Hanna Willander

Molecular biomarkers in idiopathic pulmonary fibrosis

Protein Misfolding, Amyloid Formation, and Human Disease: A Summary of Progress Over the Last Decade

Efficient protein production inspired by how spiders make silk

Idiopathic pulmonary fibrosis

Kinetic fingerprints differentiate the mechanisms of action of anti-Aβ antibodies

Idiopathic pulmonary fibrosis

Systemic amyloidosis

The S/T-Rich Motif in the DNAJB6 Chaperone Delays Polyglutamine Aggregation and the Onset of Disease in a Mouse Model

Design of amyloidogenic peptide traps

Amyloid fibril protein nomenclature: 2012 recommendations from the Nomenclature Committee of the International Society of Amyloidosis

Bri2 BRICHOS client specificity and chaperone activity are governed by assembly state

A molecular chaperone breaks the catalytic cycle that generates toxic Aβ oligomers

Charge‐Separated Fmoc‐Peptide β‐Sheets: Sequence‐Secondary Structure Relationship for Arranging Charged Side Chains on Both Sides

Supramolecular Hydrogelators and Hydrogels: From Soft Matter to Molecular Biomaterials

Exosomal cellular prion protein drives fibrillization of amyloid beta and counteracts amyloid beta‐mediated neurotoxicity

Klebsiella pneumoniae: Going on the Offense with a Strong Defense

Natural Anti-Infective Pulmonary Proteins: In Vivo Cooperative Action of Surfactant Protein SP-A and the Lung Antimicrobial Peptide SP-BN

Pathogenesis of Idiopathic Pulmonary Fibrosis

The biology , function , and biomedical applications of exosomes

On the lag phase in amyloid fibril formation

Genetic studies provide clues on the pathogenesis of idiopathic pulmonary fibrosis

Lost after translation: insights from pulmonary surfactant for understanding the role of alveolar epithelial dysfunction and cellular quality control in fibrotic lung disease

The Biomedical Use of Silk: Past, Present, Future

Surfactant Protein B Propeptide Contains a Saposin-Like Protein Domain with Antimicrobial Activity at Low pH

BRICHOS Domains Efficiently Delay Fibrillation of Amyloid β-Peptide

Separate mechanisms act concurrently to shed and release the prion protein from the cell

Conformational preferences of non-polar amino acid residues: An additional factor in amyloid formation

BRICHOS domain associated with lung fibrosis, dementia and cancer – a chaperone that prevents amyloid fibril formation?

High-resolution structure of a BRICHOS domain and its implications for anti-amyloid chaperone activity on lung surfactant protein C