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A F Hill

Showing results (11-20 of 30) with videos related to

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Neurochemistry International|December 27, 2011
Generating recombinant C-terminal prion protein fragments of exact native sequenceV A Johanssen, K J Barnham, C L Masters, et al.
Nature Cell Biology|November 13, 1999
Strain-specific prion-protein conformation determined by metal ionsJ D Wadsworth, A F Hill, S Joiner, et al.
Neurology|July 13, 2005
Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profilesV Lewis, A F Hill, G M Klug, et al.
Neuroscience Letters|December 1, 1998
Molecular screening of sheep for bovine spongiform encephalopathyA F Hill, K C Sidle, S Joiner, et al.
The Journal of Pathology|March 6, 2007
Packaging of prions into exosomes is associated with a novel pathway of PrP processingL J Vella, R A Sharples, V A Lawson, et al.
Neurology|May 29, 2003
Novel prion protein insert mutation associated with prolonged neurodegenerative illnessV Lewis, S Collins, A F Hill, et al.
Lancet (London, England)|July 31, 2001
Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assayJ D Wadsworth, S Joiner, A F Hill, et al.
Nature|October 23, 1997
The same prion strain causes vCJD and BSEA F Hill, M Desbruslais, S Joiner, et al.
Human Molecular Genetics|May 1, 1993
Deletions in the prion protein gene are not associated with CJDM S Palmer, S P Mahal, T A Campbell, et al.
Biochimica Et Biophysica Acta|April 21, 1999
Multiple folding pathways for heterologously expressed human prion proteinG S Jackson, A F Hill, C Joseph, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Neurochemistry International|December 27, 2011
Generating recombinant C-terminal prion protein fragments of exact native sequenceV A Johanssen, K J Barnham, C L Masters, et al.
Nature Cell Biology|November 13, 1999
Strain-specific prion-protein conformation determined by metal ionsJ D Wadsworth, A F Hill, S Joiner, et al.
Neurology|July 13, 2005
Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profilesV Lewis, A F Hill, G M Klug, et al.
Neuroscience Letters|December 1, 1998
Molecular screening of sheep for bovine spongiform encephalopathyA F Hill, K C Sidle, S Joiner, et al.
The Journal of Pathology|March 6, 2007
Packaging of prions into exosomes is associated with a novel pathway of PrP processingL J Vella, R A Sharples, V A Lawson, et al.
Neurology|May 29, 2003
Novel prion protein insert mutation associated with prolonged neurodegenerative illnessV Lewis, S Collins, A F Hill, et al.
Lancet (London, England)|July 31, 2001
Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assayJ D Wadsworth, S Joiner, A F Hill, et al.
Nature|October 23, 1997
The same prion strain causes vCJD and BSEA F Hill, M Desbruslais, S Joiner, et al.
Human Molecular Genetics|May 1, 1993
Deletions in the prion protein gene are not associated with CJDM S Palmer, S P Mahal, T A Campbell, et al.
Biochimica Et Biophysica Acta|April 21, 1999
Multiple folding pathways for heterologously expressed human prion proteinG S Jackson, A F Hill, C Joseph, et al.
Pageof 3