TURTURICI, Giuseppina
 Distribuzione geografica
Continente #
NA - Nord America 5.244
EU - Europa 3.247
AS - Asia 2.697
SA - Sud America 1.044
Continente sconosciuto - Info sul continente non disponibili 289
AF - Africa 98
OC - Oceania 2
Totale 12.621
Nazione #
US - Stati Uniti d'America 4.948
SG - Singapore 863
CN - Cina 754
RU - Federazione Russa 714
FI - Finlandia 483
IT - Italia 469
UA - Ucraina 376
DE - Germania 324
HK - Hong Kong 316
BR - Brasile 297
VN - Vietnam 268
PE - Perù 218
PL - Polonia 170
IE - Irlanda 165
MX - Messico 164
FR - Francia 158
GB - Regno Unito 150
CL - Cile 131
CO - Colombia 128
JP - Giappone 127
EC - Ecuador 124
SE - Svezia 91
KR - Corea 81
AR - Argentina 64
BD - Bangladesh 48
CA - Canada 44
IN - India 43
IQ - Iraq 38
CI - Costa d'Avorio 29
ES - Italia 29
BE - Belgio 27
BO - Bolivia 26
GT - Guatemala 26
NL - Olanda 26
PY - Paraguay 25
PK - Pakistan 24
CR - Costa Rica 22
TR - Turchia 22
VE - Venezuela 22
AT - Austria 15
UZ - Uzbekistan 15
ZA - Sudafrica 15
JM - Giamaica 14
CZ - Repubblica Ceca 13
SA - Arabia Saudita 11
DZ - Algeria 10
MA - Marocco 10
RO - Romania 10
AZ - Azerbaigian 9
ID - Indonesia 9
IR - Iran 9
UY - Uruguay 9
MY - Malesia 8
PA - Panama 8
TN - Tunisia 8
DO - Repubblica Dominicana 7
KE - Kenya 7
NP - Nepal 7
EG - Egitto 6
IL - Israele 5
SN - Senegal 5
ET - Etiopia 4
GR - Grecia 4
JO - Giordania 4
OM - Oman 4
PH - Filippine 4
TH - Thailandia 4
CH - Svizzera 3
EU - Europa 3
GE - Georgia 3
KZ - Kazakistan 3
LB - Libano 3
LT - Lituania 3
MM - Myanmar 3
NI - Nicaragua 3
PR - Porto Rico 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
BG - Bulgaria 2
HN - Honduras 2
HR - Croazia 2
KH - Cambogia 2
MD - Moldavia 2
NG - Nigeria 2
PS - Palestinian Territory 2
QA - Qatar 2
RS - Serbia 2
SI - Slovenia 2
SV - El Salvador 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AD - Andorra 1
AL - Albania 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
CG - Congo 1
HU - Ungheria 1
KW - Kuwait 1
LK - Sri Lanka 1
Totale 12.332
Città #
Ashburn 561
Singapore 538
San Jose 452
Chandler 336
Hong Kong 301
Fairfield 289
Woodbridge 259
Ann Arbor 255
Jacksonville 206
Wilmington 180
Dublin 164
Houston 162
Zgierz 148
Frankfurt am Main 130
Beijing 128
Lima 124
Tokyo 124
Santa Clara 123
Seattle 121
Moscow 119
Medford 116
Nanjing 116
Ho Chi Minh City 100
Dallas 81
Cambridge 76
Princeton 75
Los Angeles 71
Des Moines 69
Hanoi 67
Lauterbourg 67
Palermo 67
Hefei 66
Boardman 63
Santiago 63
Tulsa 60
Helsinki 59
Redwood City 57
Quito 51
Council Bluffs 47
Buffalo 40
The Dalles 39
New York 34
Ludwigshafen am Rhein 31
Dearborn 30
Shenyang 30
Chicago 29
Abidjan 28
Altamura 26
Arequipa 26
Brussels 26
São Paulo 26
Guayaquil 25
Medellín 25
Seoul 24
Barranquilla 23
San Diego 23
Guatemala City 22
Orem 22
Lawrence 20
Talca 20
Tianjin 20
Changsha 19
Munich 19
Nanchang 19
Asunción 18
Jiaxing 18
La Paz 18
Mexico City 18
Viña del Mar 18
Bogotá 17
Clifton 17
Hebei 17
London 17
Milan 17
Atlanta 16
Cuenca 15
Da Nang 15
Montreal 14
Phoenix 14
Posadas 14
Amsterdam 13
Auburn Hills 13
Jinan 13
Ningbo 13
San José 13
Seongnam 13
Baghdad 12
Paris 11
Puebla City 11
Rome 11
San Francisco 11
Guangzhou 10
Saint Petersburg 10
Tashkent 10
Brno 9
City of London 9
Culiacán 9
Lahore 9
Montevideo 9
Redondo Beach 9
Totale 7.218
Nome #
Sistemas de endomembranas (RE y GOLGI), sistema vacuolar y lisosomas 1.022
Oxidative stress preconditioning of mouse perivascular myogenic progenitors selects a subpopulation of cells with a distinct survival advantage in vitro and in vivo 237
Heat Shock Proteins in Multiple Sclerosis Pathogenesis: Friend or Foe? 230
Armazon celulary organelos: citoesqueleto, mitocondria, peroxisomas y nucleo 226
Hsp70 localizes differently from chaperone Hsc70 in mouse mesoangioblasts under physiological growth conditions. 224
Nickel, lead, and cadmium induce differential cellular responses in sea urchin embryos by activating the synthesis of different HSP70s 220
Extracellular Hsp70 Enhances Mesoangioblast Migration via an Autocrine Signaling Pathway 219
H2O2 resistant mesoangioblast clone isolation with a distinct survival advantage in vitro and in vivo 216
Ciclo celular, apoptosis y envejecimiento 214
Mouse A6 stem cells release active FGF-2 into extracellular space through plasma membrane vesicles 212
Stress response in mesoangioblast stem cells 210
Extracellular vesicles isolated by cerebrospinal fluid as biomarkers of inflammation in multiple sclerosis and inflammatory neurological diseases. 207
Another function of Hsp70 in mesoangioblast stem cells 206
Shedding of membrane vesicles containing HSP70 and FGF-2 from A6 stem cells. 200
Extracellular membrane vesicles as a mechanism of cell-to-cell communication: advantages and disadvantages. 197
Protective Role of Heat Shock Proteins in Parkinson's Disease. 184
Hsp70 is required for optimal cell proliferation in mouse A6 mesoangioblast stem cells 183
Cell clones more resistant to oxidative stress selecte from embryonic and adult mesoangioblast stem cell population. 180
Perturbation of Developmental Regulatory Gene Expression by a G-Quadruplex DNA Inducer in the Sea Urchin Embryo 180
Autophagy and apoptosis regolate survival of mesoangioblast stem cells subjected to oxidative stress 178
Hsp70 and its molecular role in nervous system diseases 175
Isolation of cell clones from stem cell population more resistant to oxidative stress for tissue repair. 175
Cellule staminali A6 di topo producono vescicole che contengono HSP70 e FGF-2 172
Espressione basale dell’HSP70 inducibile in differenti linee staminali di topo. 171
A sub-population of mesoangioblasts displays features of resistance and proliferation confirmed by transcriptome analysis. 171
Membrane vesicles containing matrix metalloproteinase-9 and fibroblast growth factor-2 are released into the extracellular space from mouse mesoangioblast Sstem cells 170
Rapid changes in heat-shock cognate 70 levels, heat-shock cognate phosphorylation state, heat-shock transcription factor, and metal transcription factor activity levels in response to heavy metal exposure during sea urchin embryonic development. 169
Ectosomes containing HSP70 and FGF-2 are released from mouse A6 stem cells 167
Reevaluating the function of a transcription factor: MBF-1 as a sea urchin chromatin organizer ? 167
Esocitosi di Hsp70 mediante vescicole in cellule staminali di topo 161
Differentiation capability of clones of mouse mesoangioblast stem cells resistant to oxidative stress. 161
A6 stem cells release vesicles containing HSP70i 160
Capacità di differenziamento di un clone cellulare da cellule staminali resistenti allo stress ossidativo. 160
An HSF2-like factor is present in the invertebrates: characterization and purification in sea urchin ambryos and its localization in primary mesenchime cells 160
Shedding of vesicles from mesoangioblast A6 stem cells 157
Mesoangioblast stem cell population is non-omogeneous as revealed by transcriptome analysis after a severe oxidative stress. 156
Gastrulation in sea urchin and amphibian embryos 154
Regeneration in invertebrates 153
Effects of H2O2 on mesoangioblast stem cells: survival and cell death 150
Extracellular release of Hsp70 from A6 mouse stem cells 142
Analisi dell’espressione dell’HSP70 inducubile in cellule staminali ed in tessutiu adulti di topo. 139
Hsp70 functions: inside and outside the cell 139
Hsp70 in mesoangioblast A6 stem cells. 139
Positive or negative involvement of heat-shock proteins in multiple sclerosis pathogenesis: an overview. 139
Identification of an HSF2-like factor in sea urchin embryos and its localization in primary mesenchime cells 138
Mouse mesoangioblast behaviour when subjected to cellular stress 138
Role and regulation of HSP70 in A6 mesoangioblast stem cells 137
Mouse mesoangioblasts release Hsp70 in a controlled manner through membrane vesicle shedding 136
Nichel,piombo e cadmio inducono risposte cellulari differenti, attivando la sintesi di differenti HSP70 in embrioni di ricci di mare 135
Glut-3 Gene Knockdown as a Potential Strategy to Overcome Glioblastoma Radioresistance 132
Mesoangioblast stem cells membrane vesicles are carriers for molecules involved in autocrine and paracrine signals 132
Mesoangioblast A6 stem cells release vesicles containing the inducible HSP70 130
Cell clone selected from mab stem cell is more resistent to oxidative stress and retain some ability that could be useful for cell therapy. 130
Ku factor is responsible of Hsp70 basal transcription in mouse mesoangioblasts 127
Porous PLLA scaffolds are optimal substrates for internal colonization by A6 mesoangioblasts and immunocytochemical analyses 126
Hsp70 and NF-kB are involved in mouse mesoangioblast stem cells migration. 126
Stress response in mesangioblast stem cells 125
Hsp70 release from mesoangioblast A6 stem cells through vesicles 124
Intracellular and extracellular Hsp70 in A6 mouse stem cells 123
Stress response in mouse stem cells 123
Mesoangioblast behaviour in oxidative stress condition 122
Metalloproteasi nella biologia dei mesoangioblasti di topo 121
MMP2 synthesis in mouse mesoangioblast stem cells is highly regulated 121
La regolazione dell’espressione della MMP2 in mesoangioblasti è dipendente dai livelli della proteina Hsp70. 120
Stress response and apoptosis in measoangioblast stem cells 119
Hsp70 function inside and outside mouse mesoangioblast stem cells 118
Inducible HSP70 localization in mesoangioblast A6 stem cells 117
Hsp70 level regulates MMP2 expression in mesoangioblast stemj cells 116
Transcriptome analysis after a strong oxidative stress highlighted a mesoangioblast stem cell sub-population with important different capability 113
Stress response and apoptosis in mesoangioblasts stem cells 109
Mesoangioblast MMP2 regulation is dependent on Hsp70 level 109
Selezione di cloni più resistenti allo stress ossidativo dalla popolazione di cellule staminali mesoangioblasti 108
Hsp70 is involved in MMP2 level in mouse mesoangioblast stem cells 107
Intracellular and extracellular Hsp70 in mouse mesoangioblast stem cells 103
MMP2 expression in mouse mesoangioblast is dependent on Hsp70 level. 96
Mesoangioblasti di topo producono e rilasciano nello spazio extracellulare vescicole di membrana contenenti MMP9 e FGF2 in forma attiva 88
Totale 12.621
Categoria #
all - tutte 40.087
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 40.087


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022781 0 173 18 41 78 22 27 50 78 99 42 153
2022/20231.013 102 128 24 108 118 160 51 94 113 30 56 29
2023/2024659 18 120 45 44 53 54 94 15 7 41 55 113
2024/20251.544 77 85 94 127 84 71 97 61 82 160 251 355
2025/20264.551 332 115 232 306 404 624 659 455 305 827 138 154
2026/2027270 204 66 0 0 0 0 0 0 0 0 0 0
Totale 12.621