TURTURICI, Giuseppina
 Distribuzione geografica
Continente #
NA - Nord America 3.374
EU - Europa 1.861
AS - Asia 626
SA - Sud America 554
AF - Africa 28
Continente sconosciuto - Info sul continente non disponibili 4
Totale 6.447
Nazione #
US - Stati Uniti d'America 3.211
FI - Finlandia 426
IT - Italia 404
CN - Cina 366
UA - Ucraina 366
SG - Singapore 210
PE - Perù 188
IE - Irlanda 151
DE - Germania 131
MX - Messico 124
CO - Colombia 101
GB - Regno Unito 97
CL - Cile 86
SE - Svezia 86
EC - Ecuador 85
RU - Federazione Russa 59
FR - Francia 39
AR - Argentina 33
CI - Costa d'Avorio 28
BE - Belgio 26
BR - Brasile 22
KR - Corea 18
BO - Bolivia 17
PY - Paraguay 15
CR - Costa Rica 13
CZ - Repubblica Ceca 13
NL - Olanda 13
ES - Italia 12
GT - Guatemala 11
HK - Hong Kong 11
RO - Romania 10
AT - Austria 9
PL - Polonia 8
CA - Canada 6
IN - India 6
UY - Uruguay 6
IR - Iran 5
PA - Panama 4
EU - Europa 3
JP - Giappone 3
NI - Nicaragua 3
CH - Svizzera 2
GR - Grecia 2
HR - Croazia 2
UZ - Uzbekistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BG - Bulgaria 1
GE - Georgia 1
HU - Ungheria 1
KH - Cambogia 1
LB - Libano 1
LU - Lussemburgo 1
PR - Porto Rico 1
RS - Serbia 1
SA - Arabia Saudita 1
SI - Slovenia 1
SV - El Salvador 1
VE - Venezuela 1
Totale 6.447
Città #
Chandler 336
Fairfield 289
Woodbridge 259
Ann Arbor 255
Jacksonville 206
Ashburn 191
Wilmington 179
Singapore 165
Houston 157
Dublin 151
Seattle 119
Nanjing 116
Medford 115
Lima 106
Cambridge 76
Princeton 75
Tulsa 60
Palermo 58
Redwood City 57
Des Moines 54
Quito 42
Santiago 40
Boardman 38
Beijing 33
Ludwigshafen am Rhein 31
Dearborn 30
Shenyang 30
Abidjan 28
Altamura 26
Arequipa 26
Brussels 26
Barranquilla 23
San Diego 22
Medellín 21
Lawrence 20
Santa Clara 20
Changsha 19
Nanchang 19
Jiaxing 18
Clifton 17
Hebei 17
Guayaquil 16
Asunción 15
La Paz 15
Tianjin 14
Auburn Hills 13
New York 13
Ningbo 13
Posadas 13
Seongnam 13
Viña del Mar 13
Jinan 12
Milan 12
Bogotá 11
Guatemala City 11
Munich 11
Dallas 10
Saint Petersburg 10
Brno 9
Helsinki 9
London 9
Talca 9
Atlanta 8
Chicago 8
Cuauhtémoc 8
Culiacán 8
Gustavo Adolfo Madero 8
Mexico City 8
Piura 8
San Mateo 8
Zhengzhou 8
Ancona 7
Kilburn 7
Puebla City 7
Taizhou 7
Valparaíso 7
Verona 7
Central 6
Cusco 6
Montevideo 6
San José 6
Ciudad Nezahualcoyotl 5
Concepción 5
Frankfurt 5
Goiânia 5
Guadalajara 5
Guangzhou 5
Hefei 5
Loja 5
Manta 5
Moscow 5
Norwalk 5
Orange 5
Sullana 5
Temuco 5
Tepic 5
Trujillo 5
Tumbes 5
Cartago 4
Ciudad del Carmen 4
Totale 4.052
Nome #
Sistemas de endomembranas (RE y GOLGI), sistema vacuolar y lisosomas 776
Oxidative stress preconditioning of mouse perivascular myogenic progenitors selects a subpopulation of cells with a distinct survival advantage in vitro and in vivo 166
Hsp70 localizes differently from chaperone Hsc70 in mouse mesoangioblasts under physiological growth conditions. 159
Heat Shock Proteins in Multiple Sclerosis Pathogenesis: Friend or Foe? 156
Hsp70 is required for optimal cell proliferation in mouse A6 mesoangioblast stem cells 148
Stress response in mesoangioblast stem cells 142
Nickel, lead, and cadmium induce differential cellular responses in sea urchin embryos by activating the synthesis of different HSP70s 140
Armazon celulary organelos: citoesqueleto, mitocondria, peroxisomas y nucleo 138
Extracellular Hsp70 Enhances Mesoangioblast Migration via an Autocrine Signaling Pathway 128
Regeneration in invertebrates 122
Mouse A6 stem cells release active FGF-2 into extracellular space through plasma membrane vesicles 118
Extracellular vesicles isolated by cerebrospinal fluid as biomarkers of inflammation in multiple sclerosis and inflammatory neurological diseases. 118
H2O2 resistant mesoangioblast clone isolation with a distinct survival advantage in vitro and in vivo 117
Perturbation of Developmental Regulatory Gene Expression by a G-Quadruplex DNA Inducer in the Sea Urchin Embryo 117
Protective Role of Heat Shock Proteins in Parkinson's Disease. 114
Ciclo celular, apoptosis y envejecimiento 111
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. 106
Extracellular membrane vesicles as a mechanism of cell-to-cell communication: advantages and disadvantages. 106
Membrane vesicles containing matrix metalloproteinase-9 and fibroblast growth factor-2 are released into the extracellular space from mouse mesoangioblast Sstem cells 101
Hsp70 and its molecular role in nervous system diseases 99
Shedding of vesicles from mesoangioblast A6 stem cells 94
Isolation of cell clones from stem cell population more resistant to oxidative stress for tissue repair. 86
Espressione basale dell’HSP70 inducibile in differenti linee staminali di topo. 84
Porous PLLA scaffolds are optimal substrates for internal colonization by A6 mesoangioblasts and immunocytochemical analyses 84
Cellule staminali A6 di topo producono vescicole che contengono HSP70 e FGF-2 83
Gastrulation in sea urchin and amphibian embryos 82
Esocitosi di Hsp70 mediante vescicole in cellule staminali di topo 81
Ectosomes containing HSP70 and FGF-2 are released from mouse A6 stem cells 80
Reevaluating the function of a transcription factor: MBF-1 as a sea urchin chromatin organizer ? 80
Another function of Hsp70 in mesoangioblast stem cells 77
Shedding of membrane vesicles containing HSP70 and FGF-2 from A6 stem cells. 76
Autophagy and apoptosis regolate survival of mesoangioblast stem cells subjected to oxidative stress 76
A6 stem cells release vesicles containing HSP70i 75
Role and regulation of HSP70 in A6 mesoangioblast stem cells 72
Mouse mesoangioblast behaviour when subjected to cellular stress 72
Stress response in mesangioblast stem cells 71
Stress response in mouse stem cells 71
Cell clones more resistant to oxidative stress selecte from embryonic and adult mesoangioblast stem cell population. 71
Positive or negative involvement of heat-shock proteins in multiple sclerosis pathogenesis: an overview. 70
Mesoangioblast A6 stem cells release vesicles containing the inducible HSP70 69
Hsp70 in mesoangioblast A6 stem cells. 69
Effects of H2O2 on mesoangioblast stem cells: survival and cell death 67
An HSF2-like factor is present in the invertebrates: characterization and purification in sea urchin ambryos and its localization in primary mesenchime cells 67
Stress response and apoptosis in measoangioblast stem cells 66
Extracellular release of Hsp70 from A6 mouse stem cells 66
Mouse mesoangioblasts release Hsp70 in a controlled manner through membrane vesicle shedding 63
Mesoangioblast behaviour in oxidative stress condition 63
Identification of an HSF2-like factor in sea urchin embryos and its localization in primary mesenchime cells 62
Hsp70 release from mesoangioblast A6 stem cells through vesicles 62
Intracellular and extracellular Hsp70 in A6 mouse stem cells 61
Transcriptome analysis after a strong oxidative stress highlighted a mesoangioblast stem cell sub-population with important different capability 61
Hsp70 functions: inside and outside the cell 60
Inducible HSP70 localization in mesoangioblast A6 stem cells 59
Analisi dell’espressione dell’HSP70 inducubile in cellule staminali ed in tessutiu adulti di topo. 59
Metalloproteasi nella biologia dei mesoangioblasti di topo 59
A sub-population of mesoangioblasts displays features of resistance and proliferation confirmed by transcriptome analysis. 58
Stress response and apoptosis in mesoangioblasts stem cells 57
Hsp70 function inside and outside mouse mesoangioblast stem cells 57
Ku factor is responsible of Hsp70 basal transcription in mouse mesoangioblasts 57
Nichel,piombo e cadmio inducono risposte cellulari differenti, attivando la sintesi di differenti HSP70 in embrioni di ricci di mare 55
Hsp70 is involved in MMP2 level in mouse mesoangioblast stem cells 55
Mesoangioblast stem cell population is non-omogeneous as revealed by transcriptome analysis after a severe oxidative stress. 55
MMP2 synthesis in mouse mesoangioblast stem cells is highly regulated 54
Hsp70 and NF-kB are involved in mouse mesoangioblast stem cells migration. 54
Capacità di differenziamento di un clone cellulare da cellule staminali resistenti allo stress ossidativo. 54
Selezione di cloni più resistenti allo stress ossidativo dalla popolazione di cellule staminali mesoangioblasti 52
La regolazione dell’espressione della MMP2 in mesoangioblasti è dipendente dai livelli della proteina Hsp70. 52
MMP2 expression in mouse mesoangioblast is dependent on Hsp70 level. 51
Intracellular and extracellular Hsp70 in mouse mesoangioblast stem cells 49
Differentiation capability of clones of mouse mesoangioblast stem cells resistant to oxidative stress. 49
Mesoangioblast MMP2 regulation is dependent on Hsp70 level 47
Cell clone selected from mab stem cell is more resistent to oxidative stress and retain some ability that could be useful for cell therapy. 47
Mesoangioblast stem cells membrane vesicles are carriers for molecules involved in autocrine and paracrine signals 44
Hsp70 level regulates MMP2 expression in mesoangioblast stemj cells 44
Mesoangioblasti di topo producono e rilasciano nello spazio extracellulare vescicole di membrana contenenti MMP9 e FGF2 in forma attiva 43
Glut-3 Gene Knockdown as a Potential Strategy to Overcome Glioblastoma Radioresistance 18
Totale 6.732
Categoria #
all - tutte 23.624
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 23.624


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020665 0 0 0 0 0 148 138 51 135 47 68 78
2020/2021790 38 78 46 94 66 24 81 30 90 43 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
2024/2025476 77 85 94 127 84 9 0 0 0 0 0 0
Totale 6.732