| scholarly article | Q13442814 |
| P2093 | author name string | Massimo Stefani | |
| Cristina Cecchi | |||
| P304 | page(s) | 30-43 | |
| P577 | publication date | 2013-06-11 | |
| P1433 | published in | Biophysical Chemistry | Q15760978 |
| P1476 | title | The amyloid-cell membrane system. The interplay between the biophysical features of oligomers/fibrils and cell membrane defines amyloid toxicity | |
| P478 | volume | 182 |
| Q42089651 | Amyloids, melanins and oxidative stress in melanomagenesis |
| Q41074727 | Binding affinity of amyloid oligomers to cellular membranes is a generic indicator of cellular dysfunction in protein misfolding diseases |
| Q30374807 | Differential effects of glycation on protein aggregation and amyloid formation. |
| Q35793465 | Endocytosed 2-Microglobulin Amyloid Fibrils Induce Necrosis and Apoptosis of Rabbit Synovial Fibroblasts by Disrupting Endosomal/Lysosomal Membranes: A Novel Mechanism on the Cytotoxicity of Amyloid Fibrils |
| Q39221178 | Force spectroscopy reveals the presence of structurally modified dimers in transthyretin amyloid annular oligomers. |
| Q92070015 | Functional Amyloids and their Possible Influence on Alzheimer Disease |
| Q42828706 | Glycation of Wild-Type Apomyoglobin Induces Formation of Highly Cytotoxic Oligomeric Species |
| Q47647902 | Insights into protein misfolding and aggregation enabled by solid-state NMR spectroscopy. |
| Q40851188 | Interaction of toxic and non-toxic HypF-N oligomers with lipid bilayers investigated at high resolution with atomic force microscopy. |
| Q30402710 | Membrane remodeling by amyloidogenic and non-amyloidogenic proteins studied by EPR. |
| Q47330831 | Membrane-mediated amyloid deposition of human islet amyloid polypeptide |
| Q37622574 | Misfolded polyglutamine, polyalanine, and superoxide dismutase 1 aggregate via distinct pathways in the cell |
| Q47625995 | Molecular dynamics simulations of β2-microglobulin interaction with hydrophobic surfaces. |
| Q38771098 | Molecular pathogenesis of human amyloidosis: Lessons from β2 -microglobulin-related amyloidosis |
| Q39808570 | Non-Invasive Imaging of Amyloid Deposits in a Mouse Model of AGel Using (99m)Tc-Modified Nanobodies and SPECT/CT. |
| Q38798563 | Polyglutamine aggregates impair lipid membrane integrity and enhance lipid membrane rigidity |
| Q91730805 | Probing the Origin of the Toxicity of Oligomeric Aggregates of α-Synuclein with Antibodies |
| Q38497014 | Proteotoxicity and cardiac dysfunction |
| Q28082714 | Role of Different Alpha-Synuclein Strains in Synucleinopathies, Similarities with other Neurodegenerative Diseases |
| Q34519909 | Sequestration of cellular interacting partners by protein aggregates: implication in a loss-of-function pathology |
| Q39338479 | The architecture of amyloid-like peptide fibrils revealed by X-ray scattering, diffraction and electron microscopy |
| Q38343014 | The effect of glycosaminoglycans (GAGs) on amyloid aggregation and toxicity |
| Q36327601 | Thermodynamic and fibril formation studies of full length immunoglobulin light chain AL-09 and its germline protein using scan rate dependent thermal unfolding |
| Q51730305 | Toxic HypF-N Oligomers Selectively Bind the Plasma Membrane to Impair Cell Adhesion Capability. |
| Q100750265 | Toxic oligomers of the amyloidogenic HypF-N protein form pores in mitochondrial membranes |
| Q35696876 | Two distinct β-sheet structures in Italian-mutant amyloid-beta fibrils: a potential link to different clinical phenotypes |
| Q58691616 | d-Amino Acid Pseudopeptides as Potential Amyloid-Beta Aggregation Inhibitors |
Search more.