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The Burden of Allergens in Surimi-Based Products Diminishes With Industrial Processing

Journal of investigational allergology & clinical immunology, 2021-01, Vol.31 (5), p.443-445

2021

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Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

Proceedings of the National Academy of Sciences - PNAS, 1993-12, Vol.90 (23), p.10962-10966

1993

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Histological staining of amyloid and pre-amyloid peptides and proteins in mouse tissue

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.411

2012

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Perturbation of the Secondary Structure of the Scrapie Prion Protein Under Conditions that Alter Infectivity

Proceedings of the National Academy of Sciences - PNAS, 1993-01, Vol.90 (1), p.1-5

1993

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Predicted α-Helical Regions of the Prion Protein when Synthesized as Peptides Form Amyloid

Proceedings of the National Academy of Sciences - PNAS, 1992-11, Vol.89 (22), p.10940-10944

1992

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Cyclic amplification of prion protein misfolding

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.199

2012

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Fish β-parvalbumin acquires allergenic properties by amyloid assembly

Swiss medical weekly, 2015-05, Vol.145, p.w14128

2015

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The Plasma Membrane Ca2+-ATPase Isoform 4 Is Localized in Lipid Rafts of Cerebellum Synaptic Plasma Membranes

The Journal of biological chemistry, 2006-01, Vol.281 (1), p.447-453

2006

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Bacterial amyloids

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.303

2012

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Measuring the kinetics of amyloid fibril elongation using quartz crystal microbalances

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.101

2012

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Cell-to-cell transmission of α-synuclein aggregates

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.347

2012

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PrPSc Incorporation to Cells Requires Endogenous Glycosaminoglycan Expression

The Journal of biological chemistry, 2005-04, Vol.280 (17), p.17057-17061

2005

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Structural studies of amyloids by quenched hydrogen-deuterium exchange by NMR

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.185

2012

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Search for amyloid-binding proteins by affinity chromatography

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.213

2012

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X-ray fibre diffraction studies of amyloid fibrils

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.121

2012

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Characterization of the antifungal protein secreted by the mould Aspergillus giganteus

Archives of biochemistry and biophysics, 1995-12, Vol.324 (2), p.273-281

1995

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Preparation of stable amyloid β-protein oligomers of defined assembly order

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.23

2012

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Inter- and intra-octarepeat Cu(II) site geometries in the prion protein: implications in Cu(II) binding cooperativity and Cu(II)-mediated assemblies

The Journal of biological chemistry, 2004-03, Vol.279 (12), p.11753-11759

2004

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In vivo magnetic resonance imaging of amyloid-β plaques in mice

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.435

2012

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Prions and their biology

Revista de neurologiá, 2000-07, Vol.31 (2), p.129-132

2000

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Prion Protein Interaction with Glycosaminoglycan Occurs with the Formation of Oligomeric Complexes Stabilized by Cu(II) Bridges

Journal of molecular biology, 2002-05, Vol.319 (2), p.527-540

2002

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Atomic force fluorescence microscopy in the characterization of amyloid fibril assembly and oligomeric intermediates

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.157

2012

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Cognitive and sensorimotor tasks for assessing functional impairments in mouse models of Alzheimer's disease and related disorders

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.529

2012

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Aβ measurement by enzyme-linked immunosorbent assay

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.507

2012

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Purification and fibrillation of full-length recombinant PrP

Methods in molecular biology (Clifton, N.J.), 2012, Vol.849, p.33

2012

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The Burden of Allergens in Surimi-Based Products Diminishes With Industrial Processing

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

Histological staining of amyloid and pre-amyloid peptides and proteins in mouse tissue

Perturbation of the Secondary Structure of the Scrapie Prion Protein Under Conditions that Alter Infectivity

Predicted α-Helical Regions of the Prion Protein when Synthesized as Peptides Form Amyloid

Cyclic amplification of prion protein misfolding

Fish β-parvalbumin acquires allergenic properties by amyloid assembly

The Plasma Membrane Ca2+-ATPase Isoform 4 Is Localized in Lipid Rafts of Cerebellum Synaptic Plasma Membranes

Bacterial amyloids

Measuring the kinetics of amyloid fibril elongation using quartz crystal microbalances

Cell-to-cell transmission of α-synuclein aggregates

PrPSc Incorporation to Cells Requires Endogenous Glycosaminoglycan Expression

Structural studies of amyloids by quenched hydrogen-deuterium exchange by NMR

Search for amyloid-binding proteins by affinity chromatography

X-ray fibre diffraction studies of amyloid fibrils

Characterization of the antifungal protein secreted by the mould Aspergillus giganteus

Preparation of stable amyloid β-protein oligomers of defined assembly order

Inter- and intra-octarepeat Cu(II) site geometries in the prion protein: implications in Cu(II) binding cooperativity and Cu(II)-mediated assemblies

In vivo magnetic resonance imaging of amyloid-β plaques in mice

Prions and their biology

Prion Protein Interaction with Glycosaminoglycan Occurs with the Formation of Oligomeric Complexes Stabilized by Cu(II) Bridges

Atomic force fluorescence microscopy in the characterization of amyloid fibril assembly and oligomeric intermediates

Cognitive and sensorimotor tasks for assessing functional impairments in mouse models of Alzheimer's disease and related disorders

Aβ measurement by enzyme-linked immunosorbent assay

Purification and fibrillation of full-length recombinant PrP

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