(Q37871074)

24 August 2017

1 reference

title

Mechanisms of amyloid fibril formation--focus on domain-swapping (English)

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24 August 2017

author

Rosemary A Staniforth

6

object named as

Rosemary A Staniforth

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24 August 2017

Eva Žerovnik

1

1 reference

24 August 2017

Veronika Stoka

2

1 reference

24 August 2017

Andreja Mirtič

3

1 reference

24 August 2017

Gregor Gunčar

4

1 reference

24 August 2017

Jože Grdadolnik

5

1 reference

24 August 2017

Dušan Turk

7

1 reference

24 August 2017

Vito Turk

8

1 reference

24 August 2017

language of work or name

English

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publication date

31 May 2011

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24 August 2017

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24 August 2017

volume

278

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24 August 2017

issue

13

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24 August 2017

page(s)

2263-2282

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Protein aggregation in the brain: the molecular basis for Alzheimer's and Parkinson's diseases

24 August 2017

cites work

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Aging and regulated protein degradation: who has the UPPer hand?

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Autophagy gone awry in neurodegenerative diseases

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Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis

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Models of beta-amyloid ion channels in the membrane suggest that channel formation in the bilayer is a dynamic process

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Are amyloid diseases caused by protein aggregates that mimic bacterial pore-forming toxins?

21 January 2018

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Protein aggregation probed by two-photon fluorescence correlation spectroscopy of native tryptophan

21 January 2018

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From the globular to the fibrous state: protein structure and structural conversion in amyloid formation.

21 January 2018

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Methods for structural characterization of prefibrillar intermediates and amyloid fibrils.

21 January 2018

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Beta(2)-microglobulin and its deamidated variant, N17D form amyloid fibrils with a range of morphologies in vitro

21 January 2018

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Self-propagating, molecular-level polymorphism in Alzheimer's beta-amyloid fibrils

21 January 2018

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Molecular structure of amyloid fibrils: insights from solid-state NMR.

21 January 2018

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Mapping the core of the beta(2)-microglobulin amyloid fibril by H/D exchange

21 January 2018

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Structural characterization of a soluble amyloid beta-peptide oligomer.

21 January 2018

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Structural classification of toxic amyloid oligomers

21 January 2018

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Pauling and Corey's alpha-pleated sheet structure may define the prefibrillar amyloidogenic intermediate in amyloid disease

21 January 2018

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Principles of protein folding in the cellular environment

21 January 2018

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Hsp104 targets multiple intermediates on the amyloid pathway and suppresses the seeding capacity of Abeta fibrils and protofibrils

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Remodeling of protein aggregates by Hsp104.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Applying Hsp104 to protein-misfolding disorders.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Dominant forces in protein folding

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Some factors in the interpretation of protein denaturation

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Electrostatic effects in proteins

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Areas, volumes, packing and protein structure

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Hydrogen bonding in globular proteins

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Contribution of hydration to protein folding thermodynamics. I. The enthalpy of hydration

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Interaction of the peptide bond with solvent water: a vapor phase analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Role of main-chain electrostatics, hydrophobic effect and side-chain conformational entropy in determining the secondary structure of proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Intrinsic backbone preferences are fully present in blocked amino acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Determination of conformational preferences of dipeptides using vibrational spectroscopy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Energetics of the interaction between water and the helical peptide group and its role in determining helix propensities

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Role of backbone solvation and electrostatics in generating preferred peptide backbone conformations: Distributions of phi

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Formation of partially ordered oligomers of amyloidogenic hexapeptide (NFGAIL) in aqueous solution observed in molecular dynamics simulations

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

The role of side-chain interactions in the early steps of aggregation: Molecular dynamics simulations of an amyloid-forming peptide from the yeast prion Sup35

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

De novo designed peptide-based amyloid fibrils

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Hierarchical self-assembly of chiral rod-like molecules as a model for peptide beta -sheet tapes, ribbons, fibrils, and fibers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid fibril-like structure underlies the aggregate structure across the pH range for beta-lactoglobulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Direct conversion of an oligopeptide from a beta-sheet to an alpha-helix: a model for amyloid formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Folding and amyloid-fibril formation for a series of human stefins' chimeras: any correlation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

In vitro study of stability and amyloid-fibril formation of two mutants of human stefin B (cystatin B) occurring in patients with EPM1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

The alternative conformations of amyloidogenic proteins and their multi-step assembly pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Evolution of amyloid: what normal protein folding may tell us about fibrillogenesis and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid fibrillogenesis: themes and variations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid-fibril formation. Proposed mechanisms and relevance to conformational disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid fibril formation by an SH3 domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

A systematic exploration of the influence of the protein stability on amyloid fibril formation in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

The yeast prion Ure2p retains its native alpha-helical conformation upon assembly into protein fibrils in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Lithostathine quadruple-helical filaments form proteinase K-resistant deposits in Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid fibrils from muscle myoglobin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Prediction of amyloid fibril-forming proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Elucidation of primary structure elements controlling early amyloid beta-protein oligomerization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Mechanism of prion propagation: amyloid growth occurs by monomer addition

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Alternative assembly pathways of the amyloidogenic yeast prion determinant Sup35-NM

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Conformational conversion may precede or follow aggregate elongation on alternative pathways of amyloid protofibril formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Polyglutamine disruption of the huntingtin exon 1 N terminus triggers a complex aggregation mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Molecular-level secondary structure, polymorphism, and dynamics of full-length alpha-synuclein fibrils studied by solid-state NMR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Hierarchical assembly of beta2-microglobulin amyloid in vitro revealed by atomic force microscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Natural beta-sheet proteins use negative design to avoid edge-to-edge aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Rationalization of the effects of mutations on peptide and protein aggregation rates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Prediction of "aggregation-prone" and "aggregation-susceptible" regions in proteins associated with neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Short amino acid stretches can mediate amyloid formation in globular proteins: the Src homology 3 (SH3) case

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Prediction of sequence-dependent and mutational effects on the aggregation of peptides and proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

The 3D profile method for identifying fibril-forming segments of proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Identifying the amylome, proteins capable of forming amyloid-like fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Mechanism of amyloidogenesis: nucleation-dependent fibrillation versus double-concerted fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Competition between folding, native-state dimerisation and amyloid aggregation in beta-lactoglobulin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Molecular mechanisms of amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Self-replication and scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Novel proteinaceous infectious particles cause scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Polar zippers: their role in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

A census of glutamine/asparagine-rich regions: implications for their conserved function and the prediction of novel prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Nucleated conformational conversion and the replication of conformational information by a prion determinant

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

alpha-synuclein fibrillogenesis is nucleation-dependent. Implications for the pathogenesis of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Kinetic theory of fibrillogenesis of amyloid beta-protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid β-protein aggregation produces highly reproducible kinetic data and occurs by a two-phase process

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

A critical role for amino-terminal glutamine/asparagine repeats in the formation and propagation of a yeast prion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Assembly of amyloid protofibrils via critical oligomers--a novel pathway of amyloid formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Conversion of yeast phosphoglycerate kinase into amyloid-like structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

The assembly of amyloidogenic yeast sup35 as assessed by scanning (atomic) force microscopy: an analogy to linear colloidal aggregation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Granular assembly of alpha-synuclein leading to the accelerated amyloid fibril formation with shear stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Phylogenomic analysis of the cystatin superfamily in eukaryotes and prokaryotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Cystatins: biochemical and structural properties, and medical relevance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Induction of autophagy by cystatin C: a mechanism that protects murine primary cortical neurons and neuronal cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

The CST3 B haplotype is associated with frontotemporal lobar degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Alzheimer disease-associated cystatin C variant undergoes impaired secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Abnormal distribution of cathepsin proteinases and endogenous inhibitors (cystatins) in the hippocampus of patients with Alzheimer's disease, parkinsonism-dementia complex on Guam, and senile dementia and in the aged.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Cystatin B deficiency sensitizes neurons to oxidative stress in progressive myoclonus epilepsy, EPM1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Human cystatin C, an amyloidogenic protein, dimerizes through three-dimensional domain swapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Three-dimensional domain swapping in the folded and molten-globule states of cystatins, an amyloid-forming structural superfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Essential role of proline isomerization in stefin B tetramer formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid fibril formation by human stefin B: influence of the initial pH-induced intermediate state

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Different propensity to form amyloid fibrils by two homologous proteins-Human stefins A and B: searching for an explanation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Human stefin B readily forms amyloid fibrils in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

The major transition state in folding need not involve the immobilization of side chains

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

A hinge region cis-proline in ribonuclease A acts as a conformational gatekeeper for C-terminal domain swapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

PABMB Lecture. Protein dynamics, folding and misfolding: from basic physical chemistry to human conformational diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

3D domain swapping: as domains continue to swap

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Crystal structure of the human prion protein reveals a mechanism for oligomerization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Identification of a subunit interface in transthyretin amyloid fibrils: evidence for self-assembly from oligomeric building blocks

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Temperature dependence of the nucleation constant rate in beta amyloid fibrillogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Characterization of the nucleation barriers for protein aggregation and amyloid formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

The mechanism of amyloid-fibril formation by stefin B: temperature and protein concentration dependence of the rates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Prevention of domain swapping inhibits dimerization and amyloid fibril formation of cystatin C: use of engineered disulfide bridges, antibodies, and carboxymethylpapain to stabilize the monomeric form of cystatin C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Non-3D domain swapped crystal structure of truncated zebrafish alphaA crystallin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Thermal aggregation of ribonuclease A. A contribution to the understanding of the role of 3D domain swapping in protein aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Three-dimensional domain swapping in p13suc1 occurs in the unfolded state and is controlled by conserved proline residues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Essential role of Pro 74 in stefin B amyloid-fibril formation: dual action of cyclophilin A on the process

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Oligomeric assembly of native-like precursors precedes amyloid formation by beta-2 microglobulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

A native to amyloidogenic transition regulated by a backbone trigger

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid formation under physiological conditions proceeds via a native-like folding intermediate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Delineating the conformational elements responsible for Cu(2+)-induced oligomerization of beta-2 microglobulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

A regulatable switch mediates self-association in an immunoglobulin fold

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

3D domain swapping: a mechanism for oligomer assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

A domain-swapped RNase A dimer with implications for amyloid formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Domain swapping in N-truncated human cystatin C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid fibril formation by human stefins: Structure, mechanism & putative functions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Cystatin forms a tetramer through structural rearrangement of domain-swapped dimers prior to amyloidogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Folding of Cu/Zn superoxide dismutase suggests structural hotspots for gain of neurotoxic function in ALS: parallels to precursors in amyloid disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Protein folding and three-dimensional domain swapping: a strained relationship?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Design of three-dimensional domain-swapped dimers and fibrous oligomers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Runaway domain swapping in amyloid-like fibrils of T7 endonuclease I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

β2-microglobulin forms three-dimensional domain-swapped amyloid fibrils with disulfide linkages

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Fibrillogenic oligomers of human cystatin C are formed by propagated domain swapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Exclusion of the native alpha-helix from the amyloid fibrils of a mixed alpha/beta protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Analysis of amylin cleavage products provides new insights into the amyloidogenic region of human amylin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Crystal structure of human cystatin C stabilized against amyloid formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

A mathematical model of the kinetics of beta-amyloid fibril growth from the denatured state

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Mechanisms of protein fibril formation: nucleated polymerization with competing off-pathway aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Size and morphology of toxic oligomers of amyloidogenic proteins: a case study of human stefin B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Protein aggregation in disease: a role for folding intermediates forming specific multimeric interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

For protein misassembly, it's the "I" decade

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Natively unfolded proteins: a point where biology waits for physics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Intrinsic disorder in proteins associated with neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Conformational constraints for amyloid fibrillation: the importance of being unfolded

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Models of amyloid seeding in Alzheimer's disease and scrapie: mechanistic truths and physiological consequences of the time-dependent solubility of amyloid proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Polyglutamine pathogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Atomic force microscopy analysis of the Huntington protein nanofibril formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Protein folding in the landscape perspective: chevron plots and non-Arrhenius kinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Cis-trans isomerization at a proline opens the pore of a neurotransmitter-gated ion channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Prolyl-isomerase Pin1 accumulates in lewy bodies of parkinson disease and facilitates formation of alpha-synuclein inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

The prolyl isomerase Pin1 regulates amyloid precursor protein processing and amyloid-beta production

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Protofibril formation of amyloid beta-protein at low pH via a non-cooperative elongation mechanism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Instantaneous amyloid fibril formation of alpha-synuclein from the oligomeric granular structures in the presence of hexane

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

What factor drives the fibrillogenic association of β-sheets?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Accessing the global minimum conformation of stefin A dimer by annealing under partially denaturing conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

3D domain-swapped human cystatin C with amyloidlike intermolecular β-sheets

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

Amyloid fibril formation by human stefin B: influence of pH and TFE on fibril growth and morphology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2011.08149.X

10.1111/J.1742-4658.2011.08149.X

21 January 2018

Identifiers

DOI

1 reference

24 August 2017

1 reference