Bicocca Open Archive

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DE GIOIA, LUCA
 Distribuzione geografica
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Continente #
NA - Nord America 31.443
AS - Asia 15.485
EU - Europa 15.192
SA - Sud America 2.260
AF - Africa 362
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 15
AN - Antartide 1
Totale 64.779
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Nazione #
US - Stati Uniti d'America 29.681
SG - Singapore 5.187
IT - Italia 3.710
CN - Cina 3.708
DE - Germania 2.206
VN - Vietnam 2.176
HK - Hong Kong 1.881
RU - Federazione Russa 1.855
BR - Brasile 1.705
CA - Canada 1.566
SE - Svezia 1.546
IE - Irlanda 1.069
UA - Ucraina 987
GB - Regno Unito 819
FR - Francia 688
PL - Polonia 635
IN - India 546
BD - Bangladesh 374
FI - Finlandia 368
AT - Austria 335
DK - Danimarca 313
KR - Corea 268
TR - Turchia 241
AR - Argentina 224
NL - Olanda 209
ID - Indonesia 164
IQ - Iraq 144
ES - Italia 124
ZA - Sudafrica 124
MX - Messico 114
JP - Giappone 103
PK - Pakistan 100
SA - Arabia Saudita 91
PH - Filippine 83
BE - Belgio 80
EC - Ecuador 79
CO - Colombia 61
UZ - Uzbekistan 61
VE - Venezuela 56
MA - Marocco 48
CH - Svizzera 47
MY - Malesia 40
PY - Paraguay 40
KE - Kenya 38
JO - Giordania 37
CL - Cile 35
RO - Romania 35
EG - Egitto 34
TN - Tunisia 33
AE - Emirati Arabi Uniti 28
NP - Nepal 27
PE - Perù 26
IL - Israele 24
IR - Iran 24
JM - Giamaica 23
OM - Oman 23
LT - Lituania 22
GR - Grecia 21
CZ - Repubblica Ceca 19
LB - Libano 19
TW - Taiwan 19
KZ - Kazakistan 18
TH - Thailandia 17
AL - Albania 16
ET - Etiopia 16
UY - Uruguay 16
AU - Australia 15
CR - Costa Rica 15
DZ - Algeria 15
BO - Bolivia 14
DO - Repubblica Dominicana 13
NO - Norvegia 13
RS - Serbia 13
PT - Portogallo 12
AZ - Azerbaigian 11
KW - Kuwait 11
BG - Bulgaria 9
PS - Palestinian Territory 9
EU - Europa 8
HN - Honduras 8
SY - Repubblica araba siriana 8
BH - Bahrain 7
NG - Nigeria 7
QA - Qatar 7
SK - Slovacchia (Repubblica Slovacca) 7
NZ - Nuova Zelanda 6
PA - Panama 6
BY - Bielorussia 5
HU - Ungheria 5
LY - Libia 5
MN - Mongolia 5
MU - Mauritius 5
SV - El Salvador 5
A2 - ???statistics.table.value.countryCode.A2??? 4
CM - Camerun 4
CY - Cipro 4
EE - Estonia 4
LU - Lussemburgo 4
MD - Moldavia 4
MM - Myanmar 4
Totale 64.698
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Città #
Ann Arbor 4.881
Singapore 3.084
Ashburn 2.712
Woodbridge 2.205
Hong Kong 1.830
Fairfield 1.750
Wilmington 1.698
San Jose 1.439
Houston 1.340
Milan 1.338
Frankfurt am Main 1.313
Chandler 1.229
Toronto 1.052
Dublin 1.025
Jacksonville 1.012
Seattle 733
Santa Clara 710
Dearborn 691
New York 606
Cambridge 573
Los Angeles 538
Kraków 531
Beijing 487
Ho Chi Minh City 462
Chicago 442
Princeton 436
Dallas 413
Hefei 393
Hanoi 381
The Dalles 362
Dong Ket 331
Nanjing 326
Vienna 307
Seoul 252
Shanghai 249
Lauterbourg 221
Buffalo 206
Altamura 199
Boardman 189
Lawrence 189
Moscow 181
Council Bluffs 178
Lachine 168
Munich 163
Rome 162
São Paulo 161
Ottawa 143
Guangzhou 136
Helsinki 133
San Diego 111
Jakarta 107
Fremont 105
Nanchang 101
Orem 100
London 93
Shenyang 90
Warsaw 82
Hebei 81
Brussels 75
Da Nang 73
Haiphong 73
Fuzhou 68
Denver 66
Tokyo 66
Kent 65
Montreal 64
Turin 64
Romola 62
Tianjin 62
Baghdad 61
Changsha 59
Jinan 59
Chennai 58
Johannesburg 57
Atlanta 56
Andover 55
Brooklyn 54
Columbus 54
Tashkent 52
Phoenix 49
Falls Church 48
Philadelphia 48
Stockholm 48
Jiaxing 47
Norwalk 47
Naples 43
Zhengzhou 43
Amsterdam 42
Rio de Janeiro 42
Brasília 41
Pune 41
Mountain View 40
Hangzhou 39
Montréal 39
Salt Lake City 39
San Francisco 39
Jeddah 38
Ningbo 38
Boston 37
Hyderabad 37
Totale 42.618
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Nome #
Selective cytotoxicity of a bicyclic Ras inhibitor in cancer cells expressing K-RasG13D 753
Inhibition of the Hexosamine Biosynthetic Pathway by targeting PGM3 causes breast cancer growth arrest and apoptosis 686
The Multi-Level Mechanism of Action of a Pan-Ras Inhibitor Explains its Antiproliferative Activity on Cetuximab-Resistant Cancer Cells 682
First experimental identification of Ras-inhibitor binding interface using a water-soluble Ras ligand 681
Structure-Activity Studies on Arylamides and Arysulfonamides Ras Inhibitors 659
Structure-Activity Studies on Arylamides and Arysulfonamides Ras Inhibitors 600
Synthetic sulfoglycolipids targeting the serine–threonine protein kinase Akt 545
Epigallocatechin-3-gallate and related phenol compounds redirect the amyloidogenic aggregation pathway of ataxin-3 towards non-toxic aggregates and prevent toxicity in neural cells and Caenorhabditis elegans animal model 520
Rigid polycycles and peptidomimetics from carbohydrate synthons 517
Theoretical study of hydration of cyanamide and carbodiimide 514
Design, Synthesis, and Preliminary Biological Evaluation of GlcNAc-6P Analogues for the Modulation of Phosphoacetylglucosamine Mutase 1 (AGM1/PGM3) 503
Reactivation of the Ready and Unready Oxidized States of [NiFe]-Hydrogenases: Mechanistic Insights from DFT Calculations 498
Arabinose-derived Bicyclic Amino Acids: Synthesis, Conformational Analysis and Construction of an avb3-selective RGD Peptide 492
Catalytic Mechanism of Fungal Lytic Polysaccharide Monooxygenases Investigated by First-Principles Calculations 461
A theoretical study on the reactivity of the Mo/Cu-containing carbon monoxide dehydrogenase with dihydrogen 447
Anomalous Intrinsic Fluorescence of HCl and NaOH Aqueous Solutions 438
Interaction of the H-cluster of FeFe hydrogenase with halides 399
H2 Activation in [FeFe]-Hydrogenase Cofactor Versus Diiron Dithiolate Models: Factors Underlying the Catalytic Success of Nature and Implications for an Improved Biomimicry 398
Investigations of the electronic-molecular structure of bio-inorganic systems using modern methods of quantum chemistry 397
First-Principles Calculations on Ni,Fe-Containing Carbon Monoxide Dehydrogenases Reveal Key Stereoelectronic Features for Binding and Release of CO2 to/from the C-Cluster 382
Comparative analysis of Polyethylene-Degrading Laccases: Redox Properties and Enzyme-Polyethylene Interaction Mechanism. 378
On the reactivity of the most efficient iron-based catalyst for CO2 hydrogenation: a DFT picture 374
Rational Design of Fe2(μ-PR2)2(L)6 Coordination Compounds Featuring Tailored Potential Inversion 374
Theoretical investigation of aerobic and anaerobic oxidative inactivation of the [NiFe]-hydrogenase active site 372
The Photochemistry of Fe2(S2C3H6)(CO)6(µ-CO) and Its Oxidized Form, Two Simple [FeFe]-Hydrogenase CO-Inhibited Models. A DFT and TDDFT Investigation 368
On the photochemistry of Fe2(edt)(CO)4(PMe3)2, a [FeFe]-hydrogenase model: A DFT/TDDFT investigation 364
DFT investigation of the CO2 activation at the active site of the Carbon Monoxide Dehydrogenases 361
Conjugation of gold nanoparticles with multidentate surfactants for enhanced stability and biological properties 355
N-Spirofused Bicyclic Derivatives of 1-Deoxynojirimycin: Synthesis and Preliminary Biological Evaluation 352
An acidic loop and cognate phosphorylation sites define a molecular switch that modulates ubiquitin charging activity in cdc34-like enzymes 349
Theory Related to [FeFe]- and [NiFe]-hydrogenases: Stereoelectronic Properties, H-cluster Oxidation, and Mechanisms for Increasing Oxygen Tolerance 346
Mechanism of RGD-conjugated nanodevice binding to its target protein integrin αVβ3 by atomistic molecular dynamics and machine learning 345
Computational approaches to the prediction of the redox potentials of iron and copper bioinorganic systems 344
Functionally relevant interplay between the Fe4S4 cluster and CN- ligands in the active site of [FeFe]-Hydrogenases 343
On the propagation of the OH radical produced by Cu-amyloid beta peptide model complexes. Insight from molecular modelling 342
Intramolecular interactions stabilizing compact conformations of the intrinsically disordered kinase-inhibitor domain of Sic1: A molecular dynamics investigation 334
Copper ion interaction with the RNase catalytic site fragment of the angiogenin protein: An experimental and theoretical investigation 333
DFT investigation of H-2 activation by [M(NHPnPr(3))(' S3 ')] (M = Ni, Pd). Insight into key factors relevant to the design of hydrogenase functional models 331
Disclosure of key stereoelectronic factors for efficient H2 binding and cleavage in the active site of [NiFe]-hydrogenases 325
Potentiation of fluoroquinolone and macrolide activities by efflux pump inhibitory effect on Staphylococcus aureus and Streptococcus pyogenes of new benzyl piperazinyl lysine derivatives 324
Mechanism of non-phenolic substrate oxidation by the fungal laccase Type 1 copper site from Trametes versicolor: the case of benzo[a]pyrene and anthracene 324
Does the environment around the H-cluster allow coordination of the pendant amine to the catalytic iron center in [FeFe] hydrogenases? Answers from theory 324
Multidentate surfactants for improving stability and biological properties 319
Towards biomimetic models of the reduced [FeFe]-hydrogenase that preserve the key structural features of the enzyme active site; A DFT investigation 318
The mammalian complement system as an epitome of host-pathogen genetic conflicts 318
Uncovering a Dynamically Formed Substrate Access Tunnel in Carbon Monoxide Dehydrogenase/Acetyl-CoA Synthase 318
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients 316
Relevance of metal ions for lipase stability: Structural rearrangements induced in the Burkholderia glumae lipase by calcium depletion 315
Structural and kinetic stability of the burkholderia glumae lipase 314
Redox potentials of small inorganic radicals and hexa-aquo complexes of first-row transition metals in water: a dft study based on the grand canonical ensemble 309
Optimization of electrostatics as a strategy for cold-adaptation: A case study of cold- and warm-active elastases 307
Catalytic H2 evolution/oxidation in [FeFe]-hydrogenase biomimetics: account from DFT on the interplay of related issues and proposed solutions 307
Compaction Properties of an Intrinsically Disordered Protein: Sic1 and Its Kinase-Inhibitor Domain 305
Copper coordination to the putative cell binding site of angiogenin: a DFT investigation 304
Excited State Properties of Diiron Dithiolate Hydrides: Implications in the Unsensitized Photocatalysis of H2 Evolution 303
Structural characterization of the nitrogenase molybdenum-iron protein with the substrate acetylene trapped near the active site 303
A conserved loop in polynucleotide phosphorylase (PNPase) essential for both RNA and ADP/phosphate binding 300
Influence of the [2Fe]H subcluster environment on the properties of key intermediates in the catalytic cycle of [FeFe] hydrogenases: Hints for the rational design of synthetic catalysts 299
A 175 Million Year History of T Cell Regulatory Molecules Reveals Widespread Selection, with Adaptive Evolution of Disease Alleles 299
A theoretical study of spin states in Ni-S-4 complexes and models of the [NiFe] hydrogenase active site 298
Dynamic Properties of a Psychrophilic alpha-Amylase in Comparison with a Mesophilic Homologue 296
DFT Dissection of the Reduction Step in H2 Catalytic Production by [FeFe]-Hydrogenase-Inspired Models: Can the Bridging Hydride Become More Reactive Than the Terminal Isomer? 296
Proton Shuttle Mediated by (SCH2)2P= O Moiety in [FeFe]-Hydrogenase Mimics: Electrochemical and DFT Studies 291
Genetic analysis of polynucleotide phosphorylase structure and functions 289
Application of site-directed lipase mutants on regioselective acylation of monosaccharides 289
Theoretical insights into [NiFe]-hydrogenases oxidation resulting in a slowly reactivating inactive state 289
Reciprocal influence of protein domains in the cold-adapted acyl aminoacyl peptidase from Sporosarcina psychrophila 286
RIG-I-like receptors evolved adaptively in mammals, with parallel evolution at LGP2 and RIG-I 285
Flexibility and enzymatic cold-adaptation: A comparative molecular dynamics investigation of the elastase family 285
Loop 7 of E2 enzymes: an ancestral conserved functional motif involved in the E2-mediated steps of the ubiquitination cascade 284
Structural investigation of the cold-adapted acylaminoacyl peptidase from Sporosarcina psychrophila by atomistic simulations and biophysical methods 284
The cold-active lipase of Pseudomonas fragi: Heterologous expression, biochemical characterization and molecular modeling 283
The oxidative inactivation of FeFe hydrogenase reveals the flexibility of the H-cluster 283
DNA-binding protects p53 from interactions with cofactors involved in transcription-independent functions 283
Chelate control of diiron(I) dithiolates relevant to the [Fe-Fe]-hydrogenase active site 282
Structural and electronic properties of the [FeFe] hydrogenase H-cluster in different redox and protonation states. A DFT investigation 282
Normal vs. Inverted Ordering of Reduction Potentials in [FeFe]-Hydrogenases Biomimetics: Effect of the Dithiolate Bulk 281
Free-energy landscape, principal component analysis, and structural clustering to identify representative conformations from molecular dynamics simulations: The myoglobin case 281
Speciation of Copper–Peptide Complexes in Water Solution Using DFTB and DFT Approaches: Case of the [Cu(HGGG)(Py)] Complex 280
C-type natriuretic peptide: structural studies, fragment synthesis and preliminary biological evaluation in human osteosarcoma cell lines 278
Oxidation of Phospholipids by OH Radical Coordinated to Copper Amyloid-β Peptide—A Density Functional Theory Modeling 276
DFT investigations of models related to the active site of [NiFe] and [Fe] hydrogenases 275
A new nerve growth factor-mimetic peptide active on neuropathic pain in rats 275
Excited state properties of a [FeFe] hydrogenase active site models. The Time-Dependent Density Functional Theory theoretical picture 275
Structural insights into the active-ready form of [FeFe]-Hydrogenase and mechanistic details of its inhibition by carbon monoxide 274
Synthesis of the H-cluster framework of iron-only hydrogenase 273
Characterization of Escherichia coli uridine phosphorylase by single-site mutagenesis 272
Excited state properties and photochemistry in [FeFe] hydrogenase research area. The Time-Dependent Density Functional Theory theoretical picture 272
C-terminal acidic domain of ubiquitin-conjugating enzymes: A multi-functional conserved intrinsically disordered domain in family 3 of E2 enzymes 272
The isolated catalytic hairpin of the Ras-specific guanine nucleotide exchange factor Cdc25Mm retains nucleotide dissociation activity but has impaired nucleotide exchange activity 271
TDDFT modelling of the CO-photolysis of Fe2(S2C3H6)(CO)6, a model of the [FeFe]-Hydrogenase catalytic site 271
Evolution of Virus-like Features and Intrinsically Disordered Regions in Retrotransposon-derived Mammalian Genes 270
Fast generation of broken-symmetry states in a large system including multiple iron-sulfur assemblies: Investigation of QM/MM energies, clusters charges, and spin populations 270
Photoinhibition of FeFe hydrogenase 270
Iminosugar Analogues of Phosphatidyl Inositol as Potential Inhibitors of Protein Kinase B (Akt) 269
Density functional theory investigation of the active site of [Fe]-hydrogenases: Effects of redox state and ligand characteristics on structural, electronic, and reactivity properties of complexes related to the [2Fe](H) subcluster 267
Molecular dynamics of Mesophilic-Like mutants of a Cold-Adapted enzyme: Insights into distal effects induced by the mutations 267
Insights into the mechanism of electrocatalytic hydrogen evolution mediated by Fe2(S2C3H6)(CO)6: The simplest functional model of the Fe-hydrogenase active site 266
DFT investigation of structural, electronic, and catalytic properties of diiron complexes related to the [2Fe]H subcluster of Fe-only hydrogenases 266
Time-dependent density functional theory study of Fe2(CO) 9 low-lying electronic excited states 266
Totale 34.910
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Categoria #
all - tutte 200.985
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 200.985
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021833 0 0 0 0 0 0 0 0 0 0 0 833
2021/20223.697 293 401 503 307 175 351 271 238 181 217 281 479
2022/20235.598 665 1.631 562 579 370 785 87 260 312 65 198 84
2023/20243.610 144 108 189 229 469 784 724 179 252 75 55 402
2024/20258.828 486 840 542 473 753 451 534 461 822 1.281 785 1.400
2025/202621.913 2.052 1.264 1.651 2.268 2.637 1.123 3.191 1.060 1.879 1.867 1.645 1.276
Totale 66.103