List of works - Suzette A Priola

A specific population of abnormal prion protein aggregates is preferentially taken up by cells and disaggregated in a strain-dependent manner

scientific article published on 21 August 2013

Acute cellular uptake of abnormal prion protein is cell type and scrapie-strain independent.

scientific article published on 08 August 2008

Acute formation of protease-resistant prion protein does not always lead to persistent scrapie infection in vitro

scientific article published on 7 May 2004

Altered distribution, aggregation, and protease resistance of cellular prion protein following intracranial inoculation

scientific article published on 10 July 2019

Amyloid formation via supramolecular peptide assemblies

scientific article published on 24 May 2007

Anchorless prion protein results in infectious amyloid disease without clinical scrapie

scientific article

Biomedicine. A view from the top--prion diseases from 10,000 feet

scientific article

Cell Biology Approaches to Studying Prion Diseases

scientific article published on January 2017

Cell biology of prion infection

scientific article published on 01 January 2018

Cells expressing anchorless prion protein are resistant to scrapie infection

scientific article published on 18 February 2009

Cellular prion protein is present in mitochondria of healthy mice

scientific article published on 02 February 2017

Co-infection with the friend retrovirus and mouse scrapie does not alter prion disease pathogenesis in susceptible mice.

scientific article

Comparative profiling of highly enriched 22L and Chandler mouse scrapie prion protein preparations

scientific article published on August 2010

Correction: Co-Infection with the Friend Retrovirus and Mouse Scrapie Does Not Alter Prion Disease Pathogenesis in Susceptible Mice

scientific article published on 12 June 2012

Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

scientific article published on 8 March 2016

Cyclic tetrapyrrole sulfonation, metals, and oligomerization in antiprion activity

scientific article published on 20 August 2007

DNA aptamers that bind to PrP(C) and not PrP(Sc) show sequence and structure specificity

scientific article published on February 2006

Disinfection and sterilization of prion-contaminated medical instruments

scientific article published on 01 December 2010

Endocytosis of prion protein is required for ERK1/2 signaling induced by stress-inducible protein 1.

scientific article published on June 2008

Flexible N-terminal region of prion protein influences conformation of protease-resistant prion protein isoforms associated with cross-species scrapie infection in vivo and in vitro

scientific article published on 21 January 2004

Identification and removal of proteins that co-purify with infectious prion protein improves the analysis of its secondary structure

scientific article published on 07 September 2011

Identification of possible animal origins of prion disease in human beings

scientific article published in June 2004

Lack of prion infectivity in fixed heart tissue from patients with Creutzfeldt-Jakob disease or amyloid heart disease

scientific article published on 19 June 2013

Mitochondrial Respiration Is Impaired during Late-Stage Hamster Prion Infection

scientific article published on 28 June 2017

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

scientific article published on January 2004

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

scientific article published on 01 May 2006

Molecular basis of scrapie strain glycoform variation

scientific article published on 23 July 2002

Multiple amino acid residues within the rabbit prion protein inhibit formation of its abnormal isoform

scientific article

Nonpsychoactive cannabidiol prevents prion accumulation and protects neurons against prion toxicity.

scientific article

Octapeptide repeat insertions increase the rate of protease-resistant prion protein formation

scientific article

PrP Knockout Cells Expressing Transmembrane PrP Resist Prion Infection

scientific article

Prion protein misfolding and disease

scientific article published on 20 January 2009

Prion strains depend on different endocytic routes for productive infection.

scientific article

Processing of high-titer prions for mass spectrometry inactivates prion infectivity

scientific article published on 20 August 2018

Prophylactic and therapeutic effects of phthalocyanine tetrasulfonate in scrapie-infected mice

scientific article published on 14 August 2003

Proteomics analysis of amyloid and nonamyloid prion disease phenotypes reveals both common and divergent mechanisms of neuropathogenesis

scientific article

Proteomics applications in prion biology and structure.

scientific article published on April 2015

Rabbits are not resistant to prion infection

scientific article published on 13 March 2012

Recombinant prion protein refolded with lipid and RNA has the biochemical hallmarks of a prion but lacks in vivo infectivity

scientific article (publication date: 2013)

Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes

scientific article

Self-propagating, protease-resistant, recombinant prion protein conformers with or without in vivo pathogenicity.

scientific article published on 12 July 2017

Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking

scientific article published in March 2008

Susceptibilities of nonhuman primates to chronic wasting disease

scientific article

Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents

scientific article published on 21 January 2004

The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

scientific article published on 3 February 2016

The role of the prion protein membrane anchor in prion infection

scientific article

Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes

scientific article published on 09 June 2020

Treatment of Prion Disease with Heterologous Prion Proteins

scientific article

Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein

scientific article

Uptake and degradation of protease-sensitive and -resistant forms of abnormal human prion protein aggregates by human astrocytes

scientific article

β-Barrel proteins tether the outer membrane in many Gram-negative bacteria

scientific article published on 02 November 2020

List of works by Suzette A Priola

A specific population of abnormal prion protein aggregates is preferentially taken up by cells and disaggregated in a strain-dependent manner

Acute cellular uptake of abnormal prion protein is cell type and scrapie-strain independent.

Acute formation of protease-resistant prion protein does not always lead to persistent scrapie infection in vitro

Altered distribution, aggregation, and protease resistance of cellular prion protein following intracranial inoculation

Amyloid formation via supramolecular peptide assemblies

Anchorless prion protein results in infectious amyloid disease without clinical scrapie

Biomedicine. A view from the top--prion diseases from 10,000 feet

Cell Biology Approaches to Studying Prion Diseases

Cell biology of prion infection

Cells expressing anchorless prion protein are resistant to scrapie infection

Cellular prion protein is present in mitochondria of healthy mice

Co-infection with the friend retrovirus and mouse scrapie does not alter prion disease pathogenesis in susceptible mice.

Comparative profiling of highly enriched 22L and Chandler mouse scrapie prion protein preparations

Correction: Co-Infection with the Friend Retrovirus and Mouse Scrapie Does Not Alter Prion Disease Pathogenesis in Susceptible Mice

Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

Cyclic tetrapyrrole sulfonation, metals, and oligomerization in antiprion activity

DNA aptamers that bind to PrP(C) and not PrP(Sc) show sequence and structure specificity

Disinfection and sterilization of prion-contaminated medical instruments

Endocytosis of prion protein is required for ERK1/2 signaling induced by stress-inducible protein 1.

Flexible N-terminal region of prion protein influences conformation of protease-resistant prion protein isoforms associated with cross-species scrapie infection in vivo and in vitro

Identification and removal of proteins that co-purify with infectious prion protein improves the analysis of its secondary structure

Identification of possible animal origins of prion disease in human beings

Lack of prion infectivity in fixed heart tissue from patients with Creutzfeldt-Jakob disease or amyloid heart disease

Mitochondrial Respiration Is Impaired during Late-Stage Hamster Prion Infection

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

Molecular basis of scrapie strain glycoform variation

Multiple amino acid residues within the rabbit prion protein inhibit formation of its abnormal isoform

Nonpsychoactive cannabidiol prevents prion accumulation and protects neurons against prion toxicity.

Octapeptide repeat insertions increase the rate of protease-resistant prion protein formation

PrP Knockout Cells Expressing Transmembrane PrP Resist Prion Infection

Prion protein misfolding and disease

Prion strains depend on different endocytic routes for productive infection.

Processing of high-titer prions for mass spectrometry inactivates prion infectivity

Prophylactic and therapeutic effects of phthalocyanine tetrasulfonate in scrapie-infected mice

Proteomics analysis of amyloid and nonamyloid prion disease phenotypes reveals both common and divergent mechanisms of neuropathogenesis

Proteomics applications in prion biology and structure.

Rabbits are not resistant to prion infection

Recombinant prion protein refolded with lipid and RNA has the biochemical hallmarks of a prion but lacks in vivo infectivity

Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes

Self-propagating, protease-resistant, recombinant prion protein conformers with or without in vivo pathogenicity.

Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking

Susceptibilities of nonhuman primates to chronic wasting disease

Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents

The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

The role of the prion protein membrane anchor in prion infection

Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes

Treatment of Prion Disease with Heterologous Prion Proteins

Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein

Uptake and degradation of protease-sensitive and -resistant forms of abnormal human prion protein aggregates by human astrocytes

β-Barrel proteins tether the outer membrane in many Gram-negative bacteria