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A consensus method for the prediction of 'aggregation-prone' peptides in globular proteins

PloS one, 2013-01, Vol.8 (1), p.e54175-e54175

2013

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Analysis of non-human primate models for evaluating prion disease therapeutic efficacy

PLoS pathogens, 2022-08, Vol.18 (8), p.e1010728-e1010728

2022

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The Features of Genetic Prion Diseases Based on Chinese Surveillance Program

PloS one, 2015-10, Vol.10 (10), p.e0139552-e0139552

2015

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Large-scale survey of prion protein genetic variability in scrapie disease-free goats from the United States

PloS one, 2021-07, Vol.16 (7), p.e0254998-e0254998

2021

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The amyloid interactome: Exploring protein aggregation

PloS one, 2017-03, Vol.12 (3), p.e0173163-e0173163

2017

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Anti-Prion Screening for Acridine, Dextran, and Tannic Acid using Real Time-Quaking Induced Conversion: A Comparison with PrPSc-Infected Cell Screening

PloS one, 2017-01, Vol.12 (1), p.e0170266-e0170266

2017

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An antipsychotic drug exerts anti-prion effects by altering the localization of the cellular prion protein

PloS one, 2017-08, Vol.12 (8), p.e0182589-e0182589

2017

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Epitope mapping of the protease resistant products of RT-QuIC does not allow the discrimination of sCJD subtypes

PloS one, 2019-06, Vol.14 (6), p.e0218509-e0218509

2019

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The Copper Metabolism MURR1 domain protein 1 (COMMD1) modulates the aggregation of misfolded protein species in a client-specific manner

PloS one, 2014-04, Vol.9 (4), p.e92408-e92408

2014

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A prolonged chronological lifespan is an unexpected benefit of the [PSI+] prion in yeast

PloS one, 2017-09, Vol.12 (9), p.e0184905-e0184905

2017

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Low-volume goat milk transmission of classical scrapie to lambs and goat kids

PloS one, 2018-09, Vol.13 (9), p.e0204281-e0204281

2018

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Species barriers in prion diseases--brief review

Archives of virology. Supplementum, 2005 (19), p.187

2005

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Prion pathogenesis is unaltered in the absence of SIRPα-mediated "don't-eat-me" signaling

PloS one, 2017-05, Vol.12 (5), p.e0177876-e0177876

2017

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Extending Ripley's K-Function to Quantify Aggregation in 2-D Grayscale Images

PloS one, 2015-12, Vol.10 (12), p.e0144404-e0144404

2015

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Treatment of Prion Disease with Heterologous Prion Proteins

PloS one, 2015-07, Vol.10 (7), p.e0131993-e0131993

2015

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Anti-Prion Drug mPPIg5 Inhibits PrPC Conversion to PrPSc

PloS one, 2013-01, Vol.8 (1), p.e55282

2013

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Secondary-structure prediction revisited: Theoretical β-sheet propensity and coil propensity represent structures of amyloids and aid in elucidating phenomena involved in interspecies transmission of prions

PloS one, 2017-02, Vol.12 (2), p.e0171974-e0171974

2017

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PrPC Undergoes Basal to Apical Transcytosis in Polarized Epithelial MDCK Cells

PloS one, 2016-07, Vol.11 (7), p.e0157991-e0157991

2016

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Analyses of the survival time and the influencing factors of chinese patients with prion diseases based on the surveillance data from 2008-2011

PloS one, 2013-05, Vol.8 (5), p.e62553-e62553

2013

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Enzymatic formulation capable of degrading scrapie prion under mild digestion conditions

PloS one, 2013-07, Vol.8 (7), p.e68099-e68099

2013

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Ubiquitin ligase gp78 targets unglycosylated prion protein PrP for ubiquitylation and degradation

PloS one, 2014-04, Vol.9 (4), p.e92290-e92290

2014

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The 26S Proteasome Degrades the Soluble but Not the Fibrillar Form of the Yeast Prion Ure2p In Vitro

PloS one, 2015-06, Vol.10 (6), p.e0131789-e0131789

2015

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Distinct transmissibility features of TSE sources derived from ruminant prion diseases by the oral route in a transgenic mouse model (TgOvPrP4) overexpressing the ovine prion protein

PloS one, 2014-05, Vol.9 (5), p.e96215-e96215

2014

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Prions Ex Vivo: What Cell Culture Models Tell Us about Infectious Proteins

International Journal of Cell Biology, 2013, Vol.2013 (2013), p.442-455

2013

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Deletion of β-Strand and α-Helix Secondary Structure in Normal Prion Protein Inhibits Formation of Its Protease-Resistant Isoform

Journal of Virology, 2001-11, Vol.75 (21), p.10024-10032

2001

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A consensus method for the prediction of 'aggregation-prone' peptides in globular proteins

Analysis of non-human primate models for evaluating prion disease therapeutic efficacy

The Features of Genetic Prion Diseases Based on Chinese Surveillance Program

Large-scale survey of prion protein genetic variability in scrapie disease-free goats from the United States

The amyloid interactome: Exploring protein aggregation

Anti-Prion Screening for Acridine, Dextran, and Tannic Acid using Real Time-Quaking Induced Conversion: A Comparison with PrPSc-Infected Cell Screening

An antipsychotic drug exerts anti-prion effects by altering the localization of the cellular prion protein

Epitope mapping of the protease resistant products of RT-QuIC does not allow the discrimination of sCJD subtypes

The Copper Metabolism MURR1 domain protein 1 (COMMD1) modulates the aggregation of misfolded protein species in a client-specific manner

A prolonged chronological lifespan is an unexpected benefit of the [PSI+] prion in yeast

Low-volume goat milk transmission of classical scrapie to lambs and goat kids

Species barriers in prion diseases--brief review

Prion pathogenesis is unaltered in the absence of SIRPα-mediated "don't-eat-me" signaling

Extending Ripley's K-Function to Quantify Aggregation in 2-D Grayscale Images

Treatment of Prion Disease with Heterologous Prion Proteins

Anti-Prion Drug mPPIg5 Inhibits PrPC Conversion to PrPSc

Secondary-structure prediction revisited: Theoretical β-sheet propensity and coil propensity represent structures of amyloids and aid in elucidating phenomena involved in interspecies transmission of prions

PrPC Undergoes Basal to Apical Transcytosis in Polarized Epithelial MDCK Cells

Analyses of the survival time and the influencing factors of chinese patients with prion diseases based on the surveillance data from 2008-2011

Enzymatic formulation capable of degrading scrapie prion under mild digestion conditions

Ubiquitin ligase gp78 targets unglycosylated prion protein PrP for ubiquitylation and degradation

The 26S Proteasome Degrades the Soluble but Not the Fibrillar Form of the Yeast Prion Ure2p In Vitro

Distinct transmissibility features of TSE sources derived from ruminant prion diseases by the oral route in a transgenic mouse model (TgOvPrP4) overexpressing the ovine prion protein

Prions Ex Vivo: What Cell Culture Models Tell Us about Infectious Proteins

Deletion of β-Strand and α-Helix Secondary Structure in Normal Prion Protein Inhibits Formation of Its Protease-Resistant Isoform

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