BRIGOTTI, MAURIZIO
 Distribuzione geografica
Continente #
NA - Nord America 3.426
EU - Europa 2.365
AS - Asia 2.137
SA - Sud America 198
AF - Africa 183
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 1
Totale 8.319
Nazione #
US - Stati Uniti d'America 3.377
CN - Cina 709
SG - Singapore 704
IT - Italia 526
GB - Regno Unito 485
DE - Germania 281
SE - Svezia 260
VN - Vietnam 227
HK - Hong Kong 183
BR - Brasile 150
UA - Ucraina 135
RU - Federazione Russa 134
CH - Svizzera 128
IN - India 114
IE - Irlanda 94
FR - Francia 90
KR - Corea 59
NL - Olanda 57
TG - Togo 49
CI - Costa d'Avorio 47
ZA - Sudafrica 45
JP - Giappone 44
BG - Bulgaria 38
EE - Estonia 35
CA - Canada 34
FI - Finlandia 27
JO - Giordania 27
AR - Argentina 22
ID - Indonesia 22
SC - Seychelles 18
BE - Belgio 13
EC - Ecuador 12
HR - Croazia 12
ES - Italia 9
BD - Bangladesh 8
MX - Messico 8
AT - Austria 7
AU - Australia 7
IR - Iran 7
CO - Colombia 6
EG - Egitto 6
PL - Polonia 6
GR - Grecia 5
LB - Libano 5
AE - Emirati Arabi Uniti 4
CZ - Repubblica Ceca 4
IQ - Iraq 4
LT - Lituania 4
NG - Nigeria 4
TR - Turchia 4
MA - Marocco 3
PT - Portogallo 3
PY - Paraguay 3
UZ - Uzbekistan 3
VE - Venezuela 3
CL - Cile 2
GT - Guatemala 2
HU - Ungheria 2
IL - Israele 2
KE - Kenya 2
MY - Malesia 2
NZ - Nuova Zelanda 2
PH - Filippine 2
RO - Romania 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AD - Andorra 1
AL - Albania 1
AO - Angola 1
AZ - Azerbaigian 1
BN - Brunei Darussalam 1
BZ - Belize 1
DM - Dominica 1
ET - Etiopia 1
GA - Gabon 1
KW - Kuwait 1
LI - Liechtenstein 1
MD - Moldavia 1
ME - Montenegro 1
MK - Macedonia 1
ML - Mali 1
MN - Mongolia 1
MZ - Mozambico 1
PA - Panama 1
PK - Pakistan 1
PR - Porto Rico 1
RE - Reunion 1
SA - Arabia Saudita 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
TZ - Tanzania 1
VC - Saint Vincent e Grenadine 1
Totale 8.319
Città #
Singapore 445
Southend 416
Fairfield 363
Ashburn 345
Chandler 299
Woodbridge 201
Santa Clara 199
Bologna 195
Hong Kong 178
Seattle 154
Houston 148
Wilmington 148
Ann Arbor 147
Hefei 132
Cambridge 123
Bern 118
Princeton 116
Dublin 92
Boardman 84
Beijing 79
Dallas 77
Jacksonville 72
Seoul 59
New York 56
Los Angeles 52
Lomé 49
Nanjing 49
Abidjan 47
Ho Chi Minh City 47
Westminster 47
Milan 46
Padova 44
Berlin 43
Tokyo 42
Sofia 38
Hanoi 30
Dearborn 28
Saint Petersburg 28
Amman 27
Jinan 26
Buffalo 24
Hebei 21
Helsinki 21
San Diego 21
Dong Ket 19
Guangzhou 18
Redmond 18
Redondo Beach 17
Bengaluru 15
Frankfurt am Main 15
Rome 15
São Paulo 15
Turin 15
Zhengzhou 15
Calgary 14
Changsha 14
Shenyang 14
Brussels 13
Olalla 13
Redwood City 13
Hangzhou 12
Jakarta 12
Mülheim 12
Shanghai 12
Düsseldorf 11
Falkenstein 11
Jiaxing 10
Mahé 10
Medford 10
Nanchang 10
Ningbo 10
Phoenix 10
Poplar 10
Tianjin 10
Yubileyny 10
Chicago 9
Des Moines 9
Nuremberg 9
Zurich 9
Amsterdam 8
Bremen 8
London 8
San Francisco 8
Toronto 8
Florence 7
Lauterbourg 7
Norwalk 7
Taiyuan 7
Atlanta 6
Bari 6
Brooklyn 6
Chengdu 6
Chennai 6
Fuzhou 6
Guayaquil 6
Haikou 6
Haiphong 6
Palermo 6
Verona 6
Biên Hòa 5
Totale 5.554
Nome #
Hemidesmus indicus induces apoptosis via proteasome inhibition and generation of reactive oxygen species 243
A reconstituted cell-free assay for the evaluation of the intrinsic activity of purified human ribosomes 231
Shiga toxin 1 acting on DNA in vitro is a heat-stable enzyme not requiring proteolytic activation 224
Human ribosomes from cells with reduced dyskerin levels are intrinsically altered in translation 222
Deuterium Incorporation Protects Cells from Oxidative Damage 217
Dyskerin expression influences the level of ribosomal RNA pseudo-uridylation and telomerase RNA component in human breast cancer. 191
Change in Conformation with Reduction of α-Helix Content Causes Loss of Neutrophil Binding Activity in Fully Cytotoxic Shiga Toxin 1 191
Interactions between Shiga toxins and human polymorphonuclear leukocytes 190
Human monocytes stimulated by Shiga toxin 1a via globotriaosylceramide release proinflammatory molecules associated with hemolytic uremic syndrome. 190
Novel dyskerin-mediated mechanism of p53 inactivation through defective mRNA translation. 186
Clinical Relevance of Shiga Toxin Concentrations in the Blood of Patients With Hemolytic Uremic Syndrome 182
Cap-independent protein synthesis is enhanced by betaine under hypertonic conditions 182
Identification of TLR4 as the receptor that recognizes Shiga toxins in human neutrophils 179
5′-Untranslated region of heat shock protein 70 mRNA drives translation under hypertonic conditions 179
Shiga Toxin 1, as DNA Repair Inhibitor, Synergistically Potentiates the Activity of the Anticancer Drug, Mafosfamide, on Raji Cells 163
Inhibition by suramin of protein synthesis in vitro. Ribosomes as the target of the drug 162
Galloflavin prevents the binding of lactate dehydrogenase A to single stranded DNA and inhibits RNA synthesis in cultured cells. 159
The antibiotic polymyxin B impairs the interactions between Shiga toxins and human neutrophils 159
Shiga toxin 1 and ricin A chain bind to human polymorphonuclear leucocytes through a common receptor 157
Creatine as a compatible osmolyte in muscle cells exposed to hypertonic stress 153
Early volume expansion and outcomes of hemolytic uremic syndrome 153
Sorveglianza della sindrome emolitico-uremica in Italia 152
Soluble Toll-Like Receptor 4 Impairs the Interaction of Shiga Toxin 2a with Human Serum Amyloid P Component 150
A rapid and sensitive method to measure the functional activity of shiga toxins in human serum 149
Shiga toxin 1 and ricin inhibit the repair of H2O2-induced DNA single strand breaks in cultured mammalian cells 148
Shiga Toxins present in the gut and in the polymorphonuclear leukocytes circulating in the blood of children with hemolytic-uremic syndrome 146
Endothelial damage induced by Shiga toxins delivered by neutrophils during transmigration 146
Molecular damage and induction of pro-inflammatory cytokines in human endothelial cells exposed to Shiga toxin 1, Shiga toxin 2 and alpha-sarcin 144
An Improved Method for the Sensitive Detection of Shiga Toxin 2 in Human Serum 138
Peptides inhibiting the assembly of monomeric human l‐lactate dehydrogenase into catalytically active homotetramer decrease the synthesis of lactate in cultured cells 137
The inhibition of lactate dehydrogenase A hinders the transcription of histone 2B gene independently from the block of aerobic glycolysis 135
Particulate Shiga Toxin 2 in Blood is Associated to the Development of Hemolytic Uremic Syndrome in Children 135
Shiga toxins bound to polymorphonuclear leukocytes (STXS-PMN): clinical observations in children with hemolytic uremic syndrome (HUS) 134
Flow cytometry detection of Shiga toxins in the blood from children with hemolytic uremic syndrome 130
Shiga Toxin 2 Triggers C3a-Dependent Glomerular and Tubular Injury through Mitochondrial Dysfunction in Hemolytic Uremic Syndrome 127
Enzymatic Cleavage of Stx2a in the Gut and Identification of Pancreatic Elastase and Trypsin as Possible Main Cleavers 127
Allosteric transitions of rabbit skeletal muscle lactate dehydrogenase induced by pH-dependent dissociation of the tetrameric enzyme 122
RiboAbacus: A model trained on polyribosome images predicts ribosome density and translational efficiency from mammalian transcriptomes 114
Infezioni da Escherichia coli 0157: ruolo patogenetico delle Shiga tossine 111
Detection of Cleaved Stx2a in the Blood of STEC-Infected Patients 109
Shiga toxins bound to polymorphonuclear leukocytes (STXS-PMN) and hemolytic uremic syndrome (HUS): development of experimental models of toxin delivery by transmigration through endothelial cells 108
The structure of the Shiga toxin 2a A-subunit dictates the interactions of the toxin with blood components 108
INFEZIONI DA ESCHERICHIA COLI PRODUTTORI DI VEROCITOTOSSINA (VTEC) NEI PAZIENTI DEL REGISTRO ITALIANO DELLA SINDROME EMOLITICO UREMICA PEDIATRICA NEGLI ANNI 2005-2006 106
Kinetics of Shiga Toxins (Stx) in the Blood and Feces of Patients with Bloody Diarrhea Associated with Stx-producing Escherichia coli (STEC) 105
The Interactions of Human Neutrophils with Shiga Toxins and Related Plant Toxins: Danger or Safety? 105
Human lactate dehydrogenase A undergoes allosteric transitions under pH conditions inducing the dissociation of the tetrameric enzyme 105
Hemolytic uremic syndrome and Verocytotoxin (VT)-producing E. coli (VTEC) infection in Italy 104
SHIGA TOXIN 1, AS DNA REPAIR INHIBITOR, POTENTIATES THE EFFECT OF MAFOSFAMIDE ON RAJI CELLS 100
Dyskerin depletion increases VEGF mRNA internal ribosome entry site-mediated translation. 98
Bloody Diarrhea and Shiga Toxin–Producing Escherichia coli Hemolytic Uremic Syndrome in Children: Data from the ItalKid-HUS Network 97
Extracellular Vesicles and Renal Endothelial Cells: A Fatal Attraction in Hemolytic Uremic Syndrome 97
Plasmonic Metasurfaces for Specific SERS Detection of Shiga Toxins 93
Pathogenesis of Verocytotoxin/Shiga toxins-producing Escherichia coli infection 92
null 89
Variable biological properties of two different preparations of Shiga toxins yielding new insights into eHUS pathogenesis 89
Method for the Detection of the Cleaved Form of Shiga Toxin 2a Added to Normal Human Serum 86
Is Shigatoxin 1 protective for the development of Shigatoxin 2-related hemolytic uremic syndrome in children? Data from the ItalKid-HUS Network 80
Surveillance of Pediatric Hemolytic Uremic Syndrome (HUS) in Italy, 1988–2011 76
An antibiotic derivative as a new potential tool in the prevention of hemolytic uremic syndrome 74
Shiga toxins: the ribosome-inactivating proteins from pathogenic bacteria 72
null 72
Publisher Correction: A reconstituted cell-free assay for the evaluation of the intrinsic activity of purified human ribosomes 66
Serum Shiga toxin 2 values in patients during acute phase of diarrhoea-associated haemolytic uraemic syndrome 32
Totale 8.521
Categoria #
all - tutte 23.191
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 23.191


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021413 0 0 0 0 0 54 19 34 79 38 43 146
2021/2022962 78 30 60 90 75 48 25 61 28 94 203 170
2022/20231.291 145 183 85 139 72 93 30 78 199 38 77 152
2023/2024354 21 50 22 38 19 89 14 31 20 16 18 16
2024/20251.456 63 214 110 100 277 84 116 44 29 98 54 267
2025/20261.782 252 306 350 365 349 160 0 0 0 0 0 0
Totale 8.521