POLI, Valeria
 Distribuzione geografica
Continente #
NA - Nord America 6.984
EU - Europa 5.347
AS - Asia 4.011
OC - Oceania 102
SA - Sud America 89
AF - Africa 67
Continente sconosciuto - Info sul continente non disponibili 4
Totale 16.604
Nazione #
US - Stati Uniti d'America 6.802
CN - Cina 2.574
IT - Italia 1.112
DE - Germania 643
IE - Irlanda 566
FR - Francia 403
UA - Ucraina 388
GB - Regno Unito 387
KR - Corea 360
SE - Svezia 354
FI - Finlandia 341
AT - Austria 273
ES - Italia 246
JP - Giappone 237
SG - Singapore 224
PL - Polonia 197
CA - Canada 148
VN - Vietnam 135
IN - India 129
HK - Hong Kong 104
AU - Australia 92
NL - Olanda 89
TW - Taiwan 80
DK - Danimarca 74
BE - Belgio 67
BR - Brasile 56
CH - Svizzera 45
SN - Senegal 39
MX - Messico 33
IR - Iran 31
IL - Israele 27
TR - Turchia 27
RO - Romania 26
RU - Federazione Russa 24
CZ - Repubblica Ceca 21
PK - Pakistan 21
TH - Thailandia 20
CL - Cile 17
HU - Ungheria 16
NO - Norvegia 16
GR - Grecia 14
PT - Portogallo 13
AR - Argentina 11
NZ - Nuova Zelanda 10
LU - Lussemburgo 9
JO - Giordania 8
MY - Malesia 8
HR - Croazia 7
EG - Egitto 5
ID - Indonesia 5
IQ - Iraq 5
MU - Mauritius 5
BG - Bulgaria 4
KE - Kenya 4
MA - Marocco 4
SA - Arabia Saudita 4
IS - Islanda 3
LB - Libano 3
PE - Perù 3
RS - Serbia 3
SM - San Marino 3
ZA - Sudafrica 3
DZ - Algeria 2
EU - Europa 2
GH - Ghana 2
NG - Nigeria 2
PH - Filippine 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AP - ???statistics.table.value.countryCode.AP??? 1
BA - Bosnia-Erzegovina 1
BT - Bhutan 1
CO - Colombia 1
ET - Etiopia 1
KW - Kuwait 1
LK - Sri Lanka 1
MO - Macao, regione amministrativa speciale della Cina 1
PR - Porto Rico 1
QA - Qatar 1
SI - Slovenia 1
UY - Uruguay 1
UZ - Uzbekistan 1
VA - Santa Sede (Città del Vaticano) 1
Totale 16.604
Città #
Beijing 985
Chandler 708
Dublin 563
Fairfield 504
Houston 459
Ashburn 331
Ann Arbor 288
Wilmington 244
Jacksonville 243
Vienna 243
Shanghai 230
Woodbridge 218
Seattle 207
Cambridge 204
Villeurbanne 204
Medford 188
Torino 187
Princeton 184
Redwood City 184
Warsaw 167
Pisa 165
Milan 144
Guangzhou 126
Singapore 126
Nyköping 115
Dearborn 114
Turin 113
Boston 102
Nanjing 87
Dong Ket 78
Madrid 75
Fremont 68
Wuhan 68
Boardman 55
New York 55
Hangzhou 53
Tokyo 47
Shenyang 41
Zhengzhou 41
Brussels 40
Hefei 40
Verona 40
Chengdu 38
San Diego 38
Toronto 37
Helsinki 36
Rome 36
Taipei 33
Norwalk 32
Xian 32
Chicago 30
Seoul 29
London 28
Los Angeles 28
Nanchang 28
Phoenix 27
Lachine 26
Chongqing 25
Kunming 25
Melbourne 25
Munich 25
Barcelona 23
Hong Kong 23
Bethesda 22
Magdeburg 22
Tianjin 22
Berlin 21
Dallas 19
Falls Church 19
Frankfurt am Main 19
Jinan 19
Paris 19
Philadelphia 19
Changsha 18
Edinburgh 18
Hebei 18
Fuzhou 17
Mountain View 17
San Francisco 16
Silver Spring 16
Central District 15
Duncan 15
Ottawa 15
Pittsburgh 15
Cardiff 14
Düsseldorf 14
Upper Marlboro 14
Amsterdam 13
Birmingham 13
Hanover 13
Shenzhen 13
Brisbane 12
Cleveland 12
Essen 12
Groningen 12
Halle 12
Heidelberg 12
Nanning 12
Padova 12
Santiago 12
Totale 9.541
Nome #
IL-6, IL-17 and STAT3: a holy trinity in auto-immunity? 1.717
STAT3 labels a subpopulation of reactive astrocytes required for brain metastasis article 1.055
STAT3 induces breast cancer growth via ANGPTL4, MMP13 and STC1 secretion by cancer associated fibroblasts 689
Partial inhibition of gp130-Jak-Stat3 signaling prevents Wnt- beta-catenin-mediated intestinal tumor growth and regeneration 465
Interleukin-6 influences stress-signalling by reducing the expression of the mTOR-inhibitor REDD1 in a STAT3-dependent manner 423
STAT3 in cancer: A double edged sword 365
Genotype tunes pancreatic ductal adenocarcinoma tissue tension to induce matricellular fibrosis and tumor progression 301
Constitutive STAT3 activation in epidermal keratinocytes enhances cell clonogenicity and favors spontaneous immortalization by opposing differentiation and senescence checkpoints 273
Loss of STAT3 in murine NK cells enhances NK cell-dependent tumor surveillance 249
Diazoxide postconditioning induces mitochondrial protein S-Nitrosylation and a redox-sensitive mitochondrial phosphorylation/translocation of RISK elements:no role for SAFE 236
Magnetically enriched bone marrow-derived macrophages loaded in vitro with iron oxide can migrate to inflammation sites in mice 235
A relaxometric method for the assessment of intestinal permeability based on the oral administration of gadolinium-based MRI contrast agents 219
STAT1 and STAT3 in Tumorigenesis: Two Sides of the Same Coin? 193
STAT3 can serve as a hit in the process of malignant transformation of primary cells 193
The apical ectodermal ridge of the mouse model of ectrodactyly Dlx5;Dlx6-/- shows altered stratification and cell polarity, which are restored by exogenous Wnt5a ligand 191
STAT3 activity is necessary and sufficient for the development of immune-mediated myocarditis in mice and promotes progression to dilated cardiomyopathy 176
STAT3 regulated ARF expression suppresses prostate cancer metastasis 171
From tissue invasion to glucose metabolism: the many aspects of Signal Transducer and Activator of Transcription 3 pro-oncogenic activities. 161
Disruption of STAT3 signalling promotes KRAS-induced lung tumorigenesis 161
Tyk2 and Stat3 regulate brown adipose tissue differentiation and obesity. 157
MicroRNAs-143 and -145 induce epithelial to mesenchymal transition and modulate the expression of junction proteins 155
The SRCIN1/p140Cap adaptor protein negatively regulates the aggressiveness of neuroblastoma 155
Angptl4 is upregulated under inflammatory conditions in the bone marrow of mice, expands myeloid progenitors, and accelerates reconstitution of platelets after myelosuppressive therapy 151
Identification of Functional cis-regulatory Polymorphisms in the Human Genome 150
STAT3-mediated metabolic reprograming in cellular transformation and implications for drug resistance 148
"Activated" STAT Proteins: A Paradoxical Consequence of Inhibited JAK-STAT Signaling in Cytomegalovirus-Infected Cells 146
Mice as experimental organisms. 136
STAT3 and metabolism: How many ways to use a single molecule? 133
Il diritto alla scienza medica e le questioni di genere in Così San Tuttə. Diritto alla scienza: istruzioni per l’uso. 133
STAT3 localizes to the ER, acting as a gatekeeper for ER-mitochondrion Ca2+ fluxes and apoptotic responses 124
STAT1 and STAT3 in tumorigenesis: A matter of balance 123
STAT3 Activities and Energy Metabolism: Dangerous Liaisons 121
The role of the N-terminal domain in dimerization and nucleocytoplasmic shuttling of latent STAT3 120
Stat3 is required to maintain the full differentiation potential of mammary stem cells and the proliferative potential of mammary luminal progenitors. 116
Stat3 controls tubolointerstitial communication during CKD 112
Adenoviral vaccine targeting multiple neoantigens as strategy to eradicate large tumors combined with checkpoint blockade 112
Pro-malignant properties of STAT3 during chronic inflammation. 108
Psoriasis: A STAT3-centric view 108
The STAT3 isoforms alpha and beta have unique and specific functions 107
Manipolazioni genetiche nel topo 106
From the nucleus to the mitochondria and backThe odyssey of a multitask STAT3 103
Nucleus, mitochondrion, or reticulum? STAT3 à la carte 103
SP1 and STAT3 functionally synergize to induce the RhoU small GTPase and a subclass of non-canonical WNT responsive genes correlating with poor prognosis in breast cancer 103
Myeloid STAT3 promotes formation of colitis-associated colorectal cancer in mice 96
The analysis of the human hemopexin promoter defines a new class of liver-specific genes. 95
The primary structure of human hemopexin deduced from cDNA sequence: evidence for internal, repeating homology. 94
STAT3β controls inflammatory responses and early tumor onset in skin and colon experimental cancer models. 94
Interleukin 6 is required for the development of collagen-induced arthritis. 93
The RhoU/Wrch1 Rho GTPase gene is a common transcriptional target of both the gp130/Stat3 and Wnt-1 pathways 90
Genomic and functional approaches as powerful tools to stratify human T-cell lymphoproliferative disorders and to identify relevant tumorigenic culprits 87
Of alphas and betas: distinct and overlapping functions of STAT3 isoforms 86
Structure of the human hemopexin gene and evidence for intron-mediated evolution. 84
Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis 84
Targeting the extracellular HSP90 co-chaperone Morgana inhibits cancer cell migration and promotes anti-cancer immunity 84
Characterization of an IL-6-responsive element (IL6RE) present on liver-specific genes and identification of the cognate IL-6-dependent DNA-binding protein (IL6DBP). 82
Universal and Specific Functions of STAT3in Solid Tumours 81
Tcf3 promotes cell migration and wound repair through regulation of lipocalin 2 81
Stat3 is required for anchorage-independent growth and metastasis but not for mammary tumor development downstream of the ErbB-2 oncogene 79
A stat3-mediated metabolic switch is involved in tumour transformation and stat3 addiction 79
Ups and downs: the STAT1:STAT3 seesaw of Interferon and gp130 receptor signalling 78
Interleukin 6 causes growth impairment in transgenic mice through a decrease in insulin-like growth factor-I. A model for stunted growth in children with chronic inflammation. 74
Where Sin3a meets STAT3: Balancing STAT3-mediated transcriptional activation and repression 74
The N-terminal domain of the adaptor protein p140Cap interacts with Tiam1 and controls Tiam1/Rac1 axis 74
Critical role for Stat3 in T-dependent terminal differentiation of IgG B cells 73
Metabolic switch between oxidative phosphorylation and glycolysis: a new role for Stat3 in tumours 73
Constitutively active STAT3 triggers the development of autoimmune myocarditis 73
Dissection of critical pathways instrumental for Anaplastic Lymphoma Kinase transformation 72
PS1-67 TYK2 is required for IL-17 production by innate immune cells in response to IPS 72
Alpha interferon induces long-lasting refractoriness of JAK-STATsignaling in the mouse liver through induction of USP18/UBP43 70
Constitutively active Stat3 triggers the development of autoimmune myocarditis 70
Liver-Specific siRNA-Mediated Stat3 or C3 Knockdown Improves the Outcome of Experimental Autoimmune Myocarditis 70
Ablation of STAT3 in the B cell compartment restricts gammaherpesvirus latency in Vivo 69
The cell death regulator GRIM-19 is an inhibitor of signal transducer and activator of transcription 3 67
Tyrosine phosphorylation is required for functional activation of disulfide-containing constitutively active STAT mutants 66
Development of animal models for adeno-associated virus site-specific integration. 65
The Interleukin-6-dependent DNA-binding protein gene (transcription factor 5: TCF5) maps to human chromosome 20 and rat chromosome 3, the IL6 receptor locus (IL6R) to human chromosome 1 and rat chromosome 2, and the rat IL6 gene to rat chromosome 4. 65
Genome-wide discovery of functional transcription factor binding sites by comparative genomics: The case of Stat3 64
C/EBPbeta phosphorylation by RSK creates a functional XEXD caspase inhibitory box critical for cell survival. 63
A role of STAT3 in Rho GTPase-regulated cell migration and proliferation 63
Functional analysis of IL-6 and IL-6DBP/C/EBP beta by gene targeting. 62
Differential transcriptional pattern of the hemopexin gene. 61
Prevention of Trauma and Hemorrhagic Shock-Mediated Liver Apoptosis by Activation of Stat3alpha 60
PKM2, STAT3 and HIF-1α: The Warburg’s vicious circle 60
Nociceptive responses in interleukin-6-deficient mice to peripheral inflammation and peripheral nerve section. 59
C/EBP beta blocks p65 phosphorylation and thereby NF-kappa B-mediated transcription in TNF-tolerant cells 59
C/EBPbeta is required for the late phases of acute phase genes induction in the liver and for tumour necrosis factor-alpha, but not Interleukin-6, regulation. 58
In T lymphocytes, ablation of STAT3 expression reinstates STAT1-dependent apoptosis by both IFNg and IL-6 58
A STAT3-mediated metabolic switch is involved in tumour transformation and STAT3 addiction 57
The microrna‐143/145 cluster in tumors: A matter of where and when 57
Differential co-expression analyses allow the identification of critical signalling pathways altered during tumour transformation and progression 57
Network-based inference of tumorogenic culprits in human T-cell lymphoproliferative disorders 56
CCAAT enhancer- binding protein beta is required for normal hepatocyte proliferation in mice after partial hepatectomy. 55
Constitutively active Stat3 enhances neu-mediated migration and metastasis in mammary tumors via upregulation of Cten 55
PML depletion disrupts normal mammary gland development and skews the composition of the mammary luminal cell progenitor pool 55
IL-6 knockout mice 54
The Transcription Factor C/EBPbeta Is Essential for Inducible Expression of the cox-2 Gene in Macrophages but Not in Fibroblasts. 54
A Cathepsin D-Cleaved 16 kDa Form of Prolactin Mediates Postpartum Cardiomyopathy 54
Presence of a reduced opioid response in interleukin-6 knock out mice. 52
Inactivation of the IL-6 gene prevents development of multicentric Castleman's disease in C/EBP beta-deficient mice 52
The role of IL-6 in the inflammatory and humoral response to adenoviral vectors. 52
Totale 14.474
Categoria #
all - tutte 40.970
article - articoli 0
book - libri 0
conference - conferenze 2.000
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 42.970


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.566 121 112 194 275 187 330 294 235 304 206 191 117
2020/20212.033 161 160 170 123 148 103 219 80 229 222 136 282
2021/20222.179 120 139 152 205 120 128 178 145 118 139 323 412
2022/20232.702 269 196 60 209 254 627 254 179 284 73 156 141
2023/20242.273 235 261 120 179 197 219 162 206 66 147 205 276
2024/2025110 110 0 0 0 0 0 0 0 0 0 0 0
Totale 17.119