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Suicidal [PSIâº] is a lethal yeast prion

Proceedings of the National Academy of Sciences - PNAS, 2011-03, Vol.108 (13), p.5337-5341

2011

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Yeast [PSI+] Prion Aggregates Are Formed by Small Sup35 Polymers Fragmented by Hsp104

The Journal of biological chemistry, 2003-12, Vol.278 (49), p.49636-49643

2003

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Curing of the [URE3] prion by Btn2p, a Batten disease-related protein

The EMBO journal, 2008-10, Vol.27 (20), p.2725-2735

2008

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The Core of Ure2p Prion Fibrils Is Formed by the N-Terminal Segment in a Parallel Cross-β Structure: Evidence from Solid-State NMR

Journal of molecular biology, 2011-06, Vol.409 (2), p.263-277

2011

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Molecular chaperone Hsp104 can promote yeast prion generation

Genetics (Austin), 2011-06, Vol.188 (2), p.339-348

2011

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Sex, prions, and plasmids in yeast

Proceedings of the National Academy of Sciences - PNAS, 2012-10, Vol.109 (40), p.E2683-E2690

2012

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Complex Nature of Protein Carbonylation Specificity After Metal-Catalyzed Oxidation

Pharmaceutical research, 2017-04, Vol.34 (4), p.765-779

2017

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Nonsense Suppression in Yeast Cells Overproducing Sup35 (eRF3) Is Caused by Its Non-heritable Amyloids

The Journal of biological chemistry, 2005-03, Vol.280 (10), p.8808-8812

2005

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yeast Sup35NM domain propagates as a prion in mammalian cells

Proceedings of the National Academy of Sciences - PNAS, 2009-01, Vol.106 (2), p.462-467

2009

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Increased Expression of Hsp40 Chaperones, Transcriptional Factors, and Ribosomal Protein Rpp0 Can Cure Yeast Prions

The Journal of biological chemistry, 2002-06, Vol.277 (26), p.23702-23708

2002

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Chaperones that cure yeast artificial [ PSI+] and their prion-specific effects

Current biology, 2000-11, Vol.10 (22), p.1443-1446

2000

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Modeling ALS and FTLD proteinopathies in yeast: An efficient approach for studying protein aggregation and toxicity

Prion, 2011-10, Vol.5 (4), p.250-257

2011

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Comparative Effects of Metal-Catalyzed Oxidizing Systems on Carbonylation and Integrity of Therapeutic Proteins

Pharmaceutical research, 2016-02, Vol.33 (2), p.526-539

2016

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Non-targeted Identification of Prions and Amyloid-forming Proteins from Yeast and Mammalian Cells

The Journal of biological chemistry, 2013-09, Vol.288 (38), p.27100-27111

2013

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A yeast model of optineurin proteinopathy reveals a unique aggregation pattern associated with cellular toxicity

Molecular microbiology, 2012-12, Vol.86 (6), p.1531-1547

2012

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Nucleotide exchange factors for Hsp70s are required for [URE3] prion propagation in Saccharomyces cerevisiae

Molecular biology of the cell, 2007-06, Vol.18 (6), p.2149-2154

2007

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Yeast Prions: Evolution of the Prion Concept

Prion, 2007-04, Vol.1 (2), p.94-100

2007

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Two Prion Variants of Sup35p Have In-Register Parallel β-Sheet Structures, Independent of Hydration

Biochemistry (Easton), 2009-06, Vol.48 (23), p.5074-5082

2009

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FUS/TLS forms cytoplasmic aggregates, inhibits cell growth and interacts with TDP-43 in a yeast model of amyotrophic lateral sclerosis

Protein & cell, 2011-03, Vol.2 (3), p.223-236

2011

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Protein inheritance (prions) based on parallel in-register β-sheet amyloid structures

BioEssays, 2008-10, Vol.30 (10), p.955-964

2008

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Hepatic Expression of Serum Amyloid A1 Is Induced by Traumatic Brain Injury and Modulated by Telmisartan

The American journal of pathology, 2015-10, Vol.185 (10), p.2641-2652

2015

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Study of Amyloids Using Yeast

Methods in molecular biology (Clifton, N.J.), 2018, Vol.1779, p.313

2018

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Isolation and Analysis of Prion and Amyloid Aggregates from Yeast Cells

Cold Spring Harbor protocols, 2017-02, Vol.2017 (2), p.pdb.prot089045

2017

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Prion diseases of yeast: Amyloid structure and biology

Seminars in cell & developmental biology, 2011-07, Vol.22 (5), p.469-475

2011

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Prion Transfection of Yeast

Cold Spring Harbor protocols, 2017-02, Vol.2017 (2), p.pdb.prot089037

2017

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Suicidal [PSIâº] is a lethal yeast prion

Yeast [PSI+] Prion Aggregates Are Formed by Small Sup35 Polymers Fragmented by Hsp104

Curing of the [URE3] prion by Btn2p, a Batten disease-related protein

The Core of Ure2p Prion Fibrils Is Formed by the N-Terminal Segment in a Parallel Cross-β Structure: Evidence from Solid-State NMR

Molecular chaperone Hsp104 can promote yeast prion generation

Sex, prions, and plasmids in yeast

Complex Nature of Protein Carbonylation Specificity After Metal-Catalyzed Oxidation

Nonsense Suppression in Yeast Cells Overproducing Sup35 (eRF3) Is Caused by Its Non-heritable Amyloids

yeast Sup35NM domain propagates as a prion in mammalian cells

Increased Expression of Hsp40 Chaperones, Transcriptional Factors, and Ribosomal Protein Rpp0 Can Cure Yeast Prions

Chaperones that cure yeast artificial [ PSI+] and their prion-specific effects

Modeling ALS and FTLD proteinopathies in yeast: An efficient approach for studying protein aggregation and toxicity

Comparative Effects of Metal-Catalyzed Oxidizing Systems on Carbonylation and Integrity of Therapeutic Proteins

Non-targeted Identification of Prions and Amyloid-forming Proteins from Yeast and Mammalian Cells

A yeast model of optineurin proteinopathy reveals a unique aggregation pattern associated with cellular toxicity

Nucleotide exchange factors for Hsp70s are required for [URE3] prion propagation in Saccharomyces cerevisiae

Yeast Prions: Evolution of the Prion Concept

Two Prion Variants of Sup35p Have In-Register Parallel β-Sheet Structures, Independent of Hydration

FUS/TLS forms cytoplasmic aggregates, inhibits cell growth and interacts with TDP-43 in a yeast model of amyotrophic lateral sclerosis

Protein inheritance (prions) based on parallel in-register β-sheet amyloid structures

Hepatic Expression of Serum Amyloid A1 Is Induced by Traumatic Brain Injury and Modulated by Telmisartan

Study of Amyloids Using Yeast

Isolation and Analysis of Prion and Amyloid Aggregates from Yeast Cells

Prion diseases of yeast: Amyloid structure and biology

Prion Transfection of Yeast

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