IRIS
CAMPANELLA, ALESSANDRO
 Distribuzione geografica
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Continente #
EU - Europa 1.104
AS - Asia 993
NA - Nord America 794
SA - Sud America 204
AF - Africa 28
OC - Oceania 2
Totale 3.125
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Nazione #
US - Stati Uniti d'America 734
RU - Federazione Russa 708
SG - Singapore 367
CN - Cina 331
BR - Brasile 171
SE - Svezia 107
VN - Vietnam 101
HK - Hong Kong 85
IT - Italia 75
DE - Germania 50
FR - Francia 50
GB - Regno Unito 35
CA - Canada 34
IN - India 33
MX - Messico 18
FI - Finlandia 17
JP - Giappone 13
PL - Polonia 13
ZA - Sudafrica 11
AT - Austria 10
AR - Argentina 8
BD - Bangladesh 8
ES - Italia 8
TR - Turchia 8
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
UY - Uruguay 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
GR - Grecia 4
ID - Indonesia 4
LT - Lituania 4
CL - Cile 3
JM - Giamaica 3
KE - Kenya 3
MY - Malesia 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
CH - Svizzera 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
NP - Nepal 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
ZM - Zambia 1
Totale 3.125
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Città #
Singapore 182
Moscow 143
San Jose 107
Ashburn 101
Hong Kong 85
Dallas 77
Shanghai 65
New York 56
Beijing 53
Hefei 42
Lauterbourg 37
Los Angeles 36
Ho Chi Minh City 32
Lawrence 29
Milan 29
Princeton 29
Boardman 28
Hanoi 23
Orem 16
São Paulo 15
Montreal 13
Chennai 12
Helsinki 12
Santa Clara 11
Warsaw 11
Denver 10
Nuremberg 10
Tokyo 10
Frankfurt am Main 9
Manchester 9
Rio de Janeiro 9
Munich 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
Hangzhou 4
Jacksonville 4
Montevideo 4
New Delhi 4
Novara 4
Querétaro 4
Rome 4
San Francisco 4
Tashkent 4
Vienna 4
Wuhan 4
Ankara 3
Campinas 3
Casirate d'Adda 3
City of London 3
Dublin 3
Goiânia 3
Istanbul 3
Jiaxing 3
Karachi 3
Kingston 3
Mumbai 3
Nairobi 3
Ottawa 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
Cincinnati 2
Ciudad del Este 2
Columbus 2
Cotia 2
Cuenca 2
Curitiba 2
Dakar 2
Fortaleza 2
Totale 1.566
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Nome #
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 116
Bone marrow Tfr2 deletion improves the therapeutic efficacy of the activin-receptor ligand trap RAP-536 in β-thalassemic mice 116
Iron uptake in quiescent and inflammation-activated astrocytes: a potentially neuroprotective control of iron burden 115
Iron Induces Cell Death and Strengthens the Efficacy of Antiandrogen Therapy in Prostate Cancer Models 114
Supplementary Data from Iron Induces Cell Death and Strengthens the Efficacy of Antiandrogen Therapy in Prostate Cancer Models 107
C29G in the iron-responsive element of L-ferritin: a new mutation associated with hyperferritinemia-cataract 101
Ceruloplasmin Oxidation, a Feature of Parkinson's Disease CSF, Inhibits Ferroxidase Activity and Promotes Cellular Iron Retention 101
IκBε deficiency accelerates disease development in chronic lymphocytic leukemia 98
Iron increases the susceptibility of multiple myeloma cells to bortezomib 97
CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL 94
A new G51C mutation in the IRE of L-ferritin in hyperferritinemia cataract syndrome decreases the binding affinity of the mutant IRE to IRP. 93
Iron regulatory proteins 1 and 2 in human monocytes, macrophages and duodenum: expression and regulation in hereditary hemochromatosis and iron deficiency 92
Human mitochondrial ferritin expressed in HeLa cells incorporates iron and affects cellular iron metabolism 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 89
Erythroblast apoptosis and microenvironmental iron restriction trigger anemia in the VK*MYC model of multiple myeloma 84
A new mutation in the IRE of L-ferritin (G51C) associated with hyperferritinemia-cataract syndrome decreases the binding affinity of IRE to IRPS 82
Identification of TMPRSS6 cleavage sites of hemojuvelin 81
Iron causes lipid oxidation and inhibits proteasome function in multiple myeloma cells: A proof of concept for novel combination therapies 80
Blotting Analysis of Native IRP1: A Novel Approach to Distinguish the Different Forms of IRP1 in Cells and Tissues 79
Induction of iron excess restricts malignant plasma cells expansion and potentiates bortezomib effect in models of multiple myeloma 79
IRON UPTAKE IN RESTING AND REACTIVE ASTROCYTES: A POTENTIALLY NEUROPROTECTIVE CONTROL OF IRON BURDEN 77
Over-expression of mitochondrial ferritin affects the JAK2/STAT5 pathway in K562 cells and causes mitochondrial iron accumulation. 76
CHARACTERIZATION OF THE L-FERRITIN VARIANT 460INSA RESPONSIBLE OF A HEREDITARY FERRITINOPATHY DISORDER 75
Loss of CYLD promotes splenic marginal zone lymphoma 72
Bmp6 expression in murine liver non parenchymal cells: A mechanisms to control their high iron exporter activity and protect hepatocytes from iron overload? 71
The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload 68
Oxidative stress and cell death in cells expressing L-ferritin variants causing neuroferritinopathy 68
Polarization dictates iron handling by inflammatory and alternatively activated macrophages 65
IRON CONTRIBUTES TO BORTEZOMIB SENSITIVITY IN MULTIPLE MYELOMA CELLS 63
Skin fibroblasts from pantothenate kinase-associated neurodegeneration patients show altered cellular oxidative status and have defective iron-handling properties. 62
Limiting hepatic Bmp-Smad signaling by matriptase-2 is required for erythropoietin-mediated hepcidin suppression in mice. 60
Mitochondrial ferritin limits oxidative damage regulating mitochondrial iron availability: hypothesis for a protective role in Friedreich ataxia 59
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 58
Role of iron and ferritin in TNFalpha-induced apoptosis in HeLa cells. FEBS Lett. 2003 Feb 27;537(1-3):187-92 58
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 50
The expression of human mitochondrial ferritin rescues respiratory function in frataxin-deficient yeast 50
Pantothenate kinase-2 (Pank2) silencing causes cell growth reduction, cell-specific ferroportin upregulation and iron deregulation 49
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
The deubiquitinase activity of CYLD is required for B cell differentiation 2
UVI5008: the first reversible, non-covalent Bruton’s tyrosine kinase epi-inhibitor for B-cell malignancies 1
Totale 3.185
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Categoria #
all - tutte 17.586
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 17.586
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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
2025/20262.163 181 133 93 310 201 63 197 170 615 121 40 39
Totale 3.185