PICCOLO, STEFANO
 Distribuzione geografica
Continente #
NA - Nord America 15.005
AS - Asia 7.096
EU - Europa 3.948
AF - Africa 1.073
SA - Sud America 951
Continente sconosciuto - Info sul continente non disponibili 206
OC - Oceania 108
AN - Antartide 1
Totale 28.388
Nazione #
US - Stati Uniti d'America 14.130
SG - Singapore 2.101
CN - Cina 1.364
IT - Italia 1.101
VN - Vietnam 1.022
HK - Hong Kong 676
BR - Brasile 581
BD - Bangladesh 392
DE - Germania 373
FI - Finlandia 367
GB - Regno Unito 330
CA - Canada 250
FR - Francia 237
IN - India 199
SE - Svezia 158
PL - Polonia 141
NL - Olanda 139
UA - Ucraina 125
JP - Giappone 114
IQ - Iraq 112
RU - Federazione Russa 111
TR - Turchia 98
AR - Argentina 84
PH - Filippine 81
MX - Messico 69
ZA - Sudafrica 63
ES - Italia 61
JM - Giamaica 59
KR - Corea 58
ID - Indonesia 53
AT - Austria 52
SA - Arabia Saudita 52
PK - Pakistan 50
VE - Venezuela 47
IE - Irlanda 46
PS - Palestinian Territory 45
CR - Costa Rica 43
GT - Guatemala 43
MY - Malesia 41
NI - Nicaragua 41
UZ - Uzbekistan 41
CO - Colombia 40
DZ - Algeria 40
EC - Ecuador 40
JO - Giordania 40
PT - Portogallo 40
TW - Taiwan 38
KE - Kenya 37
PY - Paraguay 37
AL - Albania 36
PR - Porto Rico 36
TH - Thailandia 36
TN - Tunisia 36
ET - Etiopia 35
AE - Emirati Arabi Uniti 34
BJ - Benin 34
EG - Egitto 34
AM - Armenia 33
AU - Australia 33
CL - Cile 33
BE - Belgio 32
LY - Libia 32
ME - Montenegro 32
NO - Norvegia 32
SI - Slovenia 32
AO - Angola 31
BA - Bosnia-Erzegovina 31
CY - Cipro 31
GR - Grecia 31
IL - Israele 31
IR - Iran 31
HU - Ungheria 30
LB - Libano 30
MA - Marocco 30
MU - Mauritius 30
BF - Burkina Faso 29
BG - Bulgaria 29
CI - Costa d'Avorio 29
CV - Capo Verde 29
DK - Danimarca 29
MD - Moldavia 29
NE - Niger 29
UG - Uganda 29
CZ - Repubblica Ceca 28
EE - Estonia 28
NP - Nepal 28
RO - Romania 28
RS - Serbia 28
TT - Trinidad e Tobago 28
UY - Uruguay 28
BZ - Belize 27
LA - Repubblica Popolare Democratica del Laos 27
LV - Lettonia 27
MR - Mauritania 27
CM - Camerun 26
GA - Gabon 26
HN - Honduras 26
LC - Santa Lucia 26
PA - Panama 26
ZW - Zimbabwe 26
Totale 27.000
Città #
Ashburn 1.866
Fairfield 1.388
San Jose 1.362
Singapore 1.316
Woodbridge 765
Ann Arbor 713
Hong Kong 600
Chandler 587
Houston 555
Seattle 519
Cambridge 468
Wilmington 454
Jacksonville 408
Ho Chi Minh City 309
Los Angeles 305
Beijing 300
Santa Clara 248
Hanoi 246
Council Bluffs 237
Helsinki 222
Padova 184
Princeton 177
Boardman 159
New York 143
San Diego 138
Lauterbourg 108
Munich 102
Milan 92
Chicago 90
Denver 90
Shanghai 82
Dallas 80
Rome 80
Des Moines 77
Bytom 75
Buffalo 72
Orem 71
São Paulo 66
Medford 63
Montreal 61
Nanjing 60
Tokyo 57
Atlanta 48
Roxbury 45
Toronto 45
Warsaw 45
Baghdad 44
Da Nang 43
Haiphong 42
Padua 41
Phoenix 41
London 40
Managua 40
Turku 40
Kingston 39
Tashkent 39
Amman 38
Baltimore 36
San José 36
Aprilia 35
Guangzhou 35
Nairobi 35
Brooklyn 34
Dong Ket 34
Dublin 33
Frankfurt am Main 33
Guatemala City 33
Cotonou 32
Vienna 32
Johannesburg 30
Luanda 30
Addis Ababa 29
Kampala 29
Boston 28
Cardiff 28
Naples 28
Abidjan 27
Amsterdam 27
Stockholm 27
Yerevan 27
Castries 26
Chennai 26
Libreville 26
Nouakchott 26
Riga 26
Hải Dương 25
Lahore 25
Podgorica 25
Chisinau 24
Dakar 24
Falls Church 24
Hebei 24
Montevideo 24
Praia 24
Salt Lake City 24
San Francisco 24
Turin 24
Istanbul 23
Lusaka 23
Niamey 23
Totale 16.833
Nome #
YAP/TAZ upstream signals and downstream responses 896
Monitoring smad activity in vivo using the xenopus model system 520
Crosstalk between YAP/TAZ and Notch Signaling 502
Germ-Layer Specification and Control of Cell Growth by Ectodermin, a Smad4 Ubiquitin Ligase 474
Mechanobiology of YAP and TAZ in physiology and disease 462
Role of Yap/Taz in mechanotransduction 382
Transcriptional addiction in cancer cells is mediated by YAP/TAZ through BRD4 360
The Disabled homolog 2 controls pro-metastatic activity of tumor-associated macrophages 349
The SWI/SNF complex is a mechanoregulated inhibitor of YAP and TAZ 348
Cell phenotypic plasticity requires autophagic flux driven by YAP/TAZ mechanotransduction 345
Genome-wide association between YAP/TAZ/TEAD and AP-1 at enhancers drives oncogenic growth 344
Reprogramming normal cells into tumour precursors requires ECM stiffness and oncogene-mediated changes of cell mechanical properties 332
Single-cell analyses reveal YAP/TAZ as regulators of stemness and cell plasticity in glioblastoma 332
YAP/TAZ at the Roots of Cancer 323
P63, Sharp1, and HIFs: Master regulators of metastasis in triple-negative breast cance 316
Metabolic control of YAP and TAZ by the mevalonate pathway. 312
MicroRNA control of nodal signalling 309
Integration of TGF-beta and Ras/MAPK signaling through p53 phosphorylation 299
Biomaterials and engineered microenvironments to control YAP/TAZ-dependent cell behaviour 299
Self-regulation of the head-inducing properties of the Spemann organizer 297
Signaling crosstalk between TGFβ and Dishevelled/Par1b. 295
YAP/TAZ-Dependent Reprogramming of Colonic Epithelium Links ECM Remodeling to Tissue Regeneration 294
Cell type-specific transcription of the alpha 1(VI) collagen gene - Role of the AP1 binding site and of the core promoter 293
p63, Sharp1, and HIFs: Master Regulators of Metastasis in Triple-Negative Breast Cancer 293
Convergence of p53 and TGF-beta signaling networks. 291
SHARP1 suppresses breast cancer metastasis by promoting degradation of hypoxia-inducible factors 291
Mechanical cues control mutant p53 stability through a mevalonate-RhoA axis 290
A Mechanical Checkpoint Controls Multicellular Growth through YAP/TAZ Regulation by Actin-Processing Factors 285
Epithelial–mesenchymal transition in malignant mesothelioma 285
The Hippo transducer TAZ confers cancer stem cell-related traits on breast cancer cells. 285
A MicroRNA targeting dicer for metastasis control. 283
FAM/USP9x, a Deubiquitinating Enzyme Essential for TGF beta Signaling, Controls Smad4 Monoubiquitination 282
Induction of Expandable Tissue-Specific Stem/Progenitor Cells through Transient Expression of YAP/TAZ 280
A TIAM Double Hit to Oppose YAP/TAZ 280
Eradicating tumor drug resistance at its YAP-biomechanical roots 275
Redox status in a model of cancer stem cells 274
YAP/TAZ activity in stromal cells prevents ageing by controlling cGAS-STING 263
Chronic inflammation imposes aberrant cell fate in regenerating epithelia through mechanotransduction 263
YAP/TAZ as master regulators in cancer: modulation, function and therapeutic approaches 260
Negative control of Smad activity by ectodermin/Tif1 gamma patterns the mammalian embryo 259
USP15 is a deubiquitylating enzyme for receptor-activated SMADs. 257
YAP/TAZ link cell mechanics to Notch signalling to control epidermal stem cell fate 256
Simple yet effective methods to probe hydrogel stiffness for mechanobiology 254
Distinct regions control transcriptional activation of the alpha1(VI) collagen promoter in different tissues of transgenic mice. 253
YAP/TAZ as therapeutic targets in cancer 252
Mapping Wnt/beta-catenin signaling during mouse development and in colorectal tumors. 250
Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy 248
A Wnt-beta-catenin-responsive cell population that participates in the formation of olfactory connections in the mouse embryo 246
Emilin1 links TGF-beta maturation to blood pressure homeostasis 246
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 244
A mutant-p53/Smad complex opposes p63 to empower TGF-beta induced metastasis. 240
Epigenomic landscape of human colorectal cancer unveils an aberrant core of pan-cancer enhancers orchestrated by YAP/TAZ 240
Broadly Applicable Hydrogel Fabrication Procedures Guided by YAP/TAZ-Activity Reveal Stiffness, Adhesiveness, and Nuclear Projected Area as Checkpoints for Mechanosensing 240
Fat facets deubiquitylation of Medea/Smad4 modulates interpretation of a Dpp morphogen gradient. 236
De novo generation of somatic stem cells by YAP/TAZ 234
Phosphatidic Acid Enters into the YAP/TAZ Arena 231
YAP and TAZ: a signalling hub of the tumour microenvironment 228
Role of TAZ as mediator of Wnt signaling 225
YAP/TAZ Incorporation in the β-Catenin Destruction Complex Orchestrates the Wnt Response 223
Microtubule architecture connects AMOT stability to YAP/TAZ mechanotransduction and Hippo signalling 220
BMP signaling controls muscle mass. 217
A mutually stimulating loop involving emx2 and canonical wnt signalling specifically promotes expansion of occipital cortex and hippocampus. 215
Single cell-derived spheroids capture the self-renewing subpopulations of metastatic ovarian cancer 211
TGF-beta signaling: Quantitative cues, qualitative outputs 208
Mechanisms of YAP/TAZ transcriptional control 208
GSK3 Inhibits Macropinocytosis and Lysosomal Activity through the Wnt Destruction Complex Machinery 207
MicroRNA control of signal transduction 206
LifeTime and improving European healthcare through cell-based interceptive medicine 205
A YAP/TAZ-TEAD signalling module links endothelial nutrient acquisition to angiogenic growth 202
Transduction of mechanical and cytoskeletal cues by YAP and TAZ. 190
beta-catenin controls differentiation of the retinal pigment epithelium in the mouse optic cup by regulating Mitf and Otx2 expression 190
BMP-binding modules in chordin: a model for signalling regulation in the extracellular space 189
Activation of beta-catenin signaling programs embryonic epidermis to hair follicle fate 188
Links between tumor suppressors: p53 is required for TGF-beta gene responses by cooperating with Smads 188
Transcriptional activation of the a1(VI) collagen gene during myoblast differentiation is mediated by multiple GA boxes. 185
Frzb-1 is a secreted antagonist of Wnt signaling expressed in the Spemann Organizer. 184
Beta-catenin is required for endothelial-mesenchymal transformation during heart cushion development in the mouse 181
Murine alpha1(VI) collagen chain. Complete amino acid sequence and identification of the gene promoter region. 179
Mechanosignaling in vertebrate development 177
EMID2 is a novel biotherapeutic for aggressive cancers identified by in vivo screening 176
ATR is essential for preservation of cell mechanics and nuclear integrity during interstitial migration 174
Cooperating pre-T-cell receptor and TCF-1-dependent signals ensure thymocyte survival. 173
The biology of YAP/TAZ: hippo signaling and beyond. 173
Dorsoventral patterning in Xenopus: inhibition of ventral signals by direct binding of chordin to BMP-4. 170
Cerberus-like is a secreted BMP and nodal antagonist not essential for mouse development 169
Combining spatial transcriptomics and ECM imaging in 3D for mapping cellular interactions in the tumor microenvironment 168
The head inducer Cerberus is a multifunctional antagonist of Nodal, BMP and Wnt signals 168
Discovery of YAP1/TAZ pathway inhibitors through phenotypic screening with potent anti-tumor activity via blockade of Rho-GTPase signaling 168
Tissue-specific expression of promoter regions of the alpha1(VI) collagen gene in cell cultures and transgenic mice. 165
miRNAs and morphogen gradients. 162
Identification of a recognition element for CAAT-enhancer binding proteins (C/EBPs) in the elastin promoter. 159
LIF-ting Hippo averts metastasis 158
BTG2 loss and miR-21 upregulation contribute to prostate cell transformation by inducing luminal markers expression and epithelial–mesenchymal transition 157
Embracing mechanical forces in cell biology. 156
Glycogen synthase kinase-3beta haploinsufficiency mimics the behavioral and molecular effects of lithium 154
TGF-beta modulators and use thereof 153
Gene expression profiling in a retrospective real-world cohort of breast cancer brain metastases and paired primary tumors identifies biological changes with potential therapeutic implications 151
Identification of new p63 targets in human keratinocytes. 150
A PIK3CA-mutant breast cancer metastatic patient-derived organoid approach to evaluate alpelisib treatment for multiple secondary lesions 149
The Role of ECM Stiffness in the Mammary Gland Tumorigenesis 146
Totale 25.374
Categoria #
all - tutte 79.217
article - articoli 76.490
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 636
patent - brevetti 758
selected - selezionate 0
volume - volumi 936
Totale 158.037


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.139 0 0 0 86 81 99 109 168 78 23 226 269
2022/20231.253 228 130 26 162 164 173 4 120 158 17 58 13
2023/2024662 28 108 92 52 54 59 59 38 17 18 88 49
2024/20252.878 16 175 120 75 369 82 146 279 221 100 551 744
2025/202613.872 655 903 1.593 2.104 1.325 719 2.073 1.084 1.367 851 647 551
2026/20272.296 430 841 628 397 0 0 0 0 0 0 0 0
Totale 28.388