Lista de obras - Maria Andreasen - Dominio Público Uruguay

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

artículo científico publicado en 2011

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

artículo científico publicado en 2013

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

artículo científico publicado en 2018

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

artículo científico publicado en 2020

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

artículo científico publicado en 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

artículo científico publicado en 2014

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

artículo científico publicado en 2010

Hyperosmotic stress induces cell-dependent aggregation of α-synuclein

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2015

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.

artículo científico publicado en 2015

Physical Determinants of Amyloid Assembly in Biofilm Formation

artículo científico publicado en 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.

artículo científico publicado en 2012

Preventing peptide and protein misbehavior.

artículo científico publicado en 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

artículo científico publicado en 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.

artículo científico publicado en 2014

Lista de obras de 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.