IRIS
DI GIORGIO, Eros
 Distribuzione geografica
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Continente #
NA - Nord America 3.150
AS - Asia 1.506
EU - Europa 920
SA - Sud America 244
AF - Africa 26
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 5.849
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Nazione #
US - Stati Uniti d'America 3.086
SG - Singapore 714
IT - Italia 307
CN - Cina 274
BR - Brasile 193
HK - Hong Kong 148
VN - Vietnam 144
DE - Germania 104
UA - Ucraina 85
RU - Federazione Russa 67
FR - Francia 59
GB - Regno Unito 57
FI - Finlandia 55
JP - Giappone 50
IE - Irlanda 37
CA - Canada 36
SE - Svezia 36
TR - Turchia 35
IN - India 34
NL - Olanda 22
KR - Corea 19
AT - Austria 16
BD - Bangladesh 15
CZ - Repubblica Ceca 15
MX - Messico 15
AR - Argentina 14
BE - Belgio 13
ES - Italia 11
PK - Pakistan 11
ZA - Sudafrica 11
IR - Iran 9
EC - Ecuador 8
PL - Polonia 8
UZ - Uzbekistan 8
VE - Venezuela 7
CH - Svizzera 6
CO - Colombia 6
ID - Indonesia 5
KG - Kirghizistan 5
DZ - Algeria 4
KE - Kenya 4
LT - Lituania 4
PE - Perù 4
PH - Filippine 4
UY - Uruguay 4
CL - Cile 3
EG - Egitto 3
IQ - Iraq 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
HN - Honduras 2
IL - Israele 2
JM - Giamaica 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
MY - Malesia 2
PT - Portogallo 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
GY - Guiana 1
HR - Croazia 1
HU - Ungheria 1
IS - Islanda 1
KW - Kuwait 1
NO - Norvegia 1
OM - Oman 1
QA - Qatar 1
SK - Slovacchia (Repubblica Slovacca) 1
TL - Timor Orientale 1
TW - Taiwan 1
Totale 5.849
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Città #
Singapore 356
Ashburn 291
Woodbridge 222
Chandler 206
Fairfield 180
Ann Arbor 146
Hong Kong 143
Houston 140
San Jose 127
Council Bluffs 120
Beijing 118
Dallas 91
Seattle 91
Wilmington 89
Los Angeles 86
Cambridge 70
Udine 68
Chicago 66
Boardman 58
Dearborn 49
Jacksonville 47
Lauterbourg 44
Salt Lake City 41
New York 39
Dong Ket 37
Ho Chi Minh City 32
Dublin 30
Hanoi 30
Princeton 27
Santa Clara 22
Helsinki 20
São Paulo 20
Buffalo 18
Frankfurt am Main 18
Tokyo 18
Hefei 17
Seoul 17
Munich 15
Nuremberg 15
Izmir 14
Kocaeli 14
Phoenix 14
Tampa 14
The Dalles 14
Baltimore 13
Des Moines 13
Nanjing 13
Orem 13
Redondo Beach 13
Remanzacco 13
Belluno 12
Brussels 12
Falls Church 12
Milan 12
Philadelphia 12
Vienna 12
Brno 11
San Diego 11
Sterling 11
Birmingham 10
Lappeenranta 10
London 10
Miami 10
Redmond 10
Codroipo 9
Elk Grove Village 9
Osaka 9
Toronto 9
Bologna 8
Brasília 8
Chennai 8
Indianapolis 8
Manchester 8
Poplar 8
Tashkent 8
Amsterdam 7
Brooklyn 7
Cincinnati 7
Johannesburg 7
Rockville 7
San Francisco 7
Trieste 7
Warsaw 7
Atlanta 6
Boston 6
Cagliari 6
Denver 6
Detroit 6
Dulles 6
Haiphong 6
Hyderabad 6
Mexico City 6
Mumbai 6
Porto Alegre 6
Rome 6
Vancouver 6
Wuhan 6
Aachen 5
Bishkek 5
Düsseldorf 5
Totale 3.774
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Nome #
Fetal growth at term and placental oxidative stress in a tissue micro-array model: a histological and immunohistochemistry study 346
Super-enhancer landscape rewiring in cancer: The epigenetic control at distal sites 287
The co-existence of transcriptional activator and transcriptional repressor MEF2 complexes influences tumor aggressiveness 246
The control operated by the cell cycle machinery on mef2 stability contributes to the downregulation of cdkn1a and entry into s phase 228
Regulation of class IIa HDAC activities: It is not only matter of subcellular localization 198
Transformation by different oncogenes relies on specific metabolic adaptations 183
MEF2 and the tumorigenic process, hic sunt leones 181
Beside the MEF2 axis: Unconventional functions of HDAC4. 177
Potent and Selective Non-hydroxamate Histone Deacetylase 8 Inhibitors 171
Class IIa HDACs repressive activities on MEF2-depedent transcription are associated with poor prognosis of ER+ breast tumors. 164
Different class IIa HDACs repressive complexes regulate specific epigenetic responses related to cell survival in leiomyosarcoma cells 155
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. 152
METABOLIC ALTERATION AND MITOCHONDRIAL BIOENERGETIC PROFILE IN HDAC4-DRIVEN TUMORIGENESIS 145
The MEF2-HDAC axis controls proliferation of mammary epithelial cells and acini formation in vitro 143
HDAC7-mediated control of tumour microenvironment maintains proliferative and stemness competence of human mammary epithelial cells 141
MEF2 is a converging hub for HDAC4 and PI3K/Akt-induced transformation. 139
GSK3β is a key regulator of the ROS-dependent necrotic death induced by the quinone DMNQ 137
Selective class IIa HDAC inhibitors: myth or reality. 136
Quis custodiet ipsos custodes (Who controls the controllers)? two decades of studies on HDAC9 131
Genetic programs driving oncogenic transformation: Lessons from in vitro models 130
Unscheduled HDAC4 repressive activity in human fibroblasts triggers TP53-dependent senescence and favors cell transformation 128
HDAC4 degradation during senescence unleashes an epigenetic program driven by AP-1/p300 at selected enhancers and super-enhancers 124
Enhancing proteotoxic stress in leiomyosarcoma cells triggers mitochondrial dysfunctions, cell death, and antitumor activity in vivo 123
Inhibiting the coregulator CoREST impairs Foxp3+ Treg function and promotes antitumor immunity 120
A Biological Circuit Involving Mef2c, Mef2d, and Hdac9 Controls the Immunosuppressive Functions of CD4+Foxp3+ T-Regulatory Cells 119
Changes in chromatin accessibility and transcriptional landscape induced by HDAC inhibitors in TP53 mutated patient-derived colon cancer organoids 108
The Histone Code of Senescence 107
A regulative epigenetic circuit supervised by HDAC7 represses IGFBP6 and IGFBP7 expression to sustain mammary stemness 104
Cytoplasmic HDAC4 regulates the membrane repair mechanism in Duchenne muscular dystrophy 104
NRF2 interacts with distal enhancer and inhibits nitric oxide synthase 2 expression in KRAS-driven pancreatic cancer cells 100
Transcription of endogenous retroviruses in senescent cells contributes to the accumulation of double-stranded RNAs that trigger an anti-viral response that reinforces senescence 100
Transcriptomic and genomic studies classify NKL54 as a histone deacetylase inhibitor with indirect influence on MEF2-dependent transcription 100
Dual-targeting peptides@PMO, a mimetic to the pro-apoptotic protein Smac/DIABLO for selective activation of apoptosis in cancer cells 97
Endogenous Retroviruses (ERVs): Does RLR (RIG-I-Like Receptors)-MAVS Pathway Directly Control Senescence and Aging as a Consequence of ERV De-Repression? 90
The central role of creatine and polyamines in fetal growth restriction 90
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
Folding of Class IIa HDAC Derived Peptides into α-helices Upon Binding to Myocyte Enhancer Factor-2 in Complex with DNA 78
Control of nitric oxide synthase 2: Role of NRF2-regulated distal enhancer 78
HDAC4 influences the DNA damage response and counteracts senescence by assembling with HDAC1/HDAC2 to control H2BK120 acetylation and homology-directed repair 78
Suppression of the KRAS-NRF2 axis shifts arginine into the phosphocreatine energy system in pancreatic cancer cells 76
T-regulatory cells require Sin3a for stable expression of Foxp3 73
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) 69
MEF2D sustains activation of effector Foxp3+ Tregs during transplant survival and anticancer immunity 61
Post-transcriptional control of KRAS: functional roles of 5′UTR RNA G-quadruplexes, long noncoding RNA, and hnRNPA1 60
The role of nitric oxide in gemcitabine resistance of pancreatic cancer cells 58
KRAS and NRF2 drive metabolic reprogramming in pancreatic cancer cells: the influence of oxidative and nitrosatice stress 42
Class IIa HDACs forced degradation allows resensitization of oxaliplatin-resistant FBXW7-mutated colorectal cancer 38
RPA hyperphosphorylation hinders the resolution of R-loops and G-quadruplex-associated R-loops during RAS-driven senescence 19
Steroidogenic compensation and lipid deficiency with enhanced NAD+ salvage in small-for-gestational-age placenta 11
Totale 6.033
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Categoria #
all - tutte 20.548
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 20.548
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202167 0 0 0 0 0 0 0 0 0 0 0 67
2021/2022314 28 38 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
2025/20262.401 209 433 286 219 288 152 215 65 151 151 175 57
Totale 6.033