FERRARONI, MARTA
 Distribuzione geografica
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Continente #
NA - Nord America 7.861
EU - Europa 4.040
AS - Asia 3.103
SA - Sud America 578
AF - Africa 84
OC - Oceania 56
Continente sconosciuto - Info sul continente non disponibili 3
Totale 15.725
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Nazione #
US - Stati Uniti d'America 7.808
RU - Federazione Russa 1.611
SG - Singapore 895
CN - Cina 800
PL - Polonia 605
BR - Brasile 482
IT - Italia 478
HK - Hong Kong 444
IE - Irlanda 396
KR - Corea 359
SE - Svezia 332
VN - Vietnam 261
DE - Germania 172
IN - India 147
UA - Ucraina 104
FI - Finlandia 98
GB - Regno Unito 89
AU - Australia 56
AR - Argentina 47
ID - Indonesia 44
FR - Francia 43
JO - Giordania 42
ES - Italia 30
CA - Canada 27
TR - Turchia 26
CI - Costa d'Avorio 23
NL - Olanda 22
CH - Svizzera 20
BE - Belgio 18
ZA - Sudafrica 17
BD - Bangladesh 15
CO - Colombia 14
JP - Giappone 14
MX - Messico 12
EC - Ecuador 11
BJ - Benin 10
MA - Marocco 9
PY - Paraguay 9
VE - Venezuela 9
IQ - Iraq 8
AZ - Azerbaigian 6
EG - Egitto 6
SA - Arabia Saudita 6
PK - Pakistan 5
PT - Portogallo 5
AE - Emirati Arabi Uniti 4
KE - Kenya 4
TN - Tunisia 4
CL - Cile 3
CR - Costa Rica 3
CZ - Repubblica Ceca 3
DO - Repubblica Dominicana 3
LB - Libano 3
MU - Mauritius 3
MY - Malesia 3
PA - Panama 3
RO - Romania 3
RS - Serbia 3
SC - Seychelles 3
SN - Senegal 3
UZ - Uzbekistan 3
DZ - Algeria 2
HU - Ungheria 2
KG - Kirghizistan 2
LA - Repubblica Popolare Democratica del Laos 2
LT - Lituania 2
NI - Nicaragua 2
NP - Nepal 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
KZ - Kazakistan 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 15.725
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Città #
Santa Clara 1.932
Fairfield 836
Ashburn 677
Singapore 604
Warsaw 603
Woodbridge 398
Dublin 394
Hong Kong 365
Seoul 359
Seattle 354
Cambridge 346
Chandler 337
Houston 310
Wilmington 275
Hefei 265
Beijing 183
Ann Arbor 162
Jacksonville 149
Dallas 145
Altamura 138
Lawrence 132
Florence 124
Princeton 107
Mumbai 99
Dong Ket 82
Buffalo 77
Los Angeles 74
Boston 73
Ho Chi Minh City 70
Boardman 69
Moscow 68
Melbourne 56
Kent 55
The Dalles 55
San Diego 49
New York 43
São Paulo 43
Medford 40
Clifton 30
Jakarta 29
Munich 27
Hanoi 26
Abidjan 22
Norwalk 22
Shanghai 22
Barcelona 20
Paris 20
Council Bluffs 18
Brussels 17
Bern 16
Washington 16
Andover 15
Falls Church 15
Redondo Beach 15
Helsinki 14
Milan 14
Chicago 13
Frankfurt am Main 13
Izmir 13
Tokyo 13
Bengaluru 12
Hillsboro 12
Yubileyny 12
Rome 11
West Jordan 11
Cotonou 10
Haiphong 10
London 10
Atlanta 9
Frankfurt Am Main 9
Guangzhou 9
Rio de Janeiro 9
Tianjin 9
Turku 9
Brooklyn 8
Cape Town 8
Da Nang 8
Gavirate 8
Johannesburg 8
Lappeenranta 8
Phoenix 8
Toronto 8
Amsterdam 7
Belo Horizonte 7
Bogotá 7
Campinas 7
Chennai 7
Curitiba 7
Düsseldorf 7
Elk Grove Village 7
Shenzhen 7
Turin 7
Baku 6
Biên Hòa 6
Brasília 6
Dummerstorf 6
Formosa 6
Montreal 6
Saarbrücken 6
San Francisco 6
Totale 10.882
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Nome #
Biotransformation of Chloroaromatics: the Impact of Bioavailability and Substrate Specificity. 364
Structure and function of Aspergillus niger laccase McoG 282
Crystal structure of a blue laccase from Lentinus tigrinus: evidences for intermediates in the molecular oxygen reductive splitting by multicopper oxidases. 253
Crystal structure and kinetic studies of a tetrameric type II β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 247
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. 223
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 219
4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic Studies 200
(1,3-Dioxolane)- and (1,3-oxathiolane)-2-pyrrolidines: molecular hybrids with potential anti-Alzheimer activity 198
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 185
A BIOLOGICALLY ACTIVE GOLD COMPLEX: TRICHLORO[(2-PYRIDYL) METHANOL-N]GOLD(III) 183
Discovery of 4-Hydroxy-3-(3-(phenylureido)benzenesulfonamides as SLC-0111 Analogues for the Treatment of Hypoxic Tumors Overexpressing Carbonic Anhydrase IX 183
[Au(9-methylcaffein-8-ylidene)2]+/DNA Tel23 System: Solution, Computational, and Biological Studies 181
Crystal structure of the blue multicopper oxidase from the white-rot fungus Trametes trogii complexed with p-toluate 179
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 178
Antagonisti muscarinici a struttura 1,3-ossatiolano-2-pirrolidinica 177
Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells 172
SYNTHESIS, AFFINITY PROFILE AND FUNCTIONAL ACTIVITY OF MUSCARINIC ANTAGONISTS WITH A 1-METHYL-2-(2,2-ALKYLARYL-1,3-OXATHIOLAN-5-YL)PYRROLIDINE STRUCTURE 171
Cristallographic studies of reduced Cu(I)-Zn(II) bovine superoxide dismutase and its adducts with small inorganic anions 169
Salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans: crystal structure of a peculiar ring-cleaving dioxygenase. 169
Chalcogenides-incorporating carbonic anhydrase inhibitors concomitantly reverted oxaliplatin-induced neuropathy and enhanced antiproliferative action 168
Crystallographic Determination of Reduced Bovine Superoxide-Dismutase at pH-5.0 and of Anion-Binding to its Active-Site 166
Benzenesulfonamides Incorporating Flexible Triazole Moieties Are Highly Effective Carbonic Anhydrase Inhibitors: Synthesis and Kinetic, Crystallographic, Computational, and Intraocular Pressure Lowering Investigations 165
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 163
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 163
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 162
Direct and Straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors 161
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. 160
Diphenylcyclohexylamine derivatives as new potent multidrug resistance (MDR) modulators 159
Solution and Solid-State Analysis of Binding of 13-Substituted Berberine Analogues to Human Telomeric G-quadruplexes 158
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. 156
Structural insights on carbonic anhydrase inhibitory action, isoform selectivity, and potency of sulfonamides and coumarins incorporating arylsulfonylureido groups. 156
Crystallization and preliminary structure analysis of the blue laccase from the ligninolytic fungus Panus tigrinus. 154
Crystal Structure Determination of a Salicylate 1,2-Dioxygenase from Pseudaminobacter salicylatoxidans 151
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 150
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 147
Crystal structure of 4-chlorocatechol 1,2-dioxygenase from the chlorophenol-utilizing gram-positive Rhodococcus opacus 1CP 145
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. 144
4-Chlorocatechol 1,2-dioxygenase fromthe chlorophenol-utilizing Gram-positive Rhodococcus opacus1CP: crystallization and preliminary crystallographic analysis. 142
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: solution and X-ray crystallographic studies. 141
Sulfonamides incorporating piperazine bioisosteres as potent human carbonic anhydrase I, II, IV and IX inhibitors 141
Polypharmacology of epacadostat: A potent and selective inhibitor of the tumor associated carbonic anhydrases IX and XII 140
Crystal analysis of aromatic sulfonamide binding to native and (Zn)2 adduct of human carbonic anhydrase I Michigan 1. 140
Azidothymidine "clicked" into 1,2,3-Triazoles: First Report on Carbonic Anhydrase-Telomerase Dual-Hybrid Inhibitors 140
Selenols: a new class of carbonic anhydrase inhibitors 139
Mechanisms of the Antiproliferative and Antitumor Activity of Novel Telomerase-Carbonic Anhydrase Dual-Hybrid Inhibitors 138
Reaction Intermediates and Redox State Changes in a Blue Laccase from Steccherinum ochraceum observed by Crystallographic High/Low X-Ray Dose Experiments 137
X-ray diffraction analyses of the natural isoquinoline alkaloids Berberine and Sanguinarine in complex with double helix DNA d(CGTACG) 135
The crystal structure of human telomeric DNA complexed with berberine: an interesting case of stacked ligand to G-tetrad ratio higher than 1:1 134
Hydroxyquinol 1,2-dioxygenase 133
Preliminary crystallographic analysis of salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans. 133
Interaction of a gold(i) dicarbene anticancer drug with human telomeric DNA G-quadruplex: solution and computationally aided X-ray diffraction analysis 133
Synthesis of different thio-scaffolds bearing sulfonamide with subnanomolar carbonic anhydrase II and IX inhibitory properties and X-ray investigations for their inhibitory mechanism 132
Anion inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 130
X-ray crystallographic and molecular docking studies on a unique chloromuconolactone dehalogenase from Rhodococcus opacus 1CP. 130
Crystal analysis of Aromatic sulfonamide binding to native and (Zn)2adduct to Human Carbonic Anhydrase I Michigan 1 129
Synthesis of Azasugar–Sulfonamide conjugates and their Evaluation as Inhibitors of Carbonic Anhydrases: the Azasugar Approach to Selectivity 127
Chlorocatechol 1, 2-dioxygenase from the Chlorophenol-utilizing Gram-positive Rhodococcus opacus 1CP: Crystallization and preliminary crystallographic analysis 127
Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activity 127
The Crystal structure of the Monomeric Human SOD Mutant F50E/G51E/E133Q at Atomic Resolution. The Enzyme mechanism Revisited 126
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 126
Fluorescent sulfonamide carbonic anhydrase inhibitors incorporating 1,2,3-triazole moieties: Kinetic and X-ray crystallographic studies 125
Structure determination of a blue laccase from Trametes Trogii at 1.5 Å 122
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. 122
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 122
Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases Inhibition 122
Benzoselenoates: A novel class of carbonic anhydrase inhibitors 121
One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase Enzymes 119
Polymeric hydrophobic membranes as a tool to control polymorphism and protein–ligand interactions 118
Thioxocoumarins Show an Alternative Carbonic Anhydrase Inhibition Mechanism Compared to Coumarins 116
Laccase isoforms with unusual properties from the basidiomycete Steccherinum ochraceum strain 1833 116
Dioxygen, an unexpected carbonic anhydrase ligand 115
The crystal structures of native hydroquinone 1,2-dioxygenase from Sphingomonas sp. TTNP3 and of substrate and inhibitor complexes 113
Interaction of Carboxypeptidase A with Anions: Crystal Structure of the Complex with the HPO42- Anion 111
Novel Carbonic Anhydrase Inhibitors with Dual-Tail Core Sulfonamide Show Potent and Lasting Effects for Glaucoma Therapy 110
Crystal structure and chemical inhibition of essential schistosome host-interactive virulence factor carbonic anhydrase SmCA 108
Pyridine Derivative of the Natural Alkaloid Berberine as Human Telomeric G4-DNA Binder: A Solution and Solid-State Study 108
Structural basis of hyaluronan degradation by Streptococcus pneumoniae hyaluronate lyase 108
X-ray structural study of human neutrophil elastase inhibition with a series of azaindoles, azaindazoles and isoxazolones 107
Crystallization and preliminary X-ray crystallographic analysis of the small subunit of the heterodimeric laccase POXA3b from Pleurotus ostreatus. 107
Mono- and three-tailed sugar and iminosugar decorated benzenesulfonamide carbonic anhydrase inhibitors 106
Selenolesterase enzyme activity of carbonic anhydrases 106
Lasamide, a Potent Human Carbonic Anhydrase Inhibitor from the Market: Inhibition Profiling and Crystallographic Studies 105
Synthetic Approaches to Novel Human Carbonic Anhydrase Isoform Inhibitors Based on Pyrrol-2-one Moiety 103
Selenocarbamates As a Prodrug-Based Approach to Carbonic Anhydrase Inhibition 103
Crystal structure of the hydroxyquinol 1,2-dioxygenase from Nocardioides simplex 3E, a key enzyme involved in polychlorinated aromatics biodegradation 103
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 101
Famotidine, an Antiulcer Agent, Strongly Inhibits Helicobacter pylori and Human Carbonic Anhydrases 100
Double helices forming unusual binding motifs: the case of the natural alkaloids coptisine and chelerythrine 100
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: Solution and X-ray crystallographic studies 100
Thia- and Seleno-Michael Reactions for the Synthesis of Carbonic Anhydrases Inhibitors 99
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 99
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 95
Sulfonamide carbonic anhydrase inhibitors: Zinc coordination and tail effects influence inhibitory efficacy and selectivity for different isoforms 94
Benzenesulfonamide decorated dihydropyrimidin(thi)ones: carbonic anhydrase profiling and antiproliferative activity 93
Study of Chalcogen Aspirin Derivatives with Carbonic Anhydrase Inhibitory Properties for Treating Inflammatory Pain 93
Molecular Basis of Pseudomonas syringae pv actinidiae Levansucrase Inhibition by a Multivalent Iminosugar 92
Induction of a Four-Way Junction Structure in the DNA Palindromic Hexanucleotide 5'-d(CGTACG)-3' by a Mononuclear Platinum Complex 92
First-in-Class Dual Targeting Compounds for the Management of Seizures in Glucose Transporter Type 1 Deficiency Syndrome 91
Anion Recognition by Proteins 90
Structural basis for the substrate specificity and the absence of dehalogenation activity in 2-chloromuconate cycloisomerase from Rhodococcus opacus 1CP 90
Totale 14.086
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Categoria #
all - tutte 44.625
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 44.625
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021695 0 0 0 0 0 99 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
2025/20263.521 565 923 710 656 626 41 0 0 0 0 0 0
Totale 15.872