Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jonathan D F Wadsworth

Showing results (11-20 of 65) with videos related to

Pageof 7
Sort By:
The Biochemical Journal|August 8, 2008
Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysinSabrina Cronier, Nathalie Gros, M Howard Tattum, et al.
The Journal of Biological Chemistry|September 15, 2005
Disease-related prion protein forms aggresomes in neuronal cells leading to caspase activation and apoptosisMark Kristiansen, Marcus J Messenger, Peter-Christian Klöhn, et al.
Lancet (London, England)|October 7, 2004
Analysis of 2000 consecutive UK tonsillectomy specimens for disease-related prion proteinAdam Frosh, Lorraine C Smith, Carl J Jackson, et al.
Archives of Neurology|December 12, 2007
Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British womanSimon Mead, Susan Joiner, Melanie Desbruslais, et al.
The Journal of General Virology|July 23, 2004
Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred miceSarah E Lloyd, Jacqueline M Linehan, Melanie Desbruslais, et al.
Archives of Neurology|August 11, 2010
Heterozygosity at polymorphic codon 219 in variant creutzfeldt-jakob diseaseAna Lukic, Jonathan Beck, Susan Joiner, et al.
Nature Communications|July 13, 2022
2.7 Å cryo-EM structure of ex vivo RML prion fibrilsSzymon W Manka, Wenjuan Zhang, Adam Wenborn, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 26, 2008
Molecular diagnosis of human prion diseaseJonathan D F Wadsworth, Caroline Powell, Jonathan A Beck, et al.
JAMA Neurology|January 22, 2014
Variant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion proteinSimon Mead, Jonathan D F Wadsworth, Marie-Claire Porter, et al.
Brain : a Journal of Neurology|January 18, 2006
Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutationsAndrew F Hill, Susan Joiner, Jonathan A Beck, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
The Biochemical Journal|August 8, 2008
Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysinSabrina Cronier, Nathalie Gros, M Howard Tattum, et al.
The Journal of Biological Chemistry|September 15, 2005
Disease-related prion protein forms aggresomes in neuronal cells leading to caspase activation and apoptosisMark Kristiansen, Marcus J Messenger, Peter-Christian Klöhn, et al.
Lancet (London, England)|October 7, 2004
Analysis of 2000 consecutive UK tonsillectomy specimens for disease-related prion proteinAdam Frosh, Lorraine C Smith, Carl J Jackson, et al.
Archives of Neurology|December 12, 2007
Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British womanSimon Mead, Susan Joiner, Melanie Desbruslais, et al.
The Journal of General Virology|July 23, 2004
Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred miceSarah E Lloyd, Jacqueline M Linehan, Melanie Desbruslais, et al.
Archives of Neurology|August 11, 2010
Heterozygosity at polymorphic codon 219 in variant creutzfeldt-jakob diseaseAna Lukic, Jonathan Beck, Susan Joiner, et al.
Nature Communications|July 13, 2022
2.7 Å cryo-EM structure of ex vivo RML prion fibrilsSzymon W Manka, Wenjuan Zhang, Adam Wenborn, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 26, 2008
Molecular diagnosis of human prion diseaseJonathan D F Wadsworth, Caroline Powell, Jonathan A Beck, et al.
JAMA Neurology|January 22, 2014
Variant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion proteinSimon Mead, Jonathan D F Wadsworth, Marie-Claire Porter, et al.
Brain : a Journal of Neurology|January 18, 2006
Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutationsAndrew F Hill, Susan Joiner, Jonathan A Beck, et al.
Pageof 7