CARNICELLI, DOMENICA
 Distribuzione geografica
Continente #
NA - Nord America 2.583
AS - Asia 1.916
EU - Europa 1.642
AF - Africa 136
SA - Sud America 126
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 1
Totale 6.412
Nazione #
US - Stati Uniti d'America 2.540
SG - Singapore 533
CN - Cina 518
VN - Vietnam 440
GB - Regno Unito 337
IT - Italia 286
SE - Svezia 208
DE - Germania 187
HK - Hong Kong 150
FR - Francia 98
CH - Svizzera 95
BR - Brasile 94
RU - Federazione Russa 92
UA - Ucraina 92
IN - India 76
IE - Irlanda 67
JP - Giappone 42
TG - Togo 41
NL - Olanda 35
ZA - Sudafrica 33
KR - Corea 32
CA - Canada 31
FI - Finlandia 31
BG - Bulgaria 29
CI - Costa d'Avorio 28
EE - Estonia 24
JO - Giordania 24
BE - Belgio 14
SC - Seychelles 13
AR - Argentina 12
BD - Bangladesh 12
PH - Filippine 12
IQ - Iraq 11
ID - Indonesia 9
TR - Turchia 9
TH - Thailandia 8
ES - Italia 7
HR - Croazia 7
MX - Messico 7
AU - Australia 6
CO - Colombia 6
EC - Ecuador 6
TW - Taiwan 6
CZ - Repubblica Ceca 5
EG - Egitto 5
IR - Iran 5
PL - Polonia 5
AT - Austria 4
DK - Danimarca 4
GR - Grecia 4
LB - Libano 4
PK - Pakistan 4
CL - Cile 3
IL - Israele 3
KE - Kenya 3
NG - Nigeria 3
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
BO - Bolivia 2
HU - Ungheria 2
MY - Malesia 2
NZ - Nuova Zelanda 2
TN - Tunisia 2
UZ - Uzbekistan 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AO - Angola 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CR - Costa Rica 1
DM - Dominica 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GA - Gabon 1
KG - Kirghizistan 1
KH - Cambogia 1
LI - Liechtenstein 1
LK - Sri Lanka 1
LT - Lituania 1
MA - Marocco 1
MD - Moldavia 1
ME - Montenegro 1
MK - Macedonia 1
MN - Mongolia 1
MZ - Mozambico 1
NP - Nepal 1
OM - Oman 1
PR - Porto Rico 1
PS - Palestinian Territory 1
PT - Portogallo 1
PY - Paraguay 1
RE - Reunion 1
RO - Romania 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
SO - Somalia 1
UG - Uganda 1
VC - Saint Vincent e Grenadine 1
Totale 6.412
Città #
Singapore 342
Southend 280
Ashburn 260
Fairfield 248
Chandler 221
Woodbridge 143
Hong Kong 142
Santa Clara 140
Bologna 123
Ann Arbor 110
San Jose 110
Seattle 105
Houston 100
Ho Chi Minh City 96
Wilmington 96
Cambridge 95
Bern 94
Hanoi 80
Princeton 76
Dublin 64
Beijing 61
Dallas 61
Hefei 56
Boardman 54
Jacksonville 51
Lomé 41
Lauterbourg 40
Tokyo 40
New York 37
Los Angeles 33
Westminster 31
Nanjing 30
Berlin 29
Helsinki 29
Sofia 29
Abidjan 28
Padova 27
Seoul 27
Milan 26
Amman 24
Haiphong 24
Saint Petersburg 24
Buffalo 17
Jinan 17
Guangzhou 16
São Paulo 16
Council Bluffs 15
Da Nang 15
Dong Ket 15
Hebei 15
Brussels 14
Dearborn 14
San Diego 14
Shanghai 14
Changsha 13
Frankfurt am Main 13
Falkenstein 11
Olalla 11
Redondo Beach 11
Shenyang 11
Redwood City 10
Tianjin 10
Calgary 9
Düsseldorf 9
Poplar 9
Zhengzhou 9
Bengaluru 8
Fuzhou 8
Hangzhou 8
London 8
Ningbo 8
Redmond 8
Taiyuan 8
The Dalles 8
Turin 8
Amsterdam 7
Bremen 7
Des Moines 7
Jiaxing 7
Johannesburg 7
Mahé 7
Montreal 7
Mülheim 7
Yubileyny 7
Biên Hòa 6
Brooklyn 6
Medford 6
Orem 6
Toronto 6
Vancouver 6
Atlanta 5
Chengdu 5
Chicago 5
Kunming 5
Nuremberg 5
Phoenix 5
Quận Bình Thạnh 5
San Francisco 5
Thái Nguyên 5
Ardabil 4
Totale 4.255
Nome #
A reconstituted cell-free assay for the evaluation of the intrinsic activity of purified human ribosomes 253
Deuterium Incorporation Protects Cells from Oxidative Damage 251
Shiga toxin 1 acting on DNA in vitro is a heat-stable enzyme not requiring proteolytic activation 244
Human ribosomes from cells with reduced dyskerin levels are intrinsically altered in translation 241
Human monocytes stimulated by Shiga toxin 1a via globotriaosylceramide release proinflammatory molecules associated with hemolytic uremic syndrome. 218
Change in Conformation with Reduction of α-Helix Content Causes Loss of Neutrophil Binding Activity in Fully Cytotoxic Shiga Toxin 1 215
Interactions between Shiga toxins and human polymorphonuclear leukocytes 214
Novel dyskerin-mediated mechanism of p53 inactivation through defective mRNA translation. 211
Cap-independent protein synthesis is enhanced by betaine under hypertonic conditions 199
Clinical Relevance of Shiga Toxin Concentrations in the Blood of Patients With Hemolytic Uremic Syndrome 198
Identification of TLR4 as the receptor that recognizes Shiga toxins in human neutrophils 192
Shiga Toxin 1, as DNA Repair Inhibitor, Synergistically Potentiates the Activity of the Anticancer Drug, Mafosfamide, on Raji Cells 181
Galloflavin prevents the binding of lactate dehydrogenase A to single stranded DNA and inhibits RNA synthesis in cultured cells. 179
The antibiotic polymyxin B impairs the interactions between Shiga toxins and human neutrophils 178
Molecular damage and induction of pro-inflammatory cytokines in human endothelial cells exposed to Shiga toxin 1, Shiga toxin 2 and alpha-sarcin 177
Inhibition by suramin of protein synthesis in vitro. Ribosomes as the target of the drug 173
Particulate Shiga Toxin 2 in Blood is Associated to the Development of Hemolytic Uremic Syndrome in Children 173
Soluble Toll-Like Receptor 4 Impairs the Interaction of Shiga Toxin 2a with Human Serum Amyloid P Component 170
Creatine as a compatible osmolyte in muscle cells exposed to hypertonic stress 169
Shiga toxin 1 and ricin A chain bind to human polymorphonuclear leucocytes through a common receptor 169
A rapid and sensitive method to measure the functional activity of shiga toxins in human serum 167
Shiga toxin 1 and ricin inhibit the repair of H2O2-induced DNA single strand breaks in cultured mammalian cells 165
Endothelial damage induced by Shiga toxins delivered by neutrophils during transmigration 160
Shiga Toxins present in the gut and in the polymorphonuclear leukocytes circulating in the blood of children with hemolytic-uremic syndrome 159
Shiga toxins bound to polymorphonuclear leukocytes (STXS-PMN): clinical observations in children with hemolytic uremic syndrome (HUS) 154
The inhibition of lactate dehydrogenase A hinders the transcription of histone 2B gene independently from the block of aerobic glycolysis 152
Flow cytometry detection of Shiga toxins in the blood from children with hemolytic uremic syndrome 141
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 132
Detection of Cleaved Stx2a in the Blood of STEC-Infected Patients 131
Plasmonic Metasurfaces for Specific SERS Detection of Shiga Toxins 129
Infezioni da Escherichia coli 0157: ruolo patogenetico delle Shiga tossine 127
The structure of the Shiga toxin 2a A-subunit dictates the interactions of the toxin with blood components 127
Extracellular Vesicles and Renal Endothelial Cells: A Fatal Attraction in Hemolytic Uremic Syndrome 121
An antibiotic derivative as a new potential tool in the prevention of hemolytic uremic syndrome 120
Kinetics of Shiga Toxins (Stx) in the Blood and Feces of Patients with Bloody Diarrhea Associated with Stx-producing Escherichia coli (STEC) 120
Method for the Detection of the Cleaved Form of Shiga Toxin 2a Added to Normal Human Serum 120
SHIGA TOXIN 1, AS DNA REPAIR INHIBITOR, POTENTIATES THE EFFECT OF MAFOSFAMIDE ON RAJI CELLS 114
Publisher Correction: A reconstituted cell-free assay for the evaluation of the intrinsic activity of purified human ribosomes 84
Purification and properties of a new ribosome-inactivation protein with RNA N-glycosidase activity suitable for immunotoxin preparation from the seeds of Momordica cochinchinensis 61
Purification and properties of new ribosome-inactivating proteins with RNA N-glycosidase activity 50
Totale 6.539
Categoria #
all - tutte 17.047
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 17.047


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021169 0 0 0 0 0 0 0 0 0 25 28 116
2021/2022676 39 22 43 64 52 26 23 39 22 72 155 119
2022/2023925 102 135 69 101 47 66 11 67 151 16 50 110
2023/2024205 14 42 13 28 12 61 0 10 7 7 5 6
2024/2025929 30 125 78 65 182 57 70 22 15 62 24 199
2025/20261.946 166 171 207 230 229 124 182 83 431 123 0 0
Totale 6.539