IRIS
BINDA, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 2.339
AS - Asia 1.881
EU - Europa 1.650
SA - Sud America 248
AF - Africa 30
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.153
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Nazione #
US - Stati Uniti d'America 2.283
CN - Cina 975
IE - Irlanda 440
SG - Singapore 391
HK - Hong Kong 226
RU - Federazione Russa 215
BR - Brasile 196
GB - Regno Unito 192
UA - Ucraina 164
FI - Finlandia 162
IT - Italia 154
DE - Germania 145
VN - Vietnam 123
IN - India 50
SE - Svezia 38
CA - Canada 31
FR - Francia 30
AR - Argentina 22
BE - Belgio 22
AT - Austria 20
JP - Giappone 19
BD - Bangladesh 17
MX - Messico 17
PL - Polonia 17
ZA - Sudafrica 16
NL - Olanda 14
TR - Turchia 13
ES - Italia 11
ID - Indonesia 10
IR - Iran 9
AZ - Azerbaigian 7
EC - Ecuador 7
IQ - Iraq 7
LT - Lituania 7
PT - Portogallo 7
PE - Perù 6
CL - Cile 5
PK - Pakistan 5
UZ - Uzbekistan 5
CO - Colombia 4
KR - Corea 4
SA - Arabia Saudita 4
AL - Albania 3
VE - Venezuela 3
CZ - Repubblica Ceca 2
DO - Repubblica Dominicana 2
EG - Egitto 2
GA - Gabon 2
KG - Kirghizistan 2
PA - Panama 2
PY - Paraguay 2
TN - Tunisia 2
UY - Uruguay 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
AU - Australia 1
BH - Bahrain 1
BO - Bolivia 1
BW - Botswana 1
BY - Bielorussia 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
DZ - Algeria 1
EE - Estonia 1
EU - Europa 1
GH - Ghana 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
IL - Israele 1
JO - Giordania 1
KE - Kenya 1
KW - Kuwait 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LV - Lettonia 1
MA - Marocco 1
ME - Montenegro 1
MU - Mauritius 1
MZ - Mozambico 1
NC - Nuova Caledonia 1
NG - Nigeria 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
OM - Oman 1
PR - Porto Rico 1
PS - Palestinian Territory 1
RS - Serbia 1
SY - Repubblica araba siriana 1
TJ - Tagikistan 1
TM - Turkmenistan 1
TT - Trinidad e Tobago 1
Totale 6.153
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Città #
Dublin 436
Chandler 279
Hong Kong 225
Jacksonville 209
Dallas 200
Nanjing 197
Ashburn 189
Beijing 189
Singapore 188
Boardman 114
New York 81
Nanchang 75
Princeton 73
Lawrence 70
Wilmington 65
Ann Arbor 64
Changsha 64
Shenyang 60
Los Angeles 55
Hebei 52
Medford 52
Helsinki 49
Buffalo 44
Jiaxing 44
Moscow 42
Pavia 41
Ho Chi Minh City 38
Shanghai 38
Munich 30
Woodbridge 28
Hangzhou 27
Redondo Beach 27
Tianjin 27
Hanoi 25
Milan 25
Brussels 22
São Paulo 19
The Dalles 19
Warsaw 17
Norwalk 16
Verona 16
Houston 14
Pune 14
Rio de Janeiro 14
Santa Clara 14
Seattle 14
Tokyo 14
Toronto 14
Chicago 13
Guangzhou 13
Denver 12
Stockholm 12
Turku 12
Atlanta 11
Brooklyn 11
San Francisco 11
Vienna 11
Piscataway 10
Zhengzhou 10
Columbus 9
Manchester 9
Montreal 9
Boston 8
Haiphong 8
Phoenix 8
Amsterdam 7
Baku 7
Belo Horizonte 7
Fairfield 7
Orem 7
Ankara 6
Biên Hòa 6
Campinas 6
Chennai 6
Johannesburg 6
London 6
Mexico City 6
Ningbo 6
Poplar 6
Potchefstroom 6
Bắc Ninh 5
Da Nang 5
Gallarate 5
Jinan 5
Padua 5
Renton 5
Tashkent 5
Voghera 5
Auburn Hills 4
Berlin 4
Kunming 4
Mumbai 4
New Delhi 4
Philadelphia 4
Seoul 4
Tappahannock 4
Washington 4
Aracaju 3
Bologna 3
Bonn 3
Totale 3.986
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Nome #
2-Carboxyquinoxalines Kill Mycobacterium tuberculosis through Noncovalent Inhibition of DprE1. 181
A Novel Mammalian Flavin-dependent Histone Demethylase 145
A 30-angstrom-long U-shaped catalytic tunnel in the crystal structure of polyamine oxidase 131
4-Aminoquinolone Piperidine Amides: Non-Covalent Inhibitors of DprE1 with Long Residence Time and Potent Antimycobacterial Activity. 128
The 'gating' residues Ile199 and Tyr326 in human monoamine oxidase B function in substrate and inhibitor recognition. 119
Structural Basis for Benzothiazinone-Mediated Killing of Mycobacterium tuberculosis. 112
8 Demethylation pathways for histone methyllysine residues 112
Binding of Rasagiline-related Inhibitors to Human Monoamine Oxidases: A Kinetic and Crystallographic Analysis 108
Monoamine Oxidases 108
Structure of the mutant E92K of [2Fe-2S] ferredoxin I from Spinacia oleracea at 1.7 A resolution. 106
Biochemical, structural, and biological evaluation of tranylcypromine derivatives as inhibitors of histone demethylases LSD1 and LSD2. 105
Alternative Splicing of the Histone Demethylase LSD1/KDM1 Contributes to the Modulation of Neurite Morphogenesis in the Mammalian Nervous System 105
Molecular Insights into Human Monoamine Oxidase B Inhibition by the Glitazone Antidiabetes Drugs 103
A highly specific mechanism of histone H3-K4 recognition by histone demethylase LSD1 103
Monoamine oxidase-A is a novel driver of stress-induced premature senescence through inhibition of parkin-mediated mitophagy 99
Crystal structures of monoamine oxidase B in complex with four inhibitors of the N-propargylaminoindan class 98
Tight-Binding Inhibition of Human Monoamine Oxidase B by Chromone Analogs: A Kinetic, Crystallographic, and Biological Analysis 97
Structural and mechanistic studies of mofegiline inhibition of recombinant human monoamine oxidase B 92
Design and synthesis of novel chalcones as potent selective monoamine oxidase-B inhibitors. 92
A cross-talk and amonia channeling between active in the unexpected domain arrangement of glutamate synthase. 90
An unprecedented NADPH domain conformation in lysine monooxygenase NbtG provides insights into uncoupling of oxygen consumption from substrate hydroxylation 90
Biocatalytic Characterization of Human FMO5: Unearthing Baeyer-Villiger Reactions in Humans 89
Structure-Based Enzyme Tailoring of 5-Hydroxymethylfurfural Oxidase 88
Biocatalytic Properties and Structural Analysis of Eugenol Oxidase from Rhodococcus jostii RHA1: A Versatile Oxidative Biocatalyst 87
Crystallization and preliminary X-ray analysis of polyamine oxidase from Zea mays L. 87
Crystal structure of human monoamine oxidase B, a drug target enzyme monotopically inserted into the mitochondrial outer membrane 86
Molecular Mimicry and Ligand Recognition in Binding and Catalysis by the Histone Demethylase LSD1-CoREST Complex 85
Kinetic Resolution of sec-Thiols by Enantioselective Oxidation with Rationally Engineered 5-(Hydroxymethyl)furfural Oxidase 84
Functional Role of the "Aromatic Cage" in Human Monoamine Oxidase B: Structures and Catalytic Properties of Tyr435 Mutant Proteins. 82
The DprE1 enzyme, one of the most vulnerable targets of Mycobacterium tuberculosis. 82
Comparative Analysis of the Neurochemical Profile and MAO Inhibition Properties of N‑(Furan-2-ylmethyl)‑N‑methylprop-2-yn-1-amine 81
The FAD Binding Sites of Human Monoamine Oxidases A and B 80
Stereoselective Activity of 1-Propargyl-4-styrylpiperidine-like Analogues That Can Discriminate between Monoamine Oxidase Isoforms A and B 80
Structure of the human mitochondrial monoamine oxidase B: New chemical implications for neuroprotectant drug design 78
Rational Redesign of Monoamine Oxidase A into a Dehydrogenase to Probe ROS in Cardiac Aging 77
Molecular and mechanistic properties of the membrane-bound mitochondrial monoamine oxidases 77
Structural properties of human monoamine oxidases A and B 76
Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders 75
Histone Demethylation Catalysed by LSD1 is a Flavin-dependent Oxidative Process 74
Structures of Human Monoamine Oxidase B Complexes with Selective Noncovalent Inhibitors: Safinamide and Coumarin Analogs 74
Structure-Based Engineering of Phanerochaete chrysosporium Alcohol Oxidase for Enhanced Oxidative Power toward Glycerol 74
New roles of flavoproteins in molecular cell biology: histone demethylase LSD1 and chromatin. 73
Structure-function relationships in flavoenzyme-dependent amine oxidations: a comparison of polyamine oxidase and monoamine oxidase. 73
Discovery and characterization of an F420-dependent glucose-6-phosphate dehydrogenase (Rh-FGD1) from Rhodococcus jostii RHA1 73
Polystyrene microbridges used in sitting-drop crystallisation release 1,4-diphenyl-2-butene, a novel inhibitor of human MAO B 72
Structural Basis of LSD1-CoREST Selectivity in Histone H3 Recognition 72
Insights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structures 72
LSD1: Oxidative Chemistry for Multifaceted Functions in Chromatin Regulation. 71
Two tyrosine residues, Tyr-108 and Tyr-503, are responsible for the deprotonation of phenolic substrates in vanillyl-alcohol oxidase. 71
Three-dimensional structure of human monoamine oxidase A (MAO A): relation to the structures of rat MAO A and human MAO B 71
Isolation and characterization of a thermostable F420:NADPH oxidoreductase from Thermobifida fusca 70
The structure of monoamine oxidases: past, present, and future 70
Demonstration of Isoleucine 199 as a Structural Determinant for the Selective Inhibition of Human Monoamine Oxidase B by Specific Reversible Inhibitors 69
Assessment of Tractable Cysteines for Covalent Targeting by Screening Covalent Fragments 68
Allosteric transitions of rabbit skeletal muscle lactate dehydrogenase induced by pH-dependent dissociation of the tetrameric enzyme 68
Discovery and structural characterization of a thermostable bacterial monoamine oxidase 68
STRUCTURE AND MECHANISM OF MONOAMINE OXIDASE 66
Monoamine Oxidases, Oxidative Stress, and Altered Mitochondrial Dynamics in Cardiac Ageing 65
Potentiation of ligand binding through cooperative effects in monoamine oxidase B 64
Human histone demethylase LSD1 reads the histone code 64
Inactivation of Purified Human Recombinant Monoamine Oxidases A and B by Rasagiline and Its Analogues 64
Diphenylene Iodonium Is a Noncovalent MAO Inhibitor: A Biochemical and Structural Analysis 64
Kinetic and structural analysis of the irreversible inhibition of human monoamine oxidases by ASS234, a multi-target compound designed for use in Alzheimer's disease 63
Dual Reversible Coumarin Inhibitors Mutually Bound to Monoamine Oxidase B and Acetylcholinesterase Crystal Structures 63
Design of Benzyl-triazolopyrimidine-Based NADPH Oxidase Inhibitors Leads to the Discovery of a Potent Dual Covalent NOX2/MAOB Inhibitor 62
Structural insights into the mechanism of amine oxidation by monoamine oxidases A and B 58
Structural based for inhibitor binding and catalysis in polyamine oxidase. 58
Interactions of Monoamine Oxidases with the Antiepileptic Drug Zonisamide: Specificity of Inhibition and Structure of the Human Monoamine Oxidase B Complex. 57
Lights and shadows on monoamine oxidase inhibition in neuroprotective pharmacological therapies 57
Structural and mechanistic studies of arylalkylhydrazine inhibition of human monoamine oxidases A and B. 57
Promising Non-cytotoxic Monosubstituted Chalcones to Target Monoamine Oxidase-B 54
Bioisosteric replacement based on 1,2,4-oxadiazoles in the discovery of 1H-indazole-bearing neuroprotective MAO B inhibitors 53
The Peroxidase-Coupled Assay to Measure MAO Enzymatic Activity 53
Measurement of MAO Enzymatic Activity by Spectrophotometric Direct Assays 52
8-Hydroxyquinolylnitrones as multifunctional ligands for the therapy of neurodegenerative diseases 50
Crystallization of Human Monoamine Oxidase B 47
Tranylcypromine-Based LSD1 Inhibitors: Structure-Activity Relationships, Antiproliferative Effects in Leukemia, and Gene Target Modulation 47
Crystallographic snapshots of UDP-glucuronic acid 4-epimerase ligand binding, rotation, and reduction 45
Monoamine Oxidase Inhibitors Prevent Glucose-Dependent Energy Production, Proliferation and Migration of Bladder Carcinoma Cells 36
Evolutionary and Functional Analysis of Monoamine Oxidase F: A Novel Member of the Monoamine Oxidase Gene Family 13
Altering substrate specificity of a thermostable bacterial monoamine oxidase by structure-based mutagenesis 12
Totale 6.325
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Categoria #
all - tutte 28.615
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 28.615
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021214 0 0 0 0 0 38 1 76 17 42 35 5
2021/2022293 8 5 17 1 3 1 2 21 14 6 56 159
2022/20231.027 111 63 9 70 79 91 0 49 491 4 33 27
2023/2024475 72 86 11 23 42 127 11 47 1 22 24 9
2024/20251.123 41 86 20 35 38 45 51 57 301 43 157 249
2025/20261.629 231 262 361 345 362 68 0 0 0 0 0 0
Totale 6.325