FERRARONI, MARTA
 Distribuzione geografica
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Continente #
NA - Nord America 8.161
EU - Europa 4.061
AS - Asia 3.226
SA - Sud America 592
AF - Africa 91
OC - Oceania 56
Continente sconosciuto - Info sul continente non disponibili 3
Totale 16.190
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Nazione #
US - Stati Uniti d'America 8.102
RU - Federazione Russa 1.612
SG - Singapore 974
CN - Cina 814
PL - Polonia 606
BR - Brasile 492
IT - Italia 478
HK - Hong Kong 447
IE - Irlanda 396
KR - Corea 359
SE - Svezia 332
VN - Vietnam 262
DE - Germania 172
IN - India 150
FI - Finlandia 111
UA - Ucraina 104
GB - Regno Unito 93
AU - Australia 56
AR - Argentina 48
JO - Giordania 45
ID - Indonesia 44
FR - Francia 43
ES - Italia 31
CA - Canada 29
TR - Turchia 26
CI - Costa d'Avorio 23
NL - Olanda 22
BD - Bangladesh 21
CH - Svizzera 20
BE - Belgio 18
ZA - Sudafrica 18
MX - Messico 16
CO - Colombia 15
JP - Giappone 15
IQ - Iraq 12
EC - Ecuador 11
BJ - Benin 10
MA - Marocco 10
PY - Paraguay 10
VE - Venezuela 9
SA - Arabia Saudita 7
AZ - Azerbaigian 6
EG - Egitto 6
KE - Kenya 6
AE - Emirati Arabi Uniti 5
PK - Pakistan 5
PT - Portogallo 5
CL - Cile 4
DZ - Algeria 4
MY - Malesia 4
NP - Nepal 4
SN - Senegal 4
TN - Tunisia 4
UZ - Uzbekistan 4
CR - Costa Rica 3
CZ - Repubblica Ceca 3
DO - Repubblica Dominicana 3
LB - Libano 3
LT - Lituania 3
MU - Mauritius 3
PA - Panama 3
RO - Romania 3
RS - Serbia 3
SC - Seychelles 3
HU - Ungheria 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
NI - Nicaragua 2
PH - Filippine 2
TW - Taiwan 2
UY - Uruguay 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
DK - Danimarca 1
EU - Europa 1
GE - Georgia 1
GR - Grecia 1
GT - Guatemala 1
IL - Israele 1
IR - Iran 1
JM - Giamaica 1
LK - Sri Lanka 1
MN - Mongolia 1
OM - Oman 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
TT - Trinidad e Tobago 1
Totale 16.190
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Città #
Santa Clara 1.932
Fairfield 836
Ashburn 763
Singapore 678
Warsaw 604
Woodbridge 398
Dublin 394
Hong Kong 368
Seoul 359
Seattle 355
Cambridge 346
Chandler 337
Houston 311
Wilmington 275
Hefei 265
Beijing 184
Ann Arbor 162
Jacksonville 149
Dallas 145
Altamura 138
San Jose 135
Lawrence 132
Florence 124
Princeton 107
Mumbai 99
The Dalles 91
Dong Ket 82
Buffalo 78
Los Angeles 77
Boston 74
Ho Chi Minh City 70
Boardman 69
Moscow 68
Melbourne 56
Kent 55
San Diego 49
New York 46
São Paulo 44
Medford 40
Clifton 30
Jakarta 29
Helsinki 27
Munich 27
Hanoi 26
Abidjan 22
Norwalk 22
Shanghai 22
Barcelona 20
Paris 20
Council Bluffs 18
Brussels 17
Bern 16
Chicago 16
Washington 16
Andover 15
Falls Church 15
Redondo Beach 15
Milan 14
Tokyo 14
Frankfurt am Main 13
Izmir 13
Bengaluru 12
Hillsboro 12
Yubileyny 12
London 11
Rome 11
West Jordan 11
Atlanta 10
Cotonou 10
Haiphong 10
Chennai 9
Frankfurt Am Main 9
Guangzhou 9
Johannesburg 9
Phoenix 9
Rio de Janeiro 9
Tianjin 9
Toronto 9
Turku 9
Brooklyn 8
Campinas 8
Cape Town 8
Curitiba 8
Da Nang 8
Gavirate 8
Lappeenranta 8
Amsterdam 7
Belo Horizonte 7
Biên Hòa 7
Bogotá 7
Düsseldorf 7
Elk Grove Village 7
Montreal 7
San Francisco 7
Shenzhen 7
Turin 7
Baku 6
Brasília 6
Denver 6
Dummerstorf 6
Totale 11.252
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Nome #
Biotransformation of Chloroaromatics: the Impact of Bioavailability and Substrate Specificity. 372
Structure and function of Aspergillus niger laccase McoG 287
Crystal structure of a blue laccase from Lentinus tigrinus: evidences for intermediates in the molecular oxygen reductive splitting by multicopper oxidases. 259
Crystal structure and kinetic studies of a tetrameric type II β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 252
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. 235
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 224
4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic Studies 205
(1,3-Dioxolane)- and (1,3-oxathiolane)-2-pyrrolidines: molecular hybrids with potential anti-Alzheimer activity 203
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 193
[Au(9-methylcaffein-8-ylidene)2]+/DNA Tel23 System: Solution, Computational, and Biological Studies 191
Discovery of 4-Hydroxy-3-(3-(phenylureido)benzenesulfonamides as SLC-0111 Analogues for the Treatment of Hypoxic Tumors Overexpressing Carbonic Anhydrase IX 189
A BIOLOGICALLY ACTIVE GOLD COMPLEX: TRICHLORO[(2-PYRIDYL) METHANOL-N]GOLD(III) 185
Crystal structure of the blue multicopper oxidase from the white-rot fungus Trametes trogii complexed with p-toluate 183
Antagonisti muscarinici a struttura 1,3-ossatiolano-2-pirrolidinica 183
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 181
Cristallographic studies of reduced Cu(I)-Zn(II) bovine superoxide dismutase and its adducts with small inorganic anions 180
Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells 180
SYNTHESIS, AFFINITY PROFILE AND FUNCTIONAL ACTIVITY OF MUSCARINIC ANTAGONISTS WITH A 1-METHYL-2-(2,2-ALKYLARYL-1,3-OXATHIOLAN-5-YL)PYRROLIDINE STRUCTURE 179
Chalcogenides-incorporating carbonic anhydrase inhibitors concomitantly reverted oxaliplatin-induced neuropathy and enhanced antiproliferative action 174
Salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans: crystal structure of a peculiar ring-cleaving dioxygenase. 172
Benzenesulfonamides Incorporating Flexible Triazole Moieties Are Highly Effective Carbonic Anhydrase Inhibitors: Synthesis and Kinetic, Crystallographic, Computational, and Intraocular Pressure Lowering Investigations 171
Crystallographic Determination of Reduced Bovine Superoxide-Dismutase at pH-5.0 and of Anion-Binding to its Active-Site 170
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 168
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 168
Direct and Straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors 165
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 165
Diphenylcyclohexylamine derivatives as new potent multidrug resistance (MDR) modulators 164
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. 164
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. 159
Solution and Solid-State Analysis of Binding of 13-Substituted Berberine Analogues to Human Telomeric G-quadruplexes 159
Structural insights on carbonic anhydrase inhibitory action, isoform selectivity, and potency of sulfonamides and coumarins incorporating arylsulfonylureido groups. 157
Crystallization and preliminary structure analysis of the blue laccase from the ligninolytic fungus Panus tigrinus. 157
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 155
Crystal Structure Determination of a Salicylate 1,2-Dioxygenase from Pseudaminobacter salicylatoxidans 152
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 149
Crystal structure of 4-chlorocatechol 1,2-dioxygenase from the chlorophenol-utilizing gram-positive Rhodococcus opacus 1CP 148
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. 148
Sulfonamides incorporating piperazine bioisosteres as potent human carbonic anhydrase I, II, IV and IX inhibitors 147
Azidothymidine "clicked" into 1,2,3-Triazoles: First Report on Carbonic Anhydrase-Telomerase Dual-Hybrid Inhibitors 147
4-Chlorocatechol 1,2-dioxygenase fromthe chlorophenol-utilizing Gram-positive Rhodococcus opacus1CP: crystallization and preliminary crystallographic analysis. 145
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: solution and X-ray crystallographic studies. 144
Mechanisms of the Antiproliferative and Antitumor Activity of Novel Telomerase-Carbonic Anhydrase Dual-Hybrid Inhibitors 142
Polypharmacology of epacadostat: A potent and selective inhibitor of the tumor associated carbonic anhydrases IX and XII 141
Crystal analysis of aromatic sulfonamide binding to native and (Zn)2 adduct of human carbonic anhydrase I Michigan 1. 141
The crystal structure of human telomeric DNA complexed with berberine: an interesting case of stacked ligand to G-tetrad ratio higher than 1:1 140
Reaction Intermediates and Redox State Changes in a Blue Laccase from Steccherinum ochraceum observed by Crystallographic High/Low X-Ray Dose Experiments 140
Selenols: a new class of carbonic anhydrase inhibitors 139
Interaction of a gold(i) dicarbene anticancer drug with human telomeric DNA G-quadruplex: solution and computationally aided X-ray diffraction analysis 138
X-ray diffraction analyses of the natural isoquinoline alkaloids Berberine and Sanguinarine in complex with double helix DNA d(CGTACG) 137
Hydroxyquinol 1,2-dioxygenase 135
Anion inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 134
Preliminary crystallographic analysis of salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans. 134
Synthesis of different thio-scaffolds bearing sulfonamide with subnanomolar carbonic anhydrase II and IX inhibitory properties and X-ray investigations for their inhibitory mechanism 133
X-ray crystallographic and molecular docking studies on a unique chloromuconolactone dehalogenase from Rhodococcus opacus 1CP. 133
Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activity 132
Crystal analysis of Aromatic sulfonamide binding to native and (Zn)2adduct to Human Carbonic Anhydrase I Michigan 1 130
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 129
Fluorescent sulfonamide carbonic anhydrase inhibitors incorporating 1,2,3-triazole moieties: Kinetic and X-ray crystallographic studies 128
Synthesis of Azasugar–Sulfonamide conjugates and their Evaluation as Inhibitors of Carbonic Anhydrases: the Azasugar Approach to Selectivity 128
Chlorocatechol 1, 2-dioxygenase from the Chlorophenol-utilizing Gram-positive Rhodococcus opacus 1CP: Crystallization and preliminary crystallographic analysis 128
Benzoselenoates: A novel class of carbonic anhydrase inhibitors 128
Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases Inhibition 127
The Crystal structure of the Monomeric Human SOD Mutant F50E/G51E/E133Q at Atomic Resolution. The Enzyme mechanism Revisited 126
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 126
Structure determination of a blue laccase from Trametes Trogii at 1.5 Å 124
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. 123
Thioxocoumarins Show an Alternative Carbonic Anhydrase Inhibition Mechanism Compared to Coumarins 122
One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase Enzymes 121
Polymeric hydrophobic membranes as a tool to control polymorphism and protein–ligand interactions 119
Laccase isoforms with unusual properties from the basidiomycete Steccherinum ochraceum strain 1833 119
Novel Carbonic Anhydrase Inhibitors with Dual-Tail Core Sulfonamide Show Potent and Lasting Effects for Glaucoma Therapy 117
Dioxygen, an unexpected carbonic anhydrase ligand 116
The crystal structures of native hydroquinone 1,2-dioxygenase from Sphingomonas sp. TTNP3 and of substrate and inhibitor complexes 116
Interaction of Carboxypeptidase A with Anions: Crystal Structure of the Complex with the HPO42- Anion 114
Pyridine Derivative of the Natural Alkaloid Berberine as Human Telomeric G4-DNA Binder: A Solution and Solid-State Study 111
Structural basis of hyaluronan degradation by Streptococcus pneumoniae hyaluronate lyase 110
Crystallization and preliminary X-ray crystallographic analysis of the small subunit of the heterodimeric laccase POXA3b from Pleurotus ostreatus. 110
Synthetic Approaches to Novel Human Carbonic Anhydrase Isoform Inhibitors Based on Pyrrol-2-one Moiety 109
Lasamide, a Potent Human Carbonic Anhydrase Inhibitor from the Market: Inhibition Profiling and Crystallographic Studies 109
Crystal structure and chemical inhibition of essential schistosome host-interactive virulence factor carbonic anhydrase SmCA 109
X-ray structural study of human neutrophil elastase inhibition with a series of azaindoles, azaindazoles and isoxazolones 107
Selenocarbamates As a Prodrug-Based Approach to Carbonic Anhydrase Inhibition 107
Mono- and three-tailed sugar and iminosugar decorated benzenesulfonamide carbonic anhydrase inhibitors 107
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 106
Selenolesterase enzyme activity of carbonic anhydrases 106
Crystal structure of the hydroxyquinol 1,2-dioxygenase from Nocardioides simplex 3E, a key enzyme involved in polychlorinated aromatics biodegradation 104
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 103
Double helices forming unusual binding motifs: the case of the natural alkaloids coptisine and chelerythrine 103
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: Solution and X-ray crystallographic studies 103
Thia- and Seleno-Michael Reactions for the Synthesis of Carbonic Anhydrases Inhibitors 102
Famotidine, an Antiulcer Agent, Strongly Inhibits Helicobacter pylori and Human Carbonic Anhydrases 100
Sintesi e affinità per i recettori colinergici degli stereoisomeri della 1-metil-2-(2-metil-1,3-diossolan-4-il)pirrolidina, della 1-metil-2-(2-metil-1,3-ossatiolan-5-il)pirrolidina e dei loro iodometilati 98
Molecular Basis of Pseudomonas syringae pv actinidiae Levansucrase Inhibition by a Multivalent Iminosugar 96
Benzenesulfonamide decorated dihydropyrimidin(thi)ones: carbonic anhydrase profiling and antiproliferative activity 96
Structural Insights into Schistosoma mansoni Carbonic Anhydrase (SmCA) Inhibition by Selenoureido-Substituted Benzenesulfonamides 96
Sulfonamide carbonic anhydrase inhibitors: Zinc coordination and tail effects influence inhibitory efficacy and selectivity for different isoforms 95
First-in-Class Dual Targeting Compounds for the Management of Seizures in Glucose Transporter Type 1 Deficiency Syndrome 94
Study of Chalcogen Aspirin Derivatives with Carbonic Anhydrase Inhibitory Properties for Treating Inflammatory Pain 94
Anion Recognition by Proteins 94
Structural basis for the substrate specificity and the absence of dehalogenation activity in 2-chloromuconate cycloisomerase from Rhodococcus opacus 1CP 94
Totale 14.452
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Categoria #
all - tutte 46.050
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 46.050
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021596 0 0 0 0 0 0 30 69 92 177 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
2025/20263.991 565 923 710 656 626 254 257 0 0 0 0 0
Totale 16.342