IRIS
SALVATORE, FRANCESCO
 Distribuzione geografica
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Continente #
EU - Europa 11.324
NA - Nord America 8.583
AS - Asia 8.230
SA - Sud America 1.287
AF - Africa 221
OC - Oceania 18
Continente sconosciuto - Info sul continente non disponibili 12
Totale 29.675
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Nazione #
US - Stati Uniti d'America 8.175
SG - Singapore 4.591
IT - Italia 4.136
RU - Federazione Russa 3.604
CN - Cina 1.648
BR - Brasile 1.049
VN - Vietnam 764
HK - Hong Kong 692
UA - Ucraina 612
DE - Germania 587
NL - Olanda 515
FI - Finlandia 393
GB - Regno Unito 343
SE - Svezia 343
CA - Canada 287
IE - Irlanda 253
FR - Francia 190
IN - India 138
AR - Argentina 99
PL - Polonia 90
ZA - Sudafrica 90
MX - Messico 82
BD - Bangladesh 62
ES - Italia 62
JP - Giappone 51
CI - Costa d'Avorio 49
EC - Ecuador 46
TR - Turchia 37
ID - Indonesia 34
BE - Belgio 31
AT - Austria 30
IQ - Iraq 30
LT - Lituania 24
IR - Iran 23
PK - Pakistan 23
CL - Cile 22
RO - Romania 22
CO - Colombia 19
CZ - Repubblica Ceca 18
VE - Venezuela 18
MA - Marocco 17
CH - Svizzera 15
AU - Australia 14
KR - Corea 12
PY - Paraguay 12
KE - Kenya 11
SA - Arabia Saudita 11
UZ - Uzbekistan 11
AE - Emirati Arabi Uniti 10
IL - Israele 10
PT - Portogallo 10
BG - Bulgaria 9
UY - Uruguay 9
EU - Europa 8
NP - Nepal 8
AZ - Azerbaigian 7
EG - Egitto 7
JM - Giamaica 7
PE - Perù 7
PS - Palestinian Territory 7
DZ - Algeria 6
SN - Senegal 6
JO - Giordania 5
KZ - Kazakistan 5
LB - Libano 5
LK - Sri Lanka 5
NO - Norvegia 5
OM - Oman 5
RS - Serbia 5
TH - Thailandia 5
TN - Tunisia 5
AL - Albania 4
AO - Angola 4
BO - Bolivia 4
DO - Repubblica Dominicana 4
MK - Macedonia 4
MY - Malesia 4
PH - Filippine 4
SV - El Salvador 4
CR - Costa Rica 3
EE - Estonia 3
ET - Etiopia 3
GT - Guatemala 3
IS - Islanda 3
KG - Kirghizistan 3
LV - Lettonia 3
PA - Panama 3
SY - Repubblica araba siriana 3
TW - Taiwan 3
UG - Uganda 3
BB - Barbados 2
BW - Botswana 2
CG - Congo 2
CW - ???statistics.table.value.countryCode.CW??? 2
DK - Danimarca 2
GE - Georgia 2
GR - Grecia 2
HN - Honduras 2
HR - Croazia 2
LA - Repubblica Popolare Democratica del Laos 2
Totale 29.626
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Città #
Singapore 2.000
Chandler 949
Moscow 857
Hong Kong 684
Ashburn 597
Beijing 582
Jacksonville 539
Amsterdam 426
Naples 411
Santa Clara 407
Los Angeles 288
Millbury 280
Princeton 279
Napoli 263
Boston 223
Munich 223
Nanjing 215
Rome 195
Ho Chi Minh City 194
Stockholm 189
Milan 161
Houston 148
Wilmington 144
San Jose 135
Buffalo 133
New York 127
Dallas 117
Hanoi 112
Ottawa 111
São Paulo 101
Dong Ket 94
Palermo 83
Woodbridge 74
Des Moines 73
The Dalles 73
Nanchang 67
Redondo Beach 64
Warsaw 63
Brooklyn 62
Helsinki 62
Mcallen 62
Montréal 62
Hefei 58
Seattle 58
Denver 53
Turku 51
Montreal 48
Turin 48
Chennai 46
Tokyo 46
Chicago 45
Johannesburg 42
London 42
Atlanta 40
Shenyang 40
Catania 39
Tianjin 38
Orem 37
Boardman 36
Rio de Janeiro 36
Falls Church 35
Norwalk 35
Hebei 34
Mexico City 34
Poplar 34
Bari 30
Augusta 29
Bologna 29
Phoenix 29
Cagliari 28
Falkenstein 27
Jiaxing 26
Redwood City 26
Manchester 25
Paris 25
Salerno 25
Florence 24
Kronberg 24
Ann Arbor 23
Biên Hòa 23
Frankfurt am Main 23
Haiphong 23
San Francisco 23
Changsha 22
Toronto 22
Belo Horizonte 21
Caserta 19
Dearborn 19
Genoa 19
Mumbai 19
Nuremberg 19
Da Nang 18
Orange 18
Dublin 17
Washington 17
Campinas 16
Kunming 16
Padova 16
Shanghai 16
Curitiba 15
Totale 13.675
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Nome #
Newborn screening: uno strumento per la diagnosi di difetti metabolici materni non diagnosticati 3.168
"Classical organic acidurias": diagnosis and pathogenesis. 534
Tools and Avenues for Nanotechnology-based Vectors Exploitation for Biomarker Signature and Therapeutical Drug Delivery 343
Diagnosi di malattie metaboliche su sospetto clinico a confronto con dati di screening metabolico allargato 315
Mutation screening of dynein genes in patients affected by primary ciliary diskinesia or Kartagener syndrome 198
Distribution of human beta-defensin polymorphisms in various control and cystic fibrosis populations. 173
Meccanismi epigenetici nella patogenesi dell'allergia al latte vaccino 172
A novel mutation in RP1 is a major cause of autosomal dominant retinitis pigmentosa in Southern Italy. 154
A child cohort study from South Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy 151
A multi-gene panel beyond BRCA1/BRCA2 to identify new breast cancer-predisposing mutations by a picodroplet PCR followed by a next-generation sequencing strategy: a pilot study 148
Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with rab geranylgeranyl transferase. 145
14-3-3 theta, a direct interactor of AF4, influences HOXA9 expression in RS4;11 leukemia cell line. 145
Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies 144
Ischemic Neoangiogenesis Enhanced by {beta}2-Adrenergic Receptor Overexpression. A Novel Role for the Endothelial Adrenergic System. 140
A role for D-aspartate oxidase in schizophrenia and in schizophrenia-related symptoms induced by phencyclidine in mice 140
Detection of colonic dysplasia in patients with ulcerative colitis using a targeted fluorescent peptide and confocal laser endomicroscopy: A pilot study 139
Epigenetic features of FoxP3 in children with cow’s milk allergy 138
Metastatic group 3 medulloblastoma is driven by PRUNE1 targeting NME1-TGF-β-OTX2-SNAIL via PTEN inhibition. 136
De novo sequencing and assembly of the whole genome of Novosphingobium Puteolanum PP1Y: a putative biotechnology engine 135
Altered miR-193a-5p expression in children with cow's milk allergy 135
The Cause of Death of a Child in the 18th Century Solved by Bone Microbiome Typing Using Laser Microdissection and Next Generation Sequencing 134
Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case Report. 134
A First Look at an Automated Pipeline for NGS-Based Breast-Cancer Diagnosis: The CArDIGAN Approach 132
Basi molecolari delle emoglobinopatie ed approcci diagnostici attraverso le metodologie del DNA ricombinante 131
Cardiac ion channel genes analysis in LQTS or Brugada families of Southern Italy revealed nineteen mutations, including nine novel ones 128
Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing 128
Genotype-phenotype correlation: A triple DNA mutational event in a boy entering sport conveys an additional pathogenicity risk 128
A paraoxonase gene polymorphism pon 1 (55) as an independent factor for increased carotid imt in women 127
Argomenti di biochimica 126
The role of the gut microbiome in the healthy adult status 125
A novel pathogenic BRCA1 splicing variant produces partial intron retention in the mature messenger RNA 125
Isolation of microRNAs from floral bud and leaf tissue of Orchis italica (Orchidaceae) 124
Adenoviral mediated gene transfer of the beta 2 adrenergic receptor (beta 2AR) corrects impaired angiogenesis in the ischemic hinlimb of hypertensive SHR rats 122
A rare case of sterol-C4-methyl oxidase deficiency in a young Italian male: Biochemical and molecular characterization 122
Yield and clinical significance of genetic screening in elite and amateur athletes 122
Unraveling the structural and functional features of an aldolase A mutant involved in the hemolytic anemia and severe rhabdomyolysis reported in a child 121
Coexistence of two distinct cell populations (CD56(+)TcRgammadelta(+) and CD56(+)TcRgammadelta(-)) in a case of aggressive CD56(+) lymphoma/leukemia. 121
Adenosylmethionine as a precursor for nucleic acids modification 121
An ancestral host defence peptide within human β-defensin 3 recapitulates the antibacterial and antiviral activity of the full-length molecule 120
Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and Perspectives 120
Partial purification and MALDI-TOF MS analysis of UN1, a tumor antigen membrane glycoprotein. 119
Mutation screening in sarcomeric genes in Italian HCM paediatric population 119
Pseudouridine and 1-ribosylpyridin-4-one-3-carboxamide (PCNR) serum concentrations in human immunodeficiency virus type 1-infected patients are independent predictors for AIDS progression 119
A deep sequencing approach to uncover the inflorescence miRNome of the orchid Orchis italica. 118
New insights into the Bcr-Abl activity-independent mechanisms of resistance to imatinib mesylate in KCL22 cells: the role of Shp1 and Shp2 117
De novo sequencing and assembly of the whole genome of Novosphingobium sp. PP1Y 117
A Novel DHPLC-Based Procedure for the Analysis of COL1A1 and COL1A2 Mutations in Osteogenesis Imperfecta. 117
A case of discordance between phenotype and genotype in malignant hyperthermia in the presence of the arg614cys mutation in the RYR1 gene 117
Differences in DNA methylation profile of Th1 and Th2 cytokine genes are associated with tolerance acquisition in children with IgE-mediated cow's milk allergy 117
The molecular analysis of BRCA1 and BRCA2: Next-generation sequencing supersedes conventional approaches 116
Cyclic beta defensins analogs fot the treatment of infections 116
Pseudouridine determination in blood serum as tumor marker 114
Cyclic beta defensisns analogs for the tratment of infections 114
Haemophilia A: molecular insights. 113
JURL-MK1 (c-kit(high)/CD30-/CD40-) and JURL-MK2 (c-kit(low)/CD30+/CD40+) cell lines: 'two-sided' model for investigating leukemic megakaryocytopoiesis. 113
DNA sequence capture and high-throughput sequencing technology: a novel approach to identify a large number of hypertrophic cardiomyopathy-causing genes 113
Digenic heterozygosity in KCNQ1 and KCNH2 genes causes severe long QT phenotype 113
PEGylated helper-dependent adenoviral vector expressing human Apo A-I for gene therapy in LDLR-deficient mice 113
Enabling cytoplasmic delivery and organelle targeting by surface modification of nanocarriers 112
DIVERSE HUMAN ALDOLASE C GENE PROMOTER REGIONS ARE REQUIRED TO DIRECT SPECIFIC LACZ EXPRESSION IN THE HIPPOCAMPUS AND PURKINJE CELLS OF TRANSGENIC MICE. 112
Red blood cells affect the margination of microparticles in synthetic microcapillaries and intravital microcirculation as a function of their size and shape 112
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss 112
Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing 112
The abundance of the long intergenic non-coding RNA 01087 differentiates between luminal and triple-negative breast cancers and predicts patient outcome 112
Nano-bio interface between human plasma and niosomes with different formulations indicates protein corona patterns for nanoparticle cell targeting and uptake 112
IgA antibodies to tissue transglutaminase: An effective diagnostic test for celiac disease. 111
Phenotypic expression of genotype-phenotype correlation in cystic fibrosis patients carrying the 852del22 mutation. 110
Novel mutations and structural implications in R-type pyruvate kinase-deficient patients from southern Italy. 110
An Altered Gut Microbiome Profile in a Child Affected by Crohn's Disease Normalized After Nutritional Therapy 110
Characterization of cholesterol biosynthesis defects: a new case of sterol-C4-methyl oxidase deficiency in Italy 109
Holt-Oram syndrome associated with anomalies of the feet 108
Natural phenylalanine hydroxylase variants that confer a mild phenotype affect the enzyme's conformational stability and oligomerization equilibrium 108
The analysis of the inflorescence miRNome of the orchid Orchis italica reveals a DEF-like MADS-box gene as a new miRNA target 108
Sex-comparative analysis of the miRNome of human amniotic stem cells during obesity 108
Characterization of deletion breakpoints within intron 50 and 51 of the dystrophin gene 107
Host defense peptide-derived privileged scaffolds for anti-infective drug discovery 107
Molecular diagnosis of Brugada syndrome via next-generation sequencing of a multigene panel in a young athlete 107
BCR/ABL genes and leukemic phenotype: from molecular mechanisms to clinical relation. 106
Complete phenotypic and genotypic lineage switch in a Philadelphia chromosome-positive acute lymphoblastic leukemia. 106
Diagnostic value of various serum antibodies detected by diverse methods in childhood celiac disease. 106
No change in the mucosal gut microbiome is associated with celiac disease-specific microbiome alteration in adult patients 106
Expression of human glyceraldehyde-3-phosphate dehydrogenase in normal and neoplastic tissues 105
Identification of two mutation within the transglutaminase 1 gene patients with lamellar ichthyosis. 105
MLL-AF4 oncoprotein up-regulates fibroblast growth factor receptor 2 (FGFR2) gene expression in hematopoietic progenitor cells 105
Denaturing HPLC procedure for factor IX gene scanning 104
Carcinoembryonic antigen mRNA analysis detects micrometsatatic cells in blood from lung cancer patients. 104
Diagnosi prenatale della sindrome nude-SCID. 104
14-3-3 θ over-expression increases both the cytosolic amount of AF4 and the expression levels of its target genes. 104
Biochemical and genetic characterization of a cholesterol biosynthesis defect: a new case of sterol-C4-methyl oxidase defect in a young Italian male 104
Detection of new mutations in hMLH1 gene in five out of ten Italian Hereditary Non Polyposis Colorectal Cancer (HNPCC) families 103
Nutritional controlled preparation and administration of different tomato purées indicate increase of β-carotene and lycopene isoforms, and of antioxidant potential in human blood bioavailability: A pilot study 103
A case of Buerger's disease associated to homozygosity of the MTHFR C677T mutation: a possible therapeutic support. 102
Prenatal diagnosis of cystic fibrosis: a case of twin pregnancy diagnosis and a review of 5 yeras experience. 102
Association of H558R Polymorphism In SCN5A Gene With Familial Dilated Cardiomyopathy 102
Interaction with 14-3-3 θ reduces AF4 transactivation function by inhibiting its nuclear translocation 101
Design and activity of a cyclic mini-β-defensin analog: a novel antimicrobial tool 101
Comparative metagenomic analysis of human gut microbiome composition using two different bioinformatic pipelines 101
The Mediterranean Diet in the Prevention of Degenerative Chronic Diseases 101
Clinical Efficacy of Isatuximab Plus Carfilzomib and Dexamethasone in Relapsed/Refractory Multiple Myeloma Patients 100
Hereditary fructose intolerance and celiac disease: a novel genetic association 100
Totale 15.811
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Categoria #
all - tutte 90.949
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 90.949
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021803 0 0 0 0 0 0 149 60 193 59 206 136
2021/20222.175 75 40 40 80 55 97 42 75 279 161 522 709
2022/20232.787 342 220 73 229 314 268 72 223 360 469 141 76
2023/20241.980 92 243 237 148 99 176 93 183 84 155 303 167
2024/20258.636 497 558 77 119 274 415 749 495 717 1.325 2.751 659
2025/20269.221 1.738 923 1.384 1.584 2.820 614 158 0 0 0 0 0
Totale 30.147