IRIS
SALVATORE, FRANCESCO
 Distribuzione geografica
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Continente #
EU - Europa 5.462
NA - Nord America 5.020
AS - Asia 828
AF - Africa 48
SA - Sud America 21
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 8
Totale 11.396
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Nazione #
US - Stati Uniti d'America 4.840
IT - Italia 3.094
CN - Cina 628
UA - Ucraina 571
NL - Olanda 431
FI - Finlandia 287
DE - Germania 269
IE - Irlanda 251
GB - Regno Unito 197
CA - Canada 180
SE - Svezia 156
FR - Francia 111
VN - Vietnam 94
CI - Costa d'Avorio 48
IN - India 42
RO - Romania 18
SG - Singapore 18
IR - Iran 16
BE - Belgio 15
PL - Polonia 15
CH - Svizzera 14
BR - Brasile 13
AU - Australia 8
EU - Europa 8
TR - Turchia 8
AR - Argentina 6
RU - Federazione Russa 6
ES - Italia 5
PK - Pakistan 5
BG - Bulgaria 4
NO - Norvegia 4
HK - Hong Kong 3
PT - Portogallo 3
CZ - Repubblica Ceca 2
DK - Danimarca 2
ID - Indonesia 2
IL - Israele 2
JP - Giappone 2
KR - Corea 2
LK - Sri Lanka 2
RS - Serbia 2
CL - Cile 1
CO - Colombia 1
GR - Grecia 1
HR - Croazia 1
KZ - Kazakistan 1
LT - Lituania 1
LV - Lettonia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PH - Filippine 1
SI - Slovenia 1
TH - Thailandia 1
Totale 11.396
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Città #
Chandler 955
Jacksonville 539
Amsterdam 419
Princeton 281
Millbury 280
Naples 267
Napoli 263
Nanjing 216
Boston 193
Ashburn 181
Wilmington 143
Houston 130
Beijing 129
Rome 119
Ottawa 108
Dong Ket 94
Woodbridge 74
Des Moines 73
Milan 68
Nanchang 67
Palermo 67
Mcallen 62
Montréal 62
Munich 51
Shenyang 39
Falls Church 36
Norwalk 35
Hebei 34
Catania 33
Turin 29
Boardman 27
Cagliari 27
Augusta 26
Redwood City 26
Jiaxing 25
Bari 24
Kronberg 24
Tianjin 23
Changsha 22
Ann Arbor 21
Florence 20
Dearborn 19
Salerno 19
Caserta 18
Orange 18
Kunming 16
Seattle 16
Nocera Superiore 15
Washington 15
Dublin 14
Lawrence 14
Torino 13
Paris 12
San Mateo 12
Hangzhou 11
Singapore 11
Trieste 11
Bologna 10
Redmond 10
Reggio Calabria 10
Helsinki 9
Indiana 9
New York 9
Padova 9
Casoria 8
Formia 8
Giugliano In Campania 8
Mumbai 8
Pune 8
San Felice A Cancello 8
Ardabil 7
Baltimore 7
Bergamo 7
Latina 7
Leawood 7
Los Angeles 7
Marano 7
Messina 7
Segrate 7
Trento 7
Valsamoggia 7
Verona 7
Ancona 6
Capaci 6
Changchun 6
Cosenza 6
Dalmine 6
Genoa 6
Marano Di Napoli 6
Toronto 6
Waanrode 6
Arad 5
Campagna 5
Camparada 5
Casalnuovo Di Napoli 5
Chennai 5
Chiaravalle 5
Foggia 5
Frankfurt am Main 5
Fremont 5
Totale 5.843
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Nome #
Newborn screening: uno strumento per la diagnosi di difetti metabolici materni non diagnosticati 2.210
Tools and Avenues for Nanotechnology-based Vectors Exploitation for Biomarker Signature and Therapeutical Drug Delivery 282
Diagnosi di malattie metaboliche su sospetto clinico a confronto con dati di screening metabolico allargato 211
Distribution of human beta-defensin polymorphisms in various control and cystic fibrosis populations. 137
Mutation screening of dynein genes in patients affected by primary ciliary diskinesia or Kartagener syndrome 132
Meccanismi epigenetici nella patogenesi dell'allergia al latte vaccino 95
Basi molecolari delle emoglobinopatie ed approcci diagnostici attraverso le metodologie del DNA ricombinante 92
Haemophilia A: molecular insights. 81
Molecular epidemiology of phenylalanine hydroxilase deficiency in Southern Italy: a 96% detection rate with ten novel mutations. 67
Metastatic group 3 medulloblastoma is driven by PRUNE1 targeting NME1-TGF-β-OTX2-SNAIL via PTEN inhibition. 66
Argomenti di biochimica 65
Cardiac ion channel genes analysis in LQTS or Brugada families of Southern Italy revealed nineteen mutations, including nine novel ones 63
Phenotypic expression of genotype-phenotype correlation in cystic fibrosis patients carrying the 852del22 mutation. 62
Association of H558R Polymorphism In SCN5A Gene With Familial Dilated Cardiomyopathy 60
14-3-3 theta, a direct interactor of AF4, influences HOXA9 expression in RS4;11 leukemia cell line. 58
Altered miR-193a-5p expression in children with cow's milk allergy 58
Mitochondrial M.T4216C (P.Y304h) and M.A4917G, (P.N150D) variations In a young patient with Maternally Inherited Diabetes and Deafness 56
A child cohort study from South Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy 54
Biochimica generale 54
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 54
The role of the gut microbiome in the healthy adult status 53
Enabling cytoplasmic delivery and organelle targeting by surface modification of nanocarriers 51
Ischemic Neoangiogenesis Enhanced by {beta}2-Adrenergic Receptor Overexpression. A Novel Role for the Endothelial Adrenergic System. 51
A deep sequencing approach to uncover the inflorescence miRNome of the orchid Orchis italica. 51
The Mediterranean Diet in the Prevention of Degenerative Chronic Diseases 51
Assignement of human aldolase C gene to chromosome 17, region cen-q21.1 50
Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing 50
The Cause of Death of a Child in the 18th Century Solved by Bone Microbiome Typing Using Laser Microdissection and Next Generation Sequencing 49
A novel pathogenic BRCA1 splicing variant produces partial intron retention in the mature messenger RNA 49
Cyclic beta defensins analogs fot the treatment of infections 49
De novo sequencing and assembly of the whole genome of Novosphingobium Puteolanum PP1Y: a putative biotechnology engine 48
Epigenetic features of FoxP3 in children with cow’s milk allergy 48
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss 48
Partial purification and MALDI-TOF MS analysis of UN1, a tumor antigen membrane glycoprotein. 47
Carcinoembryonic antigen mRNA analysis detects micrometsatatic cells in blood from lung cancer patients. 47
Unraveling the structural and functional features of an aldolase A mutant involved in the hemolytic anemia and severe rhabdomyolysis reported in a child 47
Coexistence of two distinct cell populations (CD56(+)TcRgammadelta(+) and CD56(+)TcRgammadelta(-)) in a case of aggressive CD56(+) lymphoma/leukemia. 47
A role for D-aspartate oxidase in schizophrenia and in schizophrenia-related symptoms induced by phencyclidine in mice 47
Characterization of deletion breakpoints within intron 50 and 51 of the dystrophin gene 46
A novel mutation in RP1 is a major cause of autosomal dominant retinitis pigmentosa in Southern Italy. 46
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 46
Cyclic beta defensisns analogs for the tratment of infections 46
A case of Buerger's disease associated to homozygosity of the MTHFR C677T mutation: a possible therapeutic support. 45
Citrulline blood levels as indicators of residual intestinal absorption in patients with short bowel syndrome 45
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 45
Carotid Artery Remodeling in Middle-Aged Women With the Metabolic Syndrome (from the "Progetto ATENA" Study). 44
Sequence variants of the RYR1 gene in a patient with Central Core Disease. 44
Cystic fibrosis presenting as metabolic alkalosis with hypochloremia in a boy with the rare D579G mutation 43
Hereditary fructose intolerance and celiac disease: a novel genetic association 43
A 15-year molecular analysis of Duchenne/Becker muscular dystrophy: genetic features in a large cohort 43
Digenic heterozygosity in KCNQ1 and KCNH2 genes causes severe long QT phenotype 43
Detection of colonic dysplasia in patients with ulcerative colitis using a targeted fluorescent peptide and confocal laser endomicroscopy: A pilot study 43
Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case Report. 43
Adenosylmethionine as a precursor for nucleic acids modification 42
Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with rab geranylgeranyl transferase. 42
Six novel alleles identified in Italian hereditary fructose intolerance patients enlarge the mutation spectrum of the aldolase B gene 41
DIVERSE HUMAN ALDOLASE C GENE PROMOTER REGIONS ARE REQUIRED TO DIRECT SPECIFIC LACZ EXPRESSION IN THE HIPPOCAMPUS AND PURKINJE CELLS OF TRANSGENIC MICE. 41
Liver expression in Cystic Fibrosis could be modulated by genetic factors different from the Cystic Fibrosis Transmembrane Regulator genotype. 41
Direct detection of exon deletions/duplications in female carriers of and male patients with Duchenne/Becker muscular dystrophy. 41
Analysis of dystrophin gene deletions correlates the hinge III region of the protein with the disease severity. Ann. Hum Genet. 69: 253-9. 41
Analisi molecolare e correlazioni genotipo-fenotipo per la consulenza genetica delle emoglobinopatie 41
Defensins as a therapeutic target for infectious diseases. 41
Molecular diagnosis of Brugada syndrome via next-generation sequencing of a multigene panel in a young athlete 41
RYR1 sequence variants in myopathies: expression and functional studies in two families 41
A novel nonsense mutation (Y849X) in the CFTR gene of a CF patient from Southern Italy. 40
Characterization of red cell membrane proteins as a function of red cell density: annexin VII in different forms of hereditary spherocytosis. 40
Mutation screening in sarcomeric genes in Italian HCM paediatric population 40
A Novel DHPLC-Based Procedure for the Analysis of COL1A1 and COL1A2 Mutations in Osteogenesis Imperfecta. 40
Adenoviral mediated gene transfer of the beta 2 adrenergic receptor (beta 2AR) corrects impaired angiogenesis in the ischemic hinlimb of hypertensive SHR rats 40
Red blood cells affect the margination of microparticles in synthetic microcapillaries and intravital microcirculation as a function of their size and shape 40
An ancestral host defence peptide within human β-defensin 3 recapitulates the antibacterial and antiviral activity of the full-length molecule 40
Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and Perspectives 40
The abundance of the long intergenic non-coding RNA 01087 differentiates between luminal and triple-negative breast cancers and predicts patient outcome 40
Pseudouridine determination in blood serum as tumor marker 39
A case of discordance between genotype and phenotype in a malignant hyperthermia family. 39
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. 39
The analysis of the inflorescence miRNome of the orchid Orchis italica reveals a DEF-like MADS-box gene as a new miRNA target 39
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 39
Denaturing HPLC procedure for factor IX gene scanning 38
Human aldolase B cDNA detects a Pvu II RFLP in healthy individuals 38
Transfer RNA methyltransferases: properties and role in the maturation of tRNA 38
Complete phenotypic and genotypic lineage switch in a Philadelphia chromosome-positive acute lymphoblastic leukemia. 38
The molecular analysis of BRCA1 and BRCA2: Next-generation sequencing supersedes conventional approaches 38
Characterization of cholesterol biosynthesis defects: a new case of sterol-C4-methyl oxidase deficiency in Italy 38
A First Look at an Automated Pipeline for NGS-Based Breast-Cancer Diagnosis: The CArDIGAN Approach 38
A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy 38
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 37
Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies 37
Determination of pseudouridine and other nucleosides in human blood serum by high-performance liquid chromatography. 36
A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media thickness in middle-aged women 36
Il contributo della genetica nella diagnosi in ipertermia maligna. 36
New insights into the Bcr-Abl activity-independent mechanisms of resistance to imatinib mesylate in KCL22 cells: the role of Shp1 and Shp2 36
Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing 36
Yield and clinical significance of genetic screening in elite and amateur athletes 36
BCR/ABL genes and leukemic phenotype: from molecular mechanisms to clinical relation. 35
A unique origin for Sicilian (delta beta) (0)-thalassemia in 33 unrelated families and its rapid diagnostic characterization by PCR analysis. 35
A paraoxonase gene polymorphism pon 1 (55) as an independent factor for increased carotid imt in women 35
Detection of new mutations in hMLH1 gene in five out of ten Italian Hereditary Non Polyposis Colorectal Cancer (HNPCC) families 35
BBS1, BBS10 and BBS2 are major causative genes for Bardet-Biedl syndrome in Italian patients. 35
Biochemical and genetic characterization of a cholesterol biosynthesis defect: a new case of sterol-C4-methyl oxidase defect in a young Italian male 35
Totale 7.317
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Categoria #
all - tutte 37.103
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 37.103
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019169 0 0 0 0 0 0 0 0 0 0 69 100
2019/20201.471 415 51 149 49 155 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
2022/20232.802 344 222 73 231 316 269 72 223 360 473 143 76
2023/20241.520 92 244 239 148 101 178 94 183 84 155 2 0
Totale 11.862