IRIS
CAMPANELLA, ALESSANDRO
 Distribuzione geografica
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Continente #
EU - Europa 1.090
AS - Asia 952
NA - Nord America 743
SA - Sud America 203
AF - Africa 27
OC - Oceania 2
Totale 3.017
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Nazione #
RU - Federazione Russa 708
US - Stati Uniti d'America 687
SG - Singapore 358
CN - Cina 312
BR - Brasile 171
SE - Svezia 107
VN - Vietnam 97
HK - Hong Kong 83
IT - Italia 63
DE - Germania 50
FR - Francia 50
GB - Regno Unito 35
IN - India 33
CA - Canada 31
FI - Finlandia 17
MX - Messico 17
PL - Polonia 13
JP - Giappone 11
ZA - Sudafrica 11
AT - Austria 10
AR - Argentina 8
ES - Italia 8
TR - Turchia 8
BD - Bangladesh 7
PK - Pakistan 7
CO - Colombia 6
EC - Ecuador 6
IQ - Iraq 6
UA - Ucraina 6
IE - Irlanda 5
KZ - Kazakistan 5
MA - Marocco 5
NL - Olanda 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
LT - Lituania 4
UY - Uruguay 4
CL - Cile 3
GR - Grecia 3
ID - Indonesia 3
JM - Giamaica 3
KE - Kenya 3
VE - Venezuela 3
AZ - Azerbaigian 2
PY - Paraguay 2
SN - Senegal 2
TN - Tunisia 2
TW - Taiwan 2
AL - Albania 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BS - Bahamas 1
CR - Costa Rica 1
CY - Cipro 1
DO - Repubblica Dominicana 1
EE - Estonia 1
EG - Egitto 1
ET - Etiopia 1
GA - Gabon 1
HN - Honduras 1
HU - Ungheria 1
IS - Islanda 1
JO - Giordania 1
KG - Kirghizistan 1
KR - Corea 1
ML - Mali 1
MY - Malesia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PA - Panama 1
PH - Filippine 1
PT - Portogallo 1
SA - Arabia Saudita 1
SY - Repubblica araba siriana 1
Totale 3.017
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Città #
Singapore 182
Moscow 143
Ashburn 97
San Jose 87
Hong Kong 83
Dallas 77
Shanghai 65
New York 53
Beijing 52
Hefei 41
Lauterbourg 37
Los Angeles 36
Ho Chi Minh City 30
Lawrence 29
Princeton 29
Boardman 28
Milan 27
Hanoi 23
Orem 16
São Paulo 15
Montreal 13
Chennai 12
Helsinki 12
Warsaw 11
Denver 10
Nuremberg 10
Tokyo 10
Frankfurt am Main 9
Manchester 9
Rio de Janeiro 9
Munich 8
Santa Clara 8
Toronto 8
Brooklyn 7
Houston 7
London 7
Pune 7
Stockholm 7
Atlanta 6
Falkenstein 6
Johannesburg 6
Phoenix 6
Poplar 6
The Dalles 6
Amsterdam 5
Boston 5
Council Bluffs 5
Mexico City 5
Turku 5
Almaty 4
Calgary 4
Chicago 4
Da Nang 4
Guangzhou 4
Jacksonville 4
New Delhi 4
Novara 4
Querétaro 4
Rome 4
San Francisco 4
Tashkent 4
Vienna 4
Ankara 3
Campinas 3
City of London 3
Dublin 3
Goiânia 3
Hangzhou 3
Istanbul 3
Jiaxing 3
Karachi 3
Kingston 3
Montevideo 3
Mumbai 3
Nairobi 3
Paris 3
Querétaro City 3
Seattle 3
Senador Canedo 3
Thái Nguyên 3
Vĩnh Tường 3
Abu Dhabi 2
Baghdad 2
Barueri 2
Bergamo 2
Betim 2
Bexley 2
Casablanca 2
Cesano Boscone 2
Ciudad del Este 2
Columbus 2
Cotia 2
Cuenca 2
Curitiba 2
Dakar 2
Fortaleza 2
Gorle 2
Grand Rapids 2
Guarulhos 2
Guayaquil 2
Totale 1.522
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Nome #
Iron uptake in quiescent and inflammation-activated astrocytes: a potentially neuroprotective control of iron burden 108
Iron Induces Cell Death and Strengthens the Efficacy of Antiandrogen Therapy in Prostate Cancer Models 108
Additional booster doses in patients with chronic lymphocytic leukemia induce humoral and cellular immune responses to SARS-CoV-2 similar to natural infection regardless ongoing treatments: A study by ERIC, the European Research Initiative on CLL 106
Bone marrow Tfr2 deletion improves the therapeutic efficacy of the activin-receptor ligand trap RAP-536 in β-thalassemic mice 103
Supplementary Data from Iron Induces Cell Death and Strengthens the Efficacy of Antiandrogen Therapy in Prostate Cancer Models 101
C29G in the iron-responsive element of L-ferritin: a new mutation associated with hyperferritinemia-cataract 100
Ceruloplasmin Oxidation, a Feature of Parkinson's Disease CSF, Inhibits Ferroxidase Activity and Promotes Cellular Iron Retention 100
Iron increases the susceptibility of multiple myeloma cells to bortezomib 95
IκBε deficiency accelerates disease development in chronic lymphocytic leukemia 93
A new G51C mutation in the IRE of L-ferritin in hyperferritinemia cataract syndrome decreases the binding affinity of the mutant IRE to IRP. 91
CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL 90
A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteins 88
Human mitochondrial ferritin expressed in HeLa cells incorporates iron and affects cellular iron metabolism 87
Iron regulatory proteins 1 and 2 in human monocytes, macrophages and duodenum: expression and regulation in hereditary hemochromatosis and iron deficiency 84
Identification of TMPRSS6 cleavage sites of hemojuvelin 81
A new mutation in the IRE of L-ferritin (G51C) associated with hyperferritinemia-cataract syndrome decreases the binding affinity of IRE to IRPS 81
Erythroblast apoptosis and microenvironmental iron restriction trigger anemia in the VK*MYC model of multiple myeloma 81
Induction of iron excess restricts malignant plasma cells expansion and potentiates bortezomib effect in models of multiple myeloma 79
Iron causes lipid oxidation and inhibits proteasome function in multiple myeloma cells: A proof of concept for novel combination therapies 78
Blotting Analysis of Native IRP1: A Novel Approach to Distinguish the Different Forms of IRP1 in Cells and Tissues 77
IRON UPTAKE IN RESTING AND REACTIVE ASTROCYTES: A POTENTIALLY NEUROPROTECTIVE CONTROL OF IRON BURDEN 77
CHARACTERIZATION OF THE L-FERRITIN VARIANT 460INSA RESPONSIBLE OF A HEREDITARY FERRITINOPATHY DISORDER 75
Over-expression of mitochondrial ferritin affects the JAK2/STAT5 pathway in K562 cells and causes mitochondrial iron accumulation. 73
Bmp6 expression in murine liver non parenchymal cells: A mechanisms to control their high iron exporter activity and protect hepatocytes from iron overload? 70
Oxidative stress and cell death in cells expressing L-ferritin variants causing neuroferritinopathy 67
Loss of CYLD promotes splenic marginal zone lymphoma 65
The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload 65
IRON CONTRIBUTES TO BORTEZOMIB SENSITIVITY IN MULTIPLE MYELOMA CELLS 62
Polarization dictates iron handling by inflammatory and alternatively activated macrophages 62
Skin fibroblasts from pantothenate kinase-associated neurodegeneration patients show altered cellular oxidative status and have defective iron-handling properties. 58
Limiting hepatic Bmp-Smad signaling by matriptase-2 is required for erythropoietin-mediated hepcidin suppression in mice. 58
Role of iron and ferritin in TNFalpha-induced apoptosis in HeLa cells. FEBS Lett. 2003 Feb 27;537(1-3):187-92 58
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 57
Mitochondrial ferritin limits oxidative damage regulating mitochondrial iron availability: hypothesis for a protective role in Friedreich ataxia 57
Mysteries of Mitochondrial Ferritin 57
Loss of the von Hippel Lindau tumor suppressor disrupts iron homeostasis in renal carcinoma cells 52
Targeting the BMP Receptor Inhibitor FKBP12 to Upregulate Hepcidin in Wild-Type and Hemojuvelin-Hemochromatosis Models 49
Pantothenate kinase-2 (Pank2) silencing causes cell growth reduction, cell-specific ferroportin upregulation and iron deregulation 48
The expression of human mitochondrial ferritin rescues respiratory function in frataxin-deficient yeast 48
Mitochondrial ferritin protects HeLa cells and friedreich ataxia fibroblasts by limiting oxidative stress 46
EXPLOITING IRON TOXICITY IN MULTIPLE MYELOMA: A STRATEGY TO INCREASE THE EFFICACY OF PROTEASOME INHIBITION THERAPIES 38
Oncological outcomes and prognostic factors of pulmonary metastasectomy in pancreatic cancer 3
UVI5008: the first reversible, non-covalent Bruton’s tyrosine kinase epi-inhibitor for B-cell malignancies 1
The deubiquitinase activity of CYLD is required for B cell differentiation 1
Totale 3.078
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Categoria #
all - tutte 16.336
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 16.336
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202213 0 0 0 6 3 1 0 1 0 0 0 2
2022/2023172 69 38 15 0 1 22 2 11 7 0 0 7
2023/2024165 3 1 2 23 17 31 4 21 0 17 28 18
2024/2025658 58 8 10 27 58 56 115 77 74 68 50 57
2025/20262.056 181 133 93 310 201 63 197 170 615 93 0 0
Totale 3.078