FERRARONI, MARTA
 Distribuzione geografica
Continente #
NA - Nord America 4.634
EU - Europa 2.205
AS - Asia 399
AF - Africa 6
Continente sconosciuto - Info sul continente non disponibili 1
Totale 7.245
Nazione #
US - Stati Uniti d'America 4.625
PL - Polonia 596
IE - Irlanda 438
IT - Italia 362
SE - Svezia 323
HK - Hong Kong 173
DE - Germania 115
UA - Ucraina 96
VN - Vietnam 85
GB - Regno Unito 76
FI - Finlandia 67
CN - Cina 56
JO - Giordania 41
BE - Belgio 40
ES - Italia 20
AT - Austria 19
CH - Svizzera 19
IN - India 18
FR - Francia 16
TR - Turchia 13
SG - Singapore 11
RU - Federazione Russa 10
CA - Canada 9
NL - Olanda 5
MU - Mauritius 3
SC - Seychelles 3
JP - Giappone 2
RO - Romania 2
CZ - Repubblica Ceca 1
EU - Europa 1
Totale 7.245
Città #
Fairfield 836
Warsaw 596
Dublin 436
Ashburn 430
Woodbridge 398
Seattle 351
Cambridge 346
Chandler 337
Houston 308
Wilmington 275
Ann Arbor 162
Jacksonville 148
Altamura 138
Lawrence 132
Princeton 107
Hong Kong 94
Florence 83
Dong Ket 82
Boston 66
Boardman 64
San Diego 49
Beijing 41
Brussels 40
Medford 40
New York 23
Norwalk 22
Barcelona 20
Buffalo 19
Bern 16
Andover 15
Falls Church 15
London 15
Vienna 15
Washington 15
Hillsboro 12
Izmir 12
Frankfurt Am Main 9
Gavirate 8
Milan 7
Shanghai 7
Toronto 7
Dummerstorf 6
Auburn Hills 5
Corato 5
Düsseldorf 5
Rome 5
Moscow 4
Phoenix 4
Saint-Fons 4
Serra 4
Arezzo 3
Guangzhou 3
New Bedfont 3
Siena 3
Verona 3
Bologna 2
Chengdu 2
Chieti 2
Chiswick 2
Dallas 2
Edinburgh 2
Grevenbroich 2
Islington 2
Leawood 2
Los Angeles 2
Misano Adriatico 2
Montréal 2
Monza 2
Nürnberg 2
Parma 2
Pune 2
Redwood City 2
San Mateo 2
Scandicci 2
Trumbull 2
Turin 2
Venice 2
Zurich 2
Acton 1
Arnsberg 1
Bagno A Ripoli 1
Cantagallo 1
Castel Madama 1
Catanzaro 1
Cetraro 1
Chennai 1
Chicago 1
Elmendorf 1
Fabro 1
Frosinone 1
Fuzhou 1
Gottolengo 1
Grenoble 1
Groningen 1
Hanoi 1
Hanover 1
Helsinki 1
Hounslow 1
Hyderabad 1
Kagoya 1
Totale 5.921
Nome #
Biotransformation of Chloroaromatics: the Impact of Bioavailability and Substrate Specificity. 257
Structure and function of Aspergillus niger laccase McoG 221
Crystal structure of a blue laccase from Lentinus tigrinus: evidences for intermediates in the molecular oxygen reductive splitting by multicopper oxidases. 194
Crystal structure and kinetic studies of a tetrameric type II β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 187
Discovery of 4-Hydroxy-3-(3-(phenylureido)benzenesulfonamides as SLC-0111 Analogues for the Treatment of Hypoxic Tumors Overexpressing Carbonic Anhydrase IX 125
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 118
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 112
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. 110
SYNTHESIS, AFFINITY PROFILE AND FUNCTIONAL ACTIVITY OF MUSCARINIC ANTAGONISTS WITH A 1-METHYL-2-(2,2-ALKYLARYL-1,3-OXATHIOLAN-5-YL)PYRROLIDINE STRUCTURE 108
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 106
4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic Studies 106
Structural insights on carbonic anhydrase inhibitory action, isoform selectivity, and potency of sulfonamides and coumarins incorporating arylsulfonylureido groups. 105
Crystallization and preliminary structure analysis of the blue laccase from the ligninolytic fungus Panus tigrinus. 103
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. 103
Antagonisti muscarinici a struttura 1,3-ossatiolano-2-pirrolidinica 102
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: solution and X-ray crystallographic studies. 101
Salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans: crystal structure of a peculiar ring-cleaving dioxygenase. 100
Crystal structure of the blue multicopper oxidase from the white-rot fungus Trametes trogii complexed with p-toluate 98
Crystallographic Determination of Reduced Bovine Superoxide-Dismutase at pH-5.0 and of Anion-Binding to its Active-Site 97
Cristallographic studies of reduced Cu(I)-Zn(II) bovine superoxide dismutase and its adducts with small inorganic anions 96
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. 95
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 95
Diphenylcyclohexylamine derivatives as new potent multidrug resistance (MDR) modulators 95
X-ray crystallographic and molecular docking studies on a unique chloromuconolactone dehalogenase from Rhodococcus opacus 1CP. 95
(1,3-Dioxolane)- and (1,3-oxathiolane)-2-pyrrolidines: molecular hybrids with potential anti-Alzheimer activity 94
[Au(9-methylcaffein-8-ylidene)2]+/DNA Tel23 System: Solution, Computational, and Biological Studies 94
Benzenesulfonamides Incorporating Flexible Triazole Moieties Are Highly Effective Carbonic Anhydrase Inhibitors: Synthesis and Kinetic, Crystallographic, Computational, and Intraocular Pressure Lowering Investigations 93
A BIOLOGICALLY ACTIVE GOLD COMPLEX: TRICHLORO[(2-PYRIDYL) METHANOL-N]GOLD(III) 89
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 88
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. 87
Polypharmacology of epacadostat: A potent and selective inhibitor of the tumor associated carbonic anhydrases IX and XII 86
Reaction Intermediates and Redox State Changes in a Blue Laccase from Steccherinum ochraceum observed by Crystallographic High/Low X-Ray Dose Experiments 86
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 86
The crystal structure of human telomeric DNA complexed with berberine: an interesting case of stacked ligand to G-tetrad ratio higher than 1:1 85
Sulfonamides incorporating piperazine bioisosteres as potent human carbonic anhydrase I, II, IV and IX inhibitors 84
Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells 83
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 83
Crystal analysis of aromatic sulfonamide binding to native and (Zn)2 adduct of human carbonic anhydrase I Michigan 1. 82
Crystal Structure Determination of a Salicylate 1,2-Dioxygenase from Pseudaminobacter salicylatoxidans 81
Thioxocoumarins Show an Alternative Carbonic Anhydrase Inhibition Mechanism Compared to Coumarins 81
Interaction of a gold(i) dicarbene anticancer drug with human telomeric DNA G-quadruplex: solution and computationally aided X-ray diffraction analysis 79
X-ray diffraction analyses of the natural isoquinoline alkaloids Berberine and Sanguinarine in complex with double helix DNA d(CGTACG) 78
Direct and Straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors 77
Crystal structure of 4-chlorocatechol 1,2-dioxygenase from the chlorophenol-utilizing gram-positive Rhodococcus opacus 1CP 75
Crystal analysis of Aromatic sulfonamide binding to native and (Zn)2adduct to Human Carbonic Anhydrase I Michigan 1 75
Hydroxyquinol 1,2-dioxygenase 75
Fluorescent sulfonamide carbonic anhydrase inhibitors incorporating 1,2,3-triazole moieties: Kinetic and X-ray crystallographic studies 75
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. 74
The crystal structures of native hydroquinone 1,2-dioxygenase from Sphingomonas sp. TTNP3 and of substrate and inhibitor complexes 74
Interaction of Carboxypeptidase A with Anions: Crystal Structure of the Complex with the HPO42- Anion 72
Structural basis of hyaluronan degradation by Streptococcus pneumoniae hyaluronate lyase 72
Synthesis of different thio-scaffolds bearing sulfonamide with subnanomolar carbonic anhydrase II and IX inhibitory properties and X-ray investigations for their inhibitory mechanism 71
Polymeric hydrophobic membranes as a tool to control polymorphism and protein–ligand interactions 70
Chalcogenides-incorporating carbonic anhydrase inhibitors concomitantly reverted oxaliplatin-induced neuropathy and enhanced antiproliferative action 70
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 69
Crystallization and preliminary X-ray crystallographic analysis of the small subunit of the heterodimeric laccase POXA3b from Pleurotus ostreatus. 69
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 69
Chlorocatechol 1, 2-dioxygenase from the Chlorophenol-utilizing Gram-positive Rhodococcus opacus 1CP: Crystallization and preliminary crystallographic analysis 69
Selenols: a new class of carbonic anhydrase inhibitors 68
The Crystal structure of the Monomeric Human SOD Mutant F50E/G51E/E133Q at Atomic Resolution. The Enzyme mechanism Revisited 67
Preliminary crystallographic analysis of salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans. 66
Solution and Solid-State Analysis of Binding of 13-Substituted Berberine Analogues to Human Telomeric G-quadruplexes 65
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 65
Laccase isoforms with unusual properties from the basidiomycete Steccherinum ochraceum strain 1833 64
Mechanisms of the Antiproliferative and Antitumor Activity of Novel Telomerase-Carbonic Anhydrase Dual-Hybrid Inhibitors 64
Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activity 62
Structural basis for the substrate specificity and the absence of dehalogenation activity in 2-chloromuconate cycloisomerase from Rhodococcus opacus 1CP 56
Dioxygen, an unexpected carbonic anhydrase ligand 54
Anion inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 53
Crystal structure and chemical inhibition of essential schistosome host-interactive virulence factor carbonic anhydrase SmCA 53
4-Chlorocatechol 1,2-dioxygenase fromthe chlorophenol-utilizing Gram-positive Rhodococcus opacus1CP: crystallization and preliminary crystallographic analysis. 52
Sulfonamide carbonic anhydrase inhibitors: Zinc coordination and tail effects influence inhibitory efficacy and selectivity for different isoforms 50
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 50
Crystal structure of the hydroxyquinol 1,2-dioxygenase from Nocardioides simplex 3E, a key enzyme involved in polychlorinated aromatics biodegradation 49
Azidothymidine "clicked" into 1,2,3-Triazoles: First Report on Carbonic Anhydrase-Telomerase Dual-Hybrid Inhibitors 48
Induction of a Four-Way Junction Structure in the DNA Palindromic Hexanucleotide 5'-d(CGTACG)-3' by a Mononuclear Platinum Complex 47
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae 43
Famotidine, an Antiulcer Agent, Strongly Inhibits Helicobacter pylori and Human Carbonic Anhydrases 42
Benzoselenoates: A novel class of carbonic anhydrase inhibitors 41
Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases Inhibition 40
Synthesis of Azasugar–Sulfonamide conjugates and their Evaluation as Inhibitors of Carbonic Anhydrases: the Azasugar Approach to Selectivity 39
Double helices forming unusual binding motifs: the case of the natural alkaloids coptisine and chelerythrine 36
Structure determination of a blue laccase from Trametes Trogii at 1.5 Å 34
The crystal structure of a bacterial intradiol dioxygenases involved in the biodegradation of polychlorinated aromatic compounds 34
Selenolesterase enzyme activity of carbonic anhydrases 34
Pyridine Derivative of the Natural Alkaloid Berberine as Human Telomeric G4-DNA Binder: A Solution and Solid-State Study 32
One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase Enzymes 32
Anion Recognition by Proteins 28
Nuovi modulatori della multidrug resistance (MDR) a struttura difenilcicloesilaminica 28
Crystal structure of a tetrameric type II β-carbonic anhydrase from the pathogenic bacterium burkholderia pseudomallei 27
Crystallization and preliminary X-ray crystallographic analysis of hydroquinone dioxygenase from Sphingomonas sp. TTNP3 26
X-ray structural study of human neutrophil elastase inhibition with a series of azaindoles, azaindazoles and isoxazolones 24
Structural Insights into Schistosoma mansoni Carbonic Anhydrase (SmCA) Inhibition by Selenoureido-Substituted Benzenesulfonamides 24
Experimental and theoretical affinity studies of substituted phenols tochlorocatechol 1,2-dioxygenases: A step toward the comprehension ofinhibitor/substrate binding to intradiol dioxygenases 19
Selenocarbamates As a Prodrug-Based Approach to Carbonic Anhydrase Inhibition 17
Mono- and three-tailed sugar and iminosugar decorated benzenesulfonamide carbonic anhydrase inhibitors 14
Gentisate 1,2-dioxygenase from the gram-positive bacteria Rhodococcus opacus 1CP: Identical active sites vs. different substrate selectivities 14
First-in-Class Dual Targeting Compounds for the Management of Seizures in Glucose Transporter Type 1 Deficiency Syndrome 11
Diversely substituted sulfamides for fragment-based drug discovery of carbonic anhydrase inhibitors: synthesis and inhibitory profile 11
Probing the Efficiency of 13-Pyridylalkyl Berberine Derivatives to Human Telomeric G-Quadruplexes Binding: Spectroscopic, Solid State and In Silico Analysis 10
Totale 7.317
Categoria #
all - tutte 21.008
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 21.008


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019770 0 0 0 0 0 0 0 0 24 155 309 282
2019/20201.800 150 114 38 160 211 226 215 225 193 109 133 26
2020/20211.056 83 65 72 98 43 99 30 69 92 177 84 144
2021/2022682 22 78 67 22 21 39 37 49 40 28 108 171
2022/20231.764 191 352 53 100 128 288 235 87 218 14 56 42
2023/2024533 34 61 125 43 62 81 7 110 10 0 0 0
Totale 7.357