CRIS Current Research Information System

CARNICELLI, DOMENICA
 Distribuzione geografica
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Continente #
NA - Nord America 2.791
AS - Asia 1.946
EU - Europa 1.704
AF - Africa 136
SA - Sud America 131
Continente sconosciuto - Info sul continente non disponibili 128
OC - Oceania 8
Totale 6.844
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Nazione #
US - Stati Uniti d'America 2.728
SG - Singapore 541
CN - Cina 521
VN - Vietnam 440
IT - Italia 343
GB - Regno Unito 338
SE - Svezia 208
DE - Germania 187
HK - Hong Kong 153
FR - Francia 99
BR - Brasile 95
CH - Svizzera 95
RU - Federazione Russa 92
UA - Ucraina 92
IN - India 76
IE - Irlanda 67
CA - Canada 43
JP - Giappone 42
TG - Togo 41
NL - Olanda 36
ZA - Sudafrica 33
KR - Corea 32
FI - Finlandia 31
BG - Bulgaria 29
BD - Bangladesh 28
CI - Costa d'Avorio 28
EE - Estonia 24
JO - Giordania 24
BE - Belgio 14
AR - Argentina 13
SC - Seychelles 13
PH - Filippine 12
IQ - Iraq 11
ID - Indonesia 9
TR - Turchia 9
TH - Thailandia 8
CO - Colombia 7
EC - Ecuador 7
ES - Italia 7
HR - Croazia 7
MX - Messico 7
AU - Australia 6
CZ - Repubblica Ceca 6
TW - Taiwan 6
EG - Egitto 5
IR - Iran 5
PL - Polonia 5
AT - Austria 4
CL - Cile 4
DK - Danimarca 4
GR - Grecia 4
LB - Libano 4
PK - Pakistan 4
IL - Israele 3
JM - Giamaica 3
KE - Kenya 3
NG - Nigeria 3
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
BO - Bolivia 2
CR - Costa Rica 2
HU - Ungheria 2
MY - Malesia 2
NZ - Nuova Zelanda 2
PR - Porto Rico 2
TN - Tunisia 2
UZ - Uzbekistan 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BN - Brunei Darussalam 1
DM - Dominica 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GA - Gabon 1
GT - Guatemala 1
HN - Honduras 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
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
Totale 6.713
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Città #
Singapore 349
Southend 280
Ashburn 267
Fairfield 248
Chandler 221
Santa Clara 147
Hong Kong 145
Woodbridge 143
Bologna 136
San Jose 126
Ann Arbor 110
Seattle 105
Houston 101
Wilmington 97
Ho Chi Minh City 96
Cambridge 95
Bern 94
Hanoi 80
Princeton 76
Dallas 64
Dublin 64
Beijing 62
Hefei 56
Boardman 54
Council Bluffs 54
Jacksonville 51
New York 42
Lomé 41
Lauterbourg 40
Tokyo 40
Milan 37
Los Angeles 36
Westminster 32
Nanjing 30
Berlin 29
Helsinki 29
Sofia 29
Abidjan 28
Padova 27
Seoul 27
Amman 24
Haiphong 24
Saint Petersburg 24
Buffalo 21
Jinan 17
Guangzhou 16
São Paulo 16
Da Nang 15
Dong Ket 15
Hebei 15
Brussels 14
Dearborn 14
San Diego 14
Shanghai 14
Changsha 13
Frankfurt am Main 13
Rome 13
Calgary 11
Falkenstein 11
Olalla 11
Redondo Beach 11
Shenyang 11
Redwood City 10
Tianjin 10
Düsseldorf 9
London 9
Poplar 9
Zhengzhou 9
Bengaluru 8
Brooklyn 8
Fuzhou 8
Hangzhou 8
Montreal 8
Ningbo 8
Redmond 8
Taiyuan 8
The Dalles 8
Toronto 8
Turin 8
Amsterdam 7
Bremen 7
Chicago 7
Des Moines 7
Jiaxing 7
Johannesburg 7
Mahé 7
Mülheim 7
Orem 7
Phoenix 7
Yubileyny 7
Atlanta 6
Biên Hòa 6
Medford 6
San Francisco 6
Vancouver 6
Chengdu 5
Kunming 5
Nuremberg 5
Quận Bình Thạnh 5
Thái Nguyên 5
Totale 4.401
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Nome #
Deuterium Incorporation Protects Cells from Oxidative Damage 267
A reconstituted cell-free assay for the evaluation of the intrinsic activity of purified human ribosomes 255
Human ribosomes from cells with reduced dyskerin levels are intrinsically altered in translation 248
Shiga toxin 1 acting on DNA in vitro is a heat-stable enzyme not requiring proteolytic activation 247
Human monocytes stimulated by Shiga toxin 1a via globotriaosylceramide release proinflammatory molecules associated with hemolytic uremic syndrome. 224
Interactions between Shiga toxins and human polymorphonuclear leukocytes 219
Change in Conformation with Reduction of α-Helix Content Causes Loss of Neutrophil Binding Activity in Fully Cytotoxic Shiga Toxin 1 218
Novel dyskerin-mediated mechanism of p53 inactivation through defective mRNA translation. 218
Identification of TLR4 as the receptor that recognizes Shiga toxins in human neutrophils 211
Cap-independent protein synthesis is enhanced by betaine under hypertonic conditions 205
Clinical Relevance of Shiga Toxin Concentrations in the Blood of Patients With Hemolytic Uremic Syndrome 201
Shiga Toxin 1, as DNA Repair Inhibitor, Synergistically Potentiates the Activity of the Anticancer Drug, Mafosfamide, on Raji Cells 187
Galloflavin prevents the binding of lactate dehydrogenase A to single stranded DNA and inhibits RNA synthesis in cultured cells. 186
Molecular damage and induction of pro-inflammatory cytokines in human endothelial cells exposed to Shiga toxin 1, Shiga toxin 2 and alpha-sarcin 184
The antibiotic polymyxin B impairs the interactions between Shiga toxins and human neutrophils 182
Inhibition by suramin of protein synthesis in vitro. Ribosomes as the target of the drug 179
Particulate Shiga Toxin 2 in Blood is Associated to the Development of Hemolytic Uremic Syndrome in Children 179
Shiga toxin 1 and ricin A chain bind to human polymorphonuclear leucocytes through a common receptor 177
Creatine as a compatible osmolyte in muscle cells exposed to hypertonic stress 175
Soluble Toll-Like Receptor 4 Impairs the Interaction of Shiga Toxin 2a with Human Serum Amyloid P Component 175
Shiga toxin 1 and ricin inhibit the repair of H2O2-induced DNA single strand breaks in cultured mammalian cells 171
A rapid and sensitive method to measure the functional activity of shiga toxins in human serum 168
Shiga Toxins present in the gut and in the polymorphonuclear leukocytes circulating in the blood of children with hemolytic-uremic syndrome 165
Endothelial damage induced by Shiga toxins delivered by neutrophils during transmigration 165
Shiga toxins bound to polymorphonuclear leukocytes (STXS-PMN): clinical observations in children with hemolytic uremic syndrome (HUS) 158
The inhibition of lactate dehydrogenase A hinders the transcription of histone 2B gene independently from the block of aerobic glycolysis 155
Plasmonic Metasurfaces for Specific SERS Detection of Shiga Toxins 155
An antibiotic derivative as a new potential tool in the prevention of hemolytic uremic syndrome 150
Flow cytometry detection of Shiga toxins in the blood from children with hemolytic uremic syndrome 150
Detection of Cleaved Stx2a in the Blood of STEC-Infected Patients 144
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 136
The structure of the Shiga toxin 2a A-subunit dictates the interactions of the toxin with blood components 134
Infezioni da Escherichia coli 0157: ruolo patogenetico delle Shiga tossine 132
Extracellular Vesicles and Renal Endothelial Cells: A Fatal Attraction in Hemolytic Uremic Syndrome 127
Method for the Detection of the Cleaved Form of Shiga Toxin 2a Added to Normal Human Serum 126
Kinetics of Shiga Toxins (Stx) in the Blood and Feces of Patients with Bloody Diarrhea Associated with Stx-producing Escherichia coli (STEC) 124
SHIGA TOXIN 1, AS DNA REPAIR INHIBITOR, POTENTIATES THE EFFECT OF MAFOSFAMIDE ON RAJI CELLS 118
Publisher Correction: A reconstituted cell-free assay for the evaluation of the intrinsic activity of purified human ribosomes 103
Purification and properties of a new ribosome-inactivation protein with RNA N-glycosidase activity suitable for immunotoxin preparation from the seeds of Momordica cochinchinensis 70
Purification and properties of new ribosome-inactivating proteins with RNA N-glycosidase activity 56
Totale 6.844
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Categoria #
all - tutte 18.822
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 18.822
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022637 0 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
2025/20262.148 166 171 207 230 229 124 182 83 431 156 81 88
2026/2027103 48 55 0 0 0 0 0 0 0 0 0 0
Totale 6.844