SANTORO, MASSIMO
 Distribuzione geografica
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Continente #
NA - Nord America 6.388
AS - Asia 3.442
EU - Europa 1.679
AF - Africa 771
SA - Sud America 609
Continente sconosciuto - Info sul continente non disponibili 139
OC - Oceania 49
Totale 13.077
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Nazione #
US - Stati Uniti d'America 5.929
SG - Singapore 1.027
CN - Cina 464
IT - Italia 456
VN - Vietnam 439
BR - Brasile 344
HK - Hong Kong 322
BD - Bangladesh 213
FR - Francia 141
IN - India 132
PL - Polonia 108
GB - Regno Unito 77
SE - Svezia 76
FI - Finlandia 74
IQ - Iraq 74
DE - Germania 71
RU - Federazione Russa 70
CA - Canada 61
TR - Turchia 57
JP - Giappone 50
PK - Pakistan 50
MX - Messico 46
NL - Olanda 44
SA - Arabia Saudita 44
EC - Ecuador 41
UA - Ucraina 40
AR - Argentina 39
ZA - Sudafrica 39
CO - Colombia 37
UZ - Uzbekistan 37
ID - Indonesia 35
JM - Giamaica 34
MY - Malesia 31
ET - Etiopia 30
PH - Filippine 29
YT - Mayotte 29
CI - Costa d'Avorio 28
EG - Egitto 28
KE - Kenya 27
KG - Kirghizistan 27
MA - Marocco 27
BE - Belgio 26
ES - Italia 26
IE - Irlanda 26
PR - Porto Rico 26
PT - Portogallo 26
HN - Honduras 25
KZ - Kazakistan 25
PS - Palestinian Territory 25
PY - Paraguay 25
VE - Venezuela 25
CU - Cuba 24
GR - Grecia 24
KR - Corea 24
AE - Emirati Arabi Uniti 23
AO - Angola 23
AT - Austria 23
LA - Repubblica Popolare Democratica del Laos 23
PA - Panama 23
TZ - Tanzania 23
BO - Bolivia 22
CG - Congo 22
CR - Costa Rica 22
GH - Ghana 22
JO - Giordania 22
UY - Uruguay 22
BW - Botswana 21
CZ - Repubblica Ceca 21
DO - Repubblica Dominicana 21
RO - Romania 21
UG - Uganda 21
BA - Bosnia-Erzegovina 20
CL - Cile 20
MD - Moldavia 20
NO - Norvegia 20
RS - Serbia 20
SI - Slovenia 20
TN - Tunisia 20
TW - Taiwan 20
BS - Bahamas 19
CV - Capo Verde 19
CY - Cipro 19
GE - Georgia 19
IS - Islanda 19
MR - Mauritania 19
NP - Nepal 19
RW - Ruanda 19
AL - Albania 18
CD - Congo 18
DJ - Gibuti 18
GT - Guatemala 18
LU - Lussemburgo 18
PE - Perù 18
TH - Thailandia 18
VC - Saint Vincent e Grenadine 18
ZM - Zambia 18
AZ - Azerbaigian 17
BB - Barbados 17
BY - Bielorussia 17
CW - ???statistics.table.value.countryCode.CW??? 17
Totale 12.171
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Città #
Fairfield 813
San Jose 748
Ashburn 674
Singapore 594
Woodbridge 296
Seattle 291
Cambridge 288
Hong Kong 287
Houston 270
Wilmington 261
Chandler 188
Santa Clara 151
Ann Arbor 132
Council Bluffs 128
Beijing 118
Boardman 114
Ho Chi Minh City 113
San Diego 103
Hanoi 93
Lauterbourg 80
Medford 77
Los Angeles 76
Princeton 76
Bytom 62
Des Moines 60
Milan 60
Dong Ket 59
Padova 57
Chicago 55
Helsinki 49
New York 47
São Paulo 42
Rome 40
Baghdad 35
Tashkent 32
Nanjing 31
Buffalo 30
Tokyo 29
The Dalles 27
Abidjan 26
London 25
Orem 25
Havana 23
Guayaquil 22
Kingston 22
Nairobi 22
Vientiane 22
Addis Ababa 21
Bishkek 21
Dallas 21
Dublin 21
Kampala 21
Luanda 21
Amman 20
Panama City 20
Trebaseleghe 20
Gaborone 19
Roxbury 19
Accra 18
Kigali 18
Kingstown 18
Mamoudzou 18
Nassau 18
Nouakchott 18
Padua 18
Warsaw 18
Dar es Salaam 17
Lusaka 17
Munich 17
Naples 17
Phoenix 17
San Juan 17
Vienna 17
Bridgetown 16
Conakry 16
Dakar 16
Djibouti 16
Haiphong 16
Johannesburg 16
Kinshasa 16
Montreal 16
Athens 15
Bologna 15
Castries 15
Guatemala City 15
Kuala Lumpur 15
Montevideo 15
Podgorica 15
San José 15
Willemstad 15
Baku 14
Brooklyn 14
Casablanca 14
Chisinau 14
Dushanbe 14
Praia 14
Reykjavik 14
Riyadh 14
Almaty 13
Brazzaville 13
Totale 7.761
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Nome #
Advantages and challenges of cardiovascular and lymphatic studies in zebrafish research 274
Cancer cell stiffening via CoQ10 and UBIAD1 regulates ECM signaling and ferroptosis in breast cancer 272
LKB1 loss is associated with glutathione deficiency under oxidative stress and sensitivity of cancer cells to cytotoxic drugs and γ-irradiation 267
Efficient clofilium tosylate-mediated rescue of POLG-related disease phenotypes in zebrafish 259
Cancer-Induced Metabolic Rewiring of Tumor Endothelial Cells 238
Aspartate metabolism in endothelial cells activates the mTORC1 pathway to initiate translation during angiogenesis 237
Oxidative pentose phosphate pathway controls vascular mural cell coverage by regulating extracellular matrix composition 236
Photobiomodulation at Multiple Wavelengths Differentially Modulates Oxidative Stress In Vitro and In Vivo 209
UBIAD1 and CoQ10 protect melanoma cells from lipid peroxidation-mediated cell death 202
13C-isotope-based protocol for prenyl lipid metabolic analysis in zebrafish embryos 192
Adaptive redox homeostasis in cutaneous melanoma 185
Aspartate metabolism in endothelial cells activates the mTORC1 pathway to initiate translation during angiogenesis 182
Cilia Control Vascular Mural Cell Recruitment in Vertebrates 181
LPHN2 inhibits vascular permeability by differential control of endothelial cell adhesion 178
CHARACTERIZATION OF VASCULAR MURAL CELLs DURING ZEBRAFISH DEVELOPMENT. 177
Blood flow controls bone vascular function and osteogenesis 175
Ubiad1 Is an Antioxidant Enzyme that Regulates eNOS Activity by CoQ10 Synthesis 175
Role of amino acid metabolism in angiogenesis 170
A mitochondrial contribution to anti-inflammatory shear stress signaling in vascular endothelial cells 169
An exclusive cellular and molecular network governs intestinal smooth muscle cell differentiation in vertebrates 169
Loss of pyruvate kinase M2 limits growth and triggers innate immune signaling in endothelial cells 169
Data on metabolic-dependent antioxidant response in the cardiovascular tissues of living zebrafish under stress conditions 165
Marked decrease in acquired resistance to antiretrovirals in latest years in Italy 164
Time to fight: targeting the circadian clock molecular machinery in cancer therapy 161
A SPLICING VARIANT OF THE RON TRANSCRIPT INDUCES CONSTITUTIVE TYROSINE KINASE ACTIVITY AND INVASIVE PHENOTYPE 157
Analysis of oxidative stress in zebrafish embryos 154
ROS homeostasis and metabolism: a dangerous liason in cancer cells 153
The Dlx5 and Foxg1 transcription factors, linked via miRNA-9 and -200, are required for the development of the olfactory and GnRH system 153
The circadian protein BMAL1 supports endothelial cell cycle during angiogenesis 149
ZebraBeat: a flexible platform for the analysis of the cardiac rate in zebrafish embryos 148
The heme exporter Flvcr1 regulates expansion and differentiation of committed erythroid progenitors by controlling intracellular heme accumulation 147
Antiangiogenic cancer drug using the zebrafish model 146
An α-smooth muscle actin (acta2/αsma) zebrafish transgenic line marking vascular mural cells and visceral smooth muscle cells. 145
Vascular Mural Cells Promote Noradrenergic Differentiation of Embryonic Sympathetic Neurons 144
Evaluation of post-natal angiogenesis in a mouse hind limb ischemia model 143
"Decoding" angiogenesis: New facets controlling endothelial cell behavior 141
MODELING TUMOR ANGIOGENESIS IN ZEBRAFISH 141
Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings 141
The Antioxidant Role of Non-mitochondrial CoQ10: Mystery Solved! 141
Nano-Sampling and Reporter Tools to Study Metabolic Regulation in Zebrafish 140
A transgene-assisted genetic screen identifies essential regulators of vascular development in vertebrate embryos. 139
Knock-down of Cathepsin D in zebrafish fertilized eggs determines congenital myopathy. 139
Rapid high performance liquid chromatography-high resolution mass spectrometry methodology for multiple prenol lipids analysis in zebrafish embryos 138
Exploiting the metabolic vulnerability of circulating tumour cells 137
CONSTITUTIVE ACTIVATION OF THE RON GENE INDUCES INVASIVE GROWTH BUT NOT TRANSFORMATION 136
miR-126 Regulates Angiogenic Signalingand Vascular Integrity. 136
YAP/TAZ-TEAD link angiogenesis to nutrients 134
PPFIA1 drives active α5β1 integrin recycling and controls fibronectin fibrillogenesis and vascular morphogenesis 134
Profiling, bioinformatic and functional data on the developing olfactory/GnRH system reveal cellular and molecular pathways essential for this process and potentially relevant for the Kallmann syndrome. 134
CARD-MEDIATED AUTOINHIBITION OF CIAP1'S E3 LIGASE ACTIVITY SUPPRESSES CELL PROLIFERATION AND MIGRATION 132
“FISHING" FOR ENDOTHELIAL MICRORNA FUNCTIONS AND DYSFUNCTION 131
The origin and mechanisms of smooth muscle cell development in vertebrates 131
The admiR-able advances in cardiovascular biology through the zebrafish model system 130
New models to study vascular mural cell embryonic origin: Implications in vascular diseases 129
Zebrafish as a model to explore cell metabolism. 128
ROS signaling and redox biology in endothelial cells 127
POINT MUTATIONS IN THE TYROSINE KINASE DOMAIN RELEASE THE ONCOGENIC AND METASTATIC POTENTIAL OF THE RON RECEPTOR 125
MiRNAs controlling developmental angiogenesis and vascular maturation in zebrafish 125
Knock-down of cathepsin d affects the retinal pigment epithelium, impairs swim-bladder ontogenesis and causes premature death in zebrafish 125
miRNAs in endothelial cell signaling: The endomiRNAs 124
THE RON ONCOGENIC ACTIVITY INDUCED BY THE MEN2B-LIKE SUBSTITUTION OVERCOMES THE REQUIREMENT FOR THE MULTIFUNCTIONAL DOCKING SITE 124
The glucose-to-acetate metabolic flux that drives endothelial-to-mesenchymal transition via TGF-β signaling 123
Receptor tyrosine kinases as targets for anticancer therapeutics 123
The intersection between metabolism and translation through a subcellular lens 122
Phylogeny informs ontogeny: a proposed common theme in the arterial pole of the vertebrate heart 122
Manipulating Redox signaling to block tumor angiogenesis 119
CELLULAR AND M0LECULAR FACETS OF KERATINOCYTE REEPITHELIZATION DURlNG W0UND HEALING 118
Fashioning blood vessels by ROS signalling and metabolism 117
THE CONSTITUTIVE ACTIVATION OF MET, RON, SEA GENES INDUCES DIFFERENT BIOLOGICAL RESPONSES 117
Tumor Angiogenesis: Fishing for Screening Models 117
RECEPTOR TYROSINE KINASES AS TARGET FOR ANTI-CANCER THERAPY 112
Real-time quantification of subcellular H2O2 and glutathione redox potential in living cardiovascular tissues 111
THE MSP RECEPTOR REGULATES ALPHA6BETA4 AND ALPHA3BETA1 INTEGRINS VIA 14-3-3 PROTEINS IN KERATINOCYTE RE-EPITHELIZATION 104
New findings in growth factor receptors and integrins cross-talk 104
Determination of ubiquinone and related metabolites in zebrafish embryos by LC-HRMS. 104
RON IS A HETERODIMERIC TYROSINE KINASE RECEPTOR ACTIVATED BY THE HGF HOMOLOG MSP 103
Diacylglycerol Kinase-{alpha} Mediates HGF-induced Epithelial Cell Scatter by Regulating Rac Activation and Membrane Ruffling. 100
The endocannabinoid system regulates zebrafish GnRH neuronal development 99
Peripheral Center Sparing Presentation of Schnyder Corneal Dystrophy 97
The crosstalk between metabolism and translation 93
UBIAD1 for cellular coenzyme Q10 synthesis and cardiovascular oxidative protection 93
Before the Pump 93
How to Generate a Vascular-Labelled Transgenic Zebrafish Model to Study Tumor Angiogenesis and Extravasation 88
Birc2/Iap1 regulates endothelial cell integrity and blood vessel homeostasis. 88
Motogenic growth factors: HGF/SF and MSP 88
KNOCK-DOWN OF CATHEPSIN D AFFECTS THE RETINAL PIGMENT EPITHELIUM, IMPAIRS SWIM-BLADDER ONTOGENESIS AND CAUSES TO PRAECOX DEATH IN ZEBRAFISH 87
Ubiad1 is an antioxidant enzyme that regulates eNOS activity 83
IAPs CARRY AN EVOLUTIONARILY CONSERVED UBIQUITIN-BINDING DOMAIN THAT IS INDISPENSABLE FOR NF-KB REGULATION AND CELL SURVIVAL. 83
TRANSGENIC ZEBRAFISH 82
Geldanamycin triggers a novel Ron degradative pathway hampering oncogenic signalling. 82
European Perspectives in Cardiology.Funding: Human Frontier Science Program 81
Protein phosphatase 1 binds to phospho-Ser-1394 of the macrophage- stimulating protein receptor 73
Transsulfuration metabolism is essential for ferroptosis resistance in quiescent endothelial cells 43
null 1
Totale 13.077
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Categoria #
all - tutte 40.863
article - articoli 37.339
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 282
selected - selezionate 0
volume - volumi 1.984
Totale 80.468
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022809 0 0 129 75 48 36 52 121 44 21 75 208
2022/2023462 99 3 0 47 109 63 1 35 77 3 15 10
2023/2024270 12 48 21 34 17 14 16 9 8 2 33 56
2024/20251.543 7 50 35 63 227 40 142 104 139 38 244 454
2025/20267.013 300 565 1.103 1.252 513 293 563 564 820 428 383 229
2026/2027567 290 255 22 0 0 0 0 0 0 0 0 0
Totale 13.077