UNICA IRIS Institutional Research Information System

MOI, PAOLO
 Distribuzione geografica
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Continente #
EU - Europa 106.144
NA - Nord America 5.736
AS - Asia 2.423
SA - Sud America 409
AF - Africa 65
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 1
Totale 114.788
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Nazione #
IT - Italia 104.628
US - Stati Uniti d'America 5.679
SG - Singapore 944
CN - Cina 836
UA - Ucraina 416
SE - Svezia 350
BR - Brasile 318
VN - Vietnam 245
DE - Germania 208
FI - Finlandia 152
GB - Regno Unito 133
FR - Francia 118
HK - Hong Kong 65
IN - India 58
CA - Canada 35
BD - Bangladesh 33
KR - Corea 33
AR - Argentina 27
IQ - Iraq 27
NL - Olanda 23
PK - Pakistan 23
ZA - Sudafrica 21
BE - Belgio 20
SA - Arabia Saudita 20
ES - Italia 19
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
ET - Etiopia 3
KE - Kenya 3
KG - Kirghizistan 3
LV - Lettonia 3
PT - Portogallo 3
CR - Costa Rica 2
DK - Danimarca 2
DO - Repubblica Dominicana 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
GR - Grecia 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
PR - Porto Rico 1
PS - Palestinian Territory 1
SO - Somalia 1
SR - Suriname 1
TJ - Tagikistan 1
VI - Stati Uniti Isole Vergini 1
Totale 114.787
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Città #
Cagliari 102.544
Uta 1.830
Fairfield 591
Woodbridge 546
Singapore 535
Ashburn 524
Chandler 404
Ann Arbor 310
Houston 301
San Jose 264
Wilmington 248
Nyköping 242
Boardman 240
Seattle 225
Jacksonville 219
Dallas 196
Cambridge 177
Beijing 144
Dearborn 135
Nanjing 88
Los Angeles 84
Santa Clara 83
Helsinki 81
Shanghai 78
Ho Chi Minh City 70
Lauterbourg 70
Hefei 59
Hanoi 58
Hong Kong 56
Boston 52
Buffalo 39
São Paulo 39
San Diego 36
Guangzhou 35
The Dalles 35
Seoul 33
New York 32
Hebei 28
Pune 23
Nanchang 22
Tianjin 22
Council Bluffs 21
Munich 21
Redwood City 20
Shenyang 20
Changsha 19
Jiaxing 19
Frankfurt am Main 18
London 18
Chicago 16
Dong Ket 16
Milan 16
Nuremberg 16
Sassari 16
Orem 15
Toronto 15
Brussels 13
Da Nang 13
Denver 13
Orange 13
Phoenix 13
Redondo Beach 12
Riyadh 12
Warsaw 12
Jinan 11
Mountain View 11
Norwalk 11
Tokyo 11
Haiphong 10
Islington 10
Johannesburg 10
Tashkent 10
Auburn Hills 9
Brooklyn 9
Montreal 9
Verona 9
Atlanta 8
Baghdad 8
Falls Church 8
San Francisco 8
Baku 7
Can Tho 7
Kunming 7
Manchester 7
Redmond 7
Rio de Janeiro 7
Zhengzhou 7
Biên Hòa 6
Columbus 6
Curitiba 6
Dhaka 6
Hangzhou 6
Santiago 6
Stockholm 6
Vienna 6
Amsterdam 5
Brasília 5
Erbil 5
Guayaquil 5
Indiana 5
Totale 111.439
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Nome #
Thalassemia major between liver and heart: Where we are now 4.102
Current growth patterns in children and adolescents with thalassemia major 3.008
A decisional algorithm to start iron chelation in patients with beta thalassemia 2.924
A genetic score for the prediction of beta-thalassemia severity 2.913
Earlier initiation of transfusional and iron chelation therapies in recently born children with transfusion-dependent thalassemia 2.710
Post GWAS analysis of a BCLA intronic region to define its role in regulating HbF levels 2.588
Deferasirox and children: From clinical trials to the real world 2.490
Identificazione di una nuova mutazione in posizione -52 (g->a) del beta direct repeat element del promotore del gene β-globinico 2.381
Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes 2.376
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia 2.334
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin 2.305
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation 2.275
A novel high-content immunofluorescence assay as a tool to identify at the single cell level γ-globin inducing compounds 2.111
Causes of hospital admission in children and adults with transfusion-dependent thalassemia in Sardinia, 2000-2015 2.089
In vivo activation of the human δ-globin gene: the therapeutic potential in β- thalassemic mice 2.087
A validated cellular biobank for β-thalassemia 2.075
HPFH from Klf1 haploinsufficiency combined to transcriptional heterozygous b-thalassemia 2.068
KLF1 gene mutations cause borderline HbA(2). 2.039
Thalassemia major: who is afraid of serum ferritin below 500 μg/l? 2.035
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 2.010
Quality of life in Sardinian patients with transfusion-dependent Thalassemia: a cross-sectional study 1.982
Delayed embryonic to adult globin switching in HMGB2 knock out mice 1.965
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels 1.915
Klf1 affects DNase II-alpha expression in the central macrophage of a fetal liver erythroblastic island: a non-cell-autonomous role in definitive erythropoiesis. 1.894
Regulation of the Human a-Globin Genes by GKLF 1.799
Hematological phenotypes in children according to the α-globin genotypes 1.786
null 1.759
HPFH From Klf1 Haploinsufficiency Combined to Transcriptional Heterozygous β-Thalassemia 1.728
null 1.635
null 1.567
A novel missense mutation (C84R) in a patient with type II vitamin D-dependent rickets 1.551
Towards the genetic treatment of beta-thalassemia: new disease models, new vectors, new cells 1.526
Recent advances in β-thalassemias. 1.484
Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulation 1.484
Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemia 1.459
Porfirie 1.436
Molecular pathology of haemoglobin H disease in Sardinians 1.429
Regulation of the human HBA genes by KLF4 in erythroid cell lines 1.423
The distal beta-globin CACCC box is required for maximal stimulation of the beta-globin gene by EKLF 1.334
Genetic modifier factors of ß-thalassemia [Modificatori genetici della ß-talassemia] 1.326
Phenotype-genotype correlation in haemoglobin H disease in childhood 1.316
Stem Cell engineering for the treatmentt of severe Hemoglobinopathies 1.313
cAMP differentially regulates gamma-globin gene expression in erythroleukemic cells and primary erythroblasts through c-Myb expression 1.305
DeltaN133p53 expression levels in relation to haplotypes of the TP53 internal promoter region 1.284
A novel splicing defect (IVS6+1G > T) in a patient with pseudovitamin D deficiency rickets 1.228
Nuclear factor-erythroid 2 (NF-E2) expression in normal and malignant megakaryocytopoiesis 1.171
Isolation of a differentially regulated splicing isoform of human NF-E2. 1.111
A novel silent beta-thalassemia mutation in the distal CACCC box affects the binding and responsiveness to EKLF 1.078
The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene 1.010
ΔN133p53 expression levels in relation to haplotypes of the TP53 internal promoter region 1.009
Molecular characterization of Wilson disease in the Sardinian population - Evidence of a founder effect 991
Induction of therapeutic levels of HbF in genome-edited primary β039-thalassaemia haematopoietic stem and progenitor cells 987
Regulation of the globin genes 962
A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty 941
Negative regulation of gamma-globin gene expression by cyclic AMP-dependent pathway in erythroid cells 926
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene 906
A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfism 875
hMAF, a small human transcription factor that heterodimerizes specifically with Nrf1 and Nrf2 858
Difetti enzimatici del globulo rosso e anemie megaloblastiche congenite 832
null 806
beta-Thalassemia mutation at -90C-->T impairs the interaction of the proximal CACCC box with both erythroid and nonerythroid factors 778
Synergistic enhancement of globin gene expression by activator protein-1-like proteins 775
Regulation of mouse p45 NF-E2 transcription by an erythroid-specific GATA-dependent intronic alternative promoter 738
Genetic modifying factors in β-thalassemia 722
NORMAL DELTA-GLOBIN GENE-SEQUENCES IN SARDINIAN NONDELETIONAL DELTA-BETA-THALASSEMIA 720
Long-term survival of beta thalassemia major patients treated with hematopoietic stem cell transplantation compared with survival with conventional treatment 715
Identificazione di una nuova mutazione in posizione -52 (G->A) del beta direct repeat element del promotore del gene ß globinico 708
INTERETHNIC POLYMORPHISM OF THE BETA-GLOBIN GENE LOCUS-CONTROL REGION (LCR) IN SICKLE-CELL-ANEMIA PATIENTS 698
null 644
An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype 644
Beta-thalassaemia unlinked to the beta-globin gene interacts with sickle-cell trait in a Portuguese family 643
Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian family. 633
Chromosomal localization of the human NF-E2 family of bZIP transcription factors by fluorescence in situ hybridization 607
Dissection of the enhancer activity of beta-globin 5' DNase I-hypersensitive site 2 in transgenic mice 562
Mutations in the Zn finger of EKLF that retain binding to the DNA reduce its ability to transactivate the γ-globin gene 561
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 532
null 531
CLONING OF A SMALL HUMAN MAF PROTEIN THAT HETERODIMERIZES SPECIFICALLY WITH NRF1 467
Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin gene 464
Cloning, characterization, DNA binding, mapping and mutation analysis of the human erythroid kruppel-like factor (EKLF) gene 270
Human EKLF binding and transactivation from wild type and mutant CACCC boxes 207
Reduced cyclin D3 expression in erythroid cells protects against malaria 41
Totale 114.971
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Categoria #
all - tutte 144.848
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 144.848
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.186 0 0 0 0 0 0 0 0 0 521 801 864
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
2025/20264.765 387 186 775 300 318 323 957 442 286 791 0 0
Totale 114.971