UNICA IRIS Institutional Research Information System

MOI, PAOLO
 Distribuzione geografica
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Continente #
EU - Europa 106.220
NA - Nord America 6.034
AS - Asia 2.446
SA - Sud America 409
AF - Africa 65
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 1
Totale 115.185
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Nazione #
IT - Italia 104.693
US - Stati Uniti d'America 5.969
SG - Singapore 946
CN - Cina 840
UA - Ucraina 416
SE - Svezia 352
BR - Brasile 318
VN - Vietnam 245
DE - Germania 208
FI - Finlandia 152
GB - Regno Unito 133
FR - Francia 120
HK - Hong Kong 66
IN - India 58
BD - Bangladesh 49
CA - Canada 40
KR - Corea 33
AR - Argentina 27
IQ - Iraq 27
NL - Olanda 27
PK - Pakistan 23
ES - Italia 21
ZA - Sudafrica 21
BE - Belgio 20
SA - Arabia Saudita 20
RU - Federazione Russa 18
TR - Turchia 17
JP - Giappone 16
EC - Ecuador 15
AT - Austria 14
CO - Colombia 14
PL - Polonia 14
ID - Indonesia 13
MY - Malesia 13
UZ - Uzbekistan 12
MX - Messico 11
EG - Egitto 10
MA - Marocco 10
AZ - Azerbaigian 9
VE - Venezuela 9
AU - Australia 8
CL - Cile 8
PY - Paraguay 7
NP - Nepal 6
OM - Oman 6
TH - Thailandia 6
DZ - Algeria 5
IL - Israele 5
IR - Iran 5
LT - Lituania 5
TN - Tunisia 5
AE - Emirati Arabi Uniti 4
BO - Bolivia 4
CH - Svizzera 4
CY - Cipro 4
LK - Sri Lanka 4
PE - Perù 4
PH - Filippine 4
AL - Albania 3
CR - Costa Rica 3
ET - Etiopia 3
KE - Kenya 3
KG - Kirghizistan 3
LV - Lettonia 3
PT - Portogallo 3
DK - Danimarca 2
DO - Repubblica Dominicana 2
GR - Grecia 2
GY - Guiana 2
JM - Giamaica 2
LA - Repubblica Popolare Democratica del Laos 2
ML - Mali 2
NZ - Nuova Zelanda 2
RO - Romania 2
RS - Serbia 2
SN - Senegal 2
SY - Repubblica araba siriana 2
TW - Taiwan 2
BF - Burkina Faso 1
BH - Bahrain 1
BZ - Belize 1
CG - Congo 1
CZ - Repubblica Ceca 1
EE - Estonia 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
IE - Irlanda 1
JO - Giordania 1
KH - Cambogia 1
LB - Libano 1
LU - Lussemburgo 1
MT - Malta 1
MU - Mauritius 1
NI - Nicaragua 1
PR - Porto Rico 1
PS - Palestinian Territory 1
SO - Somalia 1
SR - Suriname 1
TJ - Tagikistan 1
Totale 115.182
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Città #
Cagliari 102.588
Uta 1.830
Fairfield 591
Woodbridge 547
Singapore 536
Ashburn 529
Chandler 405
San Jose 384
Ann Arbor 310
Houston 302
Wilmington 248
Nyköping 242
Boardman 240
Seattle 228
Jacksonville 221
Dallas 199
Cambridge 177
Beijing 145
Dearborn 135
Nanjing 88
Los Angeles 86
Santa Clara 86
Helsinki 81
Shanghai 78
Ho Chi Minh City 70
Lauterbourg 70
Hefei 59
Hanoi 58
Hong Kong 57
Boston 52
New York 47
Buffalo 40
São Paulo 39
San Diego 36
Guangzhou 35
The Dalles 35
Council Bluffs 34
Seoul 33
Hebei 28
Pune 23
Nanchang 22
Tianjin 22
Munich 21
Changsha 20
Chicago 20
Redwood City 20
Shenyang 20
Jiaxing 19
Frankfurt am Main 18
London 18
Milan 17
Dong Ket 16
Nuremberg 16
Orem 16
Sassari 16
Toronto 16
Phoenix 14
Brussels 13
Da Nang 13
Denver 13
Orange 13
Redondo Beach 12
Riyadh 12
Warsaw 12
Jinan 11
Mountain View 11
Norwalk 11
Tokyo 11
Atlanta 10
Brooklyn 10
Haiphong 10
Islington 10
Johannesburg 10
Montreal 10
Tashkent 10
Auburn Hills 9
San Francisco 9
Verona 9
Baghdad 8
Falls Church 8
Baku 7
Can Tho 7
Columbus 7
Kunming 7
Manchester 7
Redmond 7
Rio de Janeiro 7
Washington 7
Zhengzhou 7
Biên Hòa 6
Curitiba 6
Dhaka 6
Hangzhou 6
Santiago 6
Stockholm 6
Vienna 6
Amsterdam 5
Brasília 5
Erbil 5
Guayaquil 5
Totale 111.673
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Nome #
Thalassemia major between liver and heart: Where we are now 4.109
Current growth patterns in children and adolescents with thalassemia major 3.015
A decisional algorithm to start iron chelation in patients with beta thalassemia 2.932
A genetic score for the prediction of beta-thalassemia severity 2.920
Earlier initiation of transfusional and iron chelation therapies in recently born children with transfusion-dependent thalassemia 2.718
Post GWAS analysis of a BCLA intronic region to define its role in regulating HbF levels 2.592
Deferasirox and children: From clinical trials to the real world 2.496
Identificazione di una nuova mutazione in posizione -52 (g->a) del beta direct repeat element del promotore del gene β-globinico 2.385
Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes 2.380
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia 2.338
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin 2.307
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation 2.279
A novel high-content immunofluorescence assay as a tool to identify at the single cell level γ-globin inducing compounds 2.114
Causes of hospital admission in children and adults with transfusion-dependent thalassemia in Sardinia, 2000-2015 2.096
In vivo activation of the human δ-globin gene: the therapeutic potential in β- thalassemic mice 2.091
A validated cellular biobank for β-thalassemia 2.082
HPFH from Klf1 haploinsufficiency combined to transcriptional heterozygous b-thalassemia 2.074
KLF1 gene mutations cause borderline HbA(2). 2.042
Thalassemia major: who is afraid of serum ferritin below 500 μg/l? 2.040
Children of a lesser god or miracles? An emotional and behavioural profile of children born to mothers on dialysis in Italy: A multicentre nationwide study 2000-12 2.012
Quality of life in Sardinian patients with transfusion-dependent Thalassemia: a cross-sectional study 1.985
Delayed embryonic to adult globin switching in HMGB2 knock out mice 1.968
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels 1.918
Klf1 affects DNase II-alpha expression in the central macrophage of a fetal liver erythroblastic island: a non-cell-autonomous role in definitive erythropoiesis. 1.907
Regulation of the Human a-Globin Genes by GKLF 1.802
Hematological phenotypes in children according to the α-globin genotypes 1.792
null 1.759
HPFH From Klf1 Haploinsufficiency Combined to Transcriptional Heterozygous β-Thalassemia 1.751
null 1.635
null 1.567
A novel missense mutation (C84R) in a patient with type II vitamin D-dependent rickets 1.555
Towards the genetic treatment of beta-thalassemia: new disease models, new vectors, new cells 1.534
Recent advances in β-thalassemias. 1.506
Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulation 1.487
Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemia 1.463
Porfirie 1.441
Molecular pathology of haemoglobin H disease in Sardinians 1.433
Regulation of the human HBA genes by KLF4 in erythroid cell lines 1.431
The distal beta-globin CACCC box is required for maximal stimulation of the beta-globin gene by EKLF 1.338
Genetic modifier factors of ß-thalassemia [Modificatori genetici della ß-talassemia] 1.332
Phenotype-genotype correlation in haemoglobin H disease in childhood 1.322
Stem Cell engineering for the treatmentt of severe Hemoglobinopathies 1.317
cAMP differentially regulates gamma-globin gene expression in erythroleukemic cells and primary erythroblasts through c-Myb expression 1.311
DeltaN133p53 expression levels in relation to haplotypes of the TP53 internal promoter region 1.287
A novel splicing defect (IVS6+1G > T) in a patient with pseudovitamin D deficiency rickets 1.234
Nuclear factor-erythroid 2 (NF-E2) expression in normal and malignant megakaryocytopoiesis 1.174
Isolation of a differentially regulated splicing isoform of human NF-E2. 1.116
A novel silent beta-thalassemia mutation in the distal CACCC box affects the binding and responsiveness to EKLF 1.081
ΔN133p53 expression levels in relation to haplotypes of the TP53 internal promoter region 1.015
The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene 1.014
Molecular characterization of Wilson disease in the Sardinian population - Evidence of a founder effect 994
Induction of therapeutic levels of HbF in genome-edited primary β039-thalassaemia haematopoietic stem and progenitor cells 988
Regulation of the globin genes 971
A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty 944
Negative regulation of gamma-globin gene expression by cyclic AMP-dependent pathway in erythroid cells 929
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene 909
A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfism 878
hMAF, a small human transcription factor that heterodimerizes specifically with Nrf1 and Nrf2 860
Difetti enzimatici del globulo rosso e anemie megaloblastiche congenite 835
null 806
beta-Thalassemia mutation at -90C-->T impairs the interaction of the proximal CACCC box with both erythroid and nonerythroid factors 781
Synergistic enhancement of globin gene expression by activator protein-1-like proteins 779
Regulation of mouse p45 NF-E2 transcription by an erythroid-specific GATA-dependent intronic alternative promoter 742
NORMAL DELTA-GLOBIN GENE-SEQUENCES IN SARDINIAN NONDELETIONAL DELTA-BETA-THALASSEMIA 724
Genetic modifying factors in β-thalassemia 724
Long-term survival of beta thalassemia major patients treated with hematopoietic stem cell transplantation compared with survival with conventional treatment 724
Identificazione di una nuova mutazione in posizione -52 (G->A) del beta direct repeat element del promotore del gene ß globinico 716
INTERETHNIC POLYMORPHISM OF THE BETA-GLOBIN GENE LOCUS-CONTROL REGION (LCR) IN SICKLE-CELL-ANEMIA PATIENTS 706
Beta-thalassaemia unlinked to the beta-globin gene interacts with sickle-cell trait in a Portuguese family 646
An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype 645
null 644
Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian family. 634
Chromosomal localization of the human NF-E2 family of bZIP transcription factors by fluorescence in situ hybridization 612
Dissection of the enhancer activity of beta-globin 5' DNase I-hypersensitive site 2 in transgenic mice 566
Mutations in the Zn finger of EKLF that retain binding to the DNA reduce its ability to transactivate the γ-globin gene 562
Isolation of NF-E2-related factor 2 (Nrf2), a NF-E2-like basic leucine zipper transcriptional activator that binds to the tandem NF-E2/AP1 repeat of the beta-globin locus control region 537
null 531
CLONING OF A SMALL HUMAN MAF PROTEIN THAT HETERODIMERIZES SPECIFICALLY WITH NRF1 468
Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin gene 466
Cloning, characterization, DNA binding, mapping and mutation analysis of the human erythroid kruppel-like factor (EKLF) gene 279
Human EKLF binding and transactivation from wild type and mutant CACCC boxes 210
Reduced cyclin D3 expression in erythroid cells protects against malaria 61
Totale 115.368
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Categoria #
all - tutte 146.759
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 146.759
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021864 0 0 0 0 0 0 0 0 0 0 0 864
2021/20225.214 470 244 298 513 366 475 334 355 566 557 516 520
2022/20239.216 565 1.151 1.118 675 854 866 569 1.138 718 576 622 364
2023/20247.635 372 329 237 529 745 1.705 872 603 459 556 701 527
2024/202529.262 10.484 9.301 3.132 1.975 860 1.341 1.471 113 170 114 145 156
2025/20265.162 387 186 775 300 318 323 957 442 286 916 209 63
Totale 115.368