TURTURICI, Giuseppina
 Distribuzione geografica
Continente #
NA - Nord America 4.869
EU - Europa 3.222
AS - Asia 2.671
SA - Sud America 1.016
AF - Africa 98
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 11.882
Nazione #
US - Stati Uniti d'America 4.609
SG - Singapore 860
CN - Cina 753
RU - Federazione Russa 714
FI - Finlandia 483
IT - Italia 455
UA - Ucraina 376
DE - Germania 322
HK - Hong Kong 315
BR - Brasile 288
VN - Vietnam 263
PE - Perù 216
PL - Polonia 170
IE - Irlanda 165
MX - Messico 163
FR - Francia 155
GB - Regno Unito 150
CL - Cile 131
JP - Giappone 127
CO - Colombia 120
EC - Ecuador 118
SE - Svezia 91
KR - Corea 81
AR - Argentina 63
BD - Bangladesh 43
IN - India 42
IQ - Iraq 38
CI - Costa d'Avorio 29
ES - Italia 29
CA - Canada 28
BE - Belgio 27
BO - Bolivia 26
GT - Guatemala 25
PY - Paraguay 25
NL - Olanda 24
PK - Pakistan 24
TR - Turchia 21
CR - Costa Rica 20
VE - Venezuela 20
AT - Austria 15
UZ - Uzbekistan 15
ZA - Sudafrica 15
CZ - Repubblica Ceca 13
DZ - Algeria 10
MA - Marocco 10
RO - Romania 10
SA - Arabia Saudita 10
IR - Iran 9
UY - Uruguay 9
AZ - Azerbaigian 8
MY - Malesia 8
TN - Tunisia 8
KE - Kenya 7
PA - Panama 7
DO - Repubblica Dominicana 6
EG - Egitto 6
NP - Nepal 6
ID - Indonesia 5
SN - Senegal 5
ET - Etiopia 4
IL - Israele 4
JO - Giordania 4
OM - Oman 4
PH - Filippine 4
TH - Thailandia 4
EU - Europa 3
GE - Georgia 3
GR - Grecia 3
JM - Giamaica 3
KZ - Kazakistan 3
LB - Libano 3
LT - Lituania 3
MM - Myanmar 3
NI - Nicaragua 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
BG - Bulgaria 2
CH - Svizzera 2
HN - Honduras 2
HR - Croazia 2
KH - Cambogia 2
MD - Moldavia 2
NG - Nigeria 2
PS - Palestinian Territory 2
RS - Serbia 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
BH - Bahrain 1
CG - Congo 1
HU - Ungheria 1
KW - Kuwait 1
LK - Sri Lanka 1
LU - Lussemburgo 1
MT - Malta 1
PR - Porto Rico 1
QA - Qatar 1
Totale 11.880
Città #
Ashburn 545
Singapore 537
Chandler 336
San Jose 334
Hong Kong 300
Fairfield 289
Woodbridge 259
Ann Arbor 255
Jacksonville 206
Wilmington 179
Dublin 164
Houston 161
Zgierz 148
Frankfurt am Main 129
Beijing 127
Tokyo 124
Lima 123
Seattle 121
Moscow 119
Nanjing 116
Medford 115
Santa Clara 112
Ho Chi Minh City 98
Dallas 79
Cambridge 76
Princeton 75
Des Moines 69
Los Angeles 68
Lauterbourg 67
Palermo 67
Hefei 66
Hanoi 64
Santiago 63
Tulsa 60
Helsinki 59
Redwood City 57
Quito 49
Council Bluffs 47
Boardman 40
Buffalo 39
The Dalles 39
New York 32
Ludwigshafen am Rhein 31
Dearborn 30
Shenyang 30
Abidjan 28
Altamura 26
Arequipa 26
Brussels 26
São Paulo 26
Seoul 24
Barranquilla 23
Medellín 23
San Diego 23
Chicago 22
Guayaquil 22
Orem 22
Guatemala City 21
Lawrence 20
Talca 20
Tianjin 20
Changsha 19
Munich 19
Nanchang 19
Asunción 18
Jiaxing 18
La Paz 18
Viña del Mar 18
Bogotá 17
Clifton 17
Hebei 17
London 17
Mexico City 17
Atlanta 15
Da Nang 15
Cuenca 14
Posadas 14
Auburn Hills 13
Jinan 13
Ningbo 13
Seongnam 13
Amsterdam 12
Baghdad 12
Milan 12
Paris 11
Phoenix 11
Puebla City 11
Rome 11
San José 11
Guangzhou 10
Montreal 10
Saint Petersburg 10
Tashkent 10
Brno 9
City of London 9
Culiacán 9
Lahore 9
Montevideo 9
Redondo Beach 9
San Francisco 9
Totale 6.994
Nome #
Sistemas de endomembranas (RE y GOLGI), sistema vacuolar y lisosomas 1.008
Oxidative stress preconditioning of mouse perivascular myogenic progenitors selects a subpopulation of cells with a distinct survival advantage in vitro and in vivo 232
Heat Shock Proteins in Multiple Sclerosis Pathogenesis: Friend or Foe? 224
Armazon celulary organelos: citoesqueleto, mitocondria, peroxisomas y nucleo 221
Hsp70 localizes differently from chaperone Hsc70 in mouse mesoangioblasts under physiological growth conditions. 216
Nickel, lead, and cadmium induce differential cellular responses in sea urchin embryos by activating the synthesis of different HSP70s 215
Extracellular Hsp70 Enhances Mesoangioblast Migration via an Autocrine Signaling Pathway 212
H2O2 resistant mesoangioblast clone isolation with a distinct survival advantage in vitro and in vivo 207
Stress response in mesoangioblast stem cells 206
Ciclo celular, apoptosis y envejecimiento 206
Mouse A6 stem cells release active FGF-2 into extracellular space through plasma membrane vesicles 204
Another function of Hsp70 in mesoangioblast stem cells 202
Extracellular vesicles isolated by cerebrospinal fluid as biomarkers of inflammation in multiple sclerosis and inflammatory neurological diseases. 199
Shedding of membrane vesicles containing HSP70 and FGF-2 from A6 stem cells. 195
Extracellular membrane vesicles as a mechanism of cell-to-cell communication: advantages and disadvantages. 191
Hsp70 is required for optimal cell proliferation in mouse A6 mesoangioblast stem cells 182
Protective Role of Heat Shock Proteins in Parkinson's Disease. 177
Cell clones more resistant to oxidative stress selecte from embryonic and adult mesoangioblast stem cell population. 173
Hsp70 and its molecular role in nervous system diseases 172
Perturbation of Developmental Regulatory Gene Expression by a G-Quadruplex DNA Inducer in the Sea Urchin Embryo 170
Espressione basale dell’HSP70 inducibile in differenti linee staminali di topo. 169
Autophagy and apoptosis regolate survival of mesoangioblast stem cells subjected to oxidative stress 169
Isolation of cell clones from stem cell population more resistant to oxidative stress for tissue repair. 169
Cellule staminali A6 di topo producono vescicole che contengono HSP70 e FGF-2 167
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. 165
Membrane vesicles containing matrix metalloproteinase-9 and fibroblast growth factor-2 are released into the extracellular space from mouse mesoangioblast Sstem cells 164
A sub-population of mesoangioblasts displays features of resistance and proliferation confirmed by transcriptome analysis. 164
Ectosomes containing HSP70 and FGF-2 are released from mouse A6 stem cells 159
Reevaluating the function of a transcription factor: MBF-1 as a sea urchin chromatin organizer ? 159
A6 stem cells release vesicles containing HSP70i 157
Differentiation capability of clones of mouse mesoangioblast stem cells resistant to oxidative stress. 156
Esocitosi di Hsp70 mediante vescicole in cellule staminali di topo 155
Shedding of vesicles from mesoangioblast A6 stem cells 154
An HSF2-like factor is present in the invertebrates: characterization and purification in sea urchin ambryos and its localization in primary mesenchime cells 154
Capacità di differenziamento di un clone cellulare da cellule staminali resistenti allo stress ossidativo. 152
Mesoangioblast stem cell population is non-omogeneous as revealed by transcriptome analysis after a severe oxidative stress. 151
Regeneration in invertebrates 150
Effects of H2O2 on mesoangioblast stem cells: survival and cell death 146
Gastrulation in sea urchin and amphibian embryos 145
Extracellular release of Hsp70 from A6 mouse stem cells 139
Hsp70 in mesoangioblast A6 stem cells. 137
Identification of an HSF2-like factor in sea urchin embryos and its localization in primary mesenchime cells 136
Hsp70 functions: inside and outside the cell 135
Analisi dell’espressione dell’HSP70 inducubile in cellule staminali ed in tessutiu adulti di topo. 133
Role and regulation of HSP70 in A6 mesoangioblast stem cells 132
Mouse mesoangioblast behaviour when subjected to cellular stress 130
Mouse mesoangioblasts release Hsp70 in a controlled manner through membrane vesicle shedding 129
Nichel,piombo e cadmio inducono risposte cellulari differenti, attivando la sintesi di differenti HSP70 in embrioni di ricci di mare 128
Glut-3 Gene Knockdown as a Potential Strategy to Overcome Glioblastoma Radioresistance 127
Mesoangioblast A6 stem cells release vesicles containing the inducible HSP70 125
Mesoangioblast stem cells membrane vesicles are carriers for molecules involved in autocrine and paracrine signals 125
Cell clone selected from mab stem cell is more resistent to oxidative stress and retain some ability that could be useful for cell therapy. 124
Positive or negative involvement of heat-shock proteins in multiple sclerosis pathogenesis: an overview. 122
Stress response in mesangioblast stem cells 121
Hsp70 release from mesoangioblast A6 stem cells through vesicles 121
Porous PLLA scaffolds are optimal substrates for internal colonization by A6 mesoangioblasts and immunocytochemical analyses 120
Mesoangioblast behaviour in oxidative stress condition 119
Stress response in mouse stem cells 118
Stress response and apoptosis in measoangioblast stem cells 117
Intracellular and extracellular Hsp70 in A6 mouse stem cells 117
Ku factor is responsible of Hsp70 basal transcription in mouse mesoangioblasts 117
Hsp70 function inside and outside mouse mesoangioblast stem cells 115
MMP2 synthesis in mouse mesoangioblast stem cells is highly regulated 115
Metalloproteasi nella biologia dei mesoangioblasti di topo 114
Hsp70 and NF-kB are involved in mouse mesoangioblast stem cells migration. 113
Hsp70 level regulates MMP2 expression in mesoangioblast stemj cells 110
La regolazione dell’espressione della MMP2 in mesoangioblasti è dipendente dai livelli della proteina Hsp70. 109
Inducible HSP70 localization in mesoangioblast A6 stem cells 108
Stress response and apoptosis in mesoangioblasts stem cells 107
Transcriptome analysis after a strong oxidative stress highlighted a mesoangioblast stem cell sub-population with important different capability 107
Selezione di cloni più resistenti allo stress ossidativo dalla popolazione di cellule staminali mesoangioblasti 103
Mesoangioblast MMP2 regulation is dependent on Hsp70 level 103
Hsp70 is involved in MMP2 level in mouse mesoangioblast stem cells 102
Intracellular and extracellular Hsp70 in mouse mesoangioblast stem cells 96
MMP2 expression in mouse mesoangioblast is dependent on Hsp70 level. 92
Mesoangioblasti di topo producono e rilasciano nello spazio extracellulare vescicole di membrana contenenti MMP9 e FGF2 in forma attiva 84
Totale 12.167
Categoria #
all - tutte 37.842
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 37.842


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021200 0 0 0 0 0 0 0 0 0 0 87 113
2021/2022814 33 173 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
2025/20264.367 332 115 232 306 404 624 659 455 305 827 108 0
Totale 12.167