FERRARONI, MARTA
 Distribuzione geografica
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Continente #
NA - Nord America 9.062
EU - Europa 4.326
AS - Asia 4.062
SA - Sud America 629
AF - Africa 134
OC - Oceania 60
Continente sconosciuto - Info sul continente non disponibili 3
Totale 18.276
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Nazione #
US - Stati Uniti d'America 8.982
RU - Federazione Russa 1.614
SG - Singapore 1.170
CN - Cina 1.039
PL - Polonia 607
IT - Italia 554
BR - Brasile 511
VN - Vietnam 509
HK - Hong Kong 467
IE - Irlanda 398
KR - Corea 361
SE - Svezia 336
DE - Germania 180
IN - India 169
FR - Francia 167
FI - Finlandia 125
UA - Ucraina 109
GB - Regno Unito 103
BD - Bangladesh 66
AU - Australia 58
AR - Argentina 52
JP - Giappone 47
ID - Indonesia 46
JO - Giordania 46
CA - Canada 43
ES - Italia 33
TR - Turchia 33
NL - Olanda 30
CI - Costa d'Avorio 24
NG - Nigeria 24
IQ - Iraq 22
ZA - Sudafrica 22
CH - Svizzera 20
CO - Colombia 20
BE - Belgio 19
MX - Messico 19
EC - Ecuador 13
MA - Marocco 12
PY - Paraguay 11
SA - Arabia Saudita 11
AE - Emirati Arabi Uniti 10
BJ - Benin 10
PK - Pakistan 10
VE - Venezuela 10
EG - Egitto 9
KE - Kenya 8
AZ - Azerbaigian 7
CL - Cile 7
PT - Portogallo 7
CR - Costa Rica 6
MY - Malesia 6
PH - Filippine 6
SN - Senegal 6
DZ - Algeria 5
TN - Tunisia 5
UZ - Uzbekistan 5
CZ - Repubblica Ceca 4
LB - Libano 4
NP - Nepal 4
RO - Romania 4
BH - Bahrain 3
DO - Repubblica Dominicana 3
KG - Kirghizistan 3
LT - Lituania 3
MU - Mauritius 3
PA - Panama 3
RS - Serbia 3
SC - Seychelles 3
UY - Uruguay 3
AL - Albania 2
BG - Bulgaria 2
HU - Ungheria 2
JM - Giamaica 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
OM - Oman 2
TH - Thailandia 2
TW - Taiwan 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
AO - Angola 1
BO - Bolivia 1
CY - Cipro 1
DK - Danimarca 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
GR - Grecia 1
GT - Guatemala 1
IL - Israele 1
IR - Iran 1
LK - Sri Lanka 1
MN - Mongolia 1
MT - Malta 1
PE - Perù 1
SK - Slovacchia (Repubblica Slovacca) 1
SO - Somalia 1
SY - Repubblica araba siriana 1
Totale 18.275
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Città #
Santa Clara 1.956
Ashburn 1.096
Singapore 849
Fairfield 836
Warsaw 604
Woodbridge 398
Dublin 396
Hong Kong 380
Seoul 359
Seattle 356
Cambridge 346
Chandler 337
Houston 315
San Jose 285
Wilmington 275
Hefei 266
Beijing 196
Ann Arbor 162
Jacksonville 151
Dallas 150
Ho Chi Minh City 143
Altamura 138
Lawrence 132
The Dalles 129
Florence 127
Lauterbourg 121
Princeton 107
Mumbai 102
Council Bluffs 98
Los Angeles 96
Hanoi 87
Buffalo 86
New York 84
Dong Ket 82
Boston 75
Boardman 69
Moscow 68
Melbourne 56
Kent 55
San Diego 49
Tokyo 45
São Paulo 44
Medford 40
Helsinki 38
Clifton 30
Jakarta 30
Munich 27
Da Nang 25
Shanghai 25
Abidjan 23
Abuja 23
Haiphong 22
Norwalk 22
Paris 22
Orem 21
Rome 21
Barcelona 20
Brussels 18
Frankfurt am Main 18
Milan 18
Chicago 17
Bern 16
Guangzhou 16
Washington 16
Andover 15
Falls Church 15
Redondo Beach 15
Chennai 14
Hillsboro 14
Izmir 14
Toronto 13
Amsterdam 12
Bengaluru 12
London 12
Yubileyny 12
Atlanta 11
Denver 11
Lappeenranta 11
West Jordan 11
Biên Hòa 10
Cape Town 10
Cotonou 10
Johannesburg 10
Phoenix 10
Bogotá 9
Brooklyn 9
Frankfurt Am Main 9
Rio de Janeiro 9
San Francisco 9
Shenzhen 9
Tianjin 9
Turin 9
Turku 9
Campinas 8
Curitiba 8
Gavirate 8
Montreal 8
Belo Horizonte 7
Düsseldorf 7
Elk Grove Village 7
Totale 12.590
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Nome #
Biotransformation of Chloroaromatics: the Impact of Bioavailability and Substrate Specificity. 386
Structure and function of Aspergillus niger laccase McoG 313
Crystal structure of a blue laccase from Lentinus tigrinus: evidences for intermediates in the molecular oxygen reductive splitting by multicopper oxidases. 286
2-Benzylpiperazine: a new scaffold for potent human Carbonic Anhydrase inhibitors. Synthesis, enzyme inhibition, enantioselectivity, computational and crystallographic studies and in vivo activity for a new class of intraocular pressure lowering agents. 272
Crystal structure and kinetic studies of a tetrameric type II β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 268
1,3-Oxazole-based selective picomolar inhibitors of cytosolic human carbonic anhydrase II alleviate ocular hypertension in rabbits: Potency is supported by X-ray crystallography of two leads 246
4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic Studies 226
Determinants for Tight and Selective Binding of a Medicinal Dicarbene Gold(I) Complex to a Telomeric DNA G-Quadruplex: a Joint ESI MS and XRD Investigation 221
(1,3-Dioxolane)- and (1,3-oxathiolane)-2-pyrrolidines: molecular hybrids with potential anti-Alzheimer activity 216
Discovery of 4-Hydroxy-3-(3-(phenylureido)benzenesulfonamides as SLC-0111 Analogues for the Treatment of Hypoxic Tumors Overexpressing Carbonic Anhydrase IX 205
Crystal structure of the blue multicopper oxidase from the white-rot fungus Trametes trogii complexed with p-toluate 204
[Au(9-methylcaffein-8-ylidene)2]+/DNA Tel23 System: Solution, Computational, and Biological Studies 203
Role of the Benzodioxole Group in the Interactions between the Natural Alkaloids Chelerythrine and Coptisine and the Human Telomeric G-Quadruplex DNA. A Multiapproach Investigation 201
Antagonisti muscarinici a struttura 1,3-ossatiolano-2-pirrolidinica 197
Cristallographic studies of reduced Cu(I)-Zn(II) bovine superoxide dismutase and its adducts with small inorganic anions 197
Chalcogenides-incorporating carbonic anhydrase inhibitors concomitantly reverted oxaliplatin-induced neuropathy and enhanced antiproliferative action 196
Benzenesulfonamides Incorporating Flexible Triazole Moieties Are Highly Effective Carbonic Anhydrase Inhibitors: Synthesis and Kinetic, Crystallographic, Computational, and Intraocular Pressure Lowering Investigations 195
SYNTHESIS, AFFINITY PROFILE AND FUNCTIONAL ACTIVITY OF MUSCARINIC ANTAGONISTS WITH A 1-METHYL-2-(2,2-ALKYLARYL-1,3-OXATHIOLAN-5-YL)PYRROLIDINE STRUCTURE 193
A BIOLOGICALLY ACTIVE GOLD COMPLEX: TRICHLORO[(2-PYRIDYL) METHANOL-N]GOLD(III) 192
Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells 191
Crystallographic Determination of Reduced Bovine Superoxide-Dismutase at pH-5.0 and of Anion-Binding to its Active-Site 185
Salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans: crystal structure of a peculiar ring-cleaving dioxygenase. 183
Synthesis and Cholinergic Affinity of Diastereomeric and Enantiomeric Isomers of 1-Methyl-2-(2-methyl-1,3-dioxolan-4-yl)-pyrrolidine, 1-Methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine and of Their Iodomethylates 182
Crystal structure of a zinc-activated variant of Human Carbonic Anhydrase I, CA I Michigan 1: evidence for a second zinc binding site involving arginine coordination 181
Direct and Straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors 179
Catechol 1,2-dioxygenase from the Gram-positive Rhodococcus opacus 1CP: Quantitative structure/activity relationship and the crystal structures of native enzyme and catechols adducts 177
X-ray structures of 4-chlorocatechol 1,2-dioxygenase adducts with substituted catechols: New perspectives in the molecular basis of intradiol ring cleaving dioxygenases specificity. 176
Crystal structure of 3-chlorocatechol 1,2-dioxygenase key enzyme of a new modified ortho-pathway from the Gram-positive Rhodococcus opacus 1CP grown on 2-chlorophenol. 173
Diphenylcyclohexylamine derivatives as new potent multidrug resistance (MDR) modulators 172
Solution and Solid-State Analysis of Binding of 13-Substituted Berberine Analogues to Human Telomeric G-quadruplexes 171
Crystallization and preliminary structure analysis of the blue laccase from the ligninolytic fungus Panus tigrinus. 170
Structural insights on carbonic anhydrase inhibitory action, isoform selectivity, and potency of sulfonamides and coumarins incorporating arylsulfonylureido groups. 169
Crystal Structure Determination of a Salicylate 1,2-Dioxygenase from Pseudaminobacter salicylatoxidans 168
The generation of a 1-hydroxy-2-naphthoate 1,2-dioxygenase by single point mutations of salicylate 1,2-dioxygenase – Rational design of mutants and the crystal structures of the A85H and W104Y variants 168
Azidothymidine "clicked" into 1,2,3-Triazoles: First Report on Carbonic Anhydrase-Telomerase Dual-Hybrid Inhibitors 166
Sulfonamides incorporating piperazine bioisosteres as potent human carbonic anhydrase I, II, IV and IX inhibitors 165
Muscarinic antagonists with multiple stereocenters: synthesis, affinity profile and functional activity of isomeric 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine sulfoxide derivatives 162
The crystal structure of human telomeric DNA complexed with berberine: an interesting case of stacked ligand to G-tetrad ratio higher than 1:1 160
Crystal structure of 4-chlorocatechol 1,2-dioxygenase from the chlorophenol-utilizing gram-positive Rhodococcus opacus 1CP 159
The salicylate 1,2-dioxygenase as a model for a conventional gentisate 1,2-dioxygenase: crystal structures of the G106A mutant and its adducts with gentisate and salicylate. 159
4-Chlorocatechol 1,2-dioxygenase fromthe chlorophenol-utilizing Gram-positive Rhodococcus opacus1CP: crystallization and preliminary crystallographic analysis. 158
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: solution and X-ray crystallographic studies. 155
Mechanisms of the Antiproliferative and Antitumor Activity of Novel Telomerase-Carbonic Anhydrase Dual-Hybrid Inhibitors 155
Reaction Intermediates and Redox State Changes in a Blue Laccase from Steccherinum ochraceum observed by Crystallographic High/Low X-Ray Dose Experiments 152
Interaction of a gold(i) dicarbene anticancer drug with human telomeric DNA G-quadruplex: solution and computationally aided X-ray diffraction analysis 151
Selenols: a new class of carbonic anhydrase inhibitors 150
Polypharmacology of epacadostat: A potent and selective inhibitor of the tumor associated carbonic anhydrases IX and XII 150
Crystal analysis of aromatic sulfonamide binding to native and (Zn)2 adduct of human carbonic anhydrase I Michigan 1. 150
Synthesis of different thio-scaffolds bearing sulfonamide with subnanomolar carbonic anhydrase II and IX inhibitory properties and X-ray investigations for their inhibitory mechanism 147
Preliminary crystallographic analysis of salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans. 147
Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activity 147
Hydroxyquinol 1,2-dioxygenase 146
Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases Inhibition 146
Anion inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 145
Benzoselenoates: A novel class of carbonic anhydrase inhibitors 145
X-ray crystallographic and molecular docking studies on a unique chloromuconolactone dehalogenase from Rhodococcus opacus 1CP. 143
X-ray diffraction analyses of the natural isoquinoline alkaloids Berberine and Sanguinarine in complex with double helix DNA d(CGTACG) 142
Crystal structures of salicylate 1,2-dioxygenase-substrates adducts: A step towards the comprehension of the structural basis for substrate selection in class III ring cleaving dioxygenases 142
Function of different amino acid residues in the reaction mechanism of gentisate 1,2-dioxygenases deduced from the analysis of mutants of the salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans 142
Crystal analysis of Aromatic sulfonamide binding to native and (Zn)2adduct to Human Carbonic Anhydrase I Michigan 1 141
Structure determination of a blue laccase from Trametes Trogii at 1.5 Å 139
Fluorescent sulfonamide carbonic anhydrase inhibitors incorporating 1,2,3-triazole moieties: Kinetic and X-ray crystallographic studies 139
Synthesis of Azasugar–Sulfonamide conjugates and their Evaluation as Inhibitors of Carbonic Anhydrases: the Azasugar Approach to Selectivity 139
Chlorocatechol 1, 2-dioxygenase from the Chlorophenol-utilizing Gram-positive Rhodococcus opacus 1CP: Crystallization and preliminary crystallographic analysis 139
One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase Enzymes 139
Preliminary Crystallographic Analysis of 3-Chlorocatechol 1,2-Dioxygenase of a New Modified Ortho-pathway from the Gram-Positive Rhodococcus opacus 1CP Grown on 2-Chlorophenol. 137
The Crystal structure of the Monomeric Human SOD Mutant F50E/G51E/E133Q at Atomic Resolution. The Enzyme mechanism Revisited 136
Thioxocoumarins Show an Alternative Carbonic Anhydrase Inhibition Mechanism Compared to Coumarins 134
Laccase isoforms with unusual properties from the basidiomycete Steccherinum ochraceum strain 1833 133
Novel Carbonic Anhydrase Inhibitors with Dual-Tail Core Sulfonamide Show Potent and Lasting Effects for Glaucoma Therapy 132
The crystal structures of native hydroquinone 1,2-dioxygenase from Sphingomonas sp. TTNP3 and of substrate and inhibitor complexes 131
Polymeric hydrophobic membranes as a tool to control polymorphism and protein–ligand interactions 129
Dioxygen, an unexpected carbonic anhydrase ligand 127
Lasamide, a Potent Human Carbonic Anhydrase Inhibitor from the Market: Inhibition Profiling and Crystallographic Studies 125
Pyridine Derivative of the Natural Alkaloid Berberine as Human Telomeric G4-DNA Binder: A Solution and Solid-State Study 125
Selenocarbamates As a Prodrug-Based Approach to Carbonic Anhydrase Inhibition 124
A new framework for novel analogues of pazopanib as potent and selective human carbonic anhydrase inhibitors: Design, repurposing rational, synthesis, crystallographic, in vivo and in vitro biological assessments 124
Interaction of Carboxypeptidase A with Anions: Crystal Structure of the Complex with the HPO42- Anion 122
Synthetic Approaches to Novel Human Carbonic Anhydrase Isoform Inhibitors Based on Pyrrol-2-one Moiety 121
Mono- and three-tailed sugar and iminosugar decorated benzenesulfonamide carbonic anhydrase inhibitors 121
Crystal structure and chemical inhibition of essential schistosome host-interactive virulence factor carbonic anhydrase SmCA 121
Benzenesulfonamide decorated dihydropyrimidin(thi)ones: carbonic anhydrase profiling and antiproliferative activity 120
Crystal structure of the hydroxyquinol 1,2-dioxygenase from Nocardioides simplex 3E, a key enzyme involved in polychlorinated aromatics biodegradation 120
Crystallization and preliminary X-ray crystallographic analysis of the small subunit of the heterodimeric laccase POXA3b from Pleurotus ostreatus. 120
Thia- and Seleno-Michael Reactions for the Synthesis of Carbonic Anhydrases Inhibitors 119
Molecular Basis of Pseudomonas syringae pv actinidiae Levansucrase Inhibition by a Multivalent Iminosugar 118
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 117
Double helices forming unusual binding motifs: the case of the natural alkaloids coptisine and chelerythrine 117
Selenolesterase enzyme activity of carbonic anhydrases 116
Structural basis of hyaluronan degradation by Streptococcus pneumoniae hyaluronate lyase 116
Diversely N-substituted benzenesulfonamides dissimilarly bind to human carbonic anhydrases: crystallographic investigations of N-nitrosulfonamides 115
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: Solution and X-ray crystallographic studies 114
Structural basis for the substrate specificity and the absence of dehalogenation activity in 2-chloromuconate cycloisomerase from Rhodococcus opacus 1CP 113
Inhibition of Pseudomonas aeruginosa Carbonic Anhydrases, Exploring Ciprofloxacin Functionalization Toward New Antibacterial Agents: An In-Depth Multidisciplinary Study 112
X-ray structural study of human neutrophil elastase inhibition with a series of azaindoles, azaindazoles and isoxazolones 112
Famotidine, an Antiulcer Agent, Strongly Inhibits Helicobacter pylori and Human Carbonic Anhydrases 112
Design, synthesis, biological evaluation and crystal structure determination of dual modulators of carbonic anhydrases and estrogen receptors 111
Structural Insights into Schistosoma mansoni Carbonic Anhydrase (SmCA) Inhibition by Selenoureido-Substituted Benzenesulfonamides 110
Sulfonamide carbonic anhydrase inhibitors: Zinc coordination and tail effects influence inhibitory efficacy and selectivity for different isoforms 108
First-in-Class Dual Targeting Compounds for the Management of Seizures in Glucose Transporter Type 1 Deficiency Syndrome 107
Totale 15.901
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Categoria #
all - tutte 50.939
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 50.939
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021228 0 0 0 0 0 0 0 0 0 0 84 144
2021/2022682 22 78 67 22 21 39 37 49 40 28 108 171
2022/20231.692 191 352 53 100 128 288 197 83 203 9 51 37
2023/2024606 28 59 119 39 54 81 7 110 14 41 37 17
2024/20254.993 128 484 309 706 1.519 798 113 260 197 101 166 212
2025/20266.089 565 923 710 656 626 254 711 372 531 467 274 0
Totale 18.440