PIUBELLI, LUCIANO
 Distribuzione geografica
Continente #
NA - Nord America 7.075
EU - Europa 4.639
AS - Asia 2.945
SA - Sud America 377
Continente sconosciuto - Info sul continente non disponibili 87
AF - Africa 44
OC - Oceania 2
Totale 15.169
Nazione #
US - Stati Uniti d'America 6.955
IT - Italia 2.430
SG - Singapore 865
CN - Cina 713
UA - Ucraina 704
TR - Turchia 429
VN - Vietnam 398
SE - Svezia 387
HK - Hong Kong 330
BR - Brasile 324
DE - Germania 212
FI - Finlandia 197
IE - Irlanda 177
GB - Regno Unito 143
FR - Francia 137
RU - Federazione Russa 107
IN - India 54
CA - Canada 42
JP - Giappone 42
MX - Messico 40
BD - Bangladesh 33
NL - Olanda 27
ES - Italia 23
AR - Argentina 19
IQ - Iraq 19
BE - Belgio 18
CZ - Repubblica Ceca 17
ZA - Sudafrica 16
PL - Polonia 15
CH - Svizzera 11
EU - Europa 10
ID - Indonesia 10
JM - Giamaica 10
AT - Austria 8
CO - Colombia 8
EC - Ecuador 8
NG - Nigeria 8
PK - Pakistan 8
CL - Cile 6
LT - Lituania 5
AE - Emirati Arabi Uniti 4
BO - Bolivia 4
CR - Costa Rica 4
GT - Guatemala 4
HN - Honduras 4
KE - Kenya 4
KZ - Kazakistan 4
MA - Marocco 4
NP - Nepal 4
PR - Porto Rico 4
SA - Arabia Saudita 4
AZ - Azerbaigian 3
BB - Barbados 3
MD - Moldavia 3
NO - Norvegia 3
PA - Panama 3
PE - Perù 3
RO - Romania 3
TN - Tunisia 3
EE - Estonia 2
IR - Iran 2
JO - Giordania 2
KH - Cambogia 2
KR - Corea 2
MN - Mongolia 2
NI - Nicaragua 2
PH - Filippine 2
RS - Serbia 2
RW - Ruanda 2
SN - Senegal 2
SV - El Salvador 2
TW - Taiwan 2
UY - Uruguay 2
UZ - Uzbekistan 2
VE - Venezuela 2
AL - Albania 1
AM - Armenia 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BY - Bielorussia 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EG - Egitto 1
ET - Etiopia 1
GE - Georgia 1
GR - Grecia 1
HU - Ungheria 1
LB - Libano 1
MK - Macedonia 1
ML - Mali 1
MY - Malesia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PS - Palestinian Territory 1
PY - Paraguay 1
QA - Qatar 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
Totale 15.090
Città #
Milan 1.491
San Jose 657
Fairfield 606
Jacksonville 553
Ashburn 509
Singapore 477
Chandler 410
Woodbridge 405
Hong Kong 328
Ann Arbor 315
Como 277
Wilmington 272
Seattle 258
Houston 243
Nyköping 214
Cambridge 213
Dallas 205
Princeton 191
Dearborn 190
Izmir 185
Dublin 177
Beijing 176
Council Bluffs 176
Boardman 116
The Dalles 108
Dong Ket 106
Rome 105
Lauterbourg 85
Chicago 84
Los Angeles 77
New York 76
Ho Chi Minh City 66
San Mateo 61
Orem 50
Santa Clara 46
Munich 43
Tokyo 40
São Paulo 39
Hanoi 34
Ogden 33
Helsinki 32
San Diego 30
Guangzhou 29
London 28
Varese 28
Chennai 23
Kunming 22
Nanjing 22
Tianjin 22
Washington 22
Mexico City 20
Atlanta 19
Hefei 19
Jinan 19
Brooklyn 18
Brussels 18
Phoenix 16
San Francisco 16
Bursa 15
Haiphong 15
Norwalk 15
Shanghai 15
Warsaw 15
Denver 14
Düsseldorf 14
Verona 14
Belo Horizonte 11
Brasília 11
Da Nang 11
Frankfurt am Main 11
Hangzhou 11
Johannesburg 11
Ponte Lambro 11
Toronto 11
Turku 11
Amsterdam 10
Manchester 10
Nanchang 10
Shenzhen 10
Stockholm 10
Baghdad 9
Boston 9
Montreal 9
Poplar 9
Querétaro 9
Redwood City 9
Abuja 8
Ankara 8
Brno 8
Buffalo 8
Kilburn 8
Nuremberg 8
Olomouc 8
Parma 8
Auburn Hills 7
Columbus 7
Des Moines 7
Gavirate 7
Kocaeli 7
Monza 7
Totale 10.526
Nome #
Structure-function relationships in human d-amino acid oxidase variants corresponding to known SNPs 281
D-amino acid oxidase-pLG72 interaction and D-serine modulation 262
Enzymatic detection of D-amino acids 253
Systems biocatalysis: An artificial metabolism for interconversion of functional groups 250
Optimizing HIV-1 protease production in Escherichia coli as fusion protein. 235
Contribution of the dimeric state to the thermal stability of the flavoprotein D-amino acid oxidase 216
Application of a rapid HILIC-UV method for synthesis optimization and stability studies of immunogenic neo-glycoconjugates 216
Liquid chromatography-mass spectrometry structural characterization of neo glycoproteins aiding the rational design and synthesis of a novel glycovaccine for protection against tuberculosis 213
Different recombinant forms of polyphenol oxidase A, a laccase from Marinomonas mediterranea 210
Investigating the role of active site residues of Rhodotorula gracilis D-amino acid oxidase on its substrate specificity. 207
Cholesterol oxidase: biotechnological applications. 206
Competition between C-terminal tyrosine and nicotinamide modulates pyridine nucleotide affinity and specificity in plant ferredoxin-NADP+ reductase 203
Assays of D-amino acid oxidase activity 203
Immobilization of L-aspartate oxidase from Sulfolobus tokodaii as biocatalyst for resolution of aspartate solutions 200
Identification of novel molecules supporting the impact of β-lactams against clinically-relevant Gram-negative multidrug resistant organisms 198
A thermostable L-aspartate oxidase from Sulfolobus tokodaii: characterization and biotechnological applications. 194
Hydrophilic interaction liquid chromatography-mass spectrometry as a new tool for the characterization of intact semi-synthetic glycoproteins 193
Is rat an appropriate animal model to study the involvement of d-serine catabolism in schizophrenia? insights from characterization of d-amino acid oxidase. 191
A "molten globule"-like intermediate in the unfolding of the peroxisomal flavoprotein D-amino acid oxidase 190
Active site of yeast D-amino acid oxidase: mutations and inferences 189
The Role of Cysteine Residues of Spinach Ferredoxin-NADP+ Reductase As Assessed by Site-Directed Mutagenesis 189
A recombinant vaccine against tuberculosis: high-level production in E. coli of antigenic proteins. 186
Production of recombinant cholesterol oxidase containing covalently bound FAD in Escherichia coli. 185
Probing the function of the invariant glutamyl residue 312 in spinach ferredoxin-NADP+ reductase 182
Cellular studies on human D-aspartate oxidase 182
Active site of yeast D-amino acid oxidase:mutations and inferences 180
"The Protein Factory": engineering and production of new enzymatic activities for industrial and biomedical applications 179
Physiological functions of D-amino acid oxidases: from yeast to humans. 177
Engineering the Properties of D-Amino Acid Oxidases by a Rational and a Directed Evolution Approach. 176
Structural, Kinetic, and Pharmacodynamic Mechanisms of d-Amino Acid Oxidase Inhibition by Small Molecules. 173
Could D-serine serum levels be considered a biomarker in Alzheimer’s disease? 171
Epitope and affinity determination of recombinant Mycobacterium tuberculosis Ag85B antigen towards anti-Ag85 antibodies using proteolytic affinity-mass spectrometry and biosensor analysis 171
Novel biosensors based on optimized glycine oxidase. 169
A "molten globule" - like intermediate in the unfolding of the flavoprotein D-amino acid oxidase 166
From new diagnostic targets to recombinant proteins and semi-synthetic protein-based vaccines 164
Ruolo della dimerizzazione nel flavoenzima D-amino acido ossidasi da Rhodotorula gracilis 161
Rational design, preparation and characterization of recombinant Ag85B variants and their glycoconjugates with T-cell antigenic activity against Mycobacterium tuberculosis 161
Enterokinase monolithic bioreactor as an efficient tool for biopharmaceuticals preparation: on-line cleavage of fusion proteins and analytical characterization of released products 159
On the oxygen reactivity of cholesterol oxidase. 157
Glycosylation of Recombinant Antigenic Proteins from Mycobacterium tuberculosis: In Silico Prediction of Protein Epitopes and Ex Vivo Biological Evaluation of New Semi-Synthetic Glycoconjugates 155
Dissection of the structural determinants involved in formation of the dimeric form of D-amino acid oxidase from Rhodotorula gracilis: role of the size of the beta F5-beta F6 loop 154
Regulation of D-amino acid oxidase expression in the yeast Rhodotorula gracilis 154
Serum D-serine levels are altered in early phases of Alzheimer’s disease: towards a precocious biomarker 153
Relevance of the flavin binding to the stability and folding of engineered cholesterol oxidase containing noncovalently bound FAD 152
Production of recombinant cholesterol oxidase containing covalently bound FAD in Escherichia coli 151
Conversion of the dimeric D-amino acid oxidase from Rhodotorula gracilis to a monomeric form. A rational mutagenesis approach 149
Biotech approach to drug rational design:a novel recombinant anti-TB vaccine 149
Effect of the oligomerization state on the thermal stability of yeast D-amino acid oxidase 147
Detection of D-amino acids by D-amino acid oxidase. 147
Unfolding intermediate in the peroxisomal flavoprotein D-amino acid oxidase 147
Glutamate synthase genes of the diazotroph Azospirillum brasilense: Cloning, sequencing, and analysis of functional domains 143
Optimizing Escherichia coli as a protein expression platform to produce Mycobacterium tuberculosis immunogenic proteins 142
SITE-DIRECTED MUTAGENESIS AND THERMODYNAMIC STUDIES REVEAL THE ROLE OF DIMERIC OLIGOMERIZATION STATE IN YEAST D-AMINO ACID OXIDASE 141
On the oxygen reactivity of flavoprotein oxidase. An oxygen access tunnel and gate in Brevibacterium sterolicum cholesterol oxidase. 141
On the mechanism of Rhodotorula gracilis D-amino acid oxidase: role of the active site serine 335 140
Optimization of production and purification of HIV-1 protease in Escherichia coli as fusion protein 140
Site-directed mutagenesis and thermodynamic studies reveal the role of dimeric oligomerization state in yeast D-amino acid oxidase 138
Rational Design, Synthesis, and Characterization of Glycoconjugates as Potential Vaccines against Tuberculosis 138
M. tuberculosis antigenic proteins: identity control and optimization of purification by ESI-MS. 134
How the specificity for pyridine nucleotides of ferredoxin-NADP+ reductase could be modified by engineering the portion of the binding site common to both coenzymes 131
EFFECT OF THE OLIGOMERIZATION STATE ON THE THERMAL STABILITY OF THE YEAST D-AMINO ACID OXIDASE 129
Erratum to: Monitoring antigenic protein integrity during glycoconjugate vaccine synthesis using capillary electrophoresis-mass spectrometry (Analytical and Bioanalytical Chemistry, (2016), 408, 22, (6123-6132), 10.1007/s00216-016-9723-5) 129
Mutations of Glu92 in ferredoxin I from spinach leaves produce proteins fully functional in electron transfer but less efficient in supporting NADP+ photoreduction 129
Role of the C-terminal portion of yeast D-amino acid oxidase in stability and in aggregation state 128
Novel drugs for schizophrenia treatment: the mechanism of human D-amino acid oxidase inhibition 128
On the oxygen reactivity of flavooxidase 128
Role of the beta12-beta13 loop of yeast D-amino acid oxidase on stability and on aggregation: a rational design and thermodynamic study 127
Thermal stability of yeast D-amino acid oxidase: Deconvoluting the contributions of the dimeric aggregation state 124
Engineering the proteins of D-amino acid oxidases by a rational and a directed evolution approach 124
Oxygen reactivity of the flavoenzyme cholesterol oxidase 123
The Role of D-Amino Acids in Alzheimer's Disease 123
Structure-function relationship in proteins 120
Unfolding intermediate in the peroxisomal flavoprotein D-amino acid oxidase of Rhodotorula gracilis 120
On the covalent link of the flavin cofactor in Cholesterol Oxidase. 118
Identification of novel molecules supporting the impact of β-lactams against clinically-relevant Gram-negative multidrug resistant organisms 115
Role of the C-terminal portion of yeast D-amino acid oxidase in stability and aggregation state 112
High-level production in E. coli of soluble, native-like immunogenic proteins from Mycobacterium tubercolosis 112
Studies on Racemic Resolution of D,L-aspartate by StLASPO. 108
The IN SIGNO project: Identification of novel molecules supporting the impact of β-lactams against clinically-relevant Gram-negative multidrug resistant organisms 107
Biotechnological approach for the rational design of new vaccines for TBC: chemoenzymatic synthesis of glycoconjugates with antigenic properties. 107
Effect of the dimeric aggregation state on the unfolding process of yeast D-amino acid oxidase 106
Oxygen reactivity of flavoxidases: a site-directed mutagenesis study of cholesterol oxidase 106
System biocatalysis: A synthetically useful artifical metabolism 105
Thermal stability of yeast D-amino acid oxidase: Deconvoluting the contributions of the dimeric aggregation state 104
Oxygen tunnel in Cholesterol Oxidase. 103
Unfolding intermediate in the peroxisomal flavoprotein D-Amino acid oxidase of Rhodotorula gracilis 102
The folding/unfolding process of yeast D-amino acid oxidase 101
On the covalent link of the flavin cofactor in cholesterol oxidase 101
Relevance of flavin binding to the stability and folding of cholesterol oxidase. 101
Glycovaccine Design: Optimization of Model and Antitubercular Carrier Glycosylation via Disuccinimidyl Homobifunctional Linker 99
Effect of the oligomerization state on the thermal stability of yeast D-amino acid oxidase 95
Role of the C-terminal loop of yeast D-amino acid oxidase in protein stability and aggregation state 94
Protein engineering of flavoprotein oxidases 93
Site-directed mutagenesis and thermodynamic studies reveal the role of dimeric oligomerization state in yeast D-amino acid oxidase 91
Effect of the dimeric aggregation state on the unfolding process of yeast D-amino acid oxidase 88
Relevance of flavin binding to the stability and folding of cholesterol oxidase. 86
Synthesis of neo-glycoproteins and their characterization by liquid chromatography-mass spectrometry peptide mapping. 83
Oxygen accessibility to the active site of flavoproteins: a site-directed mutagenesis study of B. sterolicum cholesterol oxidase 82
On the oxygen reactivity of cholesterol oxidase 79
Synthesis and structural characterization of therapeutic neo-glycoproteins: the role of liquid chromatography coupled to mass spectrometry 74
Totale 14.948
Categoria #
all - tutte 59.795
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 59.795


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022668 0 0 83 55 37 26 45 49 56 135 60 122
2022/20231.191 118 58 103 132 81 286 4 155 146 37 33 38
2023/20242.264 355 364 365 406 451 154 14 30 47 31 14 33
2024/20251.469 18 22 252 57 41 97 69 122 161 114 112 404
2025/20263.715 296 199 175 506 371 231 797 245 347 260 169 119
2026/2027378 87 180 111 0 0 0 0 0 0 0 0 0
Totale 15.169