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The expanding amyloid family: Structure, stability, function, and pathogenesis

Cell, 2021-09, Vol.184 (19), p.4857-4873

2021

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Structural Studies of Amyloid Proteins at the Molecular Level

Annual review of biochemistry, 2017-06, Vol.86 (1), p.69-95

2017

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Mechanisms and Functions of Spatial Protein Quality Control

Annual review of biochemistry, 2017-06, Vol.86 (1), p.97-122

2017

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Amyloid nomenclature 2020: update and recommendations by the International Society of Amyloidosis (ISA) nomenclature committee

Amyloid, 2020-10, Vol.27 (4), p.217-222

2020

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The amyloid cascade hypothesis: are we poised for success or failure?

Journal of neurochemistry, 2016-10, Vol.139 (S2), p.237-252

2016

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Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines

Amyloid, 2016-10, Vol.23 (4), p.209-213

2016

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Inhibition of mitochondrial fragmentation protects against Alzheimer's disease in rodent model

Human molecular genetics, 2017-11, Vol.26 (21), p.4118-4131

2017

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WALTZ-DB 2.0: an updated database containing structural information of experimentally determined amyloid-forming peptides

Nucleic acids research, 2020-01, Vol.48 (D1), p.D389-D393

2020

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Functional Amyloid and Other Protein Fibers in the Biofilm Matrix

Journal of molecular biology, 2018-10, Vol.430 (20), p.3642-3656

2018

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Regulated Formation of an Amyloid-like Translational Repressor Governs Gametogenesis

Cell, 2015-10, Vol.163 (2), p.406-418

2015

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Protein misfolding, aggregation and mechanism of amyloid cytotoxicity: An overview and therapeutic strategies to inhibit aggregation

International journal of biological macromolecules, 2019-08, Vol.134, p.1022-1037

2019

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Curli biogenesis: Order out of disorder

Biochimica et biophysica acta, 2014-08, Vol.1843 (8), p.1551-1558

2014

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Amyloid nomenclature 2022: update, novel proteins, and recommendations by the International Society of Amyloidosis (ISA) Nomenclature Committee

Amyloid, 2022-10, Vol.29 (4), p.213-219

2022

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Contagious Aggregation: Transmittable Protein Aggregation in Cellular Communities Initiated by Synthetic Cells

Journal of the American Chemical Society, 2022-03, Vol.144 (11), p.5067-5073

2022

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Amyloid PET Imaging in Self-Identified Non-Hispanic Black Participants of the Anti-Amyloid in Asymptomatic Alzheimer's Disease (A4) Study

Neurology, 2021-03, Vol.96 (11), p.e1491

2021

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Molecular properties underlying regional vulnerability to Alzheimer's disease pathology

Brain (London, England : 1878), 2018-09, Vol.141 (9), p.2755-2771

2018

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Phosphorylation-Mediated Clearance of Amyloid-like Assemblies in Meiosis

Developmental cell, 2018-05, Vol.45 (3), p.392-405.e6

2018

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Cell-to-cell transmission of pathogenic proteins in neurodegenerative diseases

Nature medicine, 2014-02, Vol.20 (2), p.130-138

2014

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The structure and phase of tau: from monomer to amyloid filament

Cellular and molecular life sciences : CMLS, 2021-03, Vol.78 (5), p.1873-1886

2021

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Amyloid precursor protein processing and Alzheimer's disease

Annual review of neuroscience, 2011-01, Vol.34 (1), p.185-204

2011

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Disruption of the CD Loop by Enzymatic Cleavage Promotes the Formation of Toxic Transthyretin Oligomers through a Common Transthyretin Misfolding Pathway

Biochemistry (Easton), 2020-06, Vol.59 (25), p.2319-2327

2020

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Natural product-based amyloid inhibitors

Biochemical pharmacology, 2017-09, Vol.139, p.40-55

2017

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The contribution of neuroinflammation to amyloid toxicity in Alzheimer's disease

Journal of neurochemistry, 2016-02, Vol.136 (3), p.457-474

2016

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The cellular modifier MOAG‐4/SERF drives amyloid formation through charge complementation

The EMBO journal, 2021-11, Vol.40 (21), p.e107568-n/a

2021

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hnRNPDL Phase Separation Is Regulated by Alternative Splicing and Disease-Causing Mutations Accelerate Its Aggregation

Cell reports (Cambridge), 2020-01, Vol.30 (4), p.1117-1128.e5

2020

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The expanding amyloid family: Structure, stability, function, and pathogenesis

Structural Studies of Amyloid Proteins at the Molecular Level

Mechanisms and Functions of Spatial Protein Quality Control

Amyloid nomenclature 2020: update and recommendations by the International Society of Amyloidosis (ISA) nomenclature committee

The amyloid cascade hypothesis: are we poised for success or failure?

Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines

Inhibition of mitochondrial fragmentation protects against Alzheimer's disease in rodent model

WALTZ-DB 2.0: an updated database containing structural information of experimentally determined amyloid-forming peptides

Functional Amyloid and Other Protein Fibers in the Biofilm Matrix

Regulated Formation of an Amyloid-like Translational Repressor Governs Gametogenesis

Protein misfolding, aggregation and mechanism of amyloid cytotoxicity: An overview and therapeutic strategies to inhibit aggregation

Curli biogenesis: Order out of disorder

Amyloid nomenclature 2022: update, novel proteins, and recommendations by the International Society of Amyloidosis (ISA) Nomenclature Committee

Contagious Aggregation: Transmittable Protein Aggregation in Cellular Communities Initiated by Synthetic Cells

Amyloid PET Imaging in Self-Identified Non-Hispanic Black Participants of the Anti-Amyloid in Asymptomatic Alzheimer's Disease (A4) Study

Molecular properties underlying regional vulnerability to Alzheimer's disease pathology

Phosphorylation-Mediated Clearance of Amyloid-like Assemblies in Meiosis

Cell-to-cell transmission of pathogenic proteins in neurodegenerative diseases

The structure and phase of tau: from monomer to amyloid filament

Amyloid precursor protein processing and Alzheimer's disease

Disruption of the CD Loop by Enzymatic Cleavage Promotes the Formation of Toxic Transthyretin Oligomers through a Common Transthyretin Misfolding Pathway

Natural product-based amyloid inhibitors

The contribution of neuroinflammation to amyloid toxicity in Alzheimer's disease

The cellular modifier MOAG‐4/SERF drives amyloid formation through charge complementation

hnRNPDL Phase Separation Is Regulated by Alternative Splicing and Disease-Causing Mutations Accelerate Its Aggregation

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