Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy von Jaunmuktane, Zane, Mead, Simon, Ellis, Matthew, Wadsworth, Jonathan D. F., Nicoll, Andrew J., Kenny, Joanna, Launchbury, Francesca, Linehan, Jacqueline, Richard-Loendt, Angela, Walker, A. Sarah, Rudge, Peter, Collinge, John, Brandner, Sebastian

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BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein von Asante, Emmanuel A., Linehan, Jacqueline M., Desbruslais, Melanie, Joiner, Susan, Gowland, Ian, Wood, Andrew L., Welch, Julie, Hill, Andrew F., Lloyd, Sarah E., Wadsworth, Jonathan D.F., Collinge, John

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Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion protein von Wadsworth, Jonathan D F, Joiner, Susan, Linehan, Jacqueline M, Balkema-Buschmann, Anne, Spiropoulos, John, Simmons, Marion M, Griffiths, Peter C, Groschup, Martin H, Hope, James, Brandner, Sebastian, Asante, Emmanuel A, Collinge, John

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Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129 von Mok, Tzehow, Jaunmuktane, Zane, Joiner, Susan, Campbell, Tracy, Morgan, Catherine, Wakerley, Benjamin, Golestani, Farhad, Rudge, Peter, Mead, Simon, Jäger, H. Rolf, Wadsworth, Jonathan D.F, Brandner, Sebastian, Collinge, John

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Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease von Brandner, Sebastian, Whitfield, Jerome, Boone, Ken, Puwa, Anderson, O'Malley, Catherine, Linehan, Jacqueline M, Joiner, Susan, Scaravilli, Francesco, Calder, Ian, P. Alpers, Michael, Wadsworth, Jonathan D.F, Collinge, John

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Strain-specific prion-protein conformation determined by metal ions von Collinge, John, Wadsworth, Jonathan D.F, Hill, Andrew F, Joiner, Susan, Jackson, Graham S, Clarke, Anthony R

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The origin of the prion agent of kuru: molecular and biological strain typing von Wadsworth, Jonathan D.F, Joiner, Susan, Linehan, Jacqueline M, Asante, Emmanuel A, Brandner, Sebastian, Collinge, John

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A Novel Prion Disease Associated with Diarrhea and Autonomic Neuropathy von Mead, Simon, Gandhi, Sonia, Beck, Jon, Caine, Diana, Gallujipali, Dillip, Carswell, Christopher, Hyare, Harpreet, Joiner, Susan, Ayling, Hilary, Lashley, Tammaryn, Linehan, Jacqueline M, Al-Doujaily, Huda, Sharps, Bernadette, Revesz, Tamas, Sandberg, Malin K, Reilly, Mary M, Koltzenburg, Martin, Forbes, Alastair, Rudge, Peter, Brandner, Sebastian, Warren, Jason D, Wadsworth, Jonathan D.F, Wood, Nicholas W, Holton, Janice L, Collinge, John

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Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein von Asante, Emmanuel A, Linehan, Jacqueline M, Smidak, Michelle, Tomlinson, Andrew, Grimshaw, Andrew, Jeelani, Asif, Jakubcova, Tatiana, Hamdan, Shyma, Powell, Caroline, Brandner, Sebastian, Wadsworth, Jonathan D F, Collinge, John

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Methods for Molecular Diagnosis of Human Prion Disease von Wadsworth, Jonathan D. F., Adamson, Gary, Joiner, Susan, Brock, Lara, Powell, Caroline, Linehan, Jacqueline M., Beck, Jonathan A., Brandner, Sebastian, Mead, Simon, Collinge, John

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Human Prion Protein with Valine 129 Prevents Expression of Variant CJD Phenotype von Jonathan D. F. Wadsworth, Asante, Emmanuel A., Desbruslais, Melanie, Linehan, Jacqueline M., Joiner, Susan, Gowland, Ian, Welch, Julie, Stone, Lisa, Lloyd, Sarah E., Hill, Andrew F., Brandner, Sebastian, Collinge, John

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Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein von Joiner, Susan, Asante, Emmanuel A., Linehan, Jacqueline M., Brock, Lara, Brandner, Sebastian, Bellworthy, Susan J., Simmons, Marion M., Hope, James, Collinge, John, Wadsworth, Jonathan D.F.

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Disease-related Prion Protein Forms Aggresomes in Neuronal Cells Leading to Caspase Activation and Apoptosis von Kristiansen, Mark, Messenger, Marcus J., Klöhn, Peter-Christian, Brandner, Sebastian, Wadsworth, Jonathan D.F., Collinge, John, Tabrizi, Sarah J.

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2.7 Å cryo-EM structure of ex vivo RML prion fibrils von Manka, Szymon W., Zhang, Wenjuan, Wenborn, Adam, Betts, Jemma, Joiner, Susan, Saibil, Helen R., Collinge, John, Wadsworth, Jonathan D. F.

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A structural basis for prion strain diversity von Manka, Szymon W., Wenborn, Adam, Betts, Jemma, Joiner, Susan, Saibil, Helen R., Collinge, John, Wadsworth, Jonathan D. F.

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Prion strains viewed through the lens of cryo-EM von Manka, Szymon W., Wenborn, Adam, Collinge, John, Wadsworth, Jonathan D. F.

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An expanded genetic code for native state, live labeling of prions von Trainer, Thomas J., Zhang, Fuquan, Wenborn, Adam, Wadsworth, Jonathan D.F., Manka, Szymon W.

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A naturally occurring variant of the human prion protein completely prevents prion disease von Asante, Emmanuel A., Smidak, Michelle, Grimshaw, Andrew, Houghton, Richard, Tomlinson, Andrew, Jeelani, Asif, Jakubcova, Tatiana, Hamdan, Shyma, Richard-Londt, Angela, Linehan, Jacqueline M., Brandner, Sebastian, Alpers, Michael, Whitfield, Jerome, Mead, Simon, Wadsworth, Jonathan D. F., Collinge, John

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Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases von Thompson, Andrew G. B., Anastasiadis, Prodromos, Druyeh, Ronald, Whitworth, Ines, Nayak, Annapurna, Nihat, Akin, Mok, Tze How, Rudge, Peter, Wadsworth, Jonathan D. F., Rohrer, Jonathan, Schott, Jonathan M., Heslegrave, Amanda, Zetterberg, Henrik, Collinge, John, Jackson, Graham S., Mead, Simon

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Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years von Rudge, Peter, Jaunmuktane, Zane, Adlard, Peter, Bjurstrom, Nina, Caine, Diana, Lowe, Jessica, Norsworthy, Penny, Hummerich, Holger, Druyeh, Ron, Wadsworth, Jonathan D F, Brandner, Sebastian, Hyare, Harpreet, Mead, Simon, Collinge, John

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