IRIS
DI GIORGIO, Eros
 Distribuzione geografica
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Continente #
NA - Nord America 3.359
AS - Asia 1.584
EU - Europa 978
SA - Sud America 254
Continente sconosciuto - Info sul continente non disponibili 188
AF - Africa 26
OC - Oceania 2
Totale 6.391
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Nazione #
US - Stati Uniti d'America 3.277
SG - Singapore 718
IT - Italia 354
CN - Cina 283
BR - Brasile 198
HK - Hong Kong 152
VN - Vietnam 146
DE - Germania 106
UA - Ucraina 85
BD - Bangladesh 67
RU - Federazione Russa 67
FR - Francia 60
GB - Regno Unito 59
FI - Finlandia 55
JP - Giappone 50
CA - Canada 43
IE - Irlanda 37
SE - Svezia 36
IN - India 35
TR - Turchia 35
NL - Olanda 24
KR - Corea 20
MX - Messico 17
AT - Austria 16
CZ - Repubblica Ceca 16
AR - Argentina 14
BE - Belgio 14
ES - Italia 11
PK - Pakistan 11
ZA - Sudafrica 11
EC - Ecuador 9
IR - Iran 9
PL - Polonia 8
UZ - Uzbekistan 8
VE - Venezuela 8
CO - Colombia 7
CH - Svizzera 6
ID - Indonesia 6
KG - Kirghizistan 5
PE - Perù 5
PH - Filippine 5
CL - Cile 4
DZ - Algeria 4
IQ - Iraq 4
KE - Kenya 4
LT - Lituania 4
MY - Malesia 4
PT - Portogallo 4
UY - Uruguay 4
CR - Costa Rica 3
EG - Egitto 3
HN - Honduras 3
JM - Giamaica 3
JO - Giordania 3
LV - Lettonia 3
PA - Panama 3
PS - Palestinian Territory 3
PY - Paraguay 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
AM - Armenia 2
AU - Australia 2
AZ - Azerbaigian 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
GR - Grecia 2
IL - Israele 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
PR - Porto Rico 2
SA - Arabia Saudita 2
SI - Slovenia 2
SV - El Salvador 2
AG - Antigua e Barbuda 1
BG - Bulgaria 1
BO - Bolivia 1
DM - Dominica 1
EE - Estonia 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
GP - Guadalupe 1
GY - Guiana 1
HR - Croazia 1
HU - Ungheria 1
IS - Islanda 1
KW - Kuwait 1
NI - Nicaragua 1
NO - Norvegia 1
OM - Oman 1
QA - Qatar 1
SK - Slovacchia (Repubblica Slovacca) 1
TL - Timor Orientale 1
TW - Taiwan 1
Totale 6.204
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Città #
Singapore 359
Ashburn 302
Woodbridge 222
Chandler 206
Fairfield 180
Council Bluffs 151
Hong Kong 147
Ann Arbor 146
San Jose 142
Houston 140
Beijing 120
Dallas 96
Seattle 93
Los Angeles 90
Wilmington 89
Cambridge 70
Chicago 68
Udine 68
Boardman 61
Dearborn 49
New York 49
Jacksonville 47
Lauterbourg 44
Santa Clara 42
Salt Lake City 41
Dong Ket 37
Ho Chi Minh City 32
Hanoi 31
Dublin 30
Princeton 27
Phoenix 23
Helsinki 20
São Paulo 20
Buffalo 19
Milan 19
Frankfurt am Main 18
Tokyo 18
Hefei 17
Seoul 17
Munich 15
Nuremberg 15
Izmir 14
Kocaeli 14
Tampa 14
The Dalles 14
Baltimore 13
Des Moines 13
Nanjing 13
Orem 13
Philadelphia 13
Redondo Beach 13
Remanzacco 13
Belluno 12
Brussels 12
Falls Church 12
San Diego 12
Vienna 12
Brno 11
Rome 11
Sterling 11
Birmingham 10
Lappeenranta 10
London 10
Miami 10
Redmond 10
Atlanta 9
Brasília 9
Brooklyn 9
Codroipo 9
Elk Grove Village 9
Osaka 9
Toronto 9
Bologna 8
Chennai 8
Denver 8
Indianapolis 8
Manchester 8
Poplar 8
Tashkent 8
Amsterdam 7
Cincinnati 7
Johannesburg 7
Mexico City 7
Rockville 7
San Francisco 7
Trieste 7
Warsaw 7
Boston 6
Cagliari 6
Detroit 6
Dulles 6
Haiphong 6
Hyderabad 6
Montreal 6
Mumbai 6
Porto Alegre 6
Sacramento 6
Vancouver 6
Wuhan 6
Aachen 5
Totale 3.922
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Nome #
Fetal growth at term and placental oxidative stress in a tissue micro-array model: a histological and immunohistochemistry study 347
Super-enhancer landscape rewiring in cancer: The epigenetic control at distal sites 290
The co-existence of transcriptional activator and transcriptional repressor MEF2 complexes influences tumor aggressiveness 254
The control operated by the cell cycle machinery on mef2 stability contributes to the downregulation of cdkn1a and entry into s phase 233
Regulation of class IIa HDAC activities: It is not only matter of subcellular localization 207
Transformation by different oncogenes relies on specific metabolic adaptations 188
MEF2 and the tumorigenic process, hic sunt leones 185
Beside the MEF2 axis: Unconventional functions of HDAC4. 181
Potent and Selective Non-hydroxamate Histone Deacetylase 8 Inhibitors 174
Class IIa HDACs repressive activities on MEF2-depedent transcription are associated with poor prognosis of ER+ breast tumors. 168
THE REPRESSION OF MEF2 TRANSCRIPTION FACTORS EXERTED BY CLASS IIA HDACS AND THEIR DEGRADATION STIMULATED BY CDK4 DETERMINE THE ACQUISITION OF HALLMARKS OF TRANSFORMATION IN FIBROBLASTS. 166
Different class IIa HDACs repressive complexes regulate specific epigenetic responses related to cell survival in leiomyosarcoma cells 161
METABOLIC ALTERATION AND MITOCHONDRIAL BIOENERGETIC PROFILE IN HDAC4-DRIVEN TUMORIGENESIS 153
The MEF2-HDAC axis controls proliferation of mammary epithelial cells and acini formation in vitro 150
A Biological Circuit Involving Mef2c, Mef2d, and Hdac9 Controls the Immunosuppressive Functions of CD4+Foxp3+ T-Regulatory Cells 146
MEF2 is a converging hub for HDAC4 and PI3K/Akt-induced transformation. 142
HDAC7-mediated control of tumour microenvironment maintains proliferative and stemness competence of human mammary epithelial cells 142
Selective class IIa HDAC inhibitors: myth or reality. 141
GSK3β is a key regulator of the ROS-dependent necrotic death induced by the quinone DMNQ 140
Quis custodiet ipsos custodes (Who controls the controllers)? two decades of studies on HDAC9 138
Genetic programs driving oncogenic transformation: Lessons from in vitro models 130
Inhibiting the coregulator CoREST impairs Foxp3+ Treg function and promotes antitumor immunity 130
Unscheduled HDAC4 repressive activity in human fibroblasts triggers TP53-dependent senescence and favors cell transformation 129
Post-transcriptional control of KRAS: functional roles of 5′UTR RNA G-quadruplexes, long noncoding RNA, and hnRNPA1 128
HDAC4 degradation during senescence unleashes an epigenetic program driven by AP-1/p300 at selected enhancers and super-enhancers 126
Enhancing proteotoxic stress in leiomyosarcoma cells triggers mitochondrial dysfunctions, cell death, and antitumor activity in vivo 125
NRF2 interacts with distal enhancer and inhibits nitric oxide synthase 2 expression in KRAS-driven pancreatic cancer cells 115
Changes in chromatin accessibility and transcriptional landscape induced by HDAC inhibitors in TP53 mutated patient-derived colon cancer organoids 110
The Histone Code of Senescence 109
Transcription of endogenous retroviruses in senescent cells contributes to the accumulation of double-stranded RNAs that trigger an anti-viral response that reinforces senescence 108
A regulative epigenetic circuit supervised by HDAC7 represses IGFBP6 and IGFBP7 expression to sustain mammary stemness 107
Cytoplasmic HDAC4 regulates the membrane repair mechanism in Duchenne muscular dystrophy 105
Transcriptomic and genomic studies classify NKL54 as a histone deacetylase inhibitor with indirect influence on MEF2-dependent transcription 104
Dual-targeting peptides@PMO, a mimetic to the pro-apoptotic protein Smac/DIABLO for selective activation of apoptosis in cancer cells 102
The central role of creatine and polyamines in fetal growth restriction 97
Endogenous Retroviruses (ERVs): Does RLR (RIG-I-Like Receptors)-MAVS Pathway Directly Control Senescence and Aging as a Consequence of ERV De-Repression? 95
Photosensitization of pancreatic cancer cells by cationic alkyl-porphyrins in free form or engrafted into POPC liposomes: The relationship between delivery mode and mechanism of cell death 88
Suppression of the KRAS-NRF2 axis shifts arginine into the phosphocreatine energy system in pancreatic cancer cells 85
Folding of Class IIa HDAC Derived Peptides into α-helices Upon Binding to Myocyte Enhancer Factor-2 in Complex with DNA 82
Control of nitric oxide synthase 2: Role of NRF2-regulated distal enhancer 82
HDAC4 influences the DNA damage response and counteracts senescence by assembling with HDAC1/HDAC2 to control H2BK120 acetylation and homology-directed repair 80
T-regulatory cells require Sin3a for stable expression of Foxp3 77
Correction: KRAS and NRF2 drive metabolic reprogramming in pancreatic cancer cells: the influence of oxidative and nitrosative stress (Frontiers in Cell and Developmental Biology, (2025), 13, (1547582), 10.3389/fcell.2025.1547582) 74
MEF2D sustains activation of effector Foxp3+ Tregs during transplant survival and anticancer immunity 62
The role of nitric oxide in gemcitabine resistance of pancreatic cancer cells 59
KRAS and NRF2 drive metabolic reprogramming in pancreatic cancer cells: the influence of oxidative and nitrosatice stress 46
Class IIa HDACs forced degradation allows resensitization of oxaliplatin-resistant FBXW7-mutated colorectal cancer 44
Experimental strategies for evaluating the impact of HDACs and HDAC inhibitors on the epigenome. ChiP-seq 34
RPA hyperphosphorylation hinders the resolution of R-loops and G-quadruplex-associated R-loops during RAS-driven senescence 33
Steroidogenic compensation and lipid deficiency with enhanced NAD+ salvage in small-for-gestational-age placenta 19
Totale 6.391
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Categoria #
all - tutte 22.574
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 22.574
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022248 0 0 8 22 10 16 27 5 28 42 58 32
2022/2023447 36 46 10 63 38 89 3 30 46 8 31 47
2023/2024379 53 24 37 15 47 25 32 53 16 19 19 39
2024/20251.001 36 50 60 52 57 59 77 72 137 76 153 172
2025/20262.512 209 433 286 219 288 152 215 65 151 151 175 168
2026/2027247 76 102 69 0 0 0 0 0 0 0 0 0
Totale 6.391