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Helen Yull

Showing results (1-10 of 7) with videos related to

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Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 9, 2019
Variably protease-sensitive prionopathy mimicking frontotemporal dementiaMiren Aizpurua, Sashika Selvackadunco, Helen Yull, et al.
Infection and Immunity|September 23, 2003
Heterogeneous surface expression of EspA translocon filaments by Escherichia coli O157:H7 is controlled at the posttranscriptional levelAndrew J Roe, Helen Yull, Stuart W Naylor, et al.
Brain Pathology (Zurich, Switzerland)|September 29, 2023
Enhanced Creutzfeldt-Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion diseaseAlexander H Peden, Adriana Libori, Diane L Ritchie, 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.
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.
Acta Neuropathologica|March 29, 2017
Amyloid-β accumulation in the CNS in human growth hormone recipients in the UKDiane L Ritchie, Peter Adlard, Alexander H Peden, et al.
Acta Neuropathologica Communications|November 21, 2013
Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Gabor G Kovacs, Alexander Peden, Serge Weis, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 9, 2019
Variably protease-sensitive prionopathy mimicking frontotemporal dementiaMiren Aizpurua, Sashika Selvackadunco, Helen Yull, et al.
Infection and Immunity|September 23, 2003
Heterogeneous surface expression of EspA translocon filaments by Escherichia coli O157:H7 is controlled at the posttranscriptional levelAndrew J Roe, Helen Yull, Stuart W Naylor, et al.
Brain Pathology (Zurich, Switzerland)|September 29, 2023
Enhanced Creutzfeldt-Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion diseaseAlexander H Peden, Adriana Libori, Diane L Ritchie, 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.
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.
Acta Neuropathologica|March 29, 2017
Amyloid-β accumulation in the CNS in human growth hormone recipients in the UKDiane L Ritchie, Peter Adlard, Alexander H Peden, et al.
Acta Neuropathologica Communications|November 21, 2013
Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Gabor G Kovacs, Alexander Peden, Serge Weis, et al.
Pageof 1