RELINI, ANNALISA
 Distribuzione geografica
Continente #
EU - Europa 11.195
Totale 11.195
Nazione #
IT - Italia 11.195
Totale 11.195
Città #
Genova 9.138
Rapallo 1.209
Genoa 815
Bordighera 33
Totale 11.195
Nome #
Effect of physical constraints on the mechanisms of membrane fusion: bolaform lipid vesicles as model systems. 163
Amyloid fibrils formation and amorphous aggregation in concanavalin A 160
Changes in the anisotropy of oriented membrane dynamics induced by myelin basic protein 144
Bipolar lipid vesicles: a model for Archaeobacteria membranes 142
Molecular packing parameters of bipolar lipids 140
Stability against temperature and external agents of vesicles composed of archaeal bolaform lipids and egg PC 136
Reversal of protein aggregation provides evidence of multiple aggregated states 135
High photoluminescence efficiency in substituted polythiophene aggregates 134
Different ataxin-3 amyloid aggregates induce intracellular Ca2+ deregulation by different mechanisms in cerebellar granule cells 133
Structure and dynamics of a partially folded protein are decoupled from its mechanism of aggregation 133
The influence of the lipid-protein interaction on the membrane dynamics 132
The (1-63) region of the p53 transactivation domain aggregates in vitro into cytotoxic amyloid assemblies 129
Organization of monolayer-formed membranes made from archaeal ether lipids 127
Embryonic stem and haematopoietic progenitor cells resist to Aβ oligomer toxicity and maintain the differentiation potency in culture 124
A thermodynamic and structural study of myelin basic protein in lipid membrane models 123
An atomic force microscopy investigation of protein crystal surface topography 123
Salt Anions Promote the Conversion of HypF-N into Amyloid-Like Oligomers and Modulate the Structure of the Oligomers and the Monomeric Precursor State 123
Measurement of the surface free energy of streptavidin crystals by atomic force microscopy 121
Natively folded HypF-N and its early amyloid aggregates interact with phospholipid monolayers and destabilize supported phospholipid bilayers 120
Lysine 58-cleaved beta2-microglobulin is not detectable by 2D electrophoresis in ex vivo amyloid fibrils of two patients affected by dialysis-related amyloidosis 119
Proteolytic cleavage of Ser52Pro variant transthyretin triggers its amyloid fibrillogenesis 119
Asymmetric black membranes formed by one monolayer of bipolar lipids at the air-water interface 119
Electroporation in symmetric and asymmetric membranes 117
A protective role for lipid raft cholesterol against amyloid-induced membrane damage in human neuroblastoma cells 117
A causative link between the structure of aberrant protein oligomers and their toxicity. 116
The Relationship between Aggregation and Toxicity of Polyglutamine-Containing Ataxin-3 in the Intracellular Environment of Escherichia coli 113
TDP-43 Inclusion Bodies Formed in Bacteria Are Structurally Amorphous, Non-Amyloid and Inherently Toxic to Neuroblastoma Cells 112
Molecular order in self-assembled multilayers of stearic acid 111
Structure and nanomechanical properties of solvent-cast stearic acid films in liquid: an atomic force microscopy study 110
Influence of subphase viscosity on Langmuir monolayer flow 110
Protein-membrane interaction: effect of myelin basic protein on the dynamics of oriented lipids 109
Enzymatically promoted release of organic molecules linked to magnetic nanoparticles 109
Structure and permeability properties of biomimetic membranes of bolaform archaeal tetraether lipids. 109
Rapid oligomer formation of human muscle acylphosphatase induced by heparan sulfate 109
Agitation and high ionic strength induce amyloidogenesis of a folded PDZ domain in native conditions 108
Toxic effects of expanded ataxin-1 involve mechanical instability of the nuclear membrane 107
Organization of bipolar lipids at the air-water interface 107
Trehalose interacts with phospholipid polar heads in Langmuir monolayers 106
Enzymatically active fibrils generated by the self-assembly of the ApoA-I fibrillogenic domain functionalized with a catalytic moiety 106
Detection of populations of amyloid-like protofibrils with different physical properties 105
Polarized electroluminescence in double layer leds with perpendicularly oriented polymers 105
Amyloid formation from HypF-N under conditions in which the protein is initially in its native state 104
Non-specific interaction of pre-fibrillar amyloid aggregates with glutamatergic receptors results in Ca2+ increase in primary neuronal cells 103
The biological and structural characterization of Mycobacterium tuberculosis UvrA provides novel insights into its mechanism of action 102
Total external reflection X-ray absorption spectroscopy reveals a zinc coordination shell in phospholipid Langmuir-Blodgett films 101
Epigallocatechin-3-gallate and related phenol compounds redirect the amyloidogenic aggregation pathway of ataxin-3 towards non-toxic aggregates and prevent toxicity in neural cells and Caenorhabditis elegans animal model 101
Conformational properties of the aggregation precursor state of HypF-N 101
An EXAFS study of the binding of Cd and Pb ions to lipid films 101
Morphology changes of Si(001) surfaces during wet chemical halogenation 100
Insights into the fate of the N-terminal amyloidogenic polypeptide of ApoA-I in cultured target cells 100
Valinomycin acts as a channel in ultrathin lipid membranes 99
Azurin immobilisation on thiol covered Au(111) 98
Protein conformational perturbations in hereditary amyloidosis: Differential impact of single point mutations in ApoAI amyloidogenic variants 98
The two-fold aspect of the interplay of amyloidogenic proteins with lipid membranes 97
Molecular mechanisms used by chaperones to reduce the toxicity of aberrant protein oligomers 97
D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profile 97
Effects of the known pathogenic mutations on the aggregation pathway of the amyloidogenic peptide of apolipoprotein A-I 97
Biochemical and Electrophysiological Modification of Amyloid Transthyretin on Cardiomyocytes 96
Effects of a lipid environment on the fibrillogenic pathway of the N-terminal polypeptide of human Apolipoprotein A-I, responsible for in vivo amyloid fibril formation 95
α-synuclein oligomers induced by docosahexaenoic acid affect membrane integrity 95
Collagen plays an active role in the aggregation of β2-microglobulin under physio-pathological conditions of dialysis-related amyloidosis 95
Structural and morphological characterization of aggregated species of alpha-synuclein induced by docosahexaenoic acid 93
Force probing of protein crystals: an atomic force microscopy study 93
Polarized electroluminescence in double layer LEDs with perpendicularly oriented polymers 93
What can Atomic Force Microscopy say about Amyloid Aggregates? 92
Monitoring the process of HypF fibrillization and liposome permeabilization by protofibrils 92
A covalent homodimer probing early oligomers along amyloid aggregation 92
Surface shear viscosity and phase transitions of monolayers at the air-water interface 91
Lipid Rafts Mediate Amyloid-Induced Calcium Dyshomeostasis and Oxidative Stress in Alzheimer’s Disease 91
A major role for side-chain polyglutamine hydrogen bonding in irreversible ataxin-3 aggregation 91
The H50Q mutation induces a 10-fold decrease in the solubility of α-synuclein 90
Molecular order in solvent-cast stearic acid films 89
Fibrillogenesis of human β2-microglobulin in three-dimensional silicon microstructures 88
Polarized electroluminescence from double-layer LEDs with active film formed by two perpendicularly oriented polymers. Chromogenic Phenomena in Polymers 88
Myelin basic protein induces changes in the anisotropy of oriented membrane dynamics: An elastic neutron scattering study 87
Ultrastructural organization of ex vivo amyloid fibrils formed by the apolipoprotein A-I Leu174Ser variant: an atomic force microscopy study 87
Effect of molecular chaperones on aberrant protein oligomers in vitro: Super-versus sub-stoichiometric chaperone concentrations 87
Amyloid disaggregation: experiencing hierarchical grades of reversibility 86
Probing the interplay between amyloidogenic proteins and membranes using lipid monolayers and bilayers 83
Nucleophosmin contains amyloidogenic regions that are able to form toxic aggregates under physiological conditions 83
Molecular motions in oriented lipid bilayers containing myelin basic protein: an incoherent neutron scattering study 83
Molecular dynamics simulation of the indentation of a crystalline surface by an atomic force microscope tip 82
Nanoscale Discrimination between Toxic and Nontoxic Protein Misfolded Oligomers with Tip-Enhanced Raman Spectroscopy 81
Optical characterization of polymethylmetacrylate-poly(3-alkylthiophene) Langmuir Blodgett films. 80
Amyloid formation by human muscle acylphosphatase in the presence of heparan sulfate 79
Increased susceptibility to amyloid toxicity in familial Alzheimer's fibroblasts 79
Heparin strongly enhances the formation of beta2-microglobulin amyloid fibrils in the presence of type I collagen 79
Imaging Biostructures with the Atomic Force Microscope 78
Surface structure of poly(3-alkylthiophene) films studied by atomic force microscopy 77
Large proteins have a great tendency to aggregate but a low propensity to form amyloid fibrils 77
Calcium induced interaction and fusion of bipolar lipid vesicles: a fluorescence study 75
Multifunctional fluorescent magnetic nanoparticles for potential biomedical applications 74
Promising applications of multifunctional magnetic nanoparticles in biomedicine 73
Epigallocatechin-3-gallate and tetracycline differently affect ataxin-3 fibrillogenesis and reduce toxicity in spinocerebellar ataxia type 3 model 72
Clinical, radiological and biochemical features of a bilateral buttock amyloidoma emerging after 27 years of haemodialysis 71
Beta-amyloid is different in normal aging and in Alzheimer's disease 71
Abeta(1-42) aggregates into non-toxic amyloid assemblies in the presence of the natural polyphenol oleuropein aglycon 70
Amyloid formation by human muscle acylphosphatase in the presence of heparan sulphate 69
Structural differences between toxic and nontoxic HypF-N oligomers 69
Structure, Folding Dynamics, and Amyloidogenesis of D76N beta2-Microglobulin: ROLES OF SHEAR FLOW, HYDROPHOBIC SURFACES, AND alpha-CRYSTALLIN. 68
Totale 10.165
Categoria #
all - tutte 31.221
article - articoli 29.563
book - libri 0
conference - conferenze 1.061
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 597
Totale 62.442


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019537 0 0 0 0 0 0 0 0 0 0 307 230
2019/20203.190 164 77 144 221 289 349 442 223 276 534 360 111
2020/2021810 64 51 102 49 48 78 65 67 85 76 76 49
2021/20221.582 35 148 197 161 53 81 108 383 56 100 104 156
2022/20231.471 143 109 32 168 192 295 1 113 255 1 137 25
2023/2024594 24 122 11 90 57 125 43 66 45 11 0 0
Totale 11.368