IRIS Institutional Research Information System

Dalla Serra, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 7.034
EU - Europa 6.738
AS - Asia 3.038
SA - Sud America 715
AF - Africa 83
Continente sconosciuto - Info sul continente non disponibili 71
OC - Oceania 8
Totale 17.687
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Nazione #
US - Stati Uniti d'America 6.893
RU - Federazione Russa 4.170
SG - Singapore 1.237
BR - Brasile 594
DE - Germania 593
SE - Svezia 520
CN - Cina 500
VN - Vietnam 465
HK - Hong Kong 436
UA - Ucraina 348
FI - Finlandia 249
FR - Francia 174
GB - Regno Unito 148
IN - India 129
NL - Olanda 124
IE - Irlanda 115
IT - Italia 108
CA - Canada 79
AR - Argentina 54
ZA - Sudafrica 51
BD - Bangladesh 50
PL - Polonia 47
MX - Messico 41
BE - Belgio 38
JP - Giappone 30
ES - Italia 27
EU - Europa 26
IQ - Iraq 24
CZ - Repubblica Ceca 22
LT - Lituania 22
TR - Turchia 21
IR - Iran 19
PH - Filippine 17
EC - Ecuador 16
PK - Pakistan 15
SA - Arabia Saudita 13
CO - Colombia 11
VE - Venezuela 11
AE - Emirati Arabi Uniti 10
AT - Austria 10
EG - Egitto 10
ID - Indonesia 10
PE - Perù 9
UZ - Uzbekistan 9
IL - Israele 8
HN - Honduras 7
KE - Kenya 7
UY - Uruguay 7
CH - Svizzera 6
KR - Corea 6
PY - Paraguay 6
AU - Australia 5
CL - Cile 5
KZ - Kazakistan 5
PT - Portogallo 5
AL - Albania 4
AZ - Azerbaigian 4
JM - Giamaica 4
MA - Marocco 4
NP - Nepal 4
TH - Thailandia 4
DO - Repubblica Dominicana 3
JO - Giordania 3
LA - Repubblica Popolare Democratica del Laos 3
MY - Malesia 3
NZ - Nuova Zelanda 3
BO - Bolivia 2
DZ - Algeria 2
GT - Guatemala 2
HU - Ungheria 2
LB - Libano 2
LY - Libia 2
OM - Oman 2
PA - Panama 2
PS - Palestinian Territory 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
CY - Cipro 1
DK - Danimarca 1
ET - Etiopia 1
GA - Gabon 1
KG - Kirghizistan 1
LK - Sri Lanka 1
MD - Moldavia 1
MM - Myanmar 1
QA - Qatar 1
RO - Romania 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TW - Taiwan 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 17.643
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Città #
Chandler 860
San Jose 788
Jacksonville 740
Council Bluffs 719
Singapore 715
Ashburn 462
Hong Kong 419
Dallas 384
Moscow 278
Wilmington 178
Beijing 171
The Dalles 168
Boardman 162
New York 154
Helsinki 130
Ho Chi Minh City 119
Dublin 113
Los Angeles 113
Hefei 110
Dong Ket 106
Ann Arbor 105
Dearborn 102
Kronberg 95
Lauterbourg 94
Hanoi 92
Santa Clara 70
Brooklyn 67
Munich 67
Woodbridge 64
Phoenix 55
São Paulo 46
Warsaw 39
Pune 37
Frankfurt am Main 34
Shanghai 34
Brussels 33
Orem 33
Seattle 33
Trento 31
Denver 29
Houston 27
Toronto 27
Rio de Janeiro 26
Montreal 24
Secaucus 23
Da Nang 22
London 22
Tokyo 22
Boston 20
Falkenstein 20
Brno 19
Johannesburg 19
St Petersburg 19
Stockholm 19
Turku 18
Amsterdam 17
Brasília 17
Chicago 17
Mumbai 16
Haiphong 15
Miami 14
Poplar 14
Buffalo 13
Chennai 13
Atlanta 12
Curitiba 12
Falls Church 12
Augusta 11
Milan 11
Norwalk 11
Campinas 10
Charlotte 10
Cologne 10
Salvador 10
San Francisco 10
Baghdad 9
Leawood 9
Portland 9
Ankara 8
Ardabil 8
Cairo 8
Erbil 8
Mexico City 8
Ottawa 8
Paris 8
Recife 8
San Mateo 8
Tashkent 8
Dhaka 7
Guangzhou 7
Nairobi 7
Nanjing 7
New Delhi 7
Nuremberg 7
Redwood City 7
Saint Petersburg 7
Tianjin 7
Belo Horizonte 6
Guarulhos 6
Hillsboro 6
Totale 8.819
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Nome #
Binding of antibodies to functional epitopes on the pore formed by Escherichia coli hemolysin in cells and model membranes. 259
Combinatorial plasma deposition of C-based films to test cell adhesion 256
A novel mechanism of pore formation: membrane penetration by the N-terminal amphipathic region of equinatoxin. 247
Activation energy of the cardiac Na+/Ca2+ exchanger in sarcolemmal vesicles and reconstituted proteoliposomes. 246
A fluorimetric assay for the effects of cytolytic toxins on the transport properties of resealed erythrocyte ghosts. 235
Alpha-synuclein pore forming activity upon membrane association 228
Antiparasite activity of sea-anemone cytolysins on Giardia duodenalis and specific targeting with anti-Giardia antibodies. 217
Anticandida activity is retained in P-113, a 12-amino-acid fragment of histatin 5. 216
Bacterial hemolysins and leukotoxins affect target cells by forming large exogenous pores into their plasma membrane: Escherichia coli hemolysin A as a case example. 214
Biochemical and cytotoxic properties of conjugates of transferrin with equinatoxin II, a cytolysin from a sea anemone. 212
Bio-hybrid interfaces to study neuromorphic functionalities: New multidisciplinary evidences of cell viability on poly(anyline) (PANI), a semiconductor polymer with memristive properties 212
Neuronal firing modulation by a membrane-targeted photoswitch 210
Cytotoxic activity of a tumor protease-activated pore-forming toxin. 206
para-sulfonato-calix[n]arenes inhibit staphylococcal bicomponent leukotoxins by supramolecular interactions. 200
Homologous versus heterologous interactions in the pore of bicomponent staphylococcal gamma-hemolysins 198
A XAS study of the geometrical arrangement of Cu(II)-binding octarepeat peptides 197
A tumor protease-activated conjugate based on a sea anemone toxin: its cytotoxic activity on cancer cells. 197
Biopolymer surface coatings for the treatment of staphylococcal infections 197
Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures. 192
γ-Hemolysin Oligomeric Structure and Effect of its Formation on Supported Lipid Bilayers: an AFM Investigation 189
Use of nanostructures for cancer care 188
Structural features of distinctin affecting peptide biological and biochemical properties 187
pH dependence of listeriolysin O aggregation and pore-forming ability 187
Effects of lipid composition on membrane permeabilization by sticholysin I and II, two cytolysins of the sea anemone Stichodactyla helianthus. 186
A tumor protease-activated pore forming toxin as a specific anticancer tool 185
Combinatorial Plasma Polymerization Approach to Produce Thin Films for Testing Cell proliferation 185
Anomalously high aggregation level of the polyene antibiotic amphotericin B in acidic medium: implications for the biological action. 183
Human perforin employs different avenues to damage membranes 181
Tolaasin I, Lipodepsipeptides from Pseudomonas reactans and Pseudomonas tolaasii, permeabilize model membranes 181
Structure and activity of the N-terminal region of the eukaryotic cytolysin equinatoxin II. 180
Synthesis and characterization of Raman active gold nanoparticles 180
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 175
Interaction with model membranes and pore formation by human stefin B; studying the native and prefibrillar states 172
N-terminal-bearing peptide derived from the pore-forming protein Sticholysin II interacts with lipid bilayer. 171
Directly assessment of drug release dynamics from gold nanoparticles 171
Multifunctional branched gold-carbon nanotube hybrid for cell imaging and drug delivery 171
Lipid modulation on structure and function abilities of two Cholesterol--Dependent Cytolysins 171
Molecular mechanism of pore formation by actinoporins 170
A molecular pin to study the dynamic of á-barrel formation in Pore Forming Toxins on erythrocytes: a sliding model 169
The interaction of Staphylococcus aureus bi-component gamma-hemolysins and leucocidins with cells and lipid membranes. 169
Mechanism of membrane permeabilization by sticholysin I, a cytolysin isolated from the venom of the sea anemone Stichodactyla helianthus. 167
Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer 167
Effects of lipid composition on membrane permeabilization by two cytolysins of the sea anemone Stichodactyla helianthus, St I and St II 165
Peptides derived from apoptotic Bax and Bid reproduce the poration activity of the parent full-length proteins 165
Perforin oligomers form arcs in cellular membranes: a locus for intracellular delivery of granzymes 165
A fluorescence-based assay for the reductase activity of protein disulfide isomerase 164
Ion channels and bacterial infection: the case of beta-barrel pore-forming protein toxins of Staphylococcus aureus. 164
Binding of antibiotic amphotericin B to lipid membranes: Monomolecular layer technique and linear dichroism-FTIR studies 163
Perforin activity at membranes leads to invaginations and vesicle formation 162
Synthesis of plasmonic gold/carbon nanotubes hybrid structures for cell imaging and drug delivery 162
Listeriolysin O pore-forming abilities on lipid membranes 162
Plasma assisted surface treatments of biomaterials 162
The mode of action of bicomponent gamma-hemolysins of Staphylococcus aureus. 161
Construction of the I18C-EqtII – avidin conjugate via a biotinylated peptide and its cytotoxic activity. 160
The Influence of Membrane Lipids in Staphylococcus aureus Gamma-Hemolysins Pore Formation 158
Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components. 158
Self-potentiation of ligand-toxin conjugates containing ricin A chain fused with viral structures. 157
Mode of action of beta-barrel pore-forming toxins of the staphylococcal alpha-hemolysin family. 157
N-terminal deletion affects catalytic activity of saporin toxin 157
Site directed mutagenesis to assess the binding capacity of class S protein of Staphylococcus aureus leucotoxins to the surface of polymorphonuclear cells 156
Potential inhibitors of Staphylococccus aureus bi-components γ-hemolysins 155
EPR and FTIR studies reveal the importance of highly ordered sterol-enriched membrane domains for ostreolysin activity. 154
Liposomes in the study of pore-forming toxins. 154
Plasticity of Listeriolysin O Pores Revealed by Mutagenesis of a Unique Histidine 154
Sizing the radius of the pore formed in erythrocytes and lipid vesicles by the toxin sticholysin I from the sea anemone Stichodactyla helianthus. 153
Characterization of anticholinesterase-active 3-alkylpyridinium polymers from the marine sponge Reniera sarai in aqueous solutions. 153
Effects of calcium and protons on the secondary structure of the nodulation protein NodO from Rhizobium leguminosarum biovar viciae. 153
Fuscopeptins, antimicrobial lipodepsipeptides from Pseudomonas fuscovaginae, are channel forming peptides active on biological and model membranes 153
Identifying the Minimal Copper- and Zinc-binding Site Sequence in Amyloid-beta Peptides 152
Biological Characterisation of WLIP produced by Pseudomonas reactans strain NCPPB1311 152
Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: Cormycin A 151
Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components. 150
XAS STUDIES OF CU(II) AND ZN(II) BINDING SITE IN AMYLOID PEPTIDES 149
Interfacing primary cortical neurons with PMCS TiO2 films to design bio-hybrid memristive device mimicking neuromorphic functionalities 148
Construction of EqtII mutants immunoconjugates and characterization of their cytotoxic activity 148
Cysteine-scanning mutagenesis of an eukaryotic pore-forming toxin from sea anemone: topology in lipid membranes. 147
HOW A METABOLITE OF DOPAMINE CAN TRANSFORM ALPHA­SYNUCLEIN IN AN ENDOTOXIN 146
Protein engineering modulates the transport properties and ion selectivity of the pores formed by staphylococcal gamma-haemolysins in lipid membranes. 145
Intrinsic tryptophan fluorescence of equinatoxin II, a pore-forming polypeptide from the sea anemone Actinia equina L, monitors its interaction with lipid membranes. 145
Deposito della beta-amiloide sulla membrana cellulare: ruolo degli ioni metallici e dei radicali liberi 144
Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores 144
In vitro investigation of doxorubicin release from gold nanoparticles coated by polyelectrolyte multilayers 144
The equinatoxin N-terminus is transferred across planar lipid membranes and helps to stabilize the transmembrane pore. 143
The adsorption of Pseudomonas aeruginosa exotoxin A to phospholipid monolayers is controlled by pH and surface potential. 143
Membrane permeabilizing activity of linusitin from flax seed 142
Les leucotoxines de staphylocoque: de l'investigation bio-structurale vers la notion d'inhibiteurs 140
The role of membrane lipid composition for the activity of Staphylococcus aureus gamma-hemolysins 139
Distinction between pore assembly by staphylococcal α-toxin versus leukotoxins 139
pH-activated doxorubicin release from polyelectrolyte complex layer coated mesoporous silica nanoparticles 138
The interaction of lipodepsipeptide toxins from Pseudomonas syringae pv. syringae with biological and model membranes: a comparison of syringotoxin, syringomycin, and two syringopeptins. 137
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 137
Reversal of charge selectivity in transmembrane protein pores by using noncovalent molecular adapters. 136
Molecular modifications of the pore forming gamma hemolysins from Staphylococcus aureus 135
Metal binding in amyloid beta-peptides shows intra- and inter-peptide coordination modes. 134
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions 131
Membrane composition effects on pore-forming ability of two cholesterol-dependent cytolysins 130
Pore-forming peptides and protein toxins 128
Metal binding in amyloids beta peptides shows both intra- and inter-peptide modes 125
Sea anemone cytolysins as toxic component of immunotoxins 125
The influence of membrane lipids in Staphylococcus aureus gamma-hemolysins pore formation 122
Totale 16.840
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Categoria #
all - tutte 74.351
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 74.351
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022499 0 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
2025/20268.337 297 597 482 541 363 306 1.315 3.353 312 315 369 87
2026/2027510 331 179 0 0 0 0 0 0 0 0 0 0
Totale 17.687