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Structural, morphological, and functional diversity of amyloid oligomers

FEBS letters, 2015-09, Vol.589 (19), p.2640-2648

2015

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Carbonyl-based blue autofluorescence of proteins and amino acids

PloS one, 2017-05, Vol.12 (5), p.e0176983-e0176983

2017

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Intrinsic disorder in proteins involved in amyotrophic lateral sclerosis

Cellular and molecular life sciences : CMLS, 2017-04, Vol.74 (7), p.1297-1318

2017

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Beyond the excluded volume effects: mechanistic complexity of the crowded milieu

Molecules, 2015-01, Vol.20 (1), p.1377-1409

2015

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Accelerated neurodegeneration through chaperone-mediated oligomerization of tau

The Journal of clinical investigation, 2013-10, Vol.123 (10), p.4158-4169

2013

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Elevated Ca2+ at the triad junction underlies dysregulation of Ca2+ signaling in dysferlin-null skeletal muscle

Frontiers in physiology, 2022-11, Vol.13, p.1032447

2022

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Intracellular processing of disease-associated α-synuclein in the human brain suggests prion-like cell-to-cell spread

Neurobiology of disease, 2014-09, Vol.69, p.76-92

2014

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Fibril specific, conformation dependent antibodies recognize a generic epitope common to amyloid fibrils and fibrillar oligomers that is absent in prefibrillar oligomers

Molecular neurodegeneration, 2007-09, Vol.2 (1), p.18-18, Article 18

2007

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Antibody association in solution: cluster distributions and mechanisms

mAbs, 2024, Vol.16 (1), p.2339582-2339582

2024

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Conformation dependent monoclonal antibodies distinguish different replicating strains or conformers of prefibrillar Aβ oligomers

Molecular neurodegeneration, 2010-12, Vol.5 (1), p.57-57, Article 57

2010

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Production and biochemical and biophysical characterization of fibrinolytic protease of a Mucor subtilissimus strain isolated from the caatinga biome

Anais da Academia Brasileira de Ciências, 2024, Vol.96 (suppl 1), p.e20230616

2024

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Polymorphism and Ultrastructural Organization of Prion Protein Amyloid Fibrils: An Insight from High Resolution Atomic Force Microscopy

Journal of molecular biology, 2006-04, Vol.358 (2), p.580-596

2006

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High throughput characterization of structural differences between closely related proteins in solution

Biochimica et biophysica acta, 2013-02, Vol.1834 (2), p.583-592

2013

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When Good Goes Awry: The Aggregation of Protein Therapeutics

Protein and peptide letters, 2017-01, Vol.24 (4), p.340-347

2017

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Converting the prion protein: What makes the protein infectious

Biochimica et biophysica acta, 2007-06, Vol.1772 (6), p.692-703

2007

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Disorder in Milk Proteins: α-Lactalbumin. Part C. Peculiarities of Metal Binding

Current protein & peptide science, 2016-01, Vol.17 (8), p.735-745

2016

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Chemoenzymatic Synthesis of HIV-1 V3 Glycopeptides Carrying Two N-Glycans and Effects of Glycosylation on the Peptide Domain

Journal of organic chemistry, 2005-11, Vol.70 (24), p.9990-9996

2005

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Disorder in Milk Proteins: ?-Lactalbumin. Part B. A Multifunctional Whey Protein Acting as an Oligomeric Molten Globular “Oil Container” in the Anti-Tumorigenic Drugs, Liprotides

Current protein & peptide science, 2016-07, Vol.17 (6), p.612-628

2016

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Disorder in Milk Proteins: ? -Lactalbumin. Part A. Structural Properties and Conformational Behavior

Current protein & peptide science, 2016-06, Vol.17 (4), p.352-367

2016

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α-Synuclein misfolding and Parkinson's disease

Biochimica et biophysica acta, 2012-02, Vol.1822 (2), p.261-285

2012

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Annealing Prion Protein Amyloid Fibrils at High Temperature Results in Extension of a Proteinase K-resistant Core

The Journal of biological chemistry, 2006-01, Vol.281 (4), p.2373-2379

2006

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Site-specific Conformational Studies of Prion Protein (PrP) Amyloid Fibrils Revealed Two Cooperative Folding Domains within Amyloid Structure

The Journal of biological chemistry, 2007-03, Vol.282 (12), p.9090-9097

2007

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Vaccination with a non-human random sequence amyloid oligomer mimic results in improved cognitive function and reduced plaque deposition and micro hemorrhage in Tg2576 mice

Molecular neurodegeneration, 2012-08, Vol.7 (1), p.37-37, Article 37

2012

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Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt‐Jakob Disease

Protein science, 2005-05, Vol.14 (5), p.1222-1232

2005

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Nonpolar Substitution at the C-Terminus of the Prion Protein, a Mimic of the Glycosylphosphatidylinositol Anchor, Partially Impairs Amyloid Fibril Formation

Biochemistry (Easton), 2007-01, Vol.46 (3), p.852-861

2007

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Structural, morphological, and functional diversity of amyloid oligomers

Carbonyl-based blue autofluorescence of proteins and amino acids

Intrinsic disorder in proteins involved in amyotrophic lateral sclerosis

Beyond the excluded volume effects: mechanistic complexity of the crowded milieu

Accelerated neurodegeneration through chaperone-mediated oligomerization of tau

Elevated Ca2+ at the triad junction underlies dysregulation of Ca2+ signaling in dysferlin-null skeletal muscle

Intracellular processing of disease-associated α-synuclein in the human brain suggests prion-like cell-to-cell spread

Fibril specific, conformation dependent antibodies recognize a generic epitope common to amyloid fibrils and fibrillar oligomers that is absent in prefibrillar oligomers

Antibody association in solution: cluster distributions and mechanisms

Conformation dependent monoclonal antibodies distinguish different replicating strains or conformers of prefibrillar Aβ oligomers

Production and biochemical and biophysical characterization of fibrinolytic protease of a Mucor subtilissimus strain isolated from the caatinga biome

Polymorphism and Ultrastructural Organization of Prion Protein Amyloid Fibrils: An Insight from High Resolution Atomic Force Microscopy

High throughput characterization of structural differences between closely related proteins in solution

When Good Goes Awry: The Aggregation of Protein Therapeutics

Converting the prion protein: What makes the protein infectious

Disorder in Milk Proteins: α-Lactalbumin. Part C. Peculiarities of Metal Binding

Chemoenzymatic Synthesis of HIV-1 V3 Glycopeptides Carrying Two N-Glycans and Effects of Glycosylation on the Peptide Domain

Disorder in Milk Proteins: ?-Lactalbumin. Part B. A Multifunctional Whey Protein Acting as an Oligomeric Molten Globular “Oil Container” in the Anti-Tumorigenic Drugs, Liprotides

Disorder in Milk Proteins: ? -Lactalbumin. Part A. Structural Properties and Conformational Behavior

α-Synuclein misfolding and Parkinson's disease

Annealing Prion Protein Amyloid Fibrils at High Temperature Results in Extension of a Proteinase K-resistant Core

Site-specific Conformational Studies of Prion Protein (PrP) Amyloid Fibrils Revealed Two Cooperative Folding Domains within Amyloid Structure

Vaccination with a non-human random sequence amyloid oligomer mimic results in improved cognitive function and reduced plaque deposition and micro hemorrhage in Tg2576 mice

Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt‐Jakob Disease

Nonpolar Substitution at the C-Terminus of the Prion Protein, a Mimic of the Glycosylphosphatidylinositol Anchor, Partially Impairs Amyloid Fibril Formation

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