Samantha Jones

发表

Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine.

Nick C Fox, J. Collinge, G. Jackson, 2016, JAMA neurology.

A highly sensitive immunoassay for the detection of prion‐infected material in whole human blood without the use of proteinase K

J. Collinge, G. Jackson, S. Jones, 2010, Transfusion.

The H187R mutation of the human prion protein induces conversion of recombinant prion protein to the PrP(Sc)-like form.

J. Collinge, A. Clarke, C. R. Trevitt, 2010, Biochemistry.

Conformational Properties of β-PrP*

J. Collinge, A. Clarke, C. R. Trevitt, 2009, The Journal of Biological Chemistry.

A reassessment of copper(II) binding in the full-length prion protein.

J. Collinge, A. Clarke, G. Jackson, 2006, The Biochemical journal.

Definable equilibrium states in the folding of human prion protein.

J. Collinge, A. Clarke, G. Jackson, 2005, Biochemistry.

The Residue 129 Polymorphism in Human Prion Protein Does Not Confer Susceptibility to Creutzfeldt-Jakob Disease by Altering the Structure or Global Stability of PrPC*

J. Collinge, A. Clarke, C. R. Trevitt, 2004, Journal of Biological Chemistry.

Superoxide Dismutase 1 and tgSOD1G93A Mouse Spinal Cord Seed Fibrils, Suggesting a Propagative Cell Death Mechanism in Amyotrophic Lateral Sclerosis

J. Collinge, G. Jackson, S. Jones, 2010, PloS one.

The C. elegans Rab Family: Identification, Classification and Toolkit Construction

Puja Patel, Nilang Gor, Danielle Jorgens, 2012, PloS one.

Crystal structure of human prion protein bound to a therapeutic antibody

J. Collinge, A. Clarke, C. R. Trevitt, 2009, Proceedings of the National Academy of Sciences.

Beta-PrP form of human prion protein stimulates production of monoclonal antibodies to epitope 91-110 that recognise native PrPSc.

J. Collinge, A. Clarke, G. Jackson, 2007, Biochimica et biophysica acta.

Codon 129 polymorphism of the human prion protein influences the kinetics of amyloid formation.

J. Collinge, A. Clarke, G. Jackson, 2006, The Journal of general virology.

Conformational Properties of β-PrP*

J. Collinge, A. Clarke, C. R. Trevitt, 2009, The Journal of Biological Chemistry.

Discrimination between prion‐infected and normal blood samples by protein misfolding cyclic amplification

J. Collinge, G. Jackson, S. Jones, 2010, Transfusion.

Recombinant prion protein does not possess SOD-1 activity.

J. Collinge, A. Clarke, G. Jackson, 2005, The Biochemical journal.