Dalla Serra, Mauro
 Distribuzione geografica
Continente #
NA - Nord America 3.466
EU - Europa 1.750
AS - Asia 531
AF - Africa 27
Continente sconosciuto - Info sul continente non disponibili 26
OC - Oceania 7
SA - Sud America 5
Totale 5.812
Nazione #
US - Stati Uniti d'America 3.457
SE - Svezia 432
DE - Germania 399
UA - Ucraina 340
FI - Finlandia 186
HK - Hong Kong 186
IE - Irlanda 113
VN - Vietnam 106
CN - Cina 102
GB - Regno Unito 81
IN - India 62
RU - Federazione Russa 58
IT - Italia 51
SG - Singapore 44
BE - Belgio 31
FR - Francia 30
ZA - Sudafrica 27
EU - Europa 26
CZ - Repubblica Ceca 20
IR - Iran 17
CA - Canada 9
ES - Italia 5
IL - Israele 5
AU - Australia 4
BR - Brasile 3
JP - Giappone 3
NZ - Nuova Zelanda 3
AR - Argentina 2
IQ - Iraq 2
KR - Corea 2
NL - Olanda 2
CH - Svizzera 1
LB - Libano 1
PL - Polonia 1
TH - Thailandia 1
Totale 5.812
Città #
Chandler 860
Jacksonville 737
Ashburn 199
Hong Kong 184
Wilmington 177
Boardman 138
Dublin 111
Dong Ket 106
Ann Arbor 105
Dearborn 102
Kronberg 95
New York 92
Helsinki 85
Woodbridge 64
Brooklyn 48
Beijing 44
Pune 36
Singapore 34
Phoenix 31
Shanghai 29
Trento 28
Brussels 27
Seattle 27
Los Angeles 24
Brno 19
Secaucus 18
Houston 16
Falls Church 12
Munich 12
Norwalk 11
Santa Clara 11
Cologne 10
Leawood 9
Portland 9
Ardabil 8
San Mateo 8
Redwood City 7
Saint Petersburg 7
Augusta 6
Monmouth Junction 6
St Petersburg 6
Auburn Hills 5
Falkenstein 5
Hanover 5
Nanjing 5
Toronto 5
Zanjan 5
Bangalore 4
Charlotte 4
Cheyenne 4
Redmond 4
Des Moines 3
Guangzhou 3
Gunzenhausen 3
Hefei 3
Roussillon 3
Stirling 3
Tokyo 3
Baghdad 2
Barcelona 2
Buenos Aires 2
Buffalo 2
Fuzhou 2
Gent 2
Ghent 2
Jinan 2
Kunming 2
Madrid 2
Mountain View 2
Mumbai 2
Sacramento 2
Sydney 2
São Luís 2
Turin 2
Wrexham 2
Wuhan 2
Xian 2
Andover 1
Auckland 1
Bad Muenstereifel 1
Berkeley 1
Borgo Valsugana 1
Brisbane 1
Castellón 1
Central District 1
Changsha 1
Costa Mesa 1
Enfield 1
Frankfurt am Main 1
Gif-sur-yvette 1
Hamilton 1
Inglewood 1
Lara 1
Las Vegas 1
Lausanne 1
Limerick 1
London 1
Milan 1
Mississauga 1
Mysiadło 1
Totale 3.686
Nome #
Combinatorial plasma deposition of C-based films to test cell adhesion 101
A novel mechanism of pore formation: membrane penetration by the N-terminal amphipathic region of equinatoxin. 85
Bio-hybrid interfaces to study neuromorphic functionalities: New multidisciplinary evidences of cell viability on poly(anyline) (PANI), a semiconductor polymer with memristive properties 85
para-sulfonato-calix[n]arenes inhibit staphylococcal bicomponent leukotoxins by supramolecular interactions. 79
A fluorimetric assay for the effects of cytolytic toxins on the transport properties of resealed erythrocyte ghosts. 78
Bacterial hemolysins and leukotoxins affect target cells by forming large exogenous pores into their plasma membrane: Escherichia coli hemolysin A as a case example. 77
N-terminal deletion affects catalytic activity of saporin toxin 76
Alpha-synuclein pore forming activity upon membrane association 76
γ-Hemolysin Oligomeric Structure and Effect of its Formation on Supported Lipid Bilayers: an AFM Investigation 75
N-terminal-bearing peptide derived from the pore-forming protein Sticholysin II interacts with lipid bilayer. 72
Effects of lipid composition on membrane permeabilization by two cytolysins of the sea anemone Stichodactyla helianthus, St I and St II 72
Cytotoxic activity of a tumor protease-activated pore-forming toxin. 70
Binding of antibodies to functional epitopes on the pore formed by Escherichia coli hemolysin in cells and model membranes. 69
Biochemical and cytotoxic properties of conjugates of transferrin with equinatoxin II, a cytolysin from a sea anemone. 68
Human perforin employs different avenues to damage membranes 68
Activation energy of the cardiac Na+/Ca2+ exchanger in sarcolemmal vesicles and reconstituted proteoliposomes. 67
Structural features of distinctin affecting peptide biological and biochemical properties 65
A XAS study of the geometrical arrangement of Cu(II)-binding octarepeat peptides 63
Antiparasite activity of sea-anemone cytolysins on Giardia duodenalis and specific targeting with anti-Giardia antibodies. 63
Homologous versus heterologous interactions in the pore of bicomponent staphylococcal gamma-hemolysins 63
Construction of the I18C-EqtII – avidin conjugate via a biotinylated peptide and its cytotoxic activity. 62
Potential inhibitors of Staphylococccus aureus bi-components γ-hemolysins 62
A tumor protease-activated conjugate based on a sea anemone toxin: its cytotoxic activity on cancer cells. 62
Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures. 62
Liposomes in the study of pore-forming toxins. 62
Interaction with model membranes and pore formation by human stefin B; studying the native and prefibrillar states 62
A tumor protease-activated pore forming toxin as a specific anticancer tool 61
HOW A METABOLITE OF DOPAMINE CAN TRANSFORM ALPHA­SYNUCLEIN IN AN ENDOTOXIN 61
Biopolymer surface coatings for the treatment of staphylococcal infections 61
Anticandida activity is retained in P-113, a 12-amino-acid fragment of histatin 5. 60
pH dependence of listeriolysin O aggregation and pore-forming ability 60
Structure and activity of the N-terminal region of the eukaryotic cytolysin equinatoxin II. 59
Characterization of anticholinesterase-active 3-alkylpyridinium polymers from the marine sponge Reniera sarai in aqueous solutions. 59
Synthesis of plasmonic gold/carbon nanotubes hybrid structures for cell imaging and drug delivery 59
The Influence of Membrane Lipids in Staphylococcus aureus Gamma-Hemolysins Pore Formation 58
Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components. 58
Anomalously high aggregation level of the polyene antibiotic amphotericin B in acidic medium: implications for the biological action. 58
Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer 58
Listeriolysin O pore-forming abilities on lipid membranes 58
Fuscopeptins, antimicrobial lipodepsipeptides from Pseudomonas fuscovaginae, are channel forming peptides active on biological and model membranes 58
Peptides derived from apoptotic Bax and Bid reproduce the poration activity of the parent full-length proteins 58
Effects of lipid composition on membrane permeabilization by sticholysin I and II, two cytolysins of the sea anemone Stichodactyla helianthus. 57
Construction of EqtII mutants immunoconjugates and characterization of their cytotoxic activity 57
The mode of action of bicomponent gamma-hemolysins of Staphylococcus aureus. 57
Synthesis and characterization of Raman active gold nanoparticles 57
A molecular pin to study the dynamic of á-barrel formation in Pore Forming Toxins on erythrocytes: a sliding model 57
A fluorescence-based assay for the reductase activity of protein disulfide isomerase 57
Tolaasin I, Lipodepsipeptides from Pseudomonas reactans and Pseudomonas tolaasii, permeabilize model membranes 57
Cysteine-scanning mutagenesis of an eukaryotic pore-forming toxin from sea anemone: topology in lipid membranes. 56
Mechanism of membrane permeabilization by sticholysin I, a cytolysin isolated from the venom of the sea anemone Stichodactyla helianthus. 56
Use of nanostructures for cancer care 55
Self-potentiation of ligand-toxin conjugates containing ricin A chain fused with viral structures. 55
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 55
Sizing the radius of the pore formed in erythrocytes and lipid vesicles by the toxin sticholysin I from the sea anemone Stichodactyla helianthus. 54
The interaction of Staphylococcus aureus bi-component gamma-hemolysins and leucocidins with cells and lipid membranes. 54
The adsorption of Pseudomonas aeruginosa exotoxin A to phospholipid monolayers is controlled by pH and surface potential. 53
Perforin activity at membranes leads to invaginations and vesicle formation 53
Site directed mutagenesis to assess the binding capacity of class S protein of Staphylococcus aureus leucotoxins to the surface of polymorphonuclear cells 53
Pore-forming peptides and protein toxins 53
Perforin oligomers form arcs in cellular membranes: a locus for intracellular delivery of granzymes 53
Multifunctional branched gold-carbon nanotube hybrid for cell imaging and drug delivery 53
Les leucotoxines de staphylocoque: de l'investigation bio-structurale vers la notion d'inhibiteurs 52
Identifying the Minimal Copper- and Zinc-binding Site Sequence in Amyloid-beta Peptides 52
Distinction between pore assembly by staphylococcal α-toxin versus leukotoxins 52
Intrinsic tryptophan fluorescence of equinatoxin II, a pore-forming polypeptide from the sea anemone Actinia equina L, monitors its interaction with lipid membranes. 52
Neuronal firing modulation by a membrane-targeted photoswitch 52
Directly assessment of drug release dynamics from gold nanoparticles 51
Protein engineering modulates the transport properties and ion selectivity of the pores formed by staphylococcal gamma-haemolysins in lipid membranes. 51
Combinatorial Plasma Polymerization Approach to Produce Thin Films for Testing Cell proliferation 51
Membrane permeabilizing activity of linusitin from flax seed 50
Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components. 50
Mode of action of beta-barrel pore-forming toxins of the staphylococcal alpha-hemolysin family. 50
Effects of calcium and protons on the secondary structure of the nodulation protein NodO from Rhizobium leguminosarum biovar viciae. 50
Molecular mechanism of pore formation by actinoporins 50
Lipid modulation on structure and function abilities of two Cholesterol--Dependent Cytolysins 50
Binding of antibiotic amphotericin B to lipid membranes: Monomolecular layer technique and linear dichroism-FTIR studies 49
pH-activated doxorubicin release from polyelectrolyte complex layer coated mesoporous silica nanoparticles 49
Plasticity of Listeriolysin O Pores Revealed by Mutagenesis of a Unique Histidine 49
Molecular modifications of the pore forming gamma hemolysins from Staphylococcus aureus 48
Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: Cormycin A 48
The influence of membrane lipids in Staphylococcus aureus gamma-hemolysins pore formation 47
Reversal of charge selectivity in transmembrane protein pores by using noncovalent molecular adapters. 47
In vitro investigation of doxorubicin release from gold nanoparticles coated by polyelectrolyte multilayers 47
Biological Characterisation of WLIP produced by Pseudomonas reactans strain NCPPB1311 47
The equinatoxin N-terminus is transferred across planar lipid membranes and helps to stabilize the transmembrane pore. 46
Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores 46
EPR and FTIR studies reveal the importance of highly ordered sterol-enriched membrane domains for ostreolysin activity. 45
Deposito della beta-amiloide sulla membrana cellulare: ruolo degli ioni metallici e dei radicali liberi 45
Metal binding in amyloids beta peptides shows both intra- and inter-peptide modes 45
Ion channels and bacterial infection: the case of beta-barrel pore-forming protein toxins of Staphylococcus aureus. 45
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 45
Conductive properties and gating of channels formed by syringopeptin 25A, a bioactive lipodepsipeptide from Pseudomonas syringae pv. syringae, in planar lipid membranes. 44
The interaction of lipodepsipeptide toxins from Pseudomonas syringae pv. syringae with biological and model membranes: a comparison of syringotoxin, syringomycin, and two syringopeptins. 44
Sea anemone cytolysins as toxic component of immunotoxins 44
Plasma assisted surface treatments of biomaterials 44
Metal binding in amyloid beta-peptides shows intra- and inter-peptide coordination modes. 43
The role of membrane lipid composition for the activity of Staphylococcus aureus gamma-hemolysins 42
XAS STUDIES OF CU(II) AND ZN(II) BINDING SITE IN AMYLOID PEPTIDES 42
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions 41
Organization of two-component monomolecular layers formed with dipalmitoylphosphatidylcholine and the carotenoid pigment, canthaxanthin 39
Totale 5.676
Categoria #
all - tutte 35.304
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 35.304


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020958 110 104 5 5 142 74 127 20 120 54 127 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
2024/202510 10 0 0 0 0 0 0 0 0 0 0 0
Totale 5.850