IRIS
AMATI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 19.730
EU - Europa 3.039
AS - Asia 808
SA - Sud America 5
AF - Africa 4
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 23.592
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Nazione #
US - Stati Uniti d'America 19.721
DE - Germania 1.100
PL - Polonia 406
SG - Singapore 351
IT - Italia 263
UA - Ucraina 257
RU - Federazione Russa 227
FR - Francia 211
CN - Cina 179
GB - Regno Unito 164
KR - Corea 163
IE - Irlanda 160
SE - Svezia 123
VN - Vietnam 72
FI - Finlandia 63
BE - Belgio 19
CZ - Repubblica Ceca 15
NL - Olanda 11
CA - Canada 7
JP - Giappone 7
KG - Kirghizistan 7
HK - Hong Kong 6
IR - Iran 6
IN - India 5
RO - Romania 5
BR - Brasile 4
DK - Danimarca 4
CH - Svizzera 3
IL - Israele 3
PK - Pakistan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AT - Austria 2
AU - Australia 2
EU - Europa 2
IQ - Iraq 2
ZA - Sudafrica 2
CL - Cile 1
DM - Dominica 1
EE - Estonia 1
EG - Egitto 1
ES - Italia 1
GR - Grecia 1
LT - Lituania 1
MX - Messico 1
NO - Norvegia 1
PH - Filippine 1
PT - Portogallo 1
SC - Seychelles 1
TR - Turchia 1
TW - Taiwan 1
UZ - Uzbekistan 1
Totale 23.592
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Città #
Woodbridge 6.297
Wilmington 4.928
Houston 4.722
Fairfield 584
Ann Arbor 514
Kraków 406
Chandler 352
Singapore 314
Ashburn 306
Seattle 262
Jacksonville 236
Cambridge 231
Dublin 148
Rome 137
Medford 132
New York 132
Dearborn 94
Beijing 76
Dong Ket 70
Santa Clara 68
Lawrence 63
Menlo Park 40
Boardman 38
San Diego 31
Mülheim 29
Milan 28
Moscow 25
Zhengzhou 20
Norwalk 19
Redwood City 18
Munich 16
Seoul 16
Brussels 15
Nürnberg 15
Falls Church 14
Mountain View 14
Brno 13
Daejeon 13
London 13
Nanjing 13
Palo Alto 11
Saint Petersburg 10
Guangzhou 9
San Mateo 9
Council Bluffs 8
Helsinki 8
Los Angeles 8
Buffalo 7
Hefei 7
Jinan 7
Auburn Hills 6
Shanghai 6
Verona 6
Kunming 5
University Park 5
Kilburn 4
Mainz 4
Parma 4
San Francisco 4
Toronto 4
Cascina 3
Chicago 3
Detroit 3
Hebei 3
Hounslow 3
Islamabad 3
Monza 3
Nuremberg 3
São Paulo 3
Tehran 3
Turin 3
Acton 2
Amsterdam 2
Baghdad 2
Braunschweig 2
Changsha 2
Chengdu 2
Del Norte 2
Engelhard 2
Enterprise 2
Esbjerg 2
Florence 2
Fuzhou 2
Gijzenzele 2
Griesstatt 2
Hangzhou 2
Ho Chi Minh City 2
Hong Kong 2
Jena 2
Johannesburg 2
Latina 2
Leawood 2
Miami 2
Monte Porzio Catone 2
Noblesville 2
Phoenix 2
Portland 2
San Jose 2
San Marcos 2
Sgurgola 2
Totale 20.685
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Nome #
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study 518
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 500
Gene expression profile study in CFTR mutated bronchial cell lines 495
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 472
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. 471
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region 466
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 466
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 463
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 460
Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways 449
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 447
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 446
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 446
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 446
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 445
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 444
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 442
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 440
The search for hemizyosity at 22q11 in patients with isolated cleft palate 439
Practical guidelines for managing patients with 22q11.2 deletion syndrome. 435
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 434
Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11? 430
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region on 8p 427
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 425
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 423
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 421
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 421
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line 420
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. 420
Functional characterization of the 5′ flanking region of human Ubiquitin Fusion Degradation 1 Like gene (UFD1L) 420
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 414
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 411
Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome 407
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome 402
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 399
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes? 394
In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction 390
Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population. 388
LOX-1 Inhibition in ApoE KO Mice Using a Schizophyllan-based Antisense Oligonucleotide Therapy. 385
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L) 383
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome 381
Epidermal growth factor-like domain 7 (EGFL7) promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways. 378
Gene expression analysis during development by high-throughput methods 368
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) 368
Hif1α down-regulation is associated with transposition of great arteries in mice treated with a retinoic acid antagonist 361
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome 359
The molecular genetics of the DiGeorge syndrome 358
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1] 356
The human rs1050286 polymorphism alters LOX-1 expression through modifying miR-24 binding 353
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene 338
Mutations of ZFPM2/FOG2 gene in sporadic cases of Tetralogy of Fallot 326
La bioinformatica come strumento per lo studio dell'espressione genica durante lo sviluppo embrionale 324
Lox-1 and its splice variants: a new challenge for atherosclerosis and cancer-targeted therapies 323
Advances in molecular analysis of congenital heart defects 307
MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 292
Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes 245
Epigenetic Modification in Coronary Atherosclerosis 243
Frataxin deficiency in Friedreich’s ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival 236
Expression profiles of the SARS-CoV-2 host invasion genes in nasopharyngeal and oropharyngeal swabs of COVID-19 patients 164
Two reck splice variants (Long and short) are differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 61
An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease 48
Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome 48
Low molecular weight heparin -induced miRNA changes in peripheral blood mononuclear cells in pregnancies with unexplained recurrent pregnancy loss 44
Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1 42
Expression profile of HERVs and inflammatory mediators detected in nasal mucosa as a predictive biomarker of COVID-19 severity 30
Recenti acquisizioni sulla genetica delle cardiopatie congenite 23
Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors 22
Downregulation of Circulating Hsa-miR-200c-3p Correlates with Dyslipidemia in Patients with Stable Coronary Artery Disease 18
Erratum: Mutations of ZFPM2/FOG2 Gene in Sporadic Cases of Tetralogy of Fallot (Human Mutation (2003) 22 (372-377)) 11
Le Basi Biologiche 10
Totale 23.841
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Categoria #
all - tutte 44.897
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 44.897
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.685 0 0 0 0 490 594 490 522 442 483 281 383
2020/20213.223 353 375 309 430 268 308 404 316 120 87 131 122
2021/2022734 51 94 31 32 29 86 38 34 60 49 48 182
2022/2023874 83 81 21 129 78 181 54 57 92 5 62 31
2023/2024414 38 13 27 8 33 143 18 23 7 11 11 82
2024/2025740 90 343 169 89 49 0 0 0 0 0 0 0
Totale 23.841