TANTINI, BENEDETTA
 Distribuzione geografica
Continente #
NA - Nord America 2.954
AS - Asia 2.569
EU - Europa 2.159
AF - Africa 220
SA - Sud America 94
OC - Oceania 5
Totale 8.001
Nazione #
US - Stati Uniti d'America 2.928
CN - Cina 734
SG - Singapore 694
VN - Vietnam 582
GB - Regno Unito 561
DE - Germania 378
IT - Italia 238
SE - Svezia 233
HK - Hong Kong 211
UA - Ucraina 186
FR - Francia 133
IN - India 125
RU - Federazione Russa 117
IE - Irlanda 71
BR - Brasile 60
FI - Finlandia 60
TG - Togo 56
JP - Giappone 49
CI - Costa d'Avorio 42
NG - Nigeria 41
ZA - Sudafrica 41
KR - Corea 39
EE - Estonia 37
SC - Seychelles 30
CH - Svizzera 27
JO - Giordania 26
NL - Olanda 25
AR - Argentina 19
BG - Bulgaria 18
BE - Belgio 15
CA - Canada 15
PL - Polonia 14
BD - Bangladesh 13
IR - Iran 13
GR - Grecia 11
TR - Turchia 10
MX - Messico 9
TW - Taiwan 9
AT - Austria 8
ID - Indonesia 8
PH - Filippine 8
PK - Pakistan 8
IQ - Iraq 7
UZ - Uzbekistan 7
CZ - Repubblica Ceca 6
ES - Italia 6
AU - Australia 5
SA - Arabia Saudita 5
TH - Thailandia 5
HU - Ungheria 4
LB - Libano 4
PY - Paraguay 4
CO - Colombia 3
HR - Croazia 3
CL - Cile 2
DZ - Algeria 2
EC - Ecuador 2
IL - Israele 2
LT - Lituania 2
MA - Marocco 2
MY - Malesia 2
VE - Venezuela 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
CR - Costa Rica 1
CY - Cipro 1
DK - Danimarca 1
EG - Egitto 1
ET - Etiopia 1
GY - Guiana 1
HN - Honduras 1
KE - Kenya 1
KH - Cambogia 1
KW - Kuwait 1
LV - Lettonia 1
MM - Myanmar 1
NA - Namibia 1
NP - Nepal 1
OM - Oman 1
PS - Palestinian Territory 1
PT - Portogallo 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TN - Tunisia 1
UY - Uruguay 1
Totale 8.001
Città #
Singapore 490
Southend 474
Ann Arbor 377
Ashburn 346
Chandler 277
Hong Kong 203
Fairfield 153
Dong Ket 147
Jacksonville 142
Santa Clara 129
San Jose 116
Wilmington 107
Beijing 106
Hefei 106
Princeton 104
Hanoi 102
Ho Chi Minh City 102
Woodbridge 89
Houston 81
Seattle 81
Dublin 71
Boardman 59
Bologna 57
Lomé 56
Cambridge 54
Helsinki 51
Padova 51
Nanjing 49
Westminster 48
Tokyo 44
Abidjan 42
Abeokuta 41
Lauterbourg 41
Los Angeles 40
Berlin 35
Medford 34
Shenyang 32
Seoul 31
Saint Petersburg 29
Buffalo 28
Mülheim 27
Amman 26
Munich 22
Frankfurt am Main 21
Shanghai 21
Bremen 20
Hebei 19
Jinan 19
Falkenstein 18
Haiphong 18
Sofia 18
Tappahannock 17
Bern 16
Guangzhou 16
Nanchang 16
Brussels 15
Changsha 15
Redwood City 15
Da Nang 13
Hangzhou 13
Mahé 13
Orem 13
Tianjin 13
Bengaluru 12
Milan 12
New York 12
San Diego 11
Verona 11
Düsseldorf 10
Redondo Beach 10
Des Moines 9
Falls Church 9
Olalla 9
Warsaw 9
Atlanta 8
Biên Hòa 8
Dallas 8
Dearborn 8
Jiaxing 8
Turku 8
Chennai 7
Haikou 7
Istanbul 7
Phoenix 7
Shijiazhuang 7
São Paulo 7
Yubileyny 7
Zanjan 7
Zhengzhou 7
Kunming 6
Lanzhou 6
Montreal 6
San Venanzo 6
Shenzhen 6
Taiyuan 6
Taizhou 6
Bexley 5
Brooklyn 5
Chengdu 5
Council Bluffs 5
Totale 5.316
Nome #
mTOR, AMPK, and Sirt1: Key Players in Metabolic Stress Management 308
Antiproliferative effect of sildenafil on human pulmonary artery smooth muscle cells 269
Antiapoptotic and Antiautophagic Effects of Eicosapentaenoic Acid in Cardiac Myoblasts Exposed to Palmitic Acid 245
Early preconditioning prevents the loss of endothelial nitric oxide synthase and enhances its activity in the ischemic/reperfused rat heart 242
A pro-survival effect of polyamine depletion on norepinephrine-mediated apoptosis in cardiac cells. Role of signalling enzymes. 232
AMP-Activated Protein Kinase can negatively modulate Ornithine Decarboxylase activity in cardiomyoblasts 207
Role of polyamines in simulated-ischemia induction of apoptosis in H9c2 cardiomyoblasts 205
PROTECTIVE EFFECT OF POLYAMINE DEPLETION ON ISCHEMIA-INDUCED APOPTOSIS OF H9c2 CARDIOMYOBLASTS 205
Simulated ischemia induces apoptosis in H9c2 cardiomyoblasts. Role of polyamines 195
Polyamines are involved in simulated ischemia induced apoptosis in H9c2 cardiomyoblasts 194
Polyamines in cardiac physiology and disease. 192
Evidence that AMP-activated protein kinase can negatively modulate Ornithine decarboxylase activity in cardiac myoblasts 191
Involvement of polyamines in ischemia-induced apoptosis of serum deprived H9c2 cardiomyoblasts 190
Experimental studies on the involvement of polyamines in cardiac remodeling 188
Attenuation of norepinephrine-mediated apoptosis in neonatal rat cardiomyocytes by an inhibitor of polyamine biosynthesis 181
Enhanced Osteoblastogenesis of Adipose-Derived Stem Cells on Spermine Delivery via β-Catenin Activation 181
3-hydroxytyrosol, signal transduction and microRNAs in chondrocytes exposed to oxidative stress 180
Polyamine biosynthesis as a target to inhibit apoptosis of non-tumoral cells 175
DFMO PROTECTS H9c2 CARDIOMYOBLASTS AGAINST ISCHEMIA-INDUCED APOPTOSIS 172
3-hydroxytyrosol protects human chondrocytes against cell death and matrix degradation 171
Effect of the polyamine analogue N(1),N(11)-diethylnorspermine on cell survival and susceptibility to apoptosis of human chondrocytes 168
MiR-33a and its SREBF2 host gene as key orchestrators of the response of cardiac cells to palmitic acid and n-3 polyunsaturated fatty acids exposure 166
Difluoromethylornithine inhibits hypertrophic, pro-fibrotic and pro-apoptotic actions of aldosterone in cardiac cells. 165
Role of polyamines in a cellular model of cardiac ischemia 164
Eicosapentaenoic acid protects against palmitate induced cell death of h9c2 cardiomyoblasts 162
Protective effect of 3-hydroxytyrosol on chondrocytes exposed to oxidative stress by promoting autophagy 162
STRATEGIE DI PROTEZIONE DA STIMOLI APOPTOTICI IN CELLULE STAMINALI CON POTENZIALITA' MIOCARDIOGENICHE 161
Involvement of polyamines in ischemia-induced apoptosis of H9c2 cardiomyoblasts 157
Are polyamines involved in apoptosis induced by norepinephrine and aldosterone in neonatal rat cardiomyocytes? 157
Meccanismi biochimici dell'osteoartrite: ruolo delle poliamine nella condrogenesi ed effetto protettivo dei nutraceutici 153
Polyamine biosynthesis as a target to inhibit apoptosis of non-tumoral cells 147
Effect of N1,N11-diethylnorspermine on cell survival and susceptibility to apoptosis of human chondrocytes 146
Protective effect of PUFA and pyrroloquinoline quinone on palmitate induced apoptosis of h9c2 cardiomyoblasts 145
EICOSAPENTAENOIC ACID EXHERTS A PROTECTIVE EFFECT ON PALMITATE INDUCED APOPTOSIS OF H9c2 CARDIOMYOBLASTS 145
Polyamine depletion protects H9c2 cardiomyoblasts against apoptosis induced by simulated ischemia. 141
N1,N11-diethylnorspermine causes apoptosis of human chondrocytes in the presence of cycloheximide independently of polyamine catabolism 139
Protective effect of eicosapentaenoic acid on palmitate induced apoptosis of h9c2 cardiomyoblasts 139
Polyamine depletion can exert a protective role against apoptosis, hypertrophy and fibrosis induced by aldosterone in cardiac cells 134
Involvement of polyamines in apoptosis induced by norepinephrine and aldosterone in neonatal rat cardiomyocytes 126
Polyamine depletion prevents ischemia-induced apoptosis of serum deprived H9c2 cardiomyoblasts 126
Involvement of Polyamines in apoptosis induced by norepinephrine in neonatal rat cardiomyocytes 124
Signal transduction pathways linking polyamines to apoptosis 122
Polyamine depletion inhibits etoposide-induced NF-kappaB activation in transformed mouse fibroblasts 121
Polyamines are required for apoptosis induced by norepinephrine and aldosterone in neonatal rat cardiomyocytes 111
LA PROTEINA CHINASI ATTIVATA DA AMP COME MODULATORE DI EVENTI PRECOCI IN UN MODELLO CELLULARE DI IPERTROFIA CARDIACA 108
PUFAs and pyrroloquinoline quinone protect from apoptosis triggered in cardiac cells by palmitate 104
REDUCED APOPTOSIS IN POLYAMINE DEPLETED RAT CARDIOMYOCYTES TREATED WITH NOREPINEPHRINE 101
Involvement of polyamines in apoptosis of cardiac myoblasts in a model of simulated ischemia 92
null 72
Totale 8.081
Categoria #
all - tutte 19.365
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 19.365


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021298 0 0 0 0 0 0 0 0 0 42 46 210
2021/20221.089 84 41 86 77 114 91 48 75 66 81 172 154
2022/20231.142 121 173 69 140 104 105 19 41 209 35 68 58
2023/2024271 21 55 19 16 23 60 14 27 0 12 12 12
2024/20251.203 51 173 92 76 220 56 81 46 7 48 51 302
2025/20262.070 209 197 181 150 307 161 208 68 448 141 0 0
Totale 8.081