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The Hsp70/Hsp90 Chaperone Machinery in Neurodegenerative Diseases

Frontiers in neuroscience, 2017-05, Vol.11, p.254-254

2017

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Highly efficient protein misfolding cyclic amplification

PLoS pathogens, 2011-02, Vol.7 (2), p.e1001277-e1001277

2011

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Domains of STIP1 responsible for regulating PrPC-dependent amyloid-β oligomer toxicity

Biochemical journal, 2016-07, Vol.473 (14), p.2119-2130

2016

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Mechanisms of neuroprotection against ischemic insult by stress‐inducible phosphoprotein‐1/prion protein complex

Journal of neurochemistry, 2018-04, Vol.145 (1), p.68-79

2018

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Conformational Switching within Individual Amyloid Fibrils

The Journal of biological chemistry, 2009-05, Vol.284 (21), p.14386-14395

2009

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Molecular structure of amyloid fibrils controls the relationship between fibrillar size and toxicity

PloS one, 2011-05, Vol.6 (5), p.e20244

2011

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Increased levels of Stress-inducible phosphoprotein-1 accelerates amyloid-β deposition in a mouse model of Alzheimer's disease

Acta neuropathologica communications, 2020-08, Vol.8 (1), p.143-19, Article 143

2020

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Two Amyloid States of the Prion Protein Display Significantly Different Folding Patterns

Journal of molecular biology, 2010-07, Vol.400 (4), p.908-921

2010

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Increased prion protein processing and expression of metabotropic glutamate receptor 1 in a mouse model of Alzheimer's disease

Journal of neurochemistry, 2013-11, Vol.127 (3), p.415-425

2013

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Brain tumor acidification using drugs simultaneously targeting multiple pH regulatory mechanisms

Journal of neuro-oncology, 2019-09, Vol.144 (3), p.453-462

2019

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The α-Helical C-Terminal Domain of Full-Length Recombinant PrP Converts to an In-Register Parallel β-Sheet Structure in PrP Fibrils: Evidence from Solid State Nuclear Magnetic Resonance

Biochemistry (Easton), 2010-11, Vol.49 (44), p.9488-9497

2010

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The Transient Receptor Potential Melastatin 2 (TRPM2) Channel Contributes to β-Amyloid Oligomer-Related Neurotoxicity and Memory Impairment

The Journal of neuroscience, 2015-11, Vol.35 (45), p.15157-15169

2015

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Highly Promiscuous Nature of Prion Polymerization

The Journal of biological chemistry, 2007-12, Vol.282 (50), p.36704-36713

2007

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A new mechanism for transmissible prion diseases

The Journal of neuroscience, 2012-05, Vol.32 (21), p.7345-7355

2012

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Regulation of Amyloid β Oligomer Binding to Neurons and Neurotoxicity by the Prion Protein-mGluR5 Complex

The Journal of biological chemistry, 2016-10, Vol.291 (42), p.21945-21955

2016

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Cholinergic Regulation of hnRNPA2/B1 Translation by M1 Muscarinic Receptors

The Journal of neuroscience, 2016-06, Vol.36 (23), p.6287-6296

2016

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The prion protein ligand, stress-inducible phosphoprotein 1, regulates amyloid-β oligomer toxicity

The Journal of neuroscience, 2013-10, Vol.33 (42), p.16552-16564

2013

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Detection of Active Caspase-3 in Mouse Models of Stroke and Alzheimer’s Disease with a Novel Dual Positron Emission Tomography/Fluorescent Tracer [68Ga]Ga-TC3-OGDOTA

Contrast media and molecular imaging, 2019-01, Vol.2019 (2019), p.1-17

2019

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The Polybasic N-Terminal Region of the Prion Protein Controls the Physical Properties of Both the Cellular and Fibrillar Forms of PrP

Journal of molecular biology, 2008-11, Vol.383 (5), p.1210-1224

2008

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Laminin‐γ1 chain and stress inducible protein 1 synergistically mediate PrPC‐dependent axonal growth via Ca2+ mobilization in dorsal root ganglia neurons

Journal of neurochemistry, 2013-01, Vol.124 (2), p.210-223

2013

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Measuring Nonapoptotic Caspase Activity with a Transgenic Reporter in Mice

eNeuro, 2022-09, Vol.9 (5), p.ENEURO.0147-21.2022-21.2022

2022

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Regulation of Stress-Inducible Phosphoprotein 1 Nuclear Retention by Protein Inhibitor of Activated STAT PIAS1

Molecular & cellular proteomics, 2013-11, Vol.12 (11), p.3253-3270

2013

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Amyloid Features and Neuronal Toxicity of Mature Prion Fibrils Are Highly Sensitive to High Pressure

The Journal of biological chemistry, 2011-04, Vol.286 (15), p.13448-13459

2011

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Expression, purification, and characterization of human enteropeptidase catalytic subunit in Escherichia coli

Protein expression and purification, 2003-09, Vol.31 (1), p.133-139

2003

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Dissecting structural basis of the unique substrate selectivity of human enteropeptidase catalytic subunit

Journal of biomolecular structure & dynamics, 2012-01, Vol.30 (1), p.62-73

2012

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The Hsp70/Hsp90 Chaperone Machinery in Neurodegenerative Diseases

Highly efficient protein misfolding cyclic amplification

Domains of STIP1 responsible for regulating PrPC-dependent amyloid-β oligomer toxicity

Mechanisms of neuroprotection against ischemic insult by stress‐inducible phosphoprotein‐1/prion protein complex

Conformational Switching within Individual Amyloid Fibrils

Molecular structure of amyloid fibrils controls the relationship between fibrillar size and toxicity

Increased levels of Stress-inducible phosphoprotein-1 accelerates amyloid-β deposition in a mouse model of Alzheimer's disease

Two Amyloid States of the Prion Protein Display Significantly Different Folding Patterns

Increased prion protein processing and expression of metabotropic glutamate receptor 1 in a mouse model of Alzheimer's disease

Brain tumor acidification using drugs simultaneously targeting multiple pH regulatory mechanisms

The α-Helical C-Terminal Domain of Full-Length Recombinant PrP Converts to an In-Register Parallel β-Sheet Structure in PrP Fibrils: Evidence from Solid State Nuclear Magnetic Resonance

The Transient Receptor Potential Melastatin 2 (TRPM2) Channel Contributes to β-Amyloid Oligomer-Related Neurotoxicity and Memory Impairment

Highly Promiscuous Nature of Prion Polymerization

A new mechanism for transmissible prion diseases

Regulation of Amyloid β Oligomer Binding to Neurons and Neurotoxicity by the Prion Protein-mGluR5 Complex

Cholinergic Regulation of hnRNPA2/B1 Translation by M1 Muscarinic Receptors

The prion protein ligand, stress-inducible phosphoprotein 1, regulates amyloid-β oligomer toxicity

Detection of Active Caspase-3 in Mouse Models of Stroke and Alzheimer’s Disease with a Novel Dual Positron Emission Tomography/Fluorescent Tracer [68Ga]Ga-TC3-OGDOTA

The Polybasic N-Terminal Region of the Prion Protein Controls the Physical Properties of Both the Cellular and Fibrillar Forms of PrP

Laminin‐γ1 chain and stress inducible protein 1 synergistically mediate PrPC‐dependent axonal growth via Ca2+ mobilization in dorsal root ganglia neurons

Measuring Nonapoptotic Caspase Activity with a Transgenic Reporter in Mice

Regulation of Stress-Inducible Phosphoprotein 1 Nuclear Retention by Protein Inhibitor of Activated STAT PIAS1

Amyloid Features and Neuronal Toxicity of Mature Prion Fibrils Are Highly Sensitive to High Pressure

Expression, purification, and characterization of human enteropeptidase catalytic subunit in Escherichia coli

Dissecting structural basis of the unique substrate selectivity of human enteropeptidase catalytic subunit

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