IRIS
BATTISTONI, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 42.399
EU - Europa 6.648
AS - Asia 4.708
SA - Sud America 751
Continente sconosciuto - Info sul continente non disponibili 639
AF - Africa 80
OC - Oceania 29
Totale 55.254
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Nazione #
US - Stati Uniti d'America 42.181
SG - Singapore 2.031
PL - Polonia 1.464
CN - Cina 962
IT - Italia 883
FR - Francia 839
DE - Germania 812
BR - Brasile 622
UA - Ucraina 586
RU - Federazione Russa 545
HK - Hong Kong 498
VN - Vietnam 391
IE - Irlanda 372
GB - Regno Unito 333
SE - Svezia 306
FI - Finlandia 216
BD - Bangladesh 188
JP - Giappone 150
KR - Corea 138
CA - Canada 122
IN - India 78
NL - Olanda 68
ID - Indonesia 65
AR - Argentina 55
BE - Belgio 50
ES - Italia 36
AT - Austria 33
MX - Messico 31
EU - Europa 28
AU - Australia 26
IQ - Iraq 25
TR - Turchia 23
ZA - Sudafrica 22
EC - Ecuador 21
MY - Malesia 21
PH - Filippine 21
SA - Arabia Saudita 18
LT - Lituania 15
PK - Pakistan 15
CH - Svizzera 13
CL - Cile 13
KE - Kenya 13
CR - Costa Rica 12
CZ - Repubblica Ceca 12
VE - Venezuela 11
AE - Emirati Arabi Uniti 10
CO - Colombia 10
UZ - Uzbekistan 10
HU - Ungheria 9
JM - Giamaica 9
MA - Marocco 9
TT - Trinidad e Tobago 9
IL - Israele 8
PY - Paraguay 8
PT - Portogallo 7
TH - Thailandia 7
TN - Tunisia 7
DZ - Algeria 6
GR - Grecia 6
HN - Honduras 6
JO - Giordania 6
OM - Oman 6
UY - Uruguay 6
AL - Albania 5
HR - Croazia 5
KG - Kirghizistan 5
SI - Slovenia 5
DK - Danimarca 4
DM - Dominica 4
DO - Repubblica Dominicana 4
EG - Egitto 4
ET - Etiopia 4
GT - Guatemala 4
LB - Libano 4
NP - Nepal 4
PA - Panama 4
PR - Porto Rico 4
PS - Palestinian Territory 4
RO - Romania 4
SN - Senegal 4
BO - Bolivia 3
BY - Bielorussia 3
GE - Georgia 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
TW - Taiwan 3
AO - Angola 2
AZ - Azerbaigian 2
BB - Barbados 2
BS - Bahamas 2
BW - Botswana 2
KH - Cambogia 2
KW - Kuwait 2
LK - Sri Lanka 2
LV - Lettonia 2
MT - Malta 2
NG - Nigeria 2
NI - Nicaragua 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
Totale 54.621
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Città #
Woodbridge 12.162
Wilmington 10.285
Houston 8.891
Kraków 1.429
Singapore 1.171
Fairfield 1.078
Ashburn 1.058
Ann Arbor 724
Chandler 702
San Jose 560
Seattle 542
Jacksonville 529
Hong Kong 490
Cambridge 426
Beijing 365
Dublin 362
Council Bluffs 352
Rome 307
Medford 274
New York 265
Dearborn 249
Santa Clara 237
The Dalles 236
Los Angeles 193
Lawrence 130
Tokyo 125
Ho Chi Minh City 108
Buffalo 94
Hanoi 91
Helsinki 91
Mülheim 86
Dallas 78
Munich 69
São Paulo 68
Milan 67
San Diego 66
Boardman 65
Creede 65
Moscow 60
Lauterbourg 55
Phoenix 51
Brussels 48
London 46
North Charleston 46
Jakarta 45
Menlo Park 44
Nuremberg 43
Orem 43
Chicago 40
Toronto 39
Falls Church 38
Montreal 36
Brooklyn 35
Guangzhou 32
Amsterdam 28
Frankfurt am Main 27
North Bergen 27
San Mateo 26
Rio de Janeiro 24
Verona 24
Dong Ket 23
Stockholm 23
Warsaw 23
Denver 22
Norwalk 21
San Francisco 21
University Park 21
Detroit 20
Philadelphia 20
Poplar 20
Turin 18
Washington 18
Zhengzhou 18
Da Nang 17
Paris 17
Belo Horizonte 16
Chennai 16
Kunming 16
Manchester 16
Redondo Beach 16
Redwood City 16
Boston 15
Curitiba 15
Del Norte 15
Johannesburg 15
Mountain View 15
Nanjing 15
Ciampino 14
Shanghai 14
Atlanta 13
Columbus 13
Hefei 13
Las Vegas 13
Norwich 12
Seongnam 12
Baghdad 11
Haiphong 11
Jeddah 11
Melbourne 11
Nürnberg 11
Totale 45.594
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Nome #
A histidine-rich metal binding domain at the N terminus of Cu,Zn-superoxide dismutases from pathogenic bacteria 654
A role for Haemophilus ducreyi Cu,ZnSOD in resistance to heme toxicity 595
Unique structural features of the monomeric Cu,Zn superoxide dismutase from Escherichia coli, revealed by X-ray crystallography 548
The Salmonella enterica ZinT structure, zinc affinity and interaction with the high-affinity uptake protein ZnuA provide insight into the management of periplasmic zinc 539
10-undecanhydroxamic acid, a hydroxamate derivative of the undecanoic acid, has strong antimicrobial activity through a mechanism that limits iron availability 535
Low-Shear Modeled Microgravity Enhances Salmonella Enterica Resistance to Hydrogen Peroxide Through a Mechanism Involving KatG and KatN 531
Structural-dynamical investigation of the ZnuA histidine-rich loop: involvement in zinc management and transport 529
Oxidative stress and antioxidant therapy in cystic fibrosis 529
Mutation of Lys-120 and Lys-134 drastically reduces the catalytic rate of Cu,Zn superoxide dismutase 523
Unfolding and inactivation of monomeric superoxide dismutase from E. coli by SDS 520
Functional and crystallographic characterization of Salmonella typhimurium Cu,Zn superoxide dismutase coded by the sodCI virulence gene 517
Copper and zinc binding properties of the N-terminal histidine-rich sequence of Haemophilus ducreyi Cu,Zn superoxide dismutase 516
An attenuated Salmonella enterica serovar Typhimurium strain lacking the ZnuABC transporter induces protection in a mouse intestinal model of Salmonella infection 515
Salmonella enterica serovar Typhimurium growth is inhibited by the concomitant binding of Zn(II) and a pyrrolyl-hydroxamate to ZnuA, the soluble component of the ZnuABC transporter 511
Salmonella enterica serovar Typhimurium exploits inflammation to modify swine intestinal microbiota 510
Three-dimensional structure of Xenopus laevis Cu,Zn superoxide dismutase b determined by X-ray crystallography at 1.5 A resolution 509
Site-directed mutagenesis of human glutathione transferase P1-1. Spectral, kinetic, and structural properties of Cys-47 and Lys-54 mutants 508
Increased expression of periplasmic Cu,Zn superoxide dismutase enhances survival of Escherichia coli invasive strains within nonphagocytic cells 505
WS2.4 Pseudomonas aeruginosa capability to colonize the CF lung may be favored by its remarkable ability to recruit zinc under conditions of limited metal availability 504
Zinc sequestration by the neutrophil protein calprotectin enhances Salmonella growth in the inflamed gut 500
Toward the engineering of a super efficient enzyme 498
Salmonella Mitigates Oxidative Stress and Thrives in the Inflamed Gut by Evading Calprotectin-Mediated Manganese Sequestration 496
Single mutations at the subunit interface modulate copper reactivity in Photobacterium leiognathi Cu,Zn superoxide dismutase 495
Unique features of the sodC-encoded superoxide dismutase from Mycobacterium tuberculosis, a fully functional copper-containing enzyme lacking zinc in the active site 495
Attenuated mutant strain of Salmonella Typhimurium lacking the ZnuABC transporter contrasts tumor growth promoting anti-cancer immune response 495
Phenotypic profile linked to inhibition of the major Zn influx system in Salmonella enterica: proteomics and ionomics investigations 493
Distinctive functional features in prokaryotic and eukaryotic Cu,Zn superoxide dismutases 492
Attenuated Salmonella enterica serovar Typhimurium lacking the ZnuABC transporter confers immune-based protection against challenge infections in mice 490
X-ray absorption investigation of a unique protein domain able to bind both copper(I) and copper(II) at adjacent sites of the N-terminus of Haemophilus ducreyi Cu,Zn superoxide dismutase 488
A study of the dual role of copper in superoxide dismutase as antioxidant and pro-oxidant in cellular models of amyotrophic lateral sclerosis 487
Regulation of CU, ZNSOD by metals in S-Cereivisiae and Zea-Mays 485
Role of ZnuABC and ZinT in Escherichia coli O157:H7 zinc acquisition and interaction with epithelial cells 485
Regulatory and structural differences in the Cu,Zn-superoxide dismutases of Salmonella enterica and their significance for virulence 484
Catalytic mechanism and role of hydroxyl residues in the active site of theta class glutathione s-transferases investigation of ser-9 and tyr-113 in a glutathione s-transferase from the australian sheep blowfly, lucilia cuprina 482
Ultrafast heme-residue bond formation in six-coordinate heme proteins: implications for functional ligand exchange 482
Parenteral administration of attenuated Salmonella Typhimurium ΔznuABC is protective against salmonellosis in piglets 482
Extracellular glutathione decreases the ability of Burkholderia cenocepacia to penetrate into epithelial cells and to induce an inflammatory response 481
Multifunctional role of Tyr 108 in the catalytic mechanism of human glutathione transferase P1-1. Crystallographic and kinetic studies on the Y108F mutant enzyme 479
Role of the electrostatic loop charged residues in Cu,Zn superoxide dismutase 477
Effect of Lys->Arg mutation on the thermal stability of Cu,Zn superoxide dismutase: Influence on the monomer-dimer equilibrium 477
Proteomic and ionomic profiling reveals significant alterations of protein expression and calcium homeostasis in cystic fibrosis cells 475
Effect of Val73->Trp mutation on the reaction of ''cambialistic'' superoxide dismutase from Propionibacterium shermanii with hydrogen peroxide 472
Single mutation induces a metal-dependent subunit association in dimeric Cu,Zn superoxide dismutase 471
NMR assignment of reduced form of copper, zinc superoxide dismutase from Salmonella enterica 468
Xenopus laevis Cu,Zn superoxide dismutase B cDNA sequence 468
Carbon monoxide binding to the heme group at the dimeric interface modulates structure and copper accessibility in the Cu,Zn superoxide dismutase from Haemophilus ducreyi: in silico and in vitro evidences. 467
Role of the electrostatic loop of Cu,Zn superoxide dismutase in the copper uptake process 464
Diversity of Salmonella spp. serovars isolated from the intestines of water buffalo calves with gastroenteritis 463
Salmonella Typhimurium infection primes a nutriprive mechanism in piglets 463
Role of prokaryotic Cu,Zn superoxide dismutase in pathogenesis 462
Growth of Pseudomonas aeruginosa in zinc poor environments is promoted by a nicotianamine-related metallophore 462
Impaired copper binding by the H46R mutant of human Cu,Zn superoxide dismutase, involved in amyotrophic lateral sclerosis 459
Cytoplasmic and periplasmic production of human placental glutathione transferase in Escherichia coli 459
CD4+CD25+ T regulatory cells limit effector T cells and favor the progression of brucellosis in BALB/c mice 459
Bovine lactoferrin inhibits the efficiency of invasion of respiratory A549 cells of different iron-regulated morphological forms of Pseudomonas aeruginosa and Burkholderia cenocepacia 459
Metal uptake of recombinant cambialistic superoxide dismutase from Propionitbacterium shermanii is affected by growth conditions of host Escherichia coli cells 457
Zinc ion coordination as a modulating factor of the ZnuA histidine-rich loop flexibility: a molecular modeling and fluorescence spectroscopy study 457
In vivo formation of Cu,Zn superoxide dismutase disulfide bond in Escherichia coli 456
The structures of human glutathione transferase P1-1 in complex with glutathione and various inhibitors at high resolution 456
An ERp57-mediated disulphide exchange promotes the interaction between Burkholderia cenocepacia and epithelial respiratory cells 455
Thermal stability and redox properties of M. tuberculosis CuSOD 452
Periplasmic Cu,Zn superoxide dismutase and cytoplasmic Dps concur in protecting Salmonella enterica serovar Typhimurium from extracellular reactive oxygen species 449
The capability of Pseudomonas aeruginosa to recruit zinc under conditions of limited metal availability is affected by inactivation of the ZnuABC transporter. 449
Temperature-dependent protein folding in vivo--lower growth temperature increases yield of two genetic variants of Xenopus laevis Cu,Zn superoxide dismutase in Escherichia coli 447
The ZupT transporter plays an important role in zinc homeostasis and contributes to Salmonella enterica virulence 444
Fe-heme structure in Cu, Zn superoxide dismutase from Haemophilus ducreyi by X-ray absorption spectroscopy 443
Iron availability influences aggregation, biofilm, adhesion and invasion of Pseudomonas aeruginosa and Burkholderia cenocepacia 440
Vibrio cholerae periplasmic superoxide dismutase: isolation of the gene and overexpression of the protein 440
Deregulation of transition metals homeostasis is a key feature of cadmium toxicity in Salmonella 440
Periplasmic competition for zinc uptake between the metallochaperone ZnuA and Cu,Zn superoxide dismutase 437
Are the steady state kinetics of glutathione transferase always dependent on the deprotonation of the bound glutathione? New insights in the kinetic mechanism of GST P 1-1 436
Role of ZupT in the mechanisms of zinc uptake in Salmonella enterica 435
Overexpression of a hydrogen peroxide-resistant periplasmic Cu,Zn superoxide dismutase protects Escherichia coli from macrophage killing 429
High-affinity Zn2+ uptake system ZnuABC is required for bacterial zinc homeostasis in intracellular environments and contributes to the virulence of Salmonella enterica 428
A free cysteine residue at the dimer interface decreases conformational stability of Xenopus laevis copper,zinc superoxide dismutase 428
The dimeric assembly of Photobacterium leiognathi and Salmonella typhimurium SodC1 Cu,Zn superoxide dismutases is affected differently by active site demetallation and pH: An analytical ultracentrifuge study 423
Reactive oxygen species and epidermal growth factor are antagonistic cues controlling SHP-2 dimerization 420
Zinc in Superoxide Dismutase 420
A novel antimicrobial approach based on the inhibition of zinc uptake in Salmonella enterica 420
Role of the dimeric structure in Cu,Zn superoxide dismutase - pH-dependent, reversible denaturation of the monomeric enzyme from Escherichia coli 419
Involvement of reactive oxygen species in bacterial killing within epithelial cells 416
Protein flexibility in monomeric Cu,Zn superoxide dismutase detected by molecular dynamics simulation and limited proteolysis 414
Purification and characterization of recombinant Caulobacter crescentus Cu,Zn superoxide dismutase 413
Isolation of an active and heat-stable monomeric form of Cu,Zn superoxide dismutase from the periplasmic space of Escherichia coli 412
Regulatory and structural properties differentiating the chromosomal and the bacteriophage-associated Escherichia coli O157:H7 Cu, Zn superoxide dismutases 407
The bacterial high affinity Zn-uptake system: a possible target for novel antibiotics 406
Conserved enzyme-substrate electrostatic attraction in prokariotic Cu,Zn superoxide dismutases 404
Evolutionary constraints for dimer formation in prokariotic Cu,Zn superoxide dismutase 402
Crystallization and preliminary X-ray analysis of the monomeric Cu,Zn superoxide dismutase from Escherichia coli 401
Structural Basis of Heme Binding in the Cu,Zn Superoxide Dismutase from Haemophilus ducreyi 400
Zinc is required to ensure the expression of flagella and the ability to form biofilms in: Salmonella enterica sv Typhimurium 400
Expression of a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis induces mitochondrial alteration and increase of cytosolic Ca2+ concentration in transfected neuroblastoma SH-SY5Y cells 398
Effect of Lys175 mutation on structure function properties of Propionibacterium shermanii superoxide dismutase 394
Conserved enzyme-substrate electrostatic attraction in prokaryotic Cu,Zn superoxide dismutases 393
Differential contribution of sodC1 and sodC2 to intracellular survival and pathogenicity of Salmonella enterica serovar Choleraesuis 392
Crystal structure of the cyanide-inhibited Xenopus laevis Cu,Zn superoxide dismutase at 98 K 392
The X-ray Structure of the Zinc Transporter ZnuA from Salmonella enterica Discloses a Unique Triad of Zinc-Coordinating Histidines 391
Competition for zinc binding in the host-pathogen interaction 390
The Cu,Zn superoxide dismutase from Escherichia coli retains monomeric structure at high protein concentration: Evidence for altered subunit interaction in all the bacteriocupreins 388
Pichia pastoris Fep1 is a [2Fe-2S] protein with a Zn finger that displays an unusual oxygen-dependent role in cluster binding 388
Totale 46.293
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Categoria #
all - tutte 128.197
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 128.197
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.620 0 75 115 84 61 129 64 50 555 80 31 376
2022/20232.058 162 147 30 289 153 410 258 221 172 7 164 45
2023/2024837 97 27 46 24 90 239 22 63 14 103 7 105
2024/20253.348 121 606 328 198 127 321 225 218 305 302 347 250
2025/20266.840 515 320 621 697 557 345 825 860 620 719 384 377
2026/2027756 426 330 0 0 0 0 0 0 0 0 0 0
Totale 55.254