IRIS
SALVATORE, FRANCESCO
 Distribuzione geografica
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Continente #
EU - Europa 12.030
NA - Nord America 12.006
AS - Asia 10.668
SA - Sud America 1.388
Continente sconosciuto - Info sul continente non disponibili 490
AF - Africa 270
OC - Oceania 19
Totale 36.871
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Nazione #
US - Stati Uniti d'America 11.465
SG - Singapore 4.780
IT - Italia 4.371
RU - Federazione Russa 3.606
VN - Vietnam 2.161
CN - Cina 1.898
BR - Brasile 1.101
HK - Hong Kong 797
UA - Ucraina 619
DE - Germania 617
NL - Olanda 540
FR - Francia 522
FI - Finlandia 402
GB - Regno Unito 366
CA - Canada 360
SE - Svezia 344
IE - Irlanda 261
IN - India 180
JP - Giappone 171
BD - Bangladesh 125
AR - Argentina 114
ZA - Sudafrica 101
MX - Messico 94
PL - Polonia 93
ES - Italia 70
PH - Filippine 60
TH - Thailandia 56
EC - Ecuador 55
IQ - Iraq 53
CI - Costa d'Avorio 51
ID - Indonesia 47
KR - Corea 42
TR - Turchia 42
PK - Pakistan 39
BE - Belgio 34
AT - Austria 33
TW - Taiwan 32
CL - Cile 26
LT - Lituania 26
VE - Venezuela 26
MA - Marocco 25
CO - Colombia 24
IR - Iran 23
RO - Romania 23
AE - Emirati Arabi Uniti 21
CH - Svizzera 19
CZ - Repubblica Ceca 19
JM - Giamaica 18
KE - Kenya 17
AU - Australia 15
PY - Paraguay 15
SA - Arabia Saudita 15
UZ - Uzbekistan 14
CR - Costa Rica 13
OM - Oman 13
PT - Portogallo 13
TN - Tunisia 13
EG - Egitto 11
IL - Israele 11
NP - Nepal 11
PE - Perù 10
UY - Uruguay 10
BG - Bulgaria 9
LB - Libano 9
DZ - Algeria 8
EU - Europa 8
JO - Giordania 8
PS - Palestinian Territory 8
AZ - Azerbaigian 7
ET - Etiopia 7
MY - Malesia 7
SN - Senegal 7
DO - Repubblica Dominicana 6
GT - Guatemala 6
KZ - Kazakistan 6
NI - Nicaragua 6
PR - Porto Rico 6
SV - El Salvador 6
HN - Honduras 5
LK - Sri Lanka 5
NO - Norvegia 5
RS - Serbia 5
AL - Albania 4
AO - Angola 4
BB - Barbados 4
BO - Bolivia 4
GE - Georgia 4
MK - Macedonia 4
SY - Repubblica araba siriana 4
TT - Trinidad e Tobago 4
EE - Estonia 3
GR - Grecia 3
IS - Islanda 3
KG - Kirghizistan 3
LV - Lettonia 3
MN - Mongolia 3
NG - Nigeria 3
PA - Panama 3
UG - Uganda 3
XK - ???statistics.table.value.countryCode.XK??? 3
Totale 36.329
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Città #
Singapore 2.145
San Jose 1.586
Chandler 949
Moscow 857
Ashburn 775
Hong Kong 757
Beijing 618
Ho Chi Minh City 556
Jacksonville 543
Hanoi 465
Santa Clara 449
Naples 441
Amsterdam 434
Los Angeles 323
Council Bluffs 321
Millbury 280
Princeton 280
The Dalles 265
Napoli 263
Lauterbourg 259
Rome 225
Boston 224
Munich 223
Nanjing 216
Stockholm 190
Milan 179
New York 173
Houston 163
Tokyo 147
Buffalo 144
Wilmington 144
Dallas 139
Ottawa 114
São Paulo 110
Dong Ket 94
Da Nang 87
Palermo 83
Haiphong 82
Brooklyn 78
Des Moines 75
Woodbridge 75
Helsinki 67
Nanchang 67
Montreal 66
Atlanta 65
Redondo Beach 64
Denver 63
Warsaw 63
Mcallen 62
Montréal 62
Chicago 60
Seattle 59
Hefei 58
Orem 57
Chennai 55
Turin 53
Turku 51
London 47
Phoenix 47
Frankfurt am Main 46
Johannesburg 45
Shenyang 42
Catania 41
Boardman 38
San Francisco 38
Tianjin 38
Bologna 37
Rio de Janeiro 37
Mexico City 36
Biên Hòa 35
Falls Church 35
Norwalk 35
Bari 34
Hebei 34
Poplar 34
Augusta 31
Manchester 30
Cagliari 29
Toronto 29
Florence 28
Falkenstein 27
Paris 27
Redwood City 27
Changsha 26
Jiaxing 26
Salerno 26
Dublin 25
Ann Arbor 24
Kronberg 24
Washington 24
Mumbai 23
Nuremberg 23
Belo Horizonte 22
Bangkok 21
Can Tho 21
Hải Dương 21
Shanghai 20
Caserta 19
Dearborn 19
Genoa 19
Totale 17.813
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Nome #
Newborn screening: uno strumento per la diagnosi di difetti metabolici materni non diagnosticati 3.361
"Classical organic acidurias": diagnosis and pathogenesis. 553
Diagnosi di malattie metaboliche su sospetto clinico a confronto con dati di screening metabolico allargato 363
Tools and Avenues for Nanotechnology-based Vectors Exploitation for Biomarker Signature and Therapeutical Drug Delivery 363
Late diagnosis of Fabry disease caused by a de novo mutation in a patient with end stage renal disease Case Reports 308
Mutation screening of dynein genes in patients affected by primary ciliary diskinesia or Kartagener syndrome 215
Meccanismi epigenetici nella patogenesi dell'allergia al latte vaccino 210
A novel mutation in RP1 is a major cause of autosomal dominant retinitis pigmentosa in Southern Italy. 200
Detection of colonic dysplasia in patients with ulcerative colitis using a targeted fluorescent peptide and confocal laser endomicroscopy: A pilot study 195
Distribution of human beta-defensin polymorphisms in various control and cystic fibrosis populations. 188
Epigenetic features of FoxP3 in children with cow’s milk allergy 181
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 181
Ischemic Neoangiogenesis Enhanced by {beta}2-Adrenergic Receptor Overexpression. A Novel Role for the Endothelial Adrenergic System. 180
A child cohort study from South Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy 176
A First Look at an Automated Pipeline for NGS-Based Breast-Cancer Diagnosis: The CArDIGAN Approach 170
Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with rab geranylgeranyl transferase. 169
Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies 169
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 168
14-3-3 theta, a direct interactor of AF4, influences HOXA9 expression in RS4;11 leukemia cell line. 167
The Cause of Death of a Child in the 18th Century Solved by Bone Microbiome Typing Using Laser Microdissection and Next Generation Sequencing 167
Metastatic group 3 medulloblastoma is driven by PRUNE1 targeting NME1-TGF-β-OTX2-SNAIL via PTEN inhibition. 167
A role for D-aspartate oxidase in schizophrenia and in schizophrenia-related symptoms induced by phencyclidine in mice 166
Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and Perspectives 165
Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case Report. 164
Altered miR-193a-5p expression in children with cow's milk allergy 163
De novo sequencing and assembly of the whole genome of Novosphingobium Puteolanum PP1Y: a putative biotechnology engine 162
Basi molecolari delle emoglobinopatie ed approcci diagnostici attraverso le metodologie del DNA ricombinante 159
Yield and clinical significance of genetic screening in elite and amateur athletes 159
Clinical Efficacy of Isatuximab Plus Carfilzomib and Dexamethasone in Relapsed/Refractory Multiple Myeloma Patients 158
Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing 158
A paraoxonase gene polymorphism pon 1 (55) as an independent factor for increased carotid imt in women 157
Unraveling the structural and functional features of an aldolase A mutant involved in the hemolytic anemia and severe rhabdomyolysis reported in a child 156
Cardiac ion channel genes analysis in LQTS or Brugada families of Southern Italy revealed nineteen mutations, including nine novel ones 156
Adenoviral mediated gene transfer of the beta 2 adrenergic receptor (beta 2AR) corrects impaired angiogenesis in the ischemic hinlimb of hypertensive SHR rats 156
Genotype-phenotype correlation: A triple DNA mutational event in a boy entering sport conveys an additional pathogenicity risk 155
The role of the gut microbiome in the healthy adult status 154
Mutation screening in sarcomeric genes in Italian HCM paediatric population 154
Digenic heterozygosity in KCNQ1 and KCNH2 genes causes severe long QT phenotype 154
Isolation of microRNAs from floral bud and leaf tissue of Orchis italica (Orchidaceae) 154
De novo sequencing and assembly of the whole genome of Novosphingobium sp. PP1Y 153
A novel pathogenic BRCA1 splicing variant produces partial intron retention in the mature messenger RNA 152
PEGylated helper-dependent adenoviral vector expressing human Apo A-I for gene therapy in LDLR-deficient mice 150
Argomenti di biochimica 149
A rare case of sterol-C4-methyl oxidase deficiency in a young Italian male: Biochemical and molecular characterization 149
A Novel DHPLC-Based Procedure for the Analysis of COL1A1 and COL1A2 Mutations in Osteogenesis Imperfecta. 148
DNA sequence capture and high-throughput sequencing technology: a novel approach to identify a large number of hypertrophic cardiomyopathy-causing genes 147
A case of discordance between phenotype and genotype in malignant hyperthermia in the presence of the arg614cys mutation in the RYR1 gene 147
A deep sequencing approach to uncover the inflorescence miRNome of the orchid Orchis italica. 147
New insights into the Bcr-Abl activity-independent mechanisms of resistance to imatinib mesylate in KCL22 cells: the role of Shp1 and Shp2 145
Adenosylmethionine as a precursor for nucleic acids modification 144
The analysis of the inflorescence miRNome of the orchid Orchis italica reveals a DEF-like MADS-box gene as a new miRNA target 144
Complete phenotypic and genotypic lineage switch in a Philadelphia chromosome-positive acute lymphoblastic leukemia. 143
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 141
Serum pseudouridine in the diagnosis of acute leukaemias and as a novel prognostic indicator in acute lymphoblastic leukaemia 141
Pseudouridine determination in blood serum as tumor marker 140
Novel mutations and structural implications in R-type pyruvate kinase-deficient patients from southern Italy. 140
14-3-3 θ over-expression increases both the cytosolic amount of AF4 and the expression levels of its target genes. 140
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss 140
Coexistence of two distinct cell populations (CD56(+)TcRgammadelta(+) and CD56(+)TcRgammadelta(-)) in a case of aggressive CD56(+) lymphoma/leukemia. 139
The molecular analysis of BRCA1 and BRCA2: Next-generation sequencing supersedes conventional approaches 139
Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing 139
Cyclic beta defensisns analogs for the tratment of infections 139
Partial purification and MALDI-TOF MS analysis of UN1, a tumor antigen membrane glycoprotein. 136
An Altered Gut Microbiome Profile in a Child Affected by Crohn's Disease Normalized After Nutritional Therapy 136
Cyclic beta defensins analogs fot the treatment of infections 136
JURL-MK1 (c-kit(high)/CD30-/CD40-) and JURL-MK2 (c-kit(low)/CD30+/CD40+) cell lines: 'two-sided' model for investigating leukemic megakaryocytopoiesis. 135
Molecular diagnosis of Brugada syndrome via next-generation sequencing of a multigene panel in a young athlete 135
MLL-AF4 oncoprotein up-regulates fibroblast growth factor receptor 2 (FGFR2) gene expression in hematopoietic progenitor cells 134
Natural phenylalanine hydroxylase variants that confer a mild phenotype affect the enzyme's conformational stability and oligomerization equilibrium 134
Red blood cells affect the margination of microparticles in synthetic microcapillaries and intravital microcirculation as a function of their size and shape 134
Characterization of cholesterol biosynthesis defects: a new case of sterol-C4-methyl oxidase deficiency in Italy 134
Nano-bio interface between human plasma and niosomes with different formulations indicates protein corona patterns for nanoparticle cell targeting and uptake 134
Holt-Oram syndrome associated with anomalies of the feet 133
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function 132
Diagnostic value of various serum antibodies detected by diverse methods in childhood celiac disease. 132
The abundance of the long intergenic non-coding RNA 01087 differentiates between luminal and triple-negative breast cancers and predicts patient outcome 132
Sex-comparative analysis of the miRNome of human amniotic stem cells during obesity 131
Prenatal diagnosis of cystic fibrosis: a case of twin pregnancy diagnosis and a review of 5 yeras experience. 130
La pseudouridina come marcatore delle neoplasie di origine retrovirale 130
An ancestral host defence peptide within human β-defensin 3 recapitulates the antibacterial and antiviral activity of the full-length molecule 130
Biochemical and genetic characterization of a cholesterol biosynthesis defect: a new case of sterol-C4-methyl oxidase defect in a young Italian male 130
Characterization of deletion breakpoints within intron 50 and 51 of the dystrophin gene 129
Haemophilia A: molecular insights. 129
BBS1, BBS10 and BBS2 are major causative genes for Bardet-Biedl syndrome in Italian patients. 129
DIVERSE HUMAN ALDOLASE C GENE PROMOTER REGIONS ARE REQUIRED TO DIRECT SPECIFIC LACZ EXPRESSION IN THE HIPPOCAMPUS AND PURKINJE CELLS OF TRANSGENIC MICE. 128
IgA antibodies to tissue transglutaminase: An effective diagnostic test for celiac disease. 128
Comparative metagenomic analysis of human gut microbiome composition using two different bioinformatic pipelines 128
BCR/ABL genes and leukemic phenotype: from molecular mechanisms to clinical relation. 127
Phenotypic expression of genotype-phenotype correlation in cystic fibrosis patients carrying the 852del22 mutation. 126
Identification of two mutation within the transglutaminase 1 gene patients with lamellar ichthyosis. 126
Interaction with 14-3-3 θ reduces AF4 transactivation function by inhibiting its nuclear translocation 126
All-trans-retinoic acid (ATRA) responsive skin relapses of acute promyelocytic leukaemia followed by ATRA-induced pseudotumour cerebri 126
No change in the mucosal gut microbiome is associated with celiac disease-specific microbiome alteration in adult patients 125
Detection of new mutations in hMLH1 gene in five out of ten Italian Hereditary Non Polyposis Colorectal Cancer (HNPCC) families 124
Host defense peptide-derived privileged scaffolds for anti-infective drug discovery 124
Decreased free D-aspartate levels in the blood serum of patients with schizophrenia 123
DIRECT-DETECTION OF PROVIRAL GAG SEGMENT OF HUMAN-IMMUNODEFICIENCY-VIRUS IN PERIPHERAL-BLOOD LYMPHOCYTES BY COLORIMETRIC PCR ASSAY AS A CLINICAL LABORATORY TOOL APPLIED TO DIFFERENT AT-RISK POPULATIONS 123
Diagnosi prenatale della sindrome nude-SCID. 123
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 122
Enabling cytoplasmic delivery and organelle targeting by surface modification of nanocarriers 121
Totale 18.932
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Categoria #
all - tutte 113.099
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 113.099
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.100 0 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
2025/202614.878 1.738 923 1.384 1.584 2.820 614 1.579 854 1.763 1.048 314 257
2026/20271.067 555 512 0 0 0 0 0 0 0 0 0 0
Totale 36.871