List of works - Maria Andreasen

Aβ1-16 can aggregate and induce the production of reactive oxygen species, nitric oxide, and inflammatory cytokines

scientific article

Coexistence of ribbon and helical fibrils originating from hIAPP(20-29) revealed by quantitative nanomechanical atomic force microscopy

scientific article published on 6 February 2013

Corneal Dystrophy Mutations Drive Pathogenesis by Targeting TGFBIp Stability and Solubility in a Latent Amyloid-forming Domain

scientific article published on 07 March 2018

Cross-talk between individual phenol soluble modulins in <i>S. aureus</i> biofilm enables rapid and efficient amyloid formation

scientific article published on 01 December 2020

Electrostatically-guided inhibition of Curli amyloid nucleation by the CsgC-like family of chaperones

scientific article published on 21 April 2016

Fabrication and Characterization of Reconstituted Silk Microgels for the Storage and Release of Small Molecules

scientific article published on 06 March 2019

High stability and cooperative unfolding of α-synuclein oligomers

scientific article

Human phenotypically distinct TGFBI corneal dystrophies are linked to the stability of the fourth FAS1 domain of TGFBIp

scientific article

Hyperosmotic stress induces cell-dependent aggregation of α-synuclein

scientific article published on 19 February 2019

Imperfect repeats in the functional amyloid protein FapC reduce the tendency to fragment during fibrillation

scientific article published on 12 January 2019

Interactions between misfolded protein oligomers and membranes: A central topic in neurodegenerative diseases?

scientific article

Modulation of fibrillation of hIAPP core fragments by chemical modification of the peptide backbone

Near-complete 1H, 13C, 15N resonance assignments of dimethylsulfoxide-denatured TGFBIp FAS1-4 A546T.

scientific article

Physical Determinants of Amyloid Assembly in Biofilm Formation

scientific article published in 2019

Polymorphic fibrillation of the destabilized fourth fasciclin-1 domain mutant A546T of the Transforming growth factor-β-induced protein (TGFBIp) occurs through multiple pathways with different oligomeric intermediates.

scientific article

Preventing peptide and protein misbehavior.

scientific article published on 20 April 2015

Scaffolded multimers of hIAPP 20–29 peptide fragments fibrillate faster and lead to different fibrils compared to the free hIAPP 20–29 peptide fragment

scientific article published on 15 August 2015

The Importance of Being Capped: Terminal Capping of an Amyloidogenic Peptide Affects Fibrillation Propensity and Fibril Morphology

scientific article published on 31 October 2014

The role of stable α-synuclein oligomers in the molecular events underlying amyloid formation.

scientific article published on 28 February 2014

List of works by Maria Andreasen

Aβ1-16 can aggregate and induce the production of reactive oxygen species, nitric oxide, and inflammatory cytokines

Coexistence of ribbon and helical fibrils originating from hIAPP(20-29) revealed by quantitative nanomechanical atomic force microscopy

Corneal Dystrophy Mutations Drive Pathogenesis by Targeting TGFBIp Stability and Solubility in a Latent Amyloid-forming Domain

Cross-talk between individual phenol soluble modulins in <i>S. aureus</i> biofilm enables rapid and efficient amyloid formation

Electrostatically-guided inhibition of Curli amyloid nucleation by the CsgC-like family of chaperones

Fabrication and Characterization of Reconstituted Silk Microgels for the Storage and Release of Small Molecules

High stability and cooperative unfolding of α-synuclein oligomers

Human phenotypically distinct TGFBI corneal dystrophies are linked to the stability of the fourth FAS1 domain of TGFBIp

Hyperosmotic stress induces cell-dependent aggregation of α-synuclein

Imperfect repeats in the functional amyloid protein FapC reduce the tendency to fragment during fibrillation

Interactions between misfolded protein oligomers and membranes: A central topic in neurodegenerative diseases?

Modulation of fibrillation of hIAPP core fragments by chemical modification of the peptide backbone

Near-complete 1H, 13C, 15N resonance assignments of dimethylsulfoxide-denatured TGFBIp FAS1-4 A546T.

Physical Determinants of Amyloid Assembly in Biofilm Formation

Polymorphic fibrillation of the destabilized fourth fasciclin-1 domain mutant A546T of the Transforming growth factor-β-induced protein (TGFBIp) occurs through multiple pathways with different oligomeric intermediates.

Preventing peptide and protein misbehavior.

Scaffolded multimers of hIAPP 20–29 peptide fragments fibrillate faster and lead to different fibrils compared to the free hIAPP 20–29 peptide fragment

The Importance of Being Capped: Terminal Capping of an Amyloidogenic Peptide Affects Fibrillation Propensity and Fibril Morphology

The role of stable α-synuclein oligomers in the molecular events underlying amyloid formation.