Susan Joiner

33 Cleveland Street, W1W 7FF
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 14 publications

Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patient.

Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patient.

Journal: PLoS pathogens
Published: October 22, 2024

A structural basis for prion strain diversity.

A structural basis for prion strain diversity.

Journal: Nature chemical biology
Published: June 21, 2022

2.7 Å cryo-EM structure of ex vivo RML prion fibrils.

2.7 Å cryo-EM structure of ex vivo RML prion fibrils.

Journal: Nature communications
Published: January 06, 2022

Humanized Transgenic Mice Are Resistant to Chronic Wasting Disease Prions From Norwegian Reindeer and Moose.

Humanized Transgenic Mice Are Resistant to Chronic Wasting Disease Prions From Norwegian Reindeer and Moose.

Journal: The Journal of infectious diseases
Published: December 01, 2020

Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitro.

Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitro.

Journal: Scientific reports
Published: July 31, 2018

Evaluating the causality of novel sequence variants in the prion protein gene by example.

Evaluating the causality of novel sequence variants in the prion protein gene by example.

Journal: Neurobiology of aging
Published: January 08, 2018

Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein.

Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein.

Journal: Journal of the neurological sciences
Published: October 02, 2017

Methods for Molecular Diagnosis of Human Prion Disease.

Methods for Molecular Diagnosis of Human Prion Disease.

Journal: Methods in molecular biology (Clifton, N.J.)
Published: September 02, 2017

Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129.

Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129.

Journal: The New England journal of medicine
Published: January 19, 2017

Ex vivo mammalian prions are formed of paired double helical prion protein fibrils.

Ex vivo mammalian prions are formed of paired double helical prion protein fibrils.

Journal: Open biology
Published: February 11, 2016

Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.

Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.

Journal: PLoS pathogens
Published: March 06, 2015

A novel and rapid method for obtaining high titre intact prion strains from mammalian brain.

A novel and rapid method for obtaining high titre intact prion strains from mammalian brain.

Journal: Scientific reports
Published: November 27, 2014
Showing 1-12 of 14

Last Updated: 09/26/2026