IRIS Institutional Research Information System

Dalla Serra, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 5.022
EU - Europa 3.316
AS - Asia 2.088
SA - Sud America 623
AF - Africa 61
Continente sconosciuto - Info sul continente non disponibili 27
OC - Oceania 7
Totale 11.144
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Nazione #
US - Stati Uniti d'America 4.921
RU - Federazione Russa 1.094
SG - Singapore 966
BR - Brasile 539
DE - Germania 510
SE - Svezia 451
CN - Cina 396
UA - Ucraina 346
HK - Hong Kong 278
FI - Finlandia 235
VN - Vietnam 167
GB - Regno Unito 138
NL - Olanda 119
IE - Irlanda 114
IN - India 103
IT - Italia 88
CA - Canada 69
FR - Francia 69
ZA - Sudafrica 44
AR - Argentina 38
BD - Bangladesh 38
BE - Belgio 37
PL - Polonia 35
EU - Europa 26
CZ - Repubblica Ceca 22
MX - Messico 21
ES - Italia 19
IR - Iran 19
JP - Giappone 19
IQ - Iraq 18
LT - Lituania 18
TR - Turchia 17
EC - Ecuador 10
AE - Emirati Arabi Uniti 9
AT - Austria 9
EG - Egitto 8
PK - Pakistan 8
SA - Arabia Saudita 8
UZ - Uzbekistan 8
VE - Venezuela 8
IL - Israele 7
PE - Perù 7
UY - Uruguay 7
CO - Colombia 6
CH - Svizzera 5
PY - Paraguay 5
AU - Australia 4
AZ - Azerbaigian 3
HN - Honduras 3
JO - Giordania 3
KE - Kenya 3
KR - Corea 3
KZ - Kazakistan 3
MA - Marocco 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
AL - Albania 2
BO - Bolivia 2
DO - Repubblica Dominicana 2
JM - Giamaica 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
PH - Filippine 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
AM - Armenia 1
BB - Barbados 1
BG - Bulgaria 1
CL - Cile 1
CY - Cipro 1
DK - Danimarca 1
DZ - Algeria 1
GA - Gabon 1
GT - Guatemala 1
LK - Sri Lanka 1
MY - Malesia 1
NP - Nepal 1
OM - Oman 1
PS - Palestinian Territory 1
TN - Tunisia 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 11.144
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Città #
Chandler 860
Jacksonville 737
Singapore 656
Dallas 379
Ashburn 355
Moscow 277
Hong Kong 276
Wilmington 177
Beijing 162
Boardman 162
New York 141
The Dalles 128
Helsinki 116
Dublin 112
Hefei 110
Dong Ket 106
Ann Arbor 105
Dearborn 102
Kronberg 95
Los Angeles 75
Munich 67
Woodbridge 64
Brooklyn 62
Santa Clara 57
Phoenix 42
São Paulo 42
Pune 37
Brussels 33
Seattle 32
Shanghai 31
Trento 29
Warsaw 29
Houston 26
Rio de Janeiro 25
Toronto 25
Secaucus 23
Montreal 22
Ho Chi Minh City 21
Denver 20
Falkenstein 20
London 20
Brno 19
St Petersburg 19
Tokyo 18
Turku 18
Boston 17
Brasília 17
Orem 17
Frankfurt am Main 16
Stockholm 16
Hanoi 14
Johannesburg 14
Chicago 13
Miami 13
Poplar 13
Amsterdam 12
Atlanta 12
Curitiba 12
Falls Church 12
Norwalk 11
Augusta 10
Campinas 10
Cologne 10
Mumbai 10
Charlotte 9
Leawood 9
Portland 9
Salvador 9
San Francisco 9
Ardabil 8
Baghdad 8
Chennai 8
Milan 8
Ottawa 8
San Mateo 8
Ankara 7
Buffalo 7
Cairo 7
Mexico City 7
Paris 7
Redwood City 7
Saint Petersburg 7
Tashkent 7
Belo Horizonte 6
Council Bluffs 6
Erbil 6
Guarulhos 6
Lima 6
Monmouth Junction 6
Montevideo 6
Nanjing 6
Niterói 6
Recife 6
Auburn Hills 5
Belém 5
Goiânia 5
Hanover 5
Manchester 5
Nuremberg 5
Porto Alegre 5
Totale 6.425
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Nome #
Combinatorial plasma deposition of C-based films to test cell adhesion 170
Binding of antibodies to functional epitopes on the pore formed by Escherichia coli hemolysin in cells and model membranes. 165
A novel mechanism of pore formation: membrane penetration by the N-terminal amphipathic region of equinatoxin. 165
Alpha-synuclein pore forming activity upon membrane association 160
Activation energy of the cardiac Na+/Ca2+ exchanger in sarcolemmal vesicles and reconstituted proteoliposomes. 159
Bio-hybrid interfaces to study neuromorphic functionalities: New multidisciplinary evidences of cell viability on poly(anyline) (PANI), a semiconductor polymer with memristive properties 157
A fluorimetric assay for the effects of cytolytic toxins on the transport properties of resealed erythrocyte ghosts. 148
Anticandida activity is retained in P-113, a 12-amino-acid fragment of histatin 5. 145
Antiparasite activity of sea-anemone cytolysins on Giardia duodenalis and specific targeting with anti-Giardia antibodies. 142
Neuronal firing modulation by a membrane-targeted photoswitch 141
A tumor protease-activated conjugate based on a sea anemone toxin: its cytotoxic activity on cancer cells. 135
A XAS study of the geometrical arrangement of Cu(II)-binding octarepeat peptides 134
para-sulfonato-calix[n]arenes inhibit staphylococcal bicomponent leukotoxins by supramolecular interactions. 134
Bacterial hemolysins and leukotoxins affect target cells by forming large exogenous pores into their plasma membrane: Escherichia coli hemolysin A as a case example. 132
Use of nanostructures for cancer care 128
Homologous versus heterologous interactions in the pore of bicomponent staphylococcal gamma-hemolysins 128
Human perforin employs different avenues to damage membranes 127
Biopolymer surface coatings for the treatment of staphylococcal infections 126
Structural features of distinctin affecting peptide biological and biochemical properties 125
Biochemical and cytotoxic properties of conjugates of transferrin with equinatoxin II, a cytolysin from a sea anemone. 125
pH dependence of listeriolysin O aggregation and pore-forming ability 125
Anomalously high aggregation level of the polyene antibiotic amphotericin B in acidic medium: implications for the biological action. 124
A tumor protease-activated pore forming toxin as a specific anticancer tool 121
γ-Hemolysin Oligomeric Structure and Effect of its Formation on Supported Lipid Bilayers: an AFM Investigation 121
Combinatorial Plasma Polymerization Approach to Produce Thin Films for Testing Cell proliferation 118
Tolaasin I, Lipodepsipeptides from Pseudomonas reactans and Pseudomonas tolaasii, permeabilize model membranes 116
Cytotoxic activity of a tumor protease-activated pore-forming toxin. 114
Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures. 114
N-terminal deletion affects catalytic activity of saporin toxin 114
A fluorescence-based assay for the reductase activity of protein disulfide isomerase 114
Effects of lipid composition on membrane permeabilization by two cytolysins of the sea anemone Stichodactyla helianthus, St I and St II 113
Synthesis and characterization of Raman active gold nanoparticles 113
N-terminal-bearing peptide derived from the pore-forming protein Sticholysin II interacts with lipid bilayer. 111
Structure and activity of the N-terminal region of the eukaryotic cytolysin equinatoxin II. 110
A molecular pin to study the dynamic of á-barrel formation in Pore Forming Toxins on erythrocytes: a sliding model 110
Peptides derived from apoptotic Bax and Bid reproduce the poration activity of the parent full-length proteins 110
Multifunctional branched gold-carbon nanotube hybrid for cell imaging and drug delivery 109
Lipid modulation on structure and function abilities of two Cholesterol--Dependent Cytolysins 109
Synthesis of plasmonic gold/carbon nanotubes hybrid structures for cell imaging and drug delivery 108
Potential inhibitors of Staphylococccus aureus bi-components γ-hemolysins 107
Directly assessment of drug release dynamics from gold nanoparticles 106
Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer 106
Interaction with model membranes and pore formation by human stefin B; studying the native and prefibrillar states 106
Effects of lipid composition on membrane permeabilization by sticholysin I and II, two cytolysins of the sea anemone Stichodactyla helianthus. 105
Fuscopeptins, antimicrobial lipodepsipeptides from Pseudomonas fuscovaginae, are channel forming peptides active on biological and model membranes 105
Binding of antibiotic amphotericin B to lipid membranes: Monomolecular layer technique and linear dichroism-FTIR studies 105
HOW A METABOLITE OF DOPAMINE CAN TRANSFORM ALPHA­SYNUCLEIN IN AN ENDOTOXIN 105
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 105
The mode of action of bicomponent gamma-hemolysins of Staphylococcus aureus. 103
Mechanism of membrane permeabilization by sticholysin I, a cytolysin isolated from the venom of the sea anemone Stichodactyla helianthus. 103
Listeriolysin O pore-forming abilities on lipid membranes 103
Biological Characterisation of WLIP produced by Pseudomonas reactans strain NCPPB1311 102
Perforin activity at membranes leads to invaginations and vesicle formation 101
Perforin oligomers form arcs in cellular membranes: a locus for intracellular delivery of granzymes 101
The Influence of Membrane Lipids in Staphylococcus aureus Gamma-Hemolysins Pore Formation 100
Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components. 100
Construction of the I18C-EqtII – avidin conjugate via a biotinylated peptide and its cytotoxic activity. 100
Site directed mutagenesis to assess the binding capacity of class S protein of Staphylococcus aureus leucotoxins to the surface of polymorphonuclear cells 100
The interaction of Staphylococcus aureus bi-component gamma-hemolysins and leucocidins with cells and lipid membranes. 100
Ion channels and bacterial infection: the case of beta-barrel pore-forming protein toxins of Staphylococcus aureus. 100
Characterization of anticholinesterase-active 3-alkylpyridinium polymers from the marine sponge Reniera sarai in aqueous solutions. 99
Construction of EqtII mutants immunoconjugates and characterization of their cytotoxic activity 97
Effects of calcium and protons on the secondary structure of the nodulation protein NodO from Rhizobium leguminosarum biovar viciae. 97
Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores 97
Molecular mechanism of pore formation by actinoporins 96
Liposomes in the study of pore-forming toxins. 95
EPR and FTIR studies reveal the importance of highly ordered sterol-enriched membrane domains for ostreolysin activity. 94
Deposito della beta-amiloide sulla membrana cellulare: ruolo degli ioni metallici e dei radicali liberi 94
Self-potentiation of ligand-toxin conjugates containing ricin A chain fused with viral structures. 94
Distinction between pore assembly by staphylococcal α-toxin versus leukotoxins 94
Plasticity of Listeriolysin O Pores Revealed by Mutagenesis of a Unique Histidine 94
Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: Cormycin A 94
Plasma assisted surface treatments of biomaterials 94
Mode of action of beta-barrel pore-forming toxins of the staphylococcal alpha-hemolysin family. 93
Les leucotoxines de staphylocoque: de l'investigation bio-structurale vers la notion d'inhibiteurs 92
The equinatoxin N-terminus is transferred across planar lipid membranes and helps to stabilize the transmembrane pore. 91
Identifying the Minimal Copper- and Zinc-binding Site Sequence in Amyloid-beta Peptides 90
Sizing the radius of the pore formed in erythrocytes and lipid vesicles by the toxin sticholysin I from the sea anemone Stichodactyla helianthus. 90
Cysteine-scanning mutagenesis of an eukaryotic pore-forming toxin from sea anemone: topology in lipid membranes. 90
In vitro investigation of doxorubicin release from gold nanoparticles coated by polyelectrolyte multilayers 90
The adsorption of Pseudomonas aeruginosa exotoxin A to phospholipid monolayers is controlled by pH and surface potential. 89
Membrane permeabilizing activity of linusitin from flax seed 89
Protein engineering modulates the transport properties and ion selectivity of the pores formed by staphylococcal gamma-haemolysins in lipid membranes. 89
Pore-forming peptides and protein toxins 89
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 89
XAS STUDIES OF CU(II) AND ZN(II) BINDING SITE IN AMYLOID PEPTIDES 86
Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components. 86
Reversal of charge selectivity in transmembrane protein pores by using noncovalent molecular adapters. 86
Metal binding in amyloid beta-peptides shows intra- and inter-peptide coordination modes. 85
pH-activated doxorubicin release from polyelectrolyte complex layer coated mesoporous silica nanoparticles 85
Intrinsic tryptophan fluorescence of equinatoxin II, a pore-forming polypeptide from the sea anemone Actinia equina L, monitors its interaction with lipid membranes. 84
Metal binding in amyloids beta peptides shows both intra- and inter-peptide modes 82
The role of membrane lipid composition for the activity of Staphylococcus aureus gamma-hemolysins 81
Molecular modifications of the pore forming gamma hemolysins from Staphylococcus aureus 77
The interaction of lipodepsipeptide toxins from Pseudomonas syringae pv. syringae with biological and model membranes: a comparison of syringotoxin, syringomycin, and two syringopeptins. 77
Sea anemone cytolysins as toxic component of immunotoxins 77
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions 76
The influence of membrane lipids in Staphylococcus aureus gamma-hemolysins pore formation 76
Membrane composition effects on pore-forming ability of two cholesterol-dependent cytolysins 71
Conductive properties and gating of channels formed by syringopeptin 25A, a bioactive lipodepsipeptide from Pseudomonas syringae pv. syringae, in planar lipid membranes. 71
Totale 10.703
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Categoria #
all - tutte 60.658
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 60.658
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021617 0 0 0 0 0 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
2024/20253.000 30 62 329 94 32 60 133 178 1.168 342 413 159
2025/20262.348 297 597 482 541 363 68 0 0 0 0 0 0
Totale 11.188