IRIS Institutional Research Information System

Dalla Serra, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 3.632
EU - Europa 1.812
AS - Asia 713
AF - Africa 31
Continente sconosciuto - Info sul continente non disponibili 26
SA - Sud America 8
OC - Oceania 7
Totale 6.229
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Nazione #
US - Stati Uniti d'America 3.612
SE - Svezia 432
DE - Germania 417
UA - Ucraina 340
HK - Hong Kong 208
FI - Finlandia 196
SG - Singapore 189
IE - Irlanda 114
VN - Vietnam 107
CN - Cina 103
GB - Regno Unito 89
IN - India 64
RU - Federazione Russa 60
IT - Italia 53
BE - Belgio 34
FR - Francia 30
ZA - Sudafrica 27
EU - Europa 26
CZ - Repubblica Ceca 21
CA - Canada 20
IR - Iran 17
LT - Lituania 9
ES - Italia 7
BR - Brasile 5
CH - Svizzera 5
IL - Israele 5
AU - Australia 4
EG - Egitto 3
JP - Giappone 3
NZ - Nuova Zelanda 3
AR - Argentina 2
IQ - Iraq 2
KR - Corea 2
LA - Repubblica Popolare Democratica del Laos 2
NL - Olanda 2
PH - Filippine 2
PL - Polonia 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
AZ - Azerbaigian 1
CY - Cipro 1
DK - Danimarca 1
KZ - Kazakistan 1
LB - Libano 1
MA - Marocco 1
PE - Perù 1
TH - Thailandia 1
Totale 6.229
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Città #
Chandler 860
Jacksonville 737
Hong Kong 206
Ashburn 199
Wilmington 177
Singapore 165
Boardman 155
Dublin 112
Dong Ket 106
Ann Arbor 105
Dearborn 102
Helsinki 95
Kronberg 95
New York 92
Woodbridge 64
Brooklyn 48
Beijing 44
Pune 36
Los Angeles 34
Phoenix 31
Brussels 30
Santa Clara 30
Shanghai 29
Trento 28
Seattle 27
Munich 24
Brno 19
Secaucus 18
Houston 16
Falls Church 12
Miami 12
Toronto 12
Norwalk 11
Cologne 10
Leawood 9
Portland 9
Ardabil 8
San Mateo 8
Frankfurt am Main 7
London 7
Redwood City 7
Saint Petersburg 7
Augusta 6
Monmouth Junction 6
St Petersburg 6
Auburn Hills 5
Falkenstein 5
Hanover 5
Nanjing 5
Ottawa 5
Zanjan 5
Bangalore 4
Charlotte 4
Cheyenne 4
Redmond 4
Zurich 4
Cairo 3
Des Moines 3
Guangzhou 3
Gunzenhausen 3
Hefei 3
Milan 3
Roussillon 3
Stirling 3
Tokyo 3
Baghdad 2
Barcelona 2
Buenos Aires 2
Buffalo 2
Fuzhou 2
Gent 2
Ghent 2
Hyderabad 2
Jinan 2
Kunming 2
Madrid 2
Manila 2
Mountain View 2
Mumbai 2
Sacramento 2
Sydney 2
São Luís 2
Tashkent 2
Turin 2
Vientiane 2
Wrexham 2
Wuhan 2
Xian 2
Almaty 1
Andover 1
Auckland 1
Bad Muenstereifel 1
Baku 1
Berkeley 1
Borgo Valsugana 1
Brisbane 1
Castellón 1
Central District 1
Changsha 1
Costa Mesa 1
Totale 3.956
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Nome #
Combinatorial plasma deposition of C-based films to test cell adhesion 107
A novel mechanism of pore formation: membrane penetration by the N-terminal amphipathic region of equinatoxin. 99
Bio-hybrid interfaces to study neuromorphic functionalities: New multidisciplinary evidences of cell viability on poly(anyline) (PANI), a semiconductor polymer with memristive properties 93
Binding of antibodies to functional epitopes on the pore formed by Escherichia coli hemolysin in cells and model membranes. 91
Alpha-synuclein pore forming activity upon membrane association 90
para-sulfonato-calix[n]arenes inhibit staphylococcal bicomponent leukotoxins by supramolecular interactions. 83
A fluorimetric assay for the effects of cytolytic toxins on the transport properties of resealed erythrocyte ghosts. 83
Bacterial hemolysins and leukotoxins affect target cells by forming large exogenous pores into their plasma membrane: Escherichia coli hemolysin A as a case example. 82
Biochemical and cytotoxic properties of conjugates of transferrin with equinatoxin II, a cytolysin from a sea anemone. 81
γ-Hemolysin Oligomeric Structure and Effect of its Formation on Supported Lipid Bilayers: an AFM Investigation 81
N-terminal deletion affects catalytic activity of saporin toxin 80
Antiparasite activity of sea-anemone cytolysins on Giardia duodenalis and specific targeting with anti-Giardia antibodies. 78
N-terminal-bearing peptide derived from the pore-forming protein Sticholysin II interacts with lipid bilayer. 74
Effects of lipid composition on membrane permeabilization by two cytolysins of the sea anemone Stichodactyla helianthus, St I and St II 74
Anticandida activity is retained in P-113, a 12-amino-acid fragment of histatin 5. 74
Cytotoxic activity of a tumor protease-activated pore-forming toxin. 73
A XAS study of the geometrical arrangement of Cu(II)-binding octarepeat peptides 72
Activation energy of the cardiac Na+/Ca2+ exchanger in sarcolemmal vesicles and reconstituted proteoliposomes. 71
Human perforin employs different avenues to damage membranes 70
Effects of lipid composition on membrane permeabilization by sticholysin I and II, two cytolysins of the sea anemone Stichodactyla helianthus. 69
Biopolymer surface coatings for the treatment of staphylococcal infections 69
Structural features of distinctin affecting peptide biological and biochemical properties 66
A tumor protease-activated conjugate based on a sea anemone toxin: its cytotoxic activity on cancer cells. 66
A tumor protease-activated pore forming toxin as a specific anticancer tool 66
Use of nanostructures for cancer care 66
Homologous versus heterologous interactions in the pore of bicomponent staphylococcal gamma-hemolysins 66
Anomalously high aggregation level of the polyene antibiotic amphotericin B in acidic medium: implications for the biological action. 65
Interaction with model membranes and pore formation by human stefin B; studying the native and prefibrillar states 65
pH dependence of listeriolysin O aggregation and pore-forming ability 65
Multifunctional branched gold-carbon nanotube hybrid for cell imaging and drug delivery 65
Potential inhibitors of Staphylococccus aureus bi-components γ-hemolysins 64
Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures. 64
Liposomes in the study of pore-forming toxins. 64
Synthesis of plasmonic gold/carbon nanotubes hybrid structures for cell imaging and drug delivery 64
Construction of the I18C-EqtII – avidin conjugate via a biotinylated peptide and its cytotoxic activity. 63
Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer 63
Structure and activity of the N-terminal region of the eukaryotic cytolysin equinatoxin II. 62
Listeriolysin O pore-forming abilities on lipid membranes 62
A molecular pin to study the dynamic of á-barrel formation in Pore Forming Toxins on erythrocytes: a sliding model 62
HOW A METABOLITE OF DOPAMINE CAN TRANSFORM ALPHA­SYNUCLEIN IN AN ENDOTOXIN 62
The Influence of Membrane Lipids in Staphylococcus aureus Gamma-Hemolysins Pore Formation 61
Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components. 61
Synthesis and characterization of Raman active gold nanoparticles 61
Characterization of anticholinesterase-active 3-alkylpyridinium polymers from the marine sponge Reniera sarai in aqueous solutions. 61
Self-potentiation of ligand-toxin conjugates containing ricin A chain fused with viral structures. 61
Distinction between pore assembly by staphylococcal α-toxin versus leukotoxins 60
Peptides derived from apoptotic Bax and Bid reproduce the poration activity of the parent full-length proteins 60
Construction of EqtII mutants immunoconjugates and characterization of their cytotoxic activity 59
Fuscopeptins, antimicrobial lipodepsipeptides from Pseudomonas fuscovaginae, are channel forming peptides active on biological and model membranes 59
A fluorescence-based assay for the reductase activity of protein disulfide isomerase 59
Tolaasin I, Lipodepsipeptides from Pseudomonas reactans and Pseudomonas tolaasii, permeabilize model membranes 59
The mode of action of bicomponent gamma-hemolysins of Staphylococcus aureus. 58
Sizing the radius of the pore formed in erythrocytes and lipid vesicles by the toxin sticholysin I from the sea anemone Stichodactyla helianthus. 57
Cysteine-scanning mutagenesis of an eukaryotic pore-forming toxin from sea anemone: topology in lipid membranes. 57
Mechanism of membrane permeabilization by sticholysin I, a cytolysin isolated from the venom of the sea anemone Stichodactyla helianthus. 57
THE STAPHYLOCOCCAL PANTON AND VALENTINE LEUKOCIDIN AND gamma-HAEMOLYSIN HLGC/HLGB SHARE C5AR AS A RECEPTOR, BUT OPERATE DIVERSE INTRACELLULAR ACTIVITIES IN HUMAN POLYMORPHONUCLEAR NEUTROPHILS 57
Les leucotoxines de staphylocoque: de l'investigation bio-structurale vers la notion d'inhibiteurs 56
Site directed mutagenesis to assess the binding capacity of class S protein of Staphylococcus aureus leucotoxins to the surface of polymorphonuclear cells 56
The interaction of Staphylococcus aureus bi-component gamma-hemolysins and leucocidins with cells and lipid membranes. 56
Perforin activity at membranes leads to invaginations and vesicle formation 55
Mode of action of beta-barrel pore-forming toxins of the staphylococcal alpha-hemolysin family. 55
Binding of antibiotic amphotericin B to lipid membranes: Monomolecular layer technique and linear dichroism-FTIR studies 55
Pore-forming peptides and protein toxins 55
Combinatorial Plasma Polymerization Approach to Produce Thin Films for Testing Cell proliferation 55
Perforin oligomers form arcs in cellular membranes: a locus for intracellular delivery of granzymes 55
Neuronal firing modulation by a membrane-targeted photoswitch 55
Directly assessment of drug release dynamics from gold nanoparticles 54
The adsorption of Pseudomonas aeruginosa exotoxin A to phospholipid monolayers is controlled by pH and surface potential. 54
Identifying the Minimal Copper- and Zinc-binding Site Sequence in Amyloid-beta Peptides 53
Molecular mechanism of pore formation by actinoporins 53
pH-activated doxorubicin release from polyelectrolyte complex layer coated mesoporous silica nanoparticles 53
Lipid modulation on structure and function abilities of two Cholesterol--Dependent Cytolysins 53
Protein engineering modulates the transport properties and ion selectivity of the pores formed by staphylococcal gamma-haemolysins in lipid membranes. 52
Intrinsic tryptophan fluorescence of equinatoxin II, a pore-forming polypeptide from the sea anemone Actinia equina L, monitors its interaction with lipid membranes. 52
Membrane permeabilizing activity of linusitin from flax seed 51
Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components. 51
Effects of calcium and protons on the secondary structure of the nodulation protein NodO from Rhizobium leguminosarum biovar viciae. 51
Plasticity of Listeriolysin O Pores Revealed by Mutagenesis of a Unique Histidine 51
In vitro investigation of doxorubicin release from gold nanoparticles coated by polyelectrolyte multilayers 51
Metal binding in amyloids beta peptides shows both intra- and inter-peptide modes 50
Molecular modifications of the pore forming gamma hemolysins from Staphylococcus aureus 49
The influence of membrane lipids in Staphylococcus aureus gamma-hemolysins pore formation 49
Reversal of charge selectivity in transmembrane protein pores by using noncovalent molecular adapters. 49
Biological Characterisation of WLIP produced by Pseudomonas reactans strain NCPPB1311 49
Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: Cormycin A 49
A multidisciplinary approach to study the functional properties of neuron-like cell models constituting a living bio-hybrid system: SH-SY5Y cells adhering to PANI substrate 49
The equinatoxin N-terminus is transferred across planar lipid membranes and helps to stabilize the transmembrane pore. 48
EPR and FTIR studies reveal the importance of highly ordered sterol-enriched membrane domains for ostreolysin activity. 48
Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores 48
Deposito della beta-amiloide sulla membrana cellulare: ruolo degli ioni metallici e dei radicali liberi 47
Conductive properties and gating of channels formed by syringopeptin 25A, a bioactive lipodepsipeptide from Pseudomonas syringae pv. syringae, in planar lipid membranes. 47
Ion channels and bacterial infection: the case of beta-barrel pore-forming protein toxins of Staphylococcus aureus. 47
The interaction of lipodepsipeptide toxins from Pseudomonas syringae pv. syringae with biological and model membranes: a comparison of syringotoxin, syringomycin, and two syringopeptins. 46
Sea anemone cytolysins as toxic component of immunotoxins 46
Metal binding in amyloid beta-peptides shows intra- and inter-peptide coordination modes. 45
Plasma assisted surface treatments of biomaterials 45
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions 43
The role of membrane lipid composition for the activity of Staphylococcus aureus gamma-hemolysins 43
XAS STUDIES OF CU(II) AND ZN(II) BINDING SITE IN AMYLOID PEPTIDES 43
Organization of two-component monomolecular layers formed with dipalmitoylphosphatidylcholine and the carotenoid pigment, canthaxanthin 40
Totale 6.073
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Categoria #
all - tutte 38.980
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 38.980
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020739 0 0 0 5 142 74 127 20 120 54 127 70
2020/20211.024 115 0 113 72 107 20 125 5 3 185 103 176
2021/2022521 22 13 5 106 13 11 7 79 42 26 61 136
2022/20231.581 32 128 27 300 80 269 8 108 407 135 53 34
2023/20241.066 76 31 120 52 88 162 40 135 14 204 10 134
2024/2025427 30 62 329 6 0 0 0 0 0 0 0 0
Totale 6.267