IRIS
SALVATORE, FRANCESCO
 Distribuzione geografica
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Continente #
EU - Europa 6.159
NA - Nord America 5.726
AS - Asia 1.770
AF - Africa 48
SA - Sud America 23
OC - Oceania 14
Continente sconosciuto - Info sul continente non disponibili 8
Totale 13.748
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Nazione #
US - Stati Uniti d'America 5.541
IT - Italia 3.625
SG - Singapore 897
CN - Cina 672
UA - Ucraina 573
NL - Olanda 445
FI - Finlandia 325
DE - Germania 320
IE - Irlanda 252
GB - Regno Unito 203
CA - Canada 185
SE - Svezia 156
FR - Francia 117
VN - Vietnam 94
CI - Costa d'Avorio 48
IN - India 46
RU - Federazione Russa 36
BE - Belgio 21
IR - Iran 21
RO - Romania 18
PL - Polonia 16
CH - Svizzera 14
AU - Australia 13
BR - Brasile 13
CZ - Repubblica Ceca 9
TR - Turchia 9
AR - Argentina 8
EU - Europa 8
HK - Hong Kong 6
ES - Italia 5
PK - Pakistan 5
BG - Bulgaria 4
NO - Norvegia 4
LT - Lituania 3
PT - Portogallo 3
AL - Albania 2
DK - Danimarca 2
ID - Indonesia 2
IL - Israele 2
JP - Giappone 2
KR - Corea 2
LK - Sri Lanka 2
PS - Palestinian Territory 2
RS - Serbia 2
TH - Thailandia 2
TW - Taiwan 2
CL - Cile 1
CO - Colombia 1
GR - Grecia 1
HR - Croazia 1
KZ - Kazakistan 1
LV - Lettonia 1
MY - Malesia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PH - Filippine 1
SI - Slovenia 1
Totale 13.748
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Città #
Chandler 948
Singapore 757
Jacksonville 539
Amsterdam 418
Santa Clara 365
Naples 328
Millbury 280
Princeton 280
Napoli 263
Nanjing 216
Ashburn 193
Boston 193
Rome 155
Wilmington 143
Beijing 130
Houston 130
Milan 116
Ottawa 109
Dong Ket 94
Munich 80
Palermo 74
Woodbridge 74
Des Moines 73
Nanchang 67
Mcallen 62
Montréal 62
Helsinki 47
Turin 43
Shenyang 40
Catania 37
Falls Church 36
Norwalk 35
Hebei 34
Boardman 33
Cagliari 27
Augusta 26
Bari 26
Redwood City 26
Jiaxing 25
Kronberg 24
Salerno 23
Tianjin 23
Changsha 22
Ann Arbor 21
Florence 21
Bologna 19
Dearborn 19
Caserta 18
Orange 18
Kunming 16
Seattle 16
Dublin 15
Nocera Superiore 15
Washington 15
Dallas 14
Lawrence 14
Falkenstein 13
Padova 13
Torino 13
Formia 12
Genoa 12
Paris 12
San Mateo 12
Hangzhou 11
Reggio Calabria 11
Trieste 11
Frankfurt am Main 10
Latina 10
Los Angeles 10
Redmond 10
Baltimore 9
Bergamo 9
Indiana 9
Messina 9
New York 9
Toronto 9
Casoria 8
Giugliano In Campania 8
London 8
Mumbai 8
Pescara 8
Pune 8
San Felice A Cancello 8
Ancona 7
Ardabil 7
Brno 7
Leawood 7
Marano 7
Moscow 7
Segrate 7
Senigallia 7
Trento 7
Valsamoggia 7
Verona 7
Alcamo 6
Brescia 6
Capaci 6
Changchun 6
Cosenza 6
Dalmine 6
Totale 7.280
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Nome #
Newborn screening: uno strumento per la diagnosi di difetti metabolici materni non diagnosticati 2.681
Tools and Avenues for Nanotechnology-based Vectors Exploitation for Biomarker Signature and Therapeutical Drug Delivery 291
Diagnosi di malattie metaboliche su sospetto clinico a confronto con dati di screening metabolico allargato 247
Distribution of human beta-defensin polymorphisms in various control and cystic fibrosis populations. 142
Mutation screening of dynein genes in patients affected by primary ciliary diskinesia or Kartagener syndrome 139
Meccanismi epigenetici nella patogenesi dell'allergia al latte vaccino 99
Basi molecolari delle emoglobinopatie ed approcci diagnostici attraverso le metodologie del DNA ricombinante 94
Haemophilia A: molecular insights. 87
Argomenti di biochimica 74
Cardiac ion channel genes analysis in LQTS or Brugada families of Southern Italy revealed nineteen mutations, including nine novel ones 71
Metastatic group 3 medulloblastoma is driven by PRUNE1 targeting NME1-TGF-β-OTX2-SNAIL via PTEN inhibition. 71
Association of H558R Polymorphism In SCN5A Gene With Familial Dilated Cardiomyopathy 70
Molecular epidemiology of phenylalanine hydroxilase deficiency in Southern Italy: a 96% detection rate with ten novel mutations. 69
Phenotypic expression of genotype-phenotype correlation in cystic fibrosis patients carrying the 852del22 mutation. 67
14-3-3 theta, a direct interactor of AF4, influences HOXA9 expression in RS4;11 leukemia cell line. 67
A child cohort study from South Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy 65
Altered miR-193a-5p expression in children with cow's milk allergy 63
Biochimica generale 62
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 62
Mitochondrial M.T4216C (P.Y304h) and M.A4917G, (P.N150D) variations In a young patient with Maternally Inherited Diabetes and Deafness 62
The role of the gut microbiome in the healthy adult status 60
De novo sequencing and assembly of the whole genome of Novosphingobium Puteolanum PP1Y: a putative biotechnology engine 60
A role for D-aspartate oxidase in schizophrenia and in schizophrenia-related symptoms induced by phencyclidine in mice 59
Ischemic Neoangiogenesis Enhanced by {beta}2-Adrenergic Receptor Overexpression. A Novel Role for the Endothelial Adrenergic System. 58
Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing 57
A novel pathogenic BRCA1 splicing variant produces partial intron retention in the mature messenger RNA 57
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 57
Enabling cytoplasmic delivery and organelle targeting by surface modification of nanocarriers 56
A case of Buerger's disease associated to homozygosity of the MTHFR C677T mutation: a possible therapeutic support. 56
Adenosylmethionine as a precursor for nucleic acids modification 56
The Cause of Death of a Child in the 18th Century Solved by Bone Microbiome Typing Using Laser Microdissection and Next Generation Sequencing 56
Cyclic beta defensins analogs fot the treatment of infections 56
Partial purification and MALDI-TOF MS analysis of UN1, a tumor antigen membrane glycoprotein. 55
Carcinoembryonic antigen mRNA analysis detects micrometsatatic cells in blood from lung cancer patients. 55
Unraveling the structural and functional features of an aldolase A mutant involved in the hemolytic anemia and severe rhabdomyolysis reported in a child 55
A deep sequencing approach to uncover the inflorescence miRNome of the orchid Orchis italica. 55
A novel mutation in RP1 is a major cause of autosomal dominant retinitis pigmentosa in Southern Italy. 55
Red blood cells affect the margination of microparticles in synthetic microcapillaries and intravital microcirculation as a function of their size and shape 55
Coexistence of two distinct cell populations (CD56(+)TcRgammadelta(+) and CD56(+)TcRgammadelta(-)) in a case of aggressive CD56(+) lymphoma/leukemia. 53
Digenic heterozygosity in KCNQ1 and KCNH2 genes causes severe long QT phenotype 53
The Mediterranean Diet in the Prevention of Degenerative Chronic Diseases 53
EXPRESSION OF ADIPONECTIN RECEPTORS IN HUMAN CAROTID ATHEROSCLEROTIC PLAQUES Abstracts from the 12th National Congress of the Italian Society of Cardiovascular Prevention (SIPREC), Naples, 6–8 March 2014 53
Assignement of human aldolase C gene to chromosome 17, region cen-q21.1 52
A Novel DHPLC-Based Procedure for the Analysis of COL1A1 and COL1A2 Mutations in Osteogenesis Imperfecta. 52
Cyclic beta defensisns analogs for the tratment of infections 52
Hereditary fructose intolerance and celiac disease: a novel genetic association 51
Epigenetic features of FoxP3 in children with cow’s milk allergy 51
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss 51
Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies 51
Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case Report. 51
RYR1 sequence variants in myopathies: expression and functional studies in two families 51
DIVERSE HUMAN ALDOLASE C GENE PROMOTER REGIONS ARE REQUIRED TO DIRECT SPECIFIC LACZ EXPRESSION IN THE HIPPOCAMPUS AND PURKINJE CELLS OF TRANSGENIC MICE. 50
Carotid Artery Remodeling in Middle-Aged Women With the Metabolic Syndrome (from the "Progetto ATENA" Study). 50
Analisi molecolare e correlazioni genotipo-fenotipo per la consulenza genetica delle emoglobinopatie 50
Sequence variants of the RYR1 gene in a patient with Central Core Disease. 50
Adenoviral mediated gene transfer of the beta 2 adrenergic receptor (beta 2AR) corrects impaired angiogenesis in the ischemic hinlimb of hypertensive SHR rats 50
Pseudouridine determination in blood serum as tumor marker 49
Citrulline blood levels as indicators of residual intestinal absorption in patients with short bowel syndrome 49
Mutation screening in sarcomeric genes in Italian HCM paediatric population 49
Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with rab geranylgeranyl transferase. 49
Characterization of deletion breakpoints within intron 50 and 51 of the dystrophin gene 48
Transfer RNA methyltransferases: properties and role in the maturation of tRNA 48
Molecular diagnosis of Brugada syndrome via next-generation sequencing of a multigene panel in a young athlete 48
Six novel alleles identified in Italian hereditary fructose intolerance patients enlarge the mutation spectrum of the aldolase B gene 47
A larger spectrum of intragenic STRs improves linkage analysis and localization of intragenic recombination detection in the dystrophin gene: an analysis of 93 families from Southern Italy. J. Mol. Diagn. 47
Knockdown of the BBS10 Gene Product Affects Apical Targeting of AQP2 in Renal Cells: A Possible Explanation for the Polyuria Associated with Bardet-Biedl Syndrome 47
Detection of colonic dysplasia in patients with ulcerative colitis using a targeted fluorescent peptide and confocal laser endomicroscopy: A pilot study 47
Denaturing HPLC procedure for factor IX gene scanning 46
Direct detection of exon deletions/duplications in female carriers of and male patients with Duchenne/Becker muscular dystrophy. 46
Characterization of red cell membrane proteins as a function of red cell density: annexin VII in different forms of hereditary spherocytosis. 46
A 15-year molecular analysis of Duchenne/Becker muscular dystrophy: genetic features in a large cohort 46
BBS1, BBS10 and BBS2 are major causative genes for Bardet-Biedl syndrome in Italian patients. 46
An ancestral host defence peptide within human β-defensin 3 recapitulates the antibacterial and antiviral activity of the full-length molecule 46
Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and Perspectives 46
Characterization of cholesterol biosynthesis defects: a new case of sterol-C4-methyl oxidase deficiency in Italy 46
A First Look at an Automated Pipeline for NGS-Based Breast-Cancer Diagnosis: The CArDIGAN Approach 46
Liver expression in Cystic Fibrosis could be modulated by genetic factors different from the Cystic Fibrosis Transmembrane Regulator genotype. 45
A novel nonsense mutation (Y849X) in the CFTR gene of a CF patient from Southern Italy. 45
Cystic fibrosis presenting as metabolic alkalosis with hypochloremia in a boy with the rare D579G mutation 45
Analysis of dystrophin gene deletions correlates the hinge III region of the protein with the disease severity. Ann. Hum Genet. 69: 253-9. 45
Complete phenotypic and genotypic lineage switch in a Philadelphia chromosome-positive acute lymphoblastic leukemia. 45
A paraoxonase gene polymorphism pon 1 (55) as an independent factor for increased carotid imt in women 45
The molecular analysis of BRCA1 and BRCA2: Next-generation sequencing supersedes conventional approaches 45
The abundance of the long intergenic non-coding RNA 01087 differentiates between luminal and triple-negative breast cancers and predicts patient outcome 45
The analysis of the inflorescence miRNome of the orchid Orchis italica reveals a DEF-like MADS-box gene as a new miRNA target 44
Determination of pseudouridine and other nucleosides in human blood serum by high-performance liquid chromatography. 43
Human aldolase B cDNA detects a Pvu II RFLP in healthy individuals 43
Defensins as a therapeutic target for infectious diseases. 43
Design and activity of a cyclic mini-β-defensin analog: a novel antimicrobial tool 43
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 43
Host defense peptide-derived privileged scaffolds for anti-infective drug discovery 43
Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing 43
A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media thickness in middle-aged women 42
New insights into the Bcr-Abl activity-independent mechanisms of resistance to imatinib mesylate in KCL22 cells: the role of Shp1 and Shp2 42
All-trans-retinoic acid (ATRA) responsive skin relapses of acute promyelocytic leukaemia followed by ATRA-induced pseudotumour cerebri 42
A rare case of sterol-C4-methyl oxidase deficiency in a young Italian male: Biochemical and molecular characterization 42
Modified nucleosides in body fluids of tumor-bearing patients 41
A case of discordance between genotype and phenotype in a malignant hyperthermia family. 41
A common polymorphism in SCN5A gene is associated with dilated cardiomyopathy 41
An Altered Gut Microbiome Profile in a Child Affected by Crohn's Disease Normalized After Nutritional Therapy 41
Totale 8.504
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Categoria #
all - tutte 52.095
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 52.095
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020652 0 0 0 0 0 46 36 43 52 119 146 210
2020/20211.822 75 165 202 160 189 228 149 60 193 59 206 136
2021/20222.183 75 40 40 80 55 98 42 75 284 162 522 710
2022/20232.791 343 220 73 229 314 268 72 223 360 471 142 76
2023/20241.984 92 244 239 148 100 176 93 183 84 155 303 167
2024/20251.900 499 562 77 119 276 367 0 0 0 0 0 0
Totale 14.215