DALLA SERRA, MAURO
 Distribuzione geografica
Continente #
AS - Asia 3.162
NA - Nord America 1.798
SA - Sud America 650
EU - Europa 632
AF - Africa 60
Continente sconosciuto - Info sul continente non disponibili 60
OC - Oceania 3
Totale 6.365
Nazione #
US - Stati Uniti d'America 1.694
SG - Singapore 1.394
CN - Cina 678
BR - Brasile 521
HK - Hong Kong 326
VN - Vietnam 319
FR - Francia 207
IT - Italia 150
KR - Corea 118
JP - Giappone 92
GB - Regno Unito 59
NL - Olanda 58
BD - Bangladesh 54
AR - Argentina 52
IN - India 44
CA - Canada 37
DE - Germania 35
MX - Messico 27
FI - Finlandia 24
ZA - Sudafrica 24
ID - Indonesia 19
CO - Colombia 18
EC - Ecuador 18
IL - Israele 14
CL - Cile 13
PL - Polonia 13
TR - Turchia 13
EG - Egitto 12
IQ - Iraq 12
UZ - Uzbekistan 12
ES - Italia 10
RU - Federazione Russa 10
AT - Austria 9
LT - Lituania 9
SA - Arabia Saudita 9
UA - Ucraina 9
CR - Costa Rica 8
JO - Giordania 8
VE - Venezuela 8
MA - Marocco 7
PY - Paraguay 7
JM - Giamaica 6
PH - Filippine 6
UY - Uruguay 6
KE - Kenya 5
OM - Oman 5
TN - Tunisia 5
BB - Barbados 4
CZ - Repubblica Ceca 4
GT - Guatemala 4
KZ - Kazakistan 4
NP - Nepal 4
PE - Perù 4
PK - Pakistan 4
PT - Portogallo 4
TW - Taiwan 4
BA - Bosnia-Erzegovina 3
BG - Bulgaria 3
CH - Svizzera 3
IE - Irlanda 3
LV - Lettonia 3
PA - Panama 3
SE - Svezia 3
SV - El Salvador 3
TH - Thailandia 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
BH - Bahrain 2
BO - Bolivia 2
CY - Cipro 2
DO - Repubblica Dominicana 2
EE - Estonia 2
GE - Georgia 2
GR - Grecia 2
KG - Kirghizistan 2
LB - Libano 2
NI - Nicaragua 2
PS - Palestinian Territory 2
QA - Qatar 2
RO - Romania 2
SC - Seychelles 2
TT - Trinidad e Tobago 2
AO - Angola 1
AZ - Azerbaigian 1
BM - Bermuda 1
BZ - Belize 1
CI - Costa d'Avorio 1
CW - ???statistics.table.value.countryCode.CW??? 1
DK - Danimarca 1
HR - Croazia 1
HU - Ungheria 1
LC - Santa Lucia 1
LY - Libia 1
MD - Moldavia 1
MF - Saint Martin 1
MK - Macedonia 1
ML - Mali 1
MN - Mongolia 1
MY - Malesia 1
NZ - Nuova Zelanda 1
Totale 6.299
Città #
Singapore 836
Santa Clara 634
Hong Kong 320
Hefei 277
San Jose 212
Ashburn 151
Lauterbourg 150
Beijing 127
Seoul 115
Ho Chi Minh City 114
Los Angeles 79
Tokyo 75
Hanoi 70
Dallas 44
São Paulo 38
Helsinki 19
New York 18
Bolzano 17
Milan 15
Minamishinagawa 15
Da Nang 14
Rio de Janeiro 14
Atlanta 13
Guangzhou 12
London 12
Belo Horizonte 11
Chicago 11
Johannesburg 11
Montreal 11
Portsmouth 11
Bengaluru 10
Brooklyn 10
Buffalo 10
Dhaka 10
Haiphong 10
Orem 10
Paris 10
Porto Alegre 10
Brasília 9
Can Tho 9
Tashkent 9
Amman 8
Buenos Aires 8
Curitiba 8
Frankfurt am Main 8
Shanghai 8
Biên Hòa 7
Bologna 7
Guayaquil 7
Phoenix 7
Quito 7
Uberlândia 7
Warsaw 7
Baghdad 6
Bogotá 6
Bắc Ninh 6
Campinas 6
Cleveland 6
Houston 6
Nuremberg 6
San Antonio 6
San José 6
Santiago 6
Santo André 6
Thái Bình 6
Toronto 6
Wuppertal 6
Boston 5
Cairo 5
Catania 5
Chennai 5
Detroit 5
Düsseldorf 5
Fortaleza 5
Goiânia 5
Guarulhos 5
Hải Dương 5
Lấp Vò 5
Manchester 5
Mexico City 5
Nairobi 5
Naples 5
Orlando 5
Palermo 5
Riyadh 5
Rome 5
Salvador 5
Shenzhen 5
Trento 5
Tây Ninh 5
Vienna 5
Alexandria 4
Asunción 4
Campo Grande 4
Caruaru 4
Charlotte 4
Colombo 4
Cà Mau 4
Guatemala City 4
Imperatriz 4
Totale 3.882
Nome #
Neuronal firing modulation by a membrane-targeted photoswitch 133
SMN-primed ribosomes modulate the translation of transcripts related to spinal muscular atrophy 100
Sustained in vitro release and cell uptake of doxorubicin adsorbed onto gold nanoparticles and covered by a polyelectrolyte complex layer 98
y-Hemolysin oligomeric structure and effect of its formation on supported lipid bilayers: an AFM investigation 93
Antifungal activity of peach defensin involves plasma membrane permeabilization 81
New insights into the structure and function of actinoporins of sea anemones 75
In memory of Gianfranco Menestrina Preface 75
Targeting the Gut: A Systematic Review of Specific Drug Nanocarriers 72
A comparison of permeabilizing activity of lipodepsipeptides from Pseudomonas spp 69
Organic electrochemical transistors based on PEDOT:PSS: biocompatible devices to sense the pore formation in bilayer lipid membranes attacked by bacterial pore forming toxins 68
Interaction of grape and peach defensins with lipids 66
Interfacing primary cortical neurons with PMCS TiO2 films to design bio-hybrid memristive device mimicking neuromorphic functionalities 65
The new COST Action European Venom Network (EUVEN)—synergy and future perspectives of modern venomics 63
Human perforin employs different avenues to damage membranes 61
Resonance energy transfer investigation of the assembly of the oligomeric pore formed by bicomponent gamma-hemolysins of Staphylococcus aureus 61
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 60
Plasticity of Lysteriolysin O Pores and its Regulation by pH and Unique Histidine. 60
The Equinatoxin N-Terminus is Transferred Across Planar Bilayers and Helps to Stabilise the Transmembrane Pore 59
Characterisation of molecular properties of pore-forming toxins with planar lipid bilayers 57
Distinction between Pore Assembly by Staphylococcal alpha-Toxin versus Leukotoxins. 57
Artificial cells drive neural differentiation 57
Fungal MACPF-like proteins and aegerolysins: bi-component pore-forming proteins? 57
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions. 54
Homologous versus heterologous interactions in the pore of bicomponent staphylococcal g -hemolysins. 54
The peach (Prunus persica) defensin PpDFN1 displays antimicrobial activity against fungal pathogens through specific lipid binding and membrane permeabilization 54
Combinatorial Plasma Polymerisation Approach to Produce thin films for Testing Cell Proliferation 53
What planar lipid membranes tell us about the pore-forming activity of cholesterol-dependent cytolysins 52
The unexpected tuners: Are LNCRNAS regulating host translation during infections? 52
The peach (Prunus persica) defensin PpDFN1 displays antifungal activity through specific interactions with the membrane lipids 52
Pore formation by actinoporins, cytolysins from sea anemones 52
Membrane composition effects on pore-forming ability of two cholesterol-dependent cytolysins 51
pH-activated doxorubicin release from polyelectrolyte complex layer coated mesoporous silica nanoparticles 51
Vitis vinifera Lipoxygenase LoxA is an Allosteric Dimer Activated by Lipidic Surfaces 51
A new cells-compatible microfluidic device for single channel recordings 51
Global translation variations in host cells upon attack of lytic and sublytic Staphylococcus aureus alpha-haemolysin. 51
Alpha-synuclein pore forming activity upon membrane association 50
Plasma assisted surface treatments of biomaterials 50
Graphene oxide nanocomposite magnetic microbeads for the remediation of positively charged aromatic compounds 49
Perforin oligomers form arcs in cellular membranes: a locus for intracellular delivery of granzymes 49
p-Sulfonato-calix[n]arenes inhibit staphylococcal bicomponent leukotoxins by supramolecular interactions 49
Properties of pores formed by cholesterol-dependent cytolysins and actinoporins 48
Permeabilizing activity of antifungal lipodepsipeptides from Pseudomonas spp. on lipid membranes. 47
Cysteine-scanning mutagenesis of an eukaryotic pore-forming toxin from sea anemone - Topology in lipid membranes 47
Non-contact mechanical and chemical analysis of single living cells by microspectroscopic techniques 47
Functional Characterization of Sticholysin I and W111C Mutant Reveals the Sequence of the Actinoporin's Pore Assembly. 47
Regional Biophysics Conference - RBC2016 47
DOPAL derived alpha-synuclein oligomers impair synaptic vesicles physiological function 47
Deposito della beta-amiloide sulla membrana cellulare: ruolo degli ioni metallici e dei radicali liberi 47
Primary cortical neurons on PMCS TiO2 films towards bio-hybrid memristive device: A morpho-functional study. 47
Pore-forming Toxins 46
pH dependence of listeriolysin O aggregation and pore-forming ability 46
Biophysical Approaches to Protein Folding and Disease, a satellite meeting to the IUPAB-EBSA congress 46
The influence of potassium and sodium ions on the aggregation process of antibiotic amphotericin B in aqueous solution 45
Biosystems interfaced to memristors: Early evidences to study neuromorphic architectures 44
Synthesis and characterization of Raman active gold nanoparticles 44
PEDOT:PSS for electrochemical sensing of drug and biophysical applications 43
Investigations on alpha-synuclein pore forming properties 43
Effects of calcium and protons on the secondary structure of the nodulation protein NodO from Rhizobium leguminosarum biovar viciae 42
Listeriolysin Pore Forming Ability in Planar Lipid Membranes at Different pH 41
Raman micro-spectroscopy study of living SH-SY5Y cells adhering on different substrates 41
Interaction with model membranes and pore formation by human stefin B; studying the native and prefibrillar states. 41
Sea anemone cytolysins as toxic component of immunotoxins. 40
Metal ions and the conformation of peptides forming amyloid deposits in Alzheimer and prion disease 40
Ion channels and bacterial infection: the case of beta-barrel pore-forming protein toxins of Staphylococcus aureus. 39
Structural features of distinctin affecting peptide biological and biochemical properties 39
Perforin activity at membranes leads to invaginations and vesicle formation 38
Antimicrobial lipodepsipeptides from Pseudomonas spp: a comparison of their activity on model membranes 38
Multifunctional Branched Gold-Carbon Nanotube Hybrid for Cell Imaging and Drug Delivery 37
Liposomes in the study of pore-forming toxins 37
Staphylococcus aureus bi-component g-hemolysins, HlgA, HlgB and HlgC can form mixed pores containing all components. 37
Pore-forming cytolysins studied with model lipid membranes 36
Fast Flow Microfluidics and Single-Molecule Fluorescence for the Rapid Characterization of alpha-Synuclein Oligomers 36
Molecular mechanism of action of syringopeptins, antifungal peptides from Pseudomonas syringae pv. syringae 36
Metal binding in amyloid beta-peptides shows intra- and inter-peptide coordination modes 36
Global translation variations in host cells upon attack of lytic and sublytic Staphylococcus aureus ?-haemolysin1 36
A molecular pin to study the dynamics of b-barrel formation in Pore Forming Toxins on erythrocytes: a sliding model 35
The phytotoxic lipodepsipeptide syringopeptin 25A from Pseudomonas syringae pv syringae forms ion channels in sugar beet vacuoles 35
La siringopeptina 25 di Pseudomonas syringae pv. syringae forma canali ionici in vacuoli di barbabietola da zucchero 35
Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: cormycin A. 35
Effects of lipid composition on membrane permeabilization by sticholysin I and II, two cytolysins of the sea anemone Stichodactyla helianthus. 34
Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures 33
Membrane Damage by an alpha-Helical Pore Forming Protein Equinatoxin II Proceeds Through Succesion of Ordered Steps 33
Staphylococcal beta-barrel pore-forming toxins: an electrical characterization 33
Bacterial hemolysins and leukotoxins affect target cells by forming large exogenous pores into their plasma membrane. Escherichia coli hemolysin A as a case example 32
A novel mechanism of pore formation - Membrane penetration by the N-terminal amphipathic region of equinatoxin 32
Lipid Composition Analysis of Detergent Resistant Membranes Through a Multi-Technique Approach 32
Mechanism of action of syringomycin structural analogues with model membranes 31
Membrane damage by an alpha-helical pore-forming protein, Equinatoxin II, proceeds through a succession of ordered steps 31
Structure and activity of the N-terminal region of the eukaryotic cytolysin equinatoxin II. 31
Incorporation of channel forming phytotoxic peptides in vacuoles from higher plant cells 31
Mechanism of membrane permeabilization by sticholysin I, a cytolysin isolated from the venom of the sea anemone Stichodactyla helianthus 30
Structural features affecting antimicrobial activity, membrane interaction and resistance to proteases of distinctin. 30
The radius of the pore formed by the sea anemone sticholysin I in erythrocytes and lipid vesicles 30
Rilevanza dell'aminoacido C-terminale della siringomicina per la sua interazione con le membrane 30
Pore-forming peptides and protein toxins 29
Architecture of human perforin pore in pure lipid bilayers 29
A tumor protease-activated conjugate based on a sea anemone toxin: its cytotoxic activity on cancer cells 29
Internalization of staphylococcal leukotoxins that bind and divert C5aR is required for intracellular Ca2+ mobilization by human neutrophils. 29
gamma-Hemolysin oligomeric structure and effect of its formation on supported lipid bilayers: An AFM Investigation 29
Role of EqTII N-terminal alfa-helix in pore formation on planar lipid bilayers 28
Totale 4.769
Categoria #
all - tutte 23.568
article - articoli 20.506
book - libri 104
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.101
Totale 45.279


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202412 0 0 0 0 0 0 0 0 0 0 11 1
2024/20252.377 10 11 175 101 572 87 31 128 81 72 593 516
2025/20263.719 176 378 339 609 624 163 621 192 233 182 98 104
2026/2027257 246 11 0 0 0 0 0 0 0 0 0 0
Totale 6.365