IRIS Institutional Research Information System

Dalla Serra, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 4.008
EU - Europa 3.096
AS - Asia 1.238
SA - Sud America 273
AF - Africa 36
Continente sconosciuto - Info sul continente non disponibili 27
OC - Oceania 7
Totale 8.685
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Nazione #
US - Stati Uniti d'America 3.966
RU - Federazione Russa 1.075
SG - Singapore 501
DE - Germania 478
SE - Svezia 435
UA - Ucraina 340
BR - Brasile 255
HK - Hong Kong 253
FI - Finlandia 230
CN - Cina 222
IE - Irlanda 114
NL - Olanda 114
VN - Vietnam 107
GB - Regno Unito 102
IT - Italia 70
IN - India 69
BE - Belgio 37
CA - Canada 37
FR - Francia 34
ZA - Sudafrica 27
EU - Europa 26
CZ - Repubblica Ceca 22
IR - Iran 18
LT - Lituania 13
PL - Polonia 10
BD - Bangladesh 9
ES - Italia 9
IQ - Iraq 9
AR - Argentina 8
TR - Turchia 7
AT - Austria 6
UZ - Uzbekistan 6
CH - Svizzera 5
EG - Egitto 5
IL - Israele 5
AE - Emirati Arabi Uniti 4
AU - Australia 4
JP - Giappone 4
PE - Perù 4
PK - Pakistan 4
JO - Giordania 3
NZ - Nuova Zelanda 3
AZ - Azerbaigian 2
EC - Ecuador 2
KR - Corea 2
LA - Repubblica Popolare Democratica del Laos 2
MA - Marocco 2
MX - Messico 2
PH - Filippine 2
PY - Paraguay 2
AM - Armenia 1
BB - Barbados 1
CY - Cipro 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
KE - Kenya 1
KZ - Kazakistan 1
LB - Libano 1
LK - Sri Lanka 1
NP - Nepal 1
PS - Palestinian Territory 1
PT - Portogallo 1
SA - Arabia Saudita 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 8.685
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Città #
Chandler 860
Jacksonville 737
Singapore 303
Moscow 277
Hong Kong 251
Ashburn 212
Wilmington 177
Boardman 155
The Dalles 123
Helsinki 116
Dublin 112
Hefei 109
Dong Ket 106
Ann Arbor 105
Dearborn 102
New York 101
Kronberg 95
Woodbridge 64
Brooklyn 51
Beijing 44
Santa Clara 44
Munich 42
Los Angeles 41
Pune 36
Brussels 33
Phoenix 32
Shanghai 31
Trento 28
Seattle 27
Falkenstein 20
Brno 19
Toronto 19
Secaucus 18
Houston 17
São Paulo 15
London 14
Turku 13
Falls Church 12
Miami 12
Norwalk 11
Brasília 10
Cologne 10
Frankfurt am Main 10
Leawood 9
Portland 9
Amsterdam 8
Ardabil 8
Curitiba 8
San Mateo 8
Charlotte 7
Milan 7
Ottawa 7
Redwood City 7
Rio de Janeiro 7
Saint Petersburg 7
Salvador 7
Warsaw 7
Augusta 6
Campinas 6
Monmouth Junction 6
Montreal 6
Nanjing 6
St Petersburg 6
Auburn Hills 5
Cairo 5
Hanover 5
Nuremberg 5
Tashkent 5
Zanjan 5
Bangalore 4
Buffalo 4
Cheyenne 4
Guangzhou 4
Paris 4
Redmond 4
Zurich 4
Amman 3
Aracaju 3
Baghdad 3
Belém 3
Chicago 3
Des Moines 3
Erbil 3
Guarulhos 3
Gunzenhausen 3
Lima 3
Mumbai 3
Recife 3
Roussillon 3
San Francisco 3
Santo André 3
Stirling 3
Stockholm 3
Tokyo 3
Vienna 3
Aparecida de Goiânia 2
Araraquara 2
Bagé 2
Baku 2
Barcelona 2
Totale 4.881
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Nome #
Combinatorial plasma deposition of C-based films to test cell adhesion 133
A novel mechanism of pore formation: membrane penetration by the N-terminal amphipathic region of equinatoxin. 127
Bio-hybrid interfaces to study neuromorphic functionalities: New multidisciplinary evidences of cell viability on poly(anyline) (PANI), a semiconductor polymer with memristive properties 123
Binding of antibodies to functional epitopes on the pore formed by Escherichia coli hemolysin in cells and model membranes. 121
Alpha-synuclein pore forming activity upon membrane association 116
para-sulfonato-calix[n]arenes inhibit staphylococcal bicomponent leukotoxins by supramolecular interactions. 111
A fluorimetric assay for the effects of cytolytic toxins on the transport properties of resealed erythrocyte ghosts. 111
Neuronal firing modulation by a membrane-targeted photoswitch 111
γ-Hemolysin Oligomeric Structure and Effect of its Formation on Supported Lipid Bilayers: an AFM Investigation 107
Antiparasite activity of sea-anemone cytolysins on Giardia duodenalis and specific targeting with anti-Giardia antibodies. 105
Bacterial hemolysins and leukotoxins affect target cells by forming large exogenous pores into their plasma membrane: Escherichia coli hemolysin A as a case example. 105
Activation energy of the cardiac Na+/Ca2+ exchanger in sarcolemmal vesicles and reconstituted proteoliposomes. 104
Biochemical and cytotoxic properties of conjugates of transferrin with equinatoxin II, a cytolysin from a sea anemone. 101
A XAS study of the geometrical arrangement of Cu(II)-binding octarepeat peptides 100
Effects of lipid composition on membrane permeabilization by two cytolysins of the sea anemone Stichodactyla helianthus, St I and St II 100
Anticandida activity is retained in P-113, a 12-amino-acid fragment of histatin 5. 98
Structural features of distinctin affecting peptide biological and biochemical properties 97
Use of nanostructures for cancer care 97
Homologous versus heterologous interactions in the pore of bicomponent staphylococcal gamma-hemolysins 96
N-terminal deletion affects catalytic activity of saporin toxin 95
Biopolymer surface coatings for the treatment of staphylococcal infections 95
Human perforin employs different avenues to damage membranes 94
N-terminal-bearing peptide derived from the pore-forming protein Sticholysin II interacts with lipid bilayer. 93
A tumor protease-activated conjugate based on a sea anemone toxin: its cytotoxic activity on cancer cells. 93
Cytotoxic activity of a tumor protease-activated pore-forming toxin. 92
pH dependence of listeriolysin O aggregation and pore-forming ability 91
A tumor protease-activated pore forming toxin as a specific anticancer tool 89
Effects of lipid composition on membrane permeabilization by sticholysin I and II, two cytolysins of the sea anemone Stichodactyla helianthus. 88
Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures. 88
HOW A METABOLITE OF DOPAMINE CAN TRANSFORM ALPHA­SYNUCLEIN IN AN ENDOTOXIN 88
Tolaasin I, Lipodepsipeptides from Pseudomonas reactans and Pseudomonas tolaasii, permeabilize model membranes 88
Construction of the I18C-EqtII – avidin conjugate via a biotinylated peptide and its cytotoxic activity. 87
Structure and activity of the N-terminal region of the eukaryotic cytolysin equinatoxin II. 86
Synthesis of plasmonic gold/carbon nanotubes hybrid structures for cell imaging and drug delivery 86
Peptides derived from apoptotic Bax and Bid reproduce the poration activity of the parent full-length proteins 86
Combinatorial Plasma Polymerization Approach to Produce Thin Films for Testing Cell proliferation 86
Multifunctional branched gold-carbon nanotube hybrid for cell imaging and drug delivery 86
Anomalously high aggregation level of the polyene antibiotic amphotericin B in acidic medium: implications for the biological action. 85
Interaction with model membranes and pore formation by human stefin B; studying the native and prefibrillar states 85
Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components. 84
Liposomes in the study of pore-forming toxins. 84
A molecular pin to study the dynamic of á-barrel formation in Pore Forming Toxins on erythrocytes: a sliding model 84
A fluorescence-based assay for the reductase activity of protein disulfide isomerase 84
The Influence of Membrane Lipids in Staphylococcus aureus Gamma-Hemolysins Pore Formation 83
Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer 83
Listeriolysin O pore-forming abilities on lipid membranes 83
Perforin oligomers form arcs in cellular membranes: a locus for intracellular delivery of granzymes 83
The interaction of Staphylococcus aureus bi-component gamma-hemolysins and leucocidins with cells and lipid membranes. 83
Characterization of anticholinesterase-active 3-alkylpyridinium polymers from the marine sponge Reniera sarai in aqueous solutions. 82
Lipid modulation on structure and function abilities of two Cholesterol--Dependent Cytolysins 82
Potential inhibitors of Staphylococccus aureus bi-components γ-hemolysins 81
Synthesis and characterization of Raman active gold nanoparticles 81
Mechanism of membrane permeabilization by sticholysin I, a cytolysin isolated from the venom of the sea anemone Stichodactyla helianthus. 81
Self-potentiation of ligand-toxin conjugates containing ricin A chain fused with viral structures. 81
Distinction between pore assembly by staphylococcal α-toxin versus leukotoxins 81
Site directed mutagenesis to assess the binding capacity of class S protein of Staphylococcus aureus leucotoxins to the surface of polymorphonuclear cells 81
The mode of action of bicomponent gamma-hemolysins of Staphylococcus aureus. 80
Binding of antibiotic amphotericin B to lipid membranes: Monomolecular layer technique and linear dichroism-FTIR studies 80
Mode of action of beta-barrel pore-forming toxins of the staphylococcal alpha-hemolysin family. 79
Plasticity of Listeriolysin O Pores Revealed by Mutagenesis of a Unique Histidine 79
Directly assessment of drug release dynamics from gold nanoparticles 78
Cysteine-scanning mutagenesis of an eukaryotic pore-forming toxin from sea anemone: topology in lipid membranes. 78
Fuscopeptins, antimicrobial lipodepsipeptides from Pseudomonas fuscovaginae, are channel forming peptides active on biological and model membranes 78
Les leucotoxines de staphylocoque: de l'investigation bio-structurale vers la notion d'inhibiteurs 77
Construction of EqtII mutants immunoconjugates and characterization of their cytotoxic activity 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
Sizing the radius of the pore formed in erythrocytes and lipid vesicles by the toxin sticholysin I from the sea anemone Stichodactyla helianthus. 76
Perforin activity at membranes leads to invaginations and vesicle formation 76
Molecular mechanism of pore formation by actinoporins 76
Pore-forming peptides and protein toxins 76
EPR and FTIR studies reveal the importance of highly ordered sterol-enriched membrane domains for ostreolysin activity. 75
Identifying the Minimal Copper- and Zinc-binding Site Sequence in Amyloid-beta Peptides 75
Ion channels and bacterial infection: the case of beta-barrel pore-forming protein toxins of Staphylococcus aureus. 75
The adsorption of Pseudomonas aeruginosa exotoxin A to phospholipid monolayers is controlled by pH and surface potential. 74
Effects of calcium and protons on the secondary structure of the nodulation protein NodO from Rhizobium leguminosarum biovar viciae. 74
Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores 74
Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: Cormycin A 74
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 74
XAS STUDIES OF CU(II) AND ZN(II) BINDING SITE IN AMYLOID PEPTIDES 73
Membrane permeabilizing activity of linusitin from flax seed 73
Biological Characterisation of WLIP produced by Pseudomonas reactans strain NCPPB1311 73
Intrinsic tryptophan fluorescence of equinatoxin II, a pore-forming polypeptide from the sea anemone Actinia equina L, monitors its interaction with lipid membranes. 73
Deposito della beta-amiloide sulla membrana cellulare: ruolo degli ioni metallici e dei radicali liberi 72
Protein engineering modulates the transport properties and ion selectivity of the pores formed by staphylococcal gamma-haemolysins in lipid membranes. 72
Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components. 71
Plasma assisted surface treatments of biomaterials 71
Metal binding in amyloid beta-peptides shows intra- and inter-peptide coordination modes. 70
Metal binding in amyloids beta peptides shows both intra- and inter-peptide modes 69
pH-activated doxorubicin release from polyelectrolyte complex layer coated mesoporous silica nanoparticles 69
Molecular modifications of the pore forming gamma hemolysins from Staphylococcus aureus 68
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 66
The interaction of lipodepsipeptide toxins from Pseudomonas syringae pv. syringae with biological and model membranes: a comparison of syringotoxin, syringomycin, and two syringopeptins. 65
The role of membrane lipid composition for the activity of Staphylococcus aureus gamma-hemolysins 64
Reversal of charge selectivity in transmembrane protein pores by using noncovalent molecular adapters. 64
Sea anemone cytolysins as toxic component of immunotoxins 64
The influence of membrane lipids in Staphylococcus aureus gamma-hemolysins pore formation 63
Conductive properties and gating of channels formed by syringopeptin 25A, a bioactive lipodepsipeptide from Pseudomonas syringae pv. syringae, in planar lipid membranes. 61
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions 59
Permeability increase induced by Escherichia coli hemolysin A in human macrophages is due to the formation of ionic pores: a patch clamp characterization. 58
Totale 8.412
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Categoria #
all - tutte 51.686
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 51.686
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202070 0 0 0 0 0 0 0 0 0 0 0 70
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
2024/20252.886 30 62 329 94 32 60 133 178 1.168 342 413 45
Totale 8.726