Hasil Pencarian - John Collinge

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  1. 1
    The retinoic acid receptor beta (Rarb) region of Mmu14 is associated with prion disease incubation time in mouse.

    The retinoic acid receptor beta (Rarb) region of Mmu14 is associated with prion disease incubation time in mouse. oleh Julia Grizenkova, Shaheen Akhtar, John Collinge, Sarah E Lloyd

    Diterbitkan 2010-12-01
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  2. 2
    Sex effects in mouse prion disease incubation time.

    Sex effects in mouse prion disease incubation time. oleh Shaheen Akhtar, Adam Wenborn, Sebastian Brandner, John Collinge, Sarah E Lloyd

    Diterbitkan 2011-01-01
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  3. 3
    Hippocampal bursts caused by changes in NMDA receptor-dependent excitation in a mouse model of variant CJD

    Hippocampal bursts caused by changes in NMDA receptor-dependent excitation in a mouse model of variant CJD oleh Stéphanie Ratté, Steven A. Prescott, John Collinge, John G.R. Jefferys

    Diterbitkan 2008-10-01
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  4. 4
    Prion protein gene mutation detection using long-read Nanopore sequencing

    Prion protein gene mutation detection using long-read Nanopore sequencing oleh François Kroll, Athanasios Dimitriadis, Tracy Campbell, Lee Darwent, John Collinge, Simon Mead, Emmanuelle Vire

    Diterbitkan 2022-05-01
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  5. 5
    The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature.

    The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature. oleh Diana Caine, Akin Nihat, Philippa Crabb, Peter Rudge, Lisa Cipolotti, John Collinge, Simon Mead

    Diterbitkan 2018-01-01
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  6. 6
    Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease

    Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease oleh Ahamad Hassan, Tracy Campbell, Lee Darwent, Hans Odd, Alison Green, John Collinge, Simon Mead

    Diterbitkan 2021-06-01
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  7. 7
    Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis.

    Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis. oleh Ruth Chia, M Howard Tattum, Samantha Jones, John Collinge, Elizabeth M C Fisher, Graham S Jackson

    Diterbitkan 2010-05-01
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  8. 8
    Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy

    Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy oleh Graham S. Jackson, Jacqueline Linehan, Sebastian Brandner, Emmanuel A. Asante, Jonathan D. F. Wadsworth, John Collinge

    Diterbitkan 2022-10-01
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  9. 9
    Familial Creutzfeldt-Jakob disease in an Indian kindred

    Familial Creutzfeldt-Jakob disease in an Indian kindred oleh Sarosh M Katrak, Apoorva Pauranik, Shrinivas B Desai, Simon Mead, Jon Beck, Sebastian Brandner, John Collinge

    Diterbitkan 2019-01-01
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  10. 10
    A high-content neuron imaging assay demonstrates inhibition of prion disease-associated neurotoxicity by an anti-prion protein antibody

    A high-content neuron imaging assay demonstrates inhibition of prion disease-associated neurotoxicity by an anti-prion protein antibody oleh Madeleine Reilly, Iryna Benilova, Azadeh Khalili-Shirazi, Christian Schmidt, Parvin Ahmed, Daniel Yip, Parmjit S. Jat, John Collinge

    Diterbitkan 2022-06-01
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  11. 11
    Isolation of proteinase K-sensitive prions using pronase E and phosphotungstic acid.

    Isolation of proteinase K-sensitive prions using pronase E and phosphotungstic acid. oleh Laura D'Castro, Adam Wenborn, Nathalie Gros, Susan Joiner, Sabrina Cronier, John Collinge, Jonathan D F Wadsworth

    Diterbitkan 2010-12-01
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  12. 12
    Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases

    Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases oleh Tze How Mok, Akin Nihat, Connie Luk, Danielle Sequeira, Mark Batchelor, Simon Mead, John Collinge, Graham S. Jackson

    Diterbitkan 2021-03-01
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  13. 13
    Sod1 deficiency reduces incubation time in mouse models of prion disease.

    Sod1 deficiency reduces incubation time in mouse models of prion disease. oleh Shaheen Akhtar, Julia Grizenkova, Adam Wenborn, Holger Hummerich, Mar Fernandez de Marco, Sebastian Brandner, John Collinge, Sarah E Lloyd

    Diterbitkan 2013-01-01
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  14. 14
    2.7 Å cryo-EM structure of ex vivo RML prion fibrils

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

    Diterbitkan 2022-07-01
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  15. 15
    NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease Progression

    NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease Progression oleh David Mengel, Tze How Mok, Akin Nihat, Wen Liu, Robert A. Rissman, Douglas Galasko, Henrik Zetterberg, Simon Mead, John Collinge, Dominic M. Walsh

    Diterbitkan 2021-12-01
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  16. 16
    Plasmacytoid dendritic cells sequester high prion titres at early stages of prion infection.

    Plasmacytoid dendritic cells sequester high prion titres at early stages of prion infection. oleh Rocio Castro-Seoane, Holger Hummerich, Trevor Sweeting, M Howard Tattum, Jacqueline M Linehan, Mar Fernandez de Marco, Sebastian Brandner, John Collinge, Peter-Christian Klöhn

    Diterbitkan 2012-02-01
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  17. 17
    HECTD2 is associated with susceptibility to mouse and human prion disease.

    HECTD2 is associated with susceptibility to mouse and human prion disease. oleh Sarah E Lloyd, Emma G Maytham, Hirva Pota, Julia Grizenkova, Eleni Molou, James Uphill, Holger Hummerich, Jerome Whitfield, Michael P Alpers, Simon Mead, John Collinge

    Diterbitkan 2009-02-01
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  18. 18
    Soluble Aβ aggregates can inhibit prion propagation

    Soluble Aβ aggregates can inhibit prion propagation oleh Claire J. Sarell, Emma Quarterman, Daniel C.-M. Yip, Cassandra Terry, Andrew J. Nicoll, Jonathan D. F. Wadsworth, Mark A. Farrow, Dominic M. Walsh, John Collinge

    Diterbitkan 2017-01-01
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  19. 19
    Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1

    Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1 oleh Christopher Carswell, Michael Rañopa, Suvankar Pal, Rebecca MacFarlane, Durre Siddique, Dafydd Thomas, Tom Webb, Steve Wroe, Sarah Walker, Janet Darbyshire, John Collinge, Simon Mead, Peter Rudge

    Diterbitkan 2012-08-01
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  20. 20
    Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.

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

    Diterbitkan 2013-01-01
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