IRIS Institutional Research Information System

Dalla Serra, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 8.278
EU - Europa 6.832
AS - Asia 3.057
SA - Sud America 725
AF - Africa 99
Continente sconosciuto - Info sul continente non disponibili 79
OC - Oceania 8
Totale 19.078
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Nazione #
US - Stati Uniti d'America 8.062
RU - Federazione Russa 4.192
SG - Singapore 1.238
BR - Brasile 599
DE - Germania 599
SE - Svezia 541
CN - Cina 501
VN - Vietnam 466
HK - Hong Kong 438
UA - Ucraina 349
FI - Finlandia 249
FR - Francia 177
GB - Regno Unito 152
IT - Italia 141
IN - India 129
NL - Olanda 124
IE - Irlanda 115
CA - Canada 114
AR - Argentina 56
BD - Bangladesh 52
ZA - Sudafrica 52
PL - Polonia 47
MX - Messico 42
BE - Belgio 39
JP - Giappone 31
ES - Italia 28
EU - Europa 26
IQ - Iraq 24
CZ - Repubblica Ceca 22
LT - Lituania 22
TR - Turchia 21
IR - Iran 19
IL - Israele 18
EC - Ecuador 17
PH - Filippine 17
PK - Pakistan 15
CR - Costa Rica 13
SA - Arabia Saudita 13
CO - Colombia 12
SC - Seychelles 12
VE - Venezuela 12
ID - Indonesia 11
AE - Emirati Arabi Uniti 10
AT - Austria 10
EG - Egitto 10
HN - Honduras 9
PE - Perù 9
UZ - Uzbekistan 9
JM - Giamaica 7
KE - Kenya 7
UY - Uruguay 7
CH - Svizzera 6
GT - Guatemala 6
KR - Corea 6
PY - Paraguay 6
TT - Trinidad e Tobago 6
AU - Australia 5
CL - Cile 5
KZ - Kazakistan 5
MA - Marocco 5
PT - Portogallo 5
AL - Albania 4
AZ - Azerbaigian 4
NP - Nepal 4
SV - El Salvador 4
TH - Thailandia 4
DO - Repubblica Dominicana 3
DZ - Algeria 3
JO - Giordania 3
LA - Repubblica Popolare Democratica del Laos 3
MY - Malesia 3
NZ - Nuova Zelanda 3
PR - Porto Rico 3
BO - Bolivia 2
HU - Ungheria 2
LB - Libano 2
LY - Libia 2
NI - Nicaragua 2
OM - Oman 2
PA - Panama 2
PS - Palestinian Territory 2
TN - Tunisia 2
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
BM - Bermuda 1
BS - Bahamas 1
BZ - Belize 1
CI - Costa d'Avorio 1
CY - Cipro 1
DK - Danimarca 1
EE - Estonia 1
ET - Etiopia 1
GA - Gabon 1
GP - Guadalupe 1
KG - Kirghizistan 1
LK - Sri Lanka 1
MD - Moldavia 1
Totale 19.017
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Città #
San Jose 903
Chandler 860
Jacksonville 743
Council Bluffs 722
Singapore 715
Ashburn 488
Hong Kong 419
Dallas 397
Moscow 278
Wilmington 184
Beijing 172
The Dalles 168
New York 167
Boardman 162
Los Angeles 143
Helsinki 130
Ho Chi Minh City 119
Dublin 113
Hefei 110
Dong Ket 106
Ann Arbor 105
Dearborn 102
Kronberg 95
Lauterbourg 94
Hanoi 93
Santa Clara 91
Munich 71
Brooklyn 70
Phoenix 65
Woodbridge 64
São Paulo 47
Tampa 47
Warsaw 39
Pune 37
Seattle 36
Frankfurt am Main 35
Houston 34
Shanghai 34
Brussels 33
Denver 33
Orem 33
Trento 32
Chicago 30
Montreal 30
Toronto 30
Rio de Janeiro 26
Buffalo 25
Secaucus 24
Garland 23
Tokyo 23
Boston 22
Da Nang 22
Lawrenceville 22
London 22
Miami 22
Falkenstein 20
Brasília 19
Brno 19
Johannesburg 19
St Petersburg 19
Stockholm 19
Atlanta 18
Charlotte 18
Turku 18
Amsterdam 17
Mumbai 16
Haiphong 15
Milan 14
Poplar 14
Chennai 13
Norwalk 13
Augusta 12
Curitiba 12
Falls Church 12
San Francisco 11
San José 11
The Bronx 11
Campinas 10
Cologne 10
Pittsburgh 10
Portland 10
Queens 10
Salvador 10
San Diego 10
Baghdad 9
Leawood 9
Paris 9
Ankara 8
Ardabil 8
Cairo 8
Erbil 8
Mexico City 8
Milwaukee 8
North Bergen 8
Ottawa 8
Philadelphia 8
Recife 8
San Mateo 8
Storo 8
Tashkent 8
Totale 9.251
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Nome #
Binding of antibodies to functional epitopes on the pore formed by Escherichia coli hemolysin in cells and model membranes. 278
Combinatorial plasma deposition of C-based films to test cell adhesion 272
A novel mechanism of pore formation: membrane penetration by the N-terminal amphipathic region of equinatoxin. 261
Activation energy of the cardiac Na+/Ca2+ exchanger in sarcolemmal vesicles and reconstituted proteoliposomes. 259
A fluorimetric assay for the effects of cytolytic toxins on the transport properties of resealed erythrocyte ghosts. 246
Alpha-synuclein pore forming activity upon membrane association 242
Antiparasite activity of sea-anemone cytolysins on Giardia duodenalis and specific targeting with anti-Giardia antibodies. 233
Anticandida activity is retained in P-113, a 12-amino-acid fragment of histatin 5. 230
Bio-hybrid interfaces to study neuromorphic functionalities: New multidisciplinary evidences of cell viability on poly(anyline) (PANI), a semiconductor polymer with memristive properties 230
Bacterial hemolysins and leukotoxins affect target cells by forming large exogenous pores into their plasma membrane: Escherichia coli hemolysin A as a case example. 229
Biochemical and cytotoxic properties of conjugates of transferrin with equinatoxin II, a cytolysin from a sea anemone. 228
Neuronal firing modulation by a membrane-targeted photoswitch 222
Cytotoxic activity of a tumor protease-activated pore-forming toxin. 218
para-sulfonato-calix[n]arenes inhibit staphylococcal bicomponent leukotoxins by supramolecular interactions. 212
A XAS study of the geometrical arrangement of Cu(II)-binding octarepeat peptides 211
Biopolymer surface coatings for the treatment of staphylococcal infections 211
A tumor protease-activated conjugate based on a sea anemone toxin: its cytotoxic activity on cancer cells. 210
Homologous versus heterologous interactions in the pore of bicomponent staphylococcal gamma-hemolysins 210
Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures. 206
Structural features of distinctin affecting peptide biological and biochemical properties 204
Use of nanostructures for cancer care 201
γ-Hemolysin Oligomeric Structure and Effect of its Formation on Supported Lipid Bilayers: an AFM Investigation 201
A tumor protease-activated pore forming toxin as a specific anticancer tool 199
Combinatorial Plasma Polymerization Approach to Produce Thin Films for Testing Cell proliferation 199
pH dependence of listeriolysin O aggregation and pore-forming ability 199
Effects of lipid composition on membrane permeabilization by sticholysin I and II, two cytolysins of the sea anemone Stichodactyla helianthus. 198
Tolaasin I, Lipodepsipeptides from Pseudomonas reactans and Pseudomonas tolaasii, permeabilize model membranes 197
Structure and activity of the N-terminal region of the eukaryotic cytolysin equinatoxin II. 196
Anomalously high aggregation level of the polyene antibiotic amphotericin B in acidic medium: implications for the biological action. 196
Synthesis and characterization of Raman active gold nanoparticles 193
Human perforin employs different avenues to damage membranes 193
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 186
Perforin oligomers form arcs in cellular membranes: a locus for intracellular delivery of granzymes 185
N-terminal-bearing peptide derived from the pore-forming protein Sticholysin II interacts with lipid bilayer. 184
Directly assessment of drug release dynamics from gold nanoparticles 184
Interaction with model membranes and pore formation by human stefin B; studying the native and prefibrillar states 184
A molecular pin to study the dynamic of á-barrel formation in Pore Forming Toxins on erythrocytes: a sliding model 183
Lipid modulation on structure and function abilities of two Cholesterol--Dependent Cytolysins 183
Multifunctional branched gold-carbon nanotube hybrid for cell imaging and drug delivery 182
Molecular mechanism of pore formation by actinoporins 180
Binding of antibiotic amphotericin B to lipid membranes: Monomolecular layer technique and linear dichroism-FTIR studies 180
The interaction of Staphylococcus aureus bi-component gamma-hemolysins and leucocidins with cells and lipid membranes. 180
Mechanism of membrane permeabilization by sticholysin I, a cytolysin isolated from the venom of the sea anemone Stichodactyla helianthus. 179
Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer 179
Effects of lipid composition on membrane permeabilization by two cytolysins of the sea anemone Stichodactyla helianthus, St I and St II 177
Listeriolysin O pore-forming abilities on lipid membranes 177
A fluorescence-based assay for the reductase activity of protein disulfide isomerase 177
Peptides derived from apoptotic Bax and Bid reproduce the poration activity of the parent full-length proteins 176
Ion channels and bacterial infection: the case of beta-barrel pore-forming protein toxins of Staphylococcus aureus. 175
Plasma assisted surface treatments of biomaterials 175
Synthesis of plasmonic gold/carbon nanotubes hybrid structures for cell imaging and drug delivery 173
The Influence of Membrane Lipids in Staphylococcus aureus Gamma-Hemolysins Pore Formation 172
The mode of action of bicomponent gamma-hemolysins of Staphylococcus aureus. 172
Perforin activity at membranes leads to invaginations and vesicle formation 171
Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components. 170
Construction of the I18C-EqtII – avidin conjugate via a biotinylated peptide and its cytotoxic activity. 169
Mode of action of beta-barrel pore-forming toxins of the staphylococcal alpha-hemolysin family. 169
Fuscopeptins, antimicrobial lipodepsipeptides from Pseudomonas fuscovaginae, are channel forming peptides active on biological and model membranes 169
N-terminal deletion affects catalytic activity of saporin toxin 168
EPR and FTIR studies reveal the importance of highly ordered sterol-enriched membrane domains for ostreolysin activity. 167
Self-potentiation of ligand-toxin conjugates containing ricin A chain fused with viral structures. 167
Site directed mutagenesis to assess the binding capacity of class S protein of Staphylococcus aureus leucotoxins to the surface of polymorphonuclear cells 166
Plasticity of Listeriolysin O Pores Revealed by Mutagenesis of a Unique Histidine 166
Potential inhibitors of Staphylococccus aureus bi-components γ-hemolysins 165
Characterization of anticholinesterase-active 3-alkylpyridinium polymers from the marine sponge Reniera sarai in aqueous solutions. 165
Liposomes in the study of pore-forming toxins. 165
Biological Characterisation of WLIP produced by Pseudomonas reactans strain NCPPB1311 165
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 165
Identifying the Minimal Copper- and Zinc-binding Site Sequence in Amyloid-beta Peptides 164
Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components. 164
Sizing the radius of the pore formed in erythrocytes and lipid vesicles by the toxin sticholysin I from the sea anemone Stichodactyla helianthus. 162
Effects of calcium and protons on the secondary structure of the nodulation protein NodO from Rhizobium leguminosarum biovar viciae. 162
Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: Cormycin A 162
XAS STUDIES OF CU(II) AND ZN(II) BINDING SITE IN AMYLOID PEPTIDES 161
Cysteine-scanning mutagenesis of an eukaryotic pore-forming toxin from sea anemone: topology in lipid membranes. 160
Construction of EqtII mutants immunoconjugates and characterization of their cytotoxic activity 159
Interfacing primary cortical neurons with PMCS TiO2 films to design bio-hybrid memristive device mimicking neuromorphic functionalities 158
Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores 157
In vitro investigation of doxorubicin release from gold nanoparticles coated by polyelectrolyte multilayers 157
HOW A METABOLITE OF DOPAMINE CAN TRANSFORM ALPHA­SYNUCLEIN IN AN ENDOTOXIN 156
Deposito della beta-amiloide sulla membrana cellulare: ruolo degli ioni metallici e dei radicali liberi 155
Intrinsic tryptophan fluorescence of equinatoxin II, a pore-forming polypeptide from the sea anemone Actinia equina L, monitors its interaction with lipid membranes. 155
The equinatoxin N-terminus is transferred across planar lipid membranes and helps to stabilize the transmembrane pore. 153
The adsorption of Pseudomonas aeruginosa exotoxin A to phospholipid monolayers is controlled by pH and surface potential. 153
Metal binding in amyloid beta-peptides shows intra- and inter-peptide coordination modes. 152
Membrane permeabilizing activity of linusitin from flax seed 152
Protein engineering modulates the transport properties and ion selectivity of the pores formed by staphylococcal gamma-haemolysins in lipid membranes. 152
pH-activated doxorubicin release from polyelectrolyte complex layer coated mesoporous silica nanoparticles 151
Les leucotoxines de staphylocoque: de l'investigation bio-structurale vers la notion d'inhibiteurs 150
The role of membrane lipid composition for the activity of Staphylococcus aureus gamma-hemolysins 149
The interaction of lipodepsipeptide toxins from Pseudomonas syringae pv. syringae with biological and model membranes: a comparison of syringotoxin, syringomycin, and two syringopeptins. 148
Distinction between pore assembly by staphylococcal α-toxin versus leukotoxins 148
Molecular modifications of the pore forming gamma hemolysins from Staphylococcus aureus 147
Reversal of charge selectivity in transmembrane protein pores by using noncovalent molecular adapters. 146
Permeability increase induced by Escherichia coli hemolysin A in human macrophages is due to the formation of ionic pores: a patch clamp characterization. 144
Membrane composition effects on pore-forming ability of two cholesterol-dependent cytolysins 142
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions 140
Pore-forming peptides and protein toxins 137
Metal binding in amyloids beta peptides shows both intra- and inter-peptide modes 133
Sea anemone cytolysins as toxic component of immunotoxins 133
Totale 18.096
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Categoria #
all - tutte 79.922
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 79.922
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022481 0 0 0 106 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
2025/20268.337 297 597 482 541 363 306 1.315 3.353 312 315 369 87
2026/20271.901 331 284 663 623 0 0 0 0 0 0 0 0
Totale 19.078