IRIS Institutional Research Information System

Dalla Serra, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 4.106
EU - Europa 3.148
AS - Asia 1.299
SA - Sud America 323
AF - Africa 37
Continente sconosciuto - Info sul continente non disponibili 27
OC - Oceania 7
Totale 8.947
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Nazione #
US - Stati Uniti d'America 4.052
RU - Federazione Russa 1.075
DE - Germania 503
SG - Singapore 503
SE - Svezia 439
UA - Ucraina 341
BR - Brasile 297
HK - Hong Kong 256
CN - Cina 245
FI - Finlandia 234
NL - Olanda 116
VN - Vietnam 116
IE - Irlanda 114
GB - Regno Unito 106
IN - India 75
IT - Italia 73
CA - Canada 43
BE - Belgio 37
FR - Francia 36
ZA - Sudafrica 28
EU - Europa 26
CZ - Repubblica Ceca 22
IR - Iran 18
PL - Polonia 14
BD - Bangladesh 13
LT - Lituania 13
ES - Italia 11
TR - Turchia 11
IQ - Iraq 10
AR - Argentina 9
UZ - Uzbekistan 7
AE - Emirati Arabi Uniti 6
AT - Austria 6
MX - Messico 6
CH - Svizzera 5
EG - Egitto 5
IL - Israele 5
AU - Australia 4
JP - Giappone 4
PE - Perù 4
PK - Pakistan 4
AZ - Azerbaigian 3
EC - Ecuador 3
JO - Giordania 3
NZ - Nuova Zelanda 3
SA - Arabia Saudita 3
UY - Uruguay 3
VE - Venezuela 3
BO - Bolivia 2
KR - Corea 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
MA - Marocco 2
PH - Filippine 2
PY - Paraguay 2
AL - Albania 1
AM - Armenia 1
BB - Barbados 1
CY - Cipro 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
HN - Honduras 1
JM - Giamaica 1
KE - Kenya 1
LK - Sri Lanka 1
NP - Nepal 1
OM - Oman 1
PS - Palestinian Territory 1
PT - Portogallo 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 8.947
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Città #
Chandler 860
Jacksonville 737
Singapore 305
Moscow 277
Hong Kong 254
Ashburn 221
Wilmington 177
Boardman 162
The Dalles 123
Helsinki 116
Dublin 112
Hefei 109
New York 108
Dong Ket 106
Ann Arbor 105
Dearborn 102
Kronberg 95
Beijing 67
Munich 67
Woodbridge 64
Brooklyn 54
Santa Clara 49
Los Angeles 44
Pune 36
Phoenix 35
Brussels 33
Shanghai 31
Seattle 28
Trento 28
São Paulo 25
Toronto 22
Falkenstein 20
Brno 19
Houston 18
Secaucus 18
Turku 17
London 15
Falls Church 12
Miami 12
Norwalk 11
Warsaw 11
Brasília 10
Cologne 10
Frankfurt am Main 10
Rio de Janeiro 10
Amsterdam 9
Curitiba 9
Leawood 9
Portland 9
Ardabil 8
Charlotte 8
Ottawa 8
San Mateo 8
Milan 7
Montreal 7
Redwood City 7
Saint Petersburg 7
Salvador 7
Augusta 6
Campinas 6
Monmouth Junction 6
Nanjing 6
St Petersburg 6
Stockholm 6
Tashkent 6
Auburn Hills 5
Boston 5
Buffalo 5
Cairo 5
Dallas 5
Hanover 5
Nuremberg 5
Paris 5
Zanjan 5
Baghdad 4
Bangalore 4
Cheyenne 4
Chicago 4
Guangzhou 4
Hanoi 4
Redmond 4
San Francisco 4
Zurich 4
Amman 3
Aracaju 3
Atlanta 3
Baku 3
Barcelona 3
Belém 3
Chandigarh 3
Cuiabá 3
Des Moines 3
Erbil 3
Guarulhos 3
Gunzenhausen 3
Hyderabad 3
Lima 3
Manchester 3
Montevideo 3
Mumbai 3
Totale 5.022
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Nome #
Combinatorial plasma deposition of C-based films to test cell adhesion 136
A novel mechanism of pore formation: membrane penetration by the N-terminal amphipathic region of equinatoxin. 130
Binding of antibodies to functional epitopes on the pore formed by Escherichia coli hemolysin in cells and model membranes. 126
Bio-hybrid interfaces to study neuromorphic functionalities: New multidisciplinary evidences of cell viability on poly(anyline) (PANI), a semiconductor polymer with memristive properties 125
Alpha-synuclein pore forming activity upon membrane association 124
Neuronal firing modulation by a membrane-targeted photoswitch 117
A fluorimetric assay for the effects of cytolytic toxins on the transport properties of resealed erythrocyte ghosts. 115
para-sulfonato-calix[n]arenes inhibit staphylococcal bicomponent leukotoxins by supramolecular interactions. 114
Bacterial hemolysins and leukotoxins affect target cells by forming large exogenous pores into their plasma membrane: Escherichia coli hemolysin A as a case example. 109
Activation energy of the cardiac Na+/Ca2+ exchanger in sarcolemmal vesicles and reconstituted proteoliposomes. 109
γ-Hemolysin Oligomeric Structure and Effect of its Formation on Supported Lipid Bilayers: an AFM Investigation 108
Antiparasite activity of sea-anemone cytolysins on Giardia duodenalis and specific targeting with anti-Giardia antibodies. 107
Anticandida activity is retained in P-113, a 12-amino-acid fragment of histatin 5. 107
A XAS study of the geometrical arrangement of Cu(II)-binding octarepeat peptides 104
Biochemical and cytotoxic properties of conjugates of transferrin with equinatoxin II, a cytolysin from a sea anemone. 103
Structural features of distinctin affecting peptide biological and biochemical properties 102
Homologous versus heterologous interactions in the pore of bicomponent staphylococcal gamma-hemolysins 102
Effects of lipid composition on membrane permeabilization by two cytolysins of the sea anemone Stichodactyla helianthus, St I and St II 101
Use of nanostructures for cancer care 99
N-terminal deletion affects catalytic activity of saporin toxin 99
Cytotoxic activity of a tumor protease-activated pore-forming toxin. 98
Biopolymer surface coatings for the treatment of staphylococcal infections 98
N-terminal-bearing peptide derived from the pore-forming protein Sticholysin II interacts with lipid bilayer. 97
Human perforin employs different avenues to damage membranes 97
A tumor protease-activated conjugate based on a sea anemone toxin: its cytotoxic activity on cancer cells. 96
A tumor protease-activated pore forming toxin as a specific anticancer tool 93
Combinatorial Plasma Polymerization Approach to Produce Thin Films for Testing Cell proliferation 93
pH dependence of listeriolysin O aggregation and pore-forming ability 92
Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures. 91
Structure and activity of the N-terminal region of the eukaryotic cytolysin equinatoxin II. 90
Effects of lipid composition on membrane permeabilization by sticholysin I and II, two cytolysins of the sea anemone Stichodactyla helianthus. 90
Tolaasin I, Lipodepsipeptides from Pseudomonas reactans and Pseudomonas tolaasii, permeabilize model membranes 90
Multifunctional branched gold-carbon nanotube hybrid for cell imaging and drug delivery 90
Construction of the I18C-EqtII – avidin conjugate via a biotinylated peptide and its cytotoxic activity. 89
Peptides derived from apoptotic Bax and Bid reproduce the poration activity of the parent full-length proteins 89
HOW A METABOLITE OF DOPAMINE CAN TRANSFORM ALPHA­SYNUCLEIN IN AN ENDOTOXIN 89
Anomalously high aggregation level of the polyene antibiotic amphotericin B in acidic medium: implications for the biological action. 87
A fluorescence-based assay for the reductase activity of protein disulfide isomerase 87
Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components. 86
The mode of action of bicomponent gamma-hemolysins of Staphylococcus aureus. 86
Synthesis of plasmonic gold/carbon nanotubes hybrid structures for cell imaging and drug delivery 86
A molecular pin to study the dynamic of á-barrel formation in Pore Forming Toxins on erythrocytes: a sliding model 86
Interaction with model membranes and pore formation by human stefin B; studying the native and prefibrillar states 86
Mechanism of membrane permeabilization by sticholysin I, a cytolysin isolated from the venom of the sea anemone Stichodactyla helianthus. 85
Liposomes in the study of pore-forming toxins. 85
Perforin oligomers form arcs in cellular membranes: a locus for intracellular delivery of granzymes 85
The interaction of Staphylococcus aureus bi-component gamma-hemolysins and leucocidins with cells and lipid membranes. 85
Lipid modulation on structure and function abilities of two Cholesterol--Dependent Cytolysins 85
The Influence of Membrane Lipids in Staphylococcus aureus Gamma-Hemolysins Pore Formation 84
Characterization of anticholinesterase-active 3-alkylpyridinium polymers from the marine sponge Reniera sarai in aqueous solutions. 84
Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer 84
Listeriolysin O pore-forming abilities on lipid membranes 84
Potential inhibitors of Staphylococccus aureus bi-components γ-hemolysins 83
Directly assessment of drug release dynamics from gold nanoparticles 83
Mode of action of beta-barrel pore-forming toxins of the staphylococcal alpha-hemolysin family. 83
Site directed mutagenesis to assess the binding capacity of class S protein of Staphylococcus aureus leucotoxins to the surface of polymorphonuclear cells 83
Construction of EqtII mutants immunoconjugates and characterization of their cytotoxic activity 82
Synthesis and characterization of Raman active gold nanoparticles 82
Self-potentiation of ligand-toxin conjugates containing ricin A chain fused with viral structures. 82
Distinction between pore assembly by staphylococcal α-toxin versus leukotoxins 82
Binding of antibiotic amphotericin B to lipid membranes: Monomolecular layer technique and linear dichroism-FTIR studies 82
Fuscopeptins, antimicrobial lipodepsipeptides from Pseudomonas fuscovaginae, are channel forming peptides active on biological and model membranes 81
Plasticity of Listeriolysin O Pores Revealed by Mutagenesis of a Unique Histidine 80
Les leucotoxines de staphylocoque: de l'investigation bio-structurale vers la notion d'inhibiteurs 79
Cysteine-scanning mutagenesis of an eukaryotic pore-forming toxin from sea anemone: topology in lipid membranes. 79
Biological Characterisation of WLIP produced by Pseudomonas reactans strain NCPPB1311 79
Sizing the radius of the pore formed in erythrocytes and lipid vesicles by the toxin sticholysin I from the sea anemone Stichodactyla helianthus. 78
Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: Cormycin A 78
EPR and FTIR studies reveal the importance of highly ordered sterol-enriched membrane domains for ostreolysin activity. 77
Perforin activity at membranes leads to invaginations and vesicle formation 77
Effects of calcium and protons on the secondary structure of the nodulation protein NodO from Rhizobium leguminosarum biovar viciae. 77
Molecular mechanism of pore formation by actinoporins 77
Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores 77
Pore-forming peptides and protein toxins 77
Plasma assisted surface treatments of biomaterials 77
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 77
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 77
Identifying the Minimal Copper- and Zinc-binding Site Sequence in Amyloid-beta Peptides 76
Membrane permeabilizing activity of linusitin from flax seed 76
Ion channels and bacterial infection: the case of beta-barrel pore-forming protein toxins of Staphylococcus aureus. 76
XAS STUDIES OF CU(II) AND ZN(II) BINDING SITE IN AMYLOID PEPTIDES 75
The adsorption of Pseudomonas aeruginosa exotoxin A to phospholipid monolayers is controlled by pH and surface potential. 75
Intrinsic tryptophan fluorescence of equinatoxin II, a pore-forming polypeptide from the sea anemone Actinia equina L, monitors its interaction with lipid membranes. 74
Deposito della beta-amiloide sulla membrana cellulare: ruolo degli ioni metallici e dei radicali liberi 73
Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components. 73
Protein engineering modulates the transport properties and ion selectivity of the pores formed by staphylococcal gamma-haemolysins in lipid membranes. 73
Metal binding in amyloid beta-peptides shows intra- and inter-peptide coordination modes. 72
Metal binding in amyloids beta peptides shows both intra- and inter-peptide modes 71
Molecular modifications of the pore forming gamma hemolysins from Staphylococcus aureus 69
pH-activated doxorubicin release from polyelectrolyte complex layer coated mesoporous silica nanoparticles 69
The equinatoxin N-terminus is transferred across planar lipid membranes and helps to stabilize the transmembrane pore. 67
In vitro investigation of doxorubicin release from gold nanoparticles coated by polyelectrolyte multilayers 67
The interaction of lipodepsipeptide toxins from Pseudomonas syringae pv. syringae with biological and model membranes: a comparison of syringotoxin, syringomycin, and two syringopeptins. 66
The role of membrane lipid composition for the activity of Staphylococcus aureus gamma-hemolysins 65
Reversal of charge selectivity in transmembrane protein pores by using noncovalent molecular adapters. 65
The influence of membrane lipids in Staphylococcus aureus gamma-hemolysins pore formation 64
Sea anemone cytolysins as toxic component of immunotoxins 64
Conductive properties and gating of channels formed by syringopeptin 25A, a bioactive lipodepsipeptide from Pseudomonas syringae pv. syringae, in planar lipid membranes. 62
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions 60
Permeability increase induced by Escherichia coli hemolysin A in human macrophages is due to the formation of ionic pores: a patch clamp characterization. 59
Totale 8.664
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Categoria #
all - tutte 53.380
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 53.380
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2024/20253.000 30 62 329 94 32 60 133 178 1.168 342 413 159
2025/2026148 148 0 0 0 0 0 0 0 0 0 0 0
Totale 8.988