular and population biology von Head, Mark W.

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Molecular barriers to zoonotic transmission of prions von Barria, Marcelo A, Balachandran, Aru, Morita, Masanori, Kitamoto, Tetsuyuki, Barron, Rona, Manson, Jean, Knight, Richard, Ironside, James W, Head, Mark W

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Sensitive and specific detection of sporadic Creutzfeldt―Jakob disease brain prion protein using real-time quaking-induced conversion von PEDEN, Alexander H, MCGUIRE, Lynne I, GREEN, Alison J. E, HEAD, Mark W, APPLEFORD, Nigel E. J, MALLINSON, Gary, WILHAM, Jason M, ORRU, Christina D, CAUGHEY, Byron, IRONSIDE, James W, KNIGHT, Richard S, WILL, Robert G

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The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients von Moore, Roger A, Head, Mark W, Ironside, James W, Ritchie, Diane L, Zanusso, Gianluigi, Choi, Young Pyo, Pyo Choi, Young, Priola, Suzette A

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Variably protease-sensitive prionopathy in the UK: a retrospective review 1991―2008 von HEAD, Mark W, YULL, Helen M, RITCHIE, Diane L, LANGEVELD, Jan P, FLETCHER, Nicholas A, KNIGHT, Richard S, IRONSIDE, James W

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Prion Protein Accumulation and Neuroprotection in Hypoxic Brain Damage von McLennan, Neil F., Brennan, Paul M., McNeill, Alisdair, Davies, Ioan, Fotheringham, Andrew, Rennison, Kathleen A., Ritchie, Diane, Brannan, Francis, Head, Mark W., Ironside, James W., Williams, Alun, Bell, Jeanne E.

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Detection of Type 1 Prion Protein in Variant Creutzfeldt-Jakob Disease von Yull, Helen M., Ritchie, Diane L., Langeveld, Jan P.M., van Zijderveld, Fred G., Bruce, Moira E., Ironside, James W., Head, Mark W.

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Rapid amplification of prions from variant Creutzfeldt–Jakob disease cerebrospinal fluid von Barria, Marcelo A, Lee, Andrew, Green, Alison JE, Knight, Richard, Head, Mark W

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Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients von Moore, Roger A, Head, Mark W, Ironside, James W, Ritchie, Diane L, Zanusso, Gianluigi, Choi, Young Pyo, Priola, Suzette A

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Distinct Stability States of Disease-Associated Human Prion Protein Identified by Conformation-Dependent Immunoassay von Choi, Young Pyo, Peden, Alexander H, Gröner, Albrecht, Ironside, James W, Head, Mark W

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Molecular model of prion transmission to humans von Jones, Michael, Wight, Darren, Barron, Rona, Jeffrey, Martin, Manson, Jean, Prowse, Christopher, Ironside, James W, Head, Mark W

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Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain von Brandel, Jean-Philippe, Heath, Craig A., Head, Mark W., Levavasseur, Etienne, Knight, Richard, Laplanche, Jean-Louis, Langeveld, Jan PM, Ironside, James W., Hauw, Jean-Jacques, Mackenzie, Jan, Alpérovitch, Annick, Will, Robert G., Haïk, Stéphane

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Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK von Ritchie, Diane L., Adlard, Peter, Peden, Alexander H., Lowrie, Suzanne, Le Grice, Margaret, Burns, Kimberley, Jackson, Rosemary J., Yull, Helen, Keogh, Michael J., Wei, Wei, Chinnery, Patrick F., Head, Mark W., Ironside, James W.

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Inter-Laboratory Assessment of PrPSc Typing in Creutzfeldt-Jakob Disease: A Western Blot Study within the NeuroPrion Consortium von Parchi, Piero, Notari, Silvio, Weber, Petra, Schimmel, Heinz, Budka, Herbert, Ferrer, Isidre, Haik, Stéphane, Hauw, Jean-Jacques, Head, Mark W, Ironside, James W, Limido, Lucia, Rodriguez, Agustin, Ströbel, Thomas, Tagliavini, Fabrizio, Kretzschmar, Hans A.

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UK Iatrogenic Creutzfeldt–Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches von Ritchie, Diane L., Barria, Marcelo A., Peden, Alexander H., Yull, Helen M., Kirkpatrick, James, Adlard, Peter, Ironside, James W., Head, Mark W.

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