IRIS Institutional Research Information System

Dalla Serra, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 5.078
EU - Europa 3.329
AS - Asia 2.107
SA - Sud America 624
AF - Africa 63
Continente sconosciuto - Info sul continente non disponibili 27
OC - Oceania 7
Totale 11.235
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Nazione #
US - Stati Uniti d'America 4.975
RU - Federazione Russa 1.094
SG - Singapore 976
BR - Brasile 540
DE - Germania 510
SE - Svezia 453
CN - Cina 400
UA - Ucraina 346
HK - Hong Kong 278
FI - Finlandia 235
VN - Vietnam 167
GB - Regno Unito 139
NL - Olanda 120
IE - Irlanda 114
IN - India 105
IT - Italia 88
CA - Canada 69
FR - Francia 69
ZA - Sudafrica 46
AR - Argentina 38
BD - Bangladesh 38
PL - Polonia 38
BE - Belgio 37
EU - Europa 26
MX - Messico 23
CZ - Repubblica Ceca 22
LT - Lituania 22
ES - Italia 21
JP - Giappone 20
IR - Iran 19
IQ - Iraq 18
TR - Turchia 18
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
ID - Indonesia 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 11.235
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Città #
Chandler 860
Jacksonville 737
Singapore 666
Dallas 379
Ashburn 367
Moscow 277
Hong Kong 276
Wilmington 177
Beijing 162
Boardman 162
New York 144
The Dalles 132
Helsinki 116
Dublin 112
Hefei 110
Dong Ket 106
Ann Arbor 105
Dearborn 102
Kronberg 95
Los Angeles 78
Munich 67
Brooklyn 64
Woodbridge 64
Santa Clara 57
Phoenix 43
São Paulo 42
Pune 37
Brussels 33
Seattle 33
Warsaw 32
Shanghai 31
Trento 29
Houston 27
Rio de Janeiro 25
Toronto 25
Denver 24
Secaucus 23
Montreal 22
Ho Chi Minh City 21
London 21
Falkenstein 20
Orem 20
Brno 19
St Petersburg 19
Tokyo 19
Boston 18
Stockholm 18
Turku 18
Brasília 17
Frankfurt am Main 16
Johannesburg 16
Hanoi 14
Amsterdam 13
Chicago 13
Miami 13
Poplar 13
Atlanta 12
Curitiba 12
Falls Church 12
Norwalk 11
Augusta 10
Campinas 10
Cologne 10
Mumbai 10
Charlotte 9
Chennai 9
Leawood 9
Portland 9
Salvador 9
San Francisco 9
Ankara 8
Ardabil 8
Baghdad 8
Milan 8
Ottawa 8
San Mateo 8
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
Guangzhou 5
Hanover 5
Manchester 5
Nuremberg 5
Totale 6.482
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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. 166
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 161
Activation energy of the cardiac Na+/Ca2+ exchanger in sarcolemmal vesicles and reconstituted proteoliposomes. 160
Bio-hybrid interfaces to study neuromorphic functionalities: New multidisciplinary evidences of cell viability on poly(anyline) (PANI), a semiconductor polymer with memristive properties 159
A fluorimetric assay for the effects of cytolytic toxins on the transport properties of resealed erythrocyte ghosts. 149
Anticandida activity is retained in P-113, a 12-amino-acid fragment of histatin 5. 146
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 142
A XAS study of the geometrical arrangement of Cu(II)-binding octarepeat peptides 135
A tumor protease-activated conjugate based on a sea anemone toxin: its cytotoxic activity on cancer cells. 135
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. 133
Homologous versus heterologous interactions in the pore of bicomponent staphylococcal gamma-hemolysins 130
Use of nanostructures for cancer care 129
Human perforin employs different avenues to damage membranes 128
Biopolymer surface coatings for the treatment of staphylococcal infections 127
Structural features of distinctin affecting peptide biological and biochemical properties 126
Biochemical and cytotoxic properties of conjugates of transferrin with equinatoxin II, a cytolysin from a sea anemone. 126
pH dependence of listeriolysin O aggregation and pore-forming ability 126
Anomalously high aggregation level of the polyene antibiotic amphotericin B in acidic medium: implications for the biological action. 125
A tumor protease-activated pore forming toxin as a specific anticancer tool 122
γ-Hemolysin Oligomeric Structure and Effect of its Formation on Supported Lipid Bilayers: an AFM Investigation 122
Combinatorial Plasma Polymerization Approach to Produce Thin Films for Testing Cell proliferation 119
Tolaasin I, Lipodepsipeptides from Pseudomonas reactans and Pseudomonas tolaasii, permeabilize model membranes 117
Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures. 116
Cytotoxic activity of a tumor protease-activated pore-forming toxin. 115
Effects of lipid composition on membrane permeabilization by two cytolysins of the sea anemone Stichodactyla helianthus, St I and St II 115
A fluorescence-based assay for the reductase activity of protein disulfide isomerase 115
Synthesis and characterization of Raman active gold nanoparticles 114
N-terminal deletion affects catalytic activity of saporin toxin 114
Structure and activity of the N-terminal region of the eukaryotic cytolysin equinatoxin II. 112
N-terminal-bearing peptide derived from the pore-forming protein Sticholysin II interacts with lipid bilayer. 112
A molecular pin to study the dynamic of á-barrel formation in Pore Forming Toxins on erythrocytes: a sliding model 111
Peptides derived from apoptotic Bax and Bid reproduce the poration activity of the parent full-length proteins 111
Lipid modulation on structure and function abilities of two Cholesterol--Dependent Cytolysins 111
Multifunctional branched gold-carbon nanotube hybrid for cell imaging and drug delivery 110
Synthesis of plasmonic gold/carbon nanotubes hybrid structures for cell imaging and drug delivery 109
Potential inhibitors of Staphylococccus aureus bi-components γ-hemolysins 108
Directly assessment of drug release dynamics from gold nanoparticles 107
Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer 107
Effects of lipid composition on membrane permeabilization by sticholysin I and II, two cytolysins of the sea anemone Stichodactyla helianthus. 106
Interaction with model membranes and pore formation by human stefin B; studying the native and prefibrillar states 106
Fuscopeptins, antimicrobial lipodepsipeptides from Pseudomonas fuscovaginae, are channel forming peptides active on biological and model membranes 106
Binding of antibiotic amphotericin B to lipid membranes: Monomolecular layer technique and linear dichroism-FTIR studies 106
Mechanism of membrane permeabilization by sticholysin I, a cytolysin isolated from the venom of the sea anemone Stichodactyla helianthus. 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
Listeriolysin O pore-forming abilities on lipid membranes 104
Perforin oligomers form arcs in cellular membranes: a locus for intracellular delivery of granzymes 104
The mode of action of bicomponent gamma-hemolysins of Staphylococcus aureus. 103
Perforin activity at membranes leads to invaginations and vesicle formation 102
Biological Characterisation of WLIP produced by Pseudomonas reactans strain NCPPB1311 102
The interaction of Staphylococcus aureus bi-component gamma-hemolysins and leucocidins with cells and lipid membranes. 102
The Influence of Membrane Lipids in Staphylococcus aureus Gamma-Hemolysins Pore Formation 101
Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components. 101
Construction of the I18C-EqtII – avidin conjugate via a biotinylated peptide and its cytotoxic activity. 101
Site directed mutagenesis to assess the binding capacity of class S protein of Staphylococcus aureus leucotoxins to the surface of polymorphonuclear cells 101
Ion channels and bacterial infection: the case of beta-barrel pore-forming protein toxins of Staphylococcus aureus. 101
Characterization of anticholinesterase-active 3-alkylpyridinium polymers from the marine sponge Reniera sarai in aqueous solutions. 100
Construction of EqtII mutants immunoconjugates and characterization of their cytotoxic activity 98
Effects of calcium and protons on the secondary structure of the nodulation protein NodO from Rhizobium leguminosarum biovar viciae. 98
Molecular mechanism of pore formation by actinoporins 97
Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores 97
Liposomes in the study of pore-forming toxins. 96
EPR and FTIR studies reveal the importance of highly ordered sterol-enriched membrane domains for ostreolysin activity. 95
Deposito della beta-amiloide sulla membrana cellulare: ruolo degli ioni metallici e dei radicali liberi 95
Self-potentiation of ligand-toxin conjugates containing ricin A chain fused with viral structures. 95
Distinction between pore assembly by staphylococcal α-toxin versus leukotoxins 95
Plasma assisted surface treatments of biomaterials 95
Mode of action of beta-barrel pore-forming toxins of the staphylococcal alpha-hemolysin family. 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
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. 92
Sizing the radius of the pore formed in erythrocytes and lipid vesicles by the toxin sticholysin I from the sea anemone Stichodactyla helianthus. 91
In vitro investigation of doxorubicin release from gold nanoparticles coated by polyelectrolyte multilayers 91
Identifying the Minimal Copper- and Zinc-binding Site Sequence in Amyloid-beta Peptides 90
Cysteine-scanning mutagenesis of an eukaryotic pore-forming toxin from sea anemone: topology in lipid membranes. 90
The adsorption of Pseudomonas aeruginosa exotoxin A to phospholipid monolayers is controlled by pH and surface potential. 90
Protein engineering modulates the transport properties and ion selectivity of the pores formed by staphylococcal gamma-haemolysins in lipid membranes. 90
Membrane permeabilizing activity of linusitin from flax seed 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 87
Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components. 87
Metal binding in amyloid beta-peptides shows intra- and inter-peptide coordination modes. 86
Reversal of charge selectivity in transmembrane protein pores by using noncovalent molecular adapters. 86
pH-activated doxorubicin release from polyelectrolyte complex layer coated mesoporous silica nanoparticles 86
Intrinsic tryptophan fluorescence of equinatoxin II, a pore-forming polypeptide from the sea anemone Actinia equina L, monitors its interaction with lipid membranes. 86
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
The interaction of lipodepsipeptide toxins from Pseudomonas syringae pv. syringae with biological and model membranes: a comparison of syringotoxin, syringomycin, and two syringopeptins. 78
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions 77
Molecular modifications of the pore forming gamma hemolysins from Staphylococcus aureus 77
Sea anemone cytolysins as toxic component of immunotoxins 77
The influence of membrane lipids in Staphylococcus aureus gamma-hemolysins pore formation 76
Conductive properties and gating of channels formed by syringopeptin 25A, a bioactive lipodepsipeptide from Pseudomonas syringae pv. syringae, in planar lipid membranes. 72
Membrane composition effects on pore-forming ability of two cholesterol-dependent cytolysins 71
Totale 10.787
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Categoria #
all - tutte 60.881
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 60.881
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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
2025/20262.439 297 597 482 541 363 159 0 0 0 0 0 0
Totale 11.279