IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

RECALCATI, STEFANIA
 Distribuzione geografica
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Continente #
EU - Europa 5.656
NA - Nord America 5.530
AS - Asia 4.950
Continente sconosciuto - Info sul continente non disponibili 751
SA - Sud America 486
AF - Africa 96
OC - Oceania 38
Totale 17.507
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Nazione #
US - Stati Uniti d'America 5.334
GB - Regno Unito 2.202
CN - Cina 1.602
SG - Singapore 1.321
IT - Italia 1.175
HK - Hong Kong 533
DE - Germania 471
SE - Svezia 439
BD - Bangladesh 437
BR - Brasile 370
RU - Federazione Russa 343
VN - Vietnam 247
FR - Francia 237
TR - Turchia 178
IN - India 151
NL - Olanda 145
CA - Canada 125
FI - Finlandia 124
IE - Irlanda 121
JP - Giappone 112
UA - Ucraina 110
KR - Corea 101
DK - Danimarca 85
ID - Indonesia 66
EU - Europa 43
CO - Colombia 38
AU - Australia 36
AR - Argentina 27
PH - Filippine 27
BE - Belgio 25
CI - Costa d'Avorio 24
MX - Messico 24
CH - Svizzera 22
GR - Grecia 22
IQ - Iraq 21
PT - Portogallo 21
ES - Italia 20
TW - Taiwan 19
AT - Austria 18
TH - Thailandia 18
PK - Pakistan 15
EC - Ecuador 14
VE - Venezuela 13
ZA - Sudafrica 13
MA - Marocco 12
UZ - Uzbekistan 12
PL - Polonia 11
IR - Iran 10
NO - Norvegia 10
NP - Nepal 10
RO - Romania 10
CL - Cile 9
EG - Egitto 9
JM - Giamaica 9
SA - Arabia Saudita 9
AZ - Azerbaigian 7
PE - Perù 7
CR - Costa Rica 6
GT - Guatemala 6
KE - Kenya 6
MY - Malesia 6
TN - Tunisia 6
AE - Emirati Arabi Uniti 5
BG - Bulgaria 5
CZ - Repubblica Ceca 5
DO - Repubblica Dominicana 5
EE - Estonia 5
GE - Georgia 5
HN - Honduras 5
IL - Israele 5
JO - Giordania 5
LB - Libano 4
LU - Lussemburgo 4
NG - Nigeria 4
PA - Panama 4
QA - Qatar 4
SI - Slovenia 4
SK - Slovacchia (Repubblica Slovacca) 4
SN - Senegal 4
UY - Uruguay 4
AL - Albania 3
CG - Congo 3
HU - Ungheria 3
LK - Sri Lanka 3
LT - Lituania 3
NI - Nicaragua 3
PR - Porto Rico 3
PY - Paraguay 3
SC - Seychelles 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
BS - Bahamas 2
DZ - Algeria 2
ET - Etiopia 2
GH - Ghana 2
HR - Croazia 2
LA - Repubblica Popolare Democratica del Laos 2
MK - Macedonia 2
MM - Myanmar 2
MO - Macao, regione amministrativa speciale della Cina 2
Totale 16.774
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Città #
Southend 2.040
Singapore 739
Ashburn 531
Hong Kong 488
Milan 459
Chandler 402
San Jose 310
Beijing 288
Seattle 257
Council Bluffs 244
Santa Clara 197
Fairfield 181
Wilmington 178
Princeton 155
Los Angeles 141
Ann Arbor 140
Dallas 140
Houston 134
Dearborn 131
Dublin 121
Frankfurt am Main 110
Woodbridge 106
New York 102
Nanjing 97
Lauterbourg 75
Boardman 72
Ho Chi Minh City 71
Shanghai 70
Buffalo 67
Guangzhou 67
Bengaluru 65
Toronto 65
Cambridge 63
Jacksonville 60
Redmond 59
Moscow 57
Grafing 56
Istanbul 54
Tokyo 53
Jinan 50
Andover 49
Des Moines 49
Hanoi 49
Jakarta 49
Mountain View 49
Phoenix 49
Munich 48
Helsinki 47
Hefei 44
Rome 43
São Paulo 41
Changsha 40
Shenyang 38
Redwood City 36
Tianjin 36
Somerville 34
Hangzhou 33
Naples 30
Bogotá 29
Sakarya 29
Serra 27
The Dalles 26
Abidjan 24
Cangzhou 24
Sunnyvale 23
Zhengzhou 23
Brussels 22
Hanover 22
Hebei 22
Eitensheim 21
Nanchang 21
Turin 21
Athens 20
Columbus 20
San Diego 20
Atlanta 19
Florence 19
Fuzhou 19
Xian 19
Berlin 18
Chicago 18
Liberty 18
Shenzhen 18
Ningbo 17
Amsterdam 16
London 16
Orem 16
Rio de Janeiro 16
Wuhan 16
Fremont 15
Jiaxing 15
Brasília 14
Como 14
Silver Spring 14
Nuremberg 13
Seoul 13
Sydney 13
Bologna 12
Brescia 12
Odernheim 12
Totale 10.245
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Nome #
Macrophages : central regulators of iron balance 663
Macrophage ferroportin is essential for stromal cell proliferation in wound healing 467
DIETARY IRON OVERLOAD INDUCES VISCERAL ADIPOSE TISSUE INSULIN RESISTANCE: SYNERGY WITH OBESITY IN INDUCING SYSTEMIC INSULIN RESISTANCE 373
Iron metabolism in liver cancer stem cells 363
Macrophage preconditioning with synthetic malaria pigment reduces cytokine production via heme iron-dependent oxidative stress 342
High fat diet subverts hepatocellular iron uptake determining dysmetabolic iron overload 327
Induction of erythroferrone in healthy humans by micro-dose recombinant erythropoietin or high-altitude exposure 316
The protease-inhibitor SerpinB3 as a critical modulator of the stem-like subset in human cholangiocarcinoma 315
DIETARY IRON OVERLOAD INDUCES VISCERAL ADIPOSE TISSUE INSULIN RESISTANCE ASSOCIATED WITH HYPER-RESISTINEMIA, AND SYNERGIZES WITH OBESITY IN INDUCING SYSTEMIC INSULIN RESISTANCE 302
Iron-induced damage in cardiomyopathy: oxidative-dependent and independent mechanisms 298
Caco2/HT-29 In Vitro Cell Co-Culture: Barrier Integrity, Permeability, and Tight Junctions’ Composition During Progressive Passages of Parental Cells 297
Erythropoietin’s inhibiting impact on hepcidin expression occurs indirectly 295
Experimental models to unravel the molecular pathogenesis, cell of origin and stem cell properties of cholangiocarcinoma 293
Dysregulation of Iron Metabolism in Cholangiocarcinoma Stem-like Cells 289
Ironing out Macrophage Immunometabolism 284
Dietary iron overload induces visceral adipose tissue insulin resistance and hyper-resistinemia, and synergizes with obesity and fatty liver in inducing systemic insulin resistance 274
Dual Role of ROS as Signal and Stress Agents : Iron Tips the Balance in favor of Toxic Effects 265
The role of iron in anthracycline cardiotoxicity 264
Kupffer cells and macrophages are not required for hepatic hepcidin activation during iron overload 258
Dietary iron overload induces visceral adipose tissue insulin resistance 257
Dysregulation of iron metabolism in cancer stem cells 257
Molecular regulation of cellular iron balance 252
Role of HIF-1 and NF-kappaB transcription factors in the modulation of transferrin receptor by inflammatory and anti-inflammatory signals 251
Mediterranean spotted fever and hearing impairment : a rare complication 242
Transcriptional modulation of transferrin receptor expression by inflammatory and anti-inflammatory signals in macrophages: role of HIF-1 and NF-kB 241
Dietary iron overload induces visceral adipose tissue insulin resistance associated with hyper-resistinemia, and synergizes with obesity and fatty liver in inducing systemic insulin resistance 240
Multifaceted Aspects of Metabolic Plasticity in Human Cholangiocarcinoma : An Overview of Current Perspectives 236
Reactive oxygen species-independent apoptosis in doxorubicin-treated H9c2 cardiomyocytes : role for heme oxygenase-1 down-modulation 234
The transferrin receptor : the cellular iron gate 230
Iron regulatory proteins 1 and 2 in human monocytes, macrophages and duodenum : expression and regulation in hereditary hemochromatosis and iron deficiency 224
Doxorubicin cardiotoxicity and the control of iron metabolism: quinone-dependent and independent mechanisms 220
Iron availability in tissue microenvironmen t: The key role of ferroportin 216
Macrophages and iron : A special relationship 211
Alterations of systemic and muscle iron metabolism in human subjects treated with low-dose recombinant erythropoietin 208
Hacat cells as a 2d experimental differentiating model to analyze the early biological effects induced by a psoriatic proinflammatory microenvironment: cell proliferation, differentiation and ferroptosis 207
Oxidative stress-mediated down-regulation of rat hydroxyacid oxidase 1, a liver-specific peroxisomal enzyme 204
Role of hypoxia-inducible factors in the dexrazoxane-mediated protection of cardiomyocytes from doxorubicin-induced toxicity 202
Loss of the von Hippel Lindau tumor suppressor disrupts iron homeostasis in renal carcinoma cells 200
Differential regulation of iron homeostasis during human macrophage polarized activation 198
Iron levels in polarized macrophages: regulation of immunity and autoimmunity 197
Alterations of systemic and muscle iron metabolism in human subjects treated with low dose recombinant erythropoietin 196
Unconventional endocytosis and trafficking of transferrin receptor induced by iron 196
New perspectives on the molecular basis of the interaction between oxygen homeostasis and iron metabolism 193
New functions for an iron storage protein : the role of ferritin in immunity and autoimmunity 188
Recent advances in iron metabolism : relevance for health, exercise, and performance 188
Inappropriately high iron regulatory protein activity in monocytes of patients with genetic hemochromatosis 185
Induction of ferritin synthesis in ischemic-reperfused rat liver: analysis of the molecular mechanisms 184
Patologia 183
Nitric oxide and peroxynitrite activate the iron regulatory protein-1 of J774A.1 macrophages by direct disassembly of the Fe-S cluster of cytoplasmic aconitase 183
Iron trafficking and metabolism in macrophages: contribution to the polarized phenotype 180
Mice lacking mitochondrial ferritin are more sensitive to doxorubicin-mediated cardiotoxicity 175
Effect of reactive oxigen species on Iron Regulatory Protein activity 174
Localizzazione e regolazione dell'enzima epato-specifico Hydrocyacid Oxidase 1 173
Iron Mining for Erythropoiesis 171
The Emerging Role of Tumor Microenvironmental Stimuli in Regulating Metabolic Rewiring of Liver Cancer Stem Cells 168
Expression of genes of iron metabolism in human macrophage differentiation and polarized activation processes 167
Response of monocyte iron regulatory protein activity to inflammation: abnormal behavior in genetic hemochromatosis 165
Iron Absorption: Molecular and Pathophysiological Aspects 164
Iron-regulatory proteins : molecular biology and pathophysiological implications 163
Nitric oxide-mediated induction of ferritin synthesis in J774 macrophages by inflammatory cytokines: role of selective iron regulatory protein-2 downregulation 161
A precious metal: iron, an essential nutrient for all cells 156
Iron regulatory proteins : from molecular mechanisms to drug development 156
Iron trapping in macrophages reshapes the homeostasis of the haematopoietic system 155
Excessive Erythrocytosis Is Not Associated With Altered Iron Homeostasis in Men From the World's Highest City 154
Preferential activation of iron regulatory protein-2 in cell lines as a result of higher sensitivity to iron 152
Mice lacking mitochondrial ferritin are more sensitive to doxorubicin-mediated cardiotoxicity 152
Diacerhein blocks Iron Regulatory Protein activation in inflammed human monocytes. 150
Role of hepcidin in the interplay between body iron metabolism and erythropoiesis 149
Liver iron modulates hepcidin expression during chronically elevated erythropoiesis in mice 147
An introduction to the metabolic determinants of anthracycline cardiotoxicity 146
The iron regulatory proteins: targets and modulators of free radical reactions and oxidative damage 146
Lack of macrophage ferroportin affects wound healing 139
The secondary alcohol metabolite of doxorubicin irreversibly inactivates aconitase/iron regulatory protein-1 in cytosolic fractions from human myocardium 136
Hepcidin as possible new indirect biomarker for blood doping : a commentary = Epcidina come possibile nuovo biomarcatore indiretto per doping ematico : commento 135
Peroxisomal targeting of mammalian hydroxyacid oxidase 1 requires the carboxy-terminal tripeptide SKI 134
Serum hepcidin levels and muscle iron proteins in humans injected with low- or high-dose erythropoietin 134
Reduced serum ceruloplasmin levels in hereditary haemochromatosis 132
Systemic and cellular consequences of macrophage control of iron metabolism 121
Editorial: Iron Metabolism at the Crossroad of Innate Immune Response and Cancer Progression 100
A proinflammatory psoriatic microenvironment has early effects on keratinocyte proliferation/differentiation and induces ferroptosis in HaCaT cells 99
The IRONic face of EMT in pancreatic ductal adenocarcinoma: preliminary results from IRONy study 99
The Interplay Between Bone Biology and Iron Metabolism: Molecular Mechanisms and Clinical Implications 46
Totale 17.507
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Categoria #
all - tutte 44.597
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 44.597
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.275 0 0 110 142 112 137 112 62 151 97 122 230
2022/20231.196 137 127 97 160 136 215 50 56 131 7 51 29
2023/2024751 21 90 46 43 151 52 31 53 22 59 81 102
2024/20252.275 98 224 66 207 164 89 145 242 109 188 205 538
2025/20265.029 417 271 418 372 449 285 616 242 527 400 537 495
2026/2027686 304 360 22 0 0 0 0 0 0 0 0 0
Totale 17.507