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JAMA Neurology
|
October 5, 2016
Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine
Connie Luk, Samantha Jones, Claire Thomas, et al.
The Journal of General Virology
|
July 19, 2006
Codon 129 polymorphism of the human prion protein influences the kinetics of amyloid formation
Patrick A Lewis, M Howard Tattum, Samantha Jones, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 27, 2009
Folding kinetics of the human prion protein probed by temperature jump
Tanya Hart, Laszlo L P Hosszu, Clare R Trevitt, et al.
Elife
|
August 7, 2024
Syntaxin-6 delays prion protein fibril formation and prolongs the presence of toxic aggregation intermediates
Daljit Sangar, Elizabeth Hill, Kezia Jack, et al.
JAMA Neurology
|
January 22, 2014
Variant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion protein
Simon Mead, Jonathan D F Wadsworth, Marie-Claire Porter, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
March 8, 2005
Protein conformation significantly influences immune responses to prion protein
Azadeh Khalili-Shirazi, Sonia Quaratino, Marco Londei, et al.
The Journal of General Virology
|
February 22, 2005
An enzyme-detergent method for effective prion decontamination of surgical steel
Graham S Jackson, Edward McKintosh, Eckhard Flechsig, et al.
The Biochemical Journal
|
July 11, 2006
A reassessment of copper(II) binding in the full-length prion protein
Mark A Wells, Graham S Jackson, Samantha Jones, et al.
Prion
|
June 11, 2016
Physical, chemical and kinetic factors affecting prion infectivity
Francesca Properzi, Anjna Badhan, Steffi Klier, et al.
The Biochemical Journal
|
August 24, 2006
Multiple forms of copper (II) co-ordination occur throughout the disordered N-terminal region of the prion protein at pH 7.4
Mark A Wells, Clare Jelinska, Laszlo L P Hosszu, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 54) with videos related to
Sort By:
Page
of 6
JAMA Neurology
|
October 5, 2016
Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine
Connie Luk, Samantha Jones, Claire Thomas, et al.
The Journal of General Virology
|
July 19, 2006
Codon 129 polymorphism of the human prion protein influences the kinetics of amyloid formation
Patrick A Lewis, M Howard Tattum, Samantha Jones, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 27, 2009
Folding kinetics of the human prion protein probed by temperature jump
Tanya Hart, Laszlo L P Hosszu, Clare R Trevitt, et al.
Elife
|
August 7, 2024
Syntaxin-6 delays prion protein fibril formation and prolongs the presence of toxic aggregation intermediates
Daljit Sangar, Elizabeth Hill, Kezia Jack, et al.
JAMA Neurology
|
January 22, 2014
Variant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion protein
Simon Mead, Jonathan D F Wadsworth, Marie-Claire Porter, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
March 8, 2005
Protein conformation significantly influences immune responses to prion protein
Azadeh Khalili-Shirazi, Sonia Quaratino, Marco Londei, et al.
The Journal of General Virology
|
February 22, 2005
An enzyme-detergent method for effective prion decontamination of surgical steel
Graham S Jackson, Edward McKintosh, Eckhard Flechsig, et al.
The Biochemical Journal
|
July 11, 2006
A reassessment of copper(II) binding in the full-length prion protein
Mark A Wells, Graham S Jackson, Samantha Jones, et al.
Prion
|
June 11, 2016
Physical, chemical and kinetic factors affecting prion infectivity
Francesca Properzi, Anjna Badhan, Steffi Klier, et al.
The Biochemical Journal
|
August 24, 2006
Multiple forms of copper (II) co-ordination occur throughout the disordered N-terminal region of the prion protein at pH 7.4
Mark A Wells, Clare Jelinska, Laszlo L P Hosszu, et al.
Page
of 6