FERRARONI, MARTA
 Distribuzione geografica
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Continente #
NA - Nord America 9.462
EU - Europa 4.999
AS - Asia 4.184
SA - Sud America 635
Continente sconosciuto - Info sul continente non disponibili 170
AF - Africa 134
OC - Oceania 60
Totale 19.644
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Nazione #
US - Stati Uniti d'America 9.308
RU - Federazione Russa 1.614
IT - Italia 1.223
SG - Singapore 1.172
CN - Cina 1.046
PL - Polonia 607
BR - Brasile 515
VN - Vietnam 509
HK - Hong Kong 468
IE - Irlanda 399
KR - Corea 361
SE - Svezia 336
DE - Germania 180
BD - Bangladesh 174
IN - India 170
FR - Francia 167
FI - Finlandia 125
UA - Ucraina 109
CA - Canada 106
GB - Regno Unito 103
AU - Australia 58
AR - Argentina 52
JP - Giappone 47
ID - Indonesia 46
JO - Giordania 46
ES - Italia 33
TR - Turchia 33
NL - Olanda 31
CI - Costa d'Avorio 24
NG - Nigeria 24
IQ - Iraq 22
ZA - Sudafrica 22
CO - Colombia 21
MX - Messico 21
CH - Svizzera 20
BE - Belgio 19
EC - Ecuador 13
MA - Marocco 12
AE - Emirati Arabi Uniti 11
PY - Paraguay 11
SA - Arabia Saudita 11
BJ - Benin 10
PK - Pakistan 10
VE - Venezuela 10
EG - Egitto 9
KE - Kenya 8
MY - Malesia 8
AZ - Azerbaigian 7
CL - Cile 7
CR - Costa Rica 7
PT - Portogallo 7
PH - Filippine 6
SN - Senegal 6
DZ - Algeria 5
TN - Tunisia 5
UZ - Uzbekistan 5
CZ - Repubblica Ceca 4
GT - Guatemala 4
LB - Libano 4
NP - Nepal 4
RO - Romania 4
RS - Serbia 4
BH - Bahrain 3
DO - Repubblica Dominicana 3
JM - Giamaica 3
KG - Kirghizistan 3
LT - Lituania 3
MU - Mauritius 3
PA - Panama 3
SC - Seychelles 3
UY - Uruguay 3
AL - Albania 2
BG - Bulgaria 2
HU - Ungheria 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
OM - Oman 2
PE - Perù 2
SV - El Salvador 2
TH - Thailandia 2
TW - Taiwan 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BO - Bolivia 1
BZ - Belize 1
CY - Cipro 1
DK - Danimarca 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
GR - Grecia 1
HR - Croazia 1
IL - Israele 1
IR - Iran 1
LK - Sri Lanka 1
MN - Mongolia 1
Totale 19.472
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Città #
Santa Clara 1.967
Ashburn 1.170
Singapore 850
Fairfield 836
Warsaw 604
Woodbridge 399
Dublin 397
Hong Kong 381
Seoul 359
Seattle 356
Cambridge 353
Chandler 337
Houston 317
San Jose 290
Wilmington 275
Hefei 266
Milan 230
Beijing 199
Ann Arbor 162
Dallas 155
Jacksonville 155
Ho Chi Minh City 143
Altamura 138
Florence 135
Lawrence 132
The Dalles 131
Los Angeles 123
Lauterbourg 121
Princeton 107
Rome 105
Mumbai 102
Council Bluffs 98
New York 89
Buffalo 88
Hanoi 87
Dong Ket 82
Boardman 76
Boston 76
Moscow 68
Melbourne 56
Kent 55
San Diego 50
Tokyo 45
São Paulo 44
Medford 40
Helsinki 38
Turin 32
Clifton 30
Jakarta 30
Munich 27
Toronto 26
Da Nang 25
Shanghai 25
Bologna 24
Abidjan 23
Abuja 23
Naples 23
Paris 23
Haiphong 22
Norwalk 22
Chicago 21
Montreal 21
Orem 21
Barcelona 20
Brussels 18
Frankfurt am Main 18
Washington 17
Bern 16
Guangzhou 16
Andover 15
Falls Church 15
Redondo Beach 15
Chennai 14
Hillsboro 14
Izmir 14
Miano 14
Amsterdam 12
Atlanta 12
Bari 12
Bengaluru 12
Denver 12
London 12
Palermo 12
Yubileyny 12
Lappeenranta 11
West Jordan 11
Biên Hòa 10
Bogotá 10
Cape Town 10
Cotonou 10
Johannesburg 10
Phoenix 10
Venice 10
Verona 10
Brooklyn 9
Frankfurt Am Main 9
Genoa 9
Newark 9
Padua 9
Rio de Janeiro 9
Totale 13.163
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Nome #
Biotransformation of Chloroaromatics: the Impact of Bioavailability and Substrate Specificity. 388
Structure and function of Aspergillus niger laccase McoG 317
Crystal structure of a blue laccase from Lentinus tigrinus: evidences for intermediates in the molecular oxygen reductive splitting by multicopper oxidases. 293
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. 281
Crystal structure and kinetic studies of a tetrameric type II β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 272
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 266
4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic Studies 243
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 239
(1,3-Dioxolane)- and (1,3-oxathiolane)-2-pyrrolidines: molecular hybrids with potential anti-Alzheimer activity 229
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 221
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 215
Discovery of 4-Hydroxy-3-(3-(phenylureido)benzenesulfonamides as SLC-0111 Analogues for the Treatment of Hypoxic Tumors Overexpressing Carbonic Anhydrase IX 215
Chalcogenides-incorporating carbonic anhydrase inhibitors concomitantly reverted oxaliplatin-induced neuropathy and enhanced antiproliferative action 213
Crystal structure of the blue multicopper oxidase from the white-rot fungus Trametes trogii complexed with p-toluate 208
SYNTHESIS, AFFINITY PROFILE AND FUNCTIONAL ACTIVITY OF MUSCARINIC ANTAGONISTS WITH A 1-METHYL-2-(2,2-ALKYLARYL-1,3-OXATHIOLAN-5-YL)PYRROLIDINE STRUCTURE 208
Cristallographic studies of reduced Cu(I)-Zn(II) bovine superoxide dismutase and its adducts with small inorganic anions 207
[Au(9-methylcaffein-8-ylidene)2]+/DNA Tel23 System: Solution, Computational, and Biological Studies 205
Antagonisti muscarinici a struttura 1,3-ossatiolano-2-pirrolidinica 204
Benzenesulfonamides Incorporating Flexible Triazole Moieties Are Highly Effective Carbonic Anhydrase Inhibitors: Synthesis and Kinetic, Crystallographic, Computational, and Intraocular Pressure Lowering Investigations 204
Crystallographic Determination of Reduced Bovine Superoxide-Dismutase at pH-5.0 and of Anion-Binding to its Active-Site 202
A BIOLOGICALLY ACTIVE GOLD COMPLEX: TRICHLORO[(2-PYRIDYL) METHANOL-N]GOLD(III) 196
Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells 196
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. 195
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 190
Salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans: crystal structure of a peculiar ring-cleaving dioxygenase. 188
Direct and Straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors 187
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 186
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 183
Diphenylcyclohexylamine derivatives as new potent multidrug resistance (MDR) modulators 182
Solution and Solid-State Analysis of Binding of 13-Substituted Berberine Analogues to Human Telomeric G-quadruplexes 178
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 178
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. 177
Crystallization and preliminary structure analysis of the blue laccase from the ligninolytic fungus Panus tigrinus. 177
Crystal Structure Determination of a Salicylate 1,2-Dioxygenase from Pseudaminobacter salicylatoxidans 174
Azidothymidine "clicked" into 1,2,3-Triazoles: First Report on Carbonic Anhydrase-Telomerase Dual-Hybrid Inhibitors 174
Benzenesulfonamide decorated dihydropyrimidin(thi)ones: carbonic anhydrase profiling and antiproliferative activity 173
Structural insights on carbonic anhydrase inhibitory action, isoform selectivity, and potency of sulfonamides and coumarins incorporating arylsulfonylureido groups. 173
The crystal structure of human telomeric DNA complexed with berberine: an interesting case of stacked ligand to G-tetrad ratio higher than 1:1 169
Sulfonamides incorporating piperazine bioisosteres as potent human carbonic anhydrase I, II, IV and IX inhibitors 169
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. 168
Mechanisms of the Antiproliferative and Antitumor Activity of Novel Telomerase-Carbonic Anhydrase Dual-Hybrid Inhibitors 167
Crystal structure of 4-chlorocatechol 1,2-dioxygenase from the chlorophenol-utilizing gram-positive Rhodococcus opacus 1CP 164
4-Chlorocatechol 1,2-dioxygenase fromthe chlorophenol-utilizing Gram-positive Rhodococcus opacus1CP: crystallization and preliminary crystallographic analysis. 163
Polypharmacology of epacadostat: A potent and selective inhibitor of the tumor associated carbonic anhydrases IX and XII 162
Synthesis of different thio-scaffolds bearing sulfonamide with subnanomolar carbonic anhydrase II and IX inhibitory properties and X-ray investigations for their inhibitory mechanism 161
X-ray diffraction analyses of the natural isoquinoline alkaloids Berberine and Sanguinarine in complex with double helix DNA d(CGTACG) 160
Reaction Intermediates and Redox State Changes in a Blue Laccase from Steccherinum ochraceum observed by Crystallographic High/Low X-Ray Dose Experiments 160
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: solution and X-ray crystallographic studies. 159
Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activity 159
X-ray crystallographic and molecular docking studies on a unique chloromuconolactone dehalogenase from Rhodococcus opacus 1CP. 157
Anion inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 156
Selenols: a new class of carbonic anhydrase inhibitors 155
Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases Inhibition 155
Synthesis of Azasugar–Sulfonamide conjugates and their Evaluation as Inhibitors of Carbonic Anhydrases: the Azasugar Approach to Selectivity 154
Hydroxyquinol 1,2-dioxygenase 153
Interaction of a gold(i) dicarbene anticancer drug with human telomeric DNA G-quadruplex: solution and computationally aided X-ray diffraction analysis 153
Study of Chalcogen Aspirin Derivatives with Carbonic Anhydrase Inhibitory Properties for Treating Inflammatory Pain 152
Crystal analysis of aromatic sulfonamide binding to native and (Zn)2 adduct of human carbonic anhydrase I Michigan 1. 152
One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase Enzymes 152
Benzoselenoates: A novel class of carbonic anhydrase inhibitors 150
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. 149
Preliminary crystallographic analysis of salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans. 147
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 146
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 146
Crystal analysis of Aromatic sulfonamide binding to native and (Zn)2adduct to Human Carbonic Anhydrase I Michigan 1 145
Structure determination of a blue laccase from Trametes Trogii at 1.5 Å 144
Fluorescent sulfonamide carbonic anhydrase inhibitors incorporating 1,2,3-triazole moieties: Kinetic and X-ray crystallographic studies 143
Thioxocoumarins Show an Alternative Carbonic Anhydrase Inhibition Mechanism Compared to Coumarins 141
Chlorocatechol 1, 2-dioxygenase from the Chlorophenol-utilizing Gram-positive Rhodococcus opacus 1CP: Crystallization and preliminary crystallographic analysis 141
Novel Carbonic Anhydrase Inhibitors with Dual-Tail Core Sulfonamide Show Potent and Lasting Effects for Glaucoma Therapy 138
The Crystal structure of the Monomeric Human SOD Mutant F50E/G51E/E133Q at Atomic Resolution. The Enzyme mechanism Revisited 137
Laccase isoforms with unusual properties from the basidiomycete Steccherinum ochraceum strain 1833 137
Pyridine Derivative of the Natural Alkaloid Berberine as Human Telomeric G4-DNA Binder: A Solution and Solid-State Study 136
Polymeric hydrophobic membranes as a tool to control polymorphism and protein–ligand interactions 135
The crystal structures of native hydroquinone 1,2-dioxygenase from Sphingomonas sp. TTNP3 and of substrate and inhibitor complexes 133
Dioxygen, an unexpected carbonic anhydrase ligand 132
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 130
Lasamide, a Potent Human Carbonic Anhydrase Inhibitor from the Market: Inhibition Profiling and Crystallographic Studies 129
Crystal structure of the hydroxyquinol 1,2-dioxygenase from Nocardioides simplex 3E, a key enzyme involved in polychlorinated aromatics biodegradation 129
Selenocarbamates As a Prodrug-Based Approach to Carbonic Anhydrase Inhibition 128
Crystal structure and chemical inhibition of essential schistosome host-interactive virulence factor carbonic anhydrase SmCA 128
Thia- and Seleno-Michael Reactions for the Synthesis of Carbonic Anhydrases Inhibitors 127
Mono- and three-tailed sugar and iminosugar decorated benzenesulfonamide carbonic anhydrase inhibitors 127
Crystallization and preliminary X-ray crystallographic analysis of the small subunit of the heterodimeric laccase POXA3b from Pleurotus ostreatus. 127
Structural basis for the substrate specificity and the absence of dehalogenation activity in 2-chloromuconate cycloisomerase from Rhodococcus opacus 1CP 126
Selenolesterase enzyme activity of carbonic anhydrases 125
Diversely N-substituted benzenesulfonamides dissimilarly bind to human carbonic anhydrases: crystallographic investigations of N-nitrosulfonamides 125
X-ray crystallographic and kinetic studies of biguanide containing aryl sulfonamides as carbonic anhydrase inhibitors 124
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 124
X-ray structural study of human neutrophil elastase inhibition with a series of azaindoles, azaindazoles and isoxazolones 123
Interaction of Carboxypeptidase A with Anions: Crystal Structure of the Complex with the HPO42- Anion 123
Synthetic Approaches to Novel Human Carbonic Anhydrase Isoform Inhibitors Based on Pyrrol-2-one Moiety 122
Molecular Basis of Pseudomonas syringae pv actinidiae Levansucrase Inhibition by a Multivalent Iminosugar 122
Famotidine, an Antiulcer Agent, Strongly Inhibits Helicobacter pylori and Human Carbonic Anhydrases 122
First-in-Class Dual Targeting Compounds for the Management of Seizures in Glucose Transporter Type 1 Deficiency Syndrome 121
Structural basis of hyaluronan degradation by Streptococcus pneumoniae hyaluronate lyase 120
Structural Insights into Schistosoma mansoni Carbonic Anhydrase (SmCA) Inhibition by Selenoureido-Substituted Benzenesulfonamides 119
Double helices forming unusual binding motifs: the case of the natural alkaloids coptisine and chelerythrine 119
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: Solution and X-ray crystallographic studies 118
Inhibition of Pseudomonas aeruginosa Carbonic Anhydrases, Exploring Ciprofloxacin Functionalization Toward New Antibacterial Agents: An In-Depth Multidisciplinary Study 117
Totale 16.812
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Categoria #
all - tutte 54.643
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 54.643
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20267.023 565 923 710 656 626 254 711 372 531 467 308 900
2026/2027270 270 0 0 0 0 0 0 0 0 0 0 0
Totale 19.644