SALVATORE, FRANCESCO
 Distribuzione geografica
Continente #
EU - Europa 11.928
NA - Nord America 10.961
AS - Asia 10.599
SA - Sud America 1.362
AF - Africa 268
OC - Oceania 19
Continente sconosciuto - Info sul continente non disponibili 13
Totale 35.150
Nazione #
US - Stati Uniti d'America 10.481
SG - Singapore 4.779
IT - Italia 4.299
RU - Federazione Russa 3.606
VN - Vietnam 2.157
CN - Cina 1.880
BR - Brasile 1.084
HK - Hong Kong 795
DE - Germania 617
UA - Ucraina 617
NL - Olanda 530
FR - Francia 517
FI - Finlandia 402
GB - Regno Unito 365
SE - Svezia 344
CA - Canada 328
IE - Irlanda 261
IN - India 178
JP - Giappone 170
AR - Argentina 113
ZA - Sudafrica 101
BD - Bangladesh 94
MX - Messico 93
PL - Polonia 92
ES - Italia 66
PH - Filippine 58
TH - Thailandia 56
EC - Ecuador 53
IQ - Iraq 53
CI - Costa d'Avorio 51
ID - Indonesia 44
KR - Corea 42
TR - Turchia 42
PK - Pakistan 38
BE - Belgio 34
AT - Austria 33
TW - Taiwan 32
CL - Cile 26
LT - Lituania 26
MA - Marocco 25
VE - Venezuela 24
IR - Iran 23
RO - Romania 23
AE - Emirati Arabi Uniti 21
CO - Colombia 21
CZ - Repubblica Ceca 18
KE - Kenya 17
CH - Svizzera 16
AU - Australia 15
PY - Paraguay 15
SA - Arabia Saudita 14
UZ - Uzbekistan 14
JM - Giamaica 13
OM - Oman 13
TN - Tunisia 13
EG - Egitto 11
IL - Israele 11
PT - Portogallo 11
NP - Nepal 10
PE - Perù 10
BG - Bulgaria 9
LB - Libano 9
UY - Uruguay 9
DZ - Algeria 8
EU - Europa 8
JO - Giordania 8
PS - Palestinian Territory 8
AZ - Azerbaigian 7
ET - Etiopia 7
SN - Senegal 7
CR - Costa Rica 6
DO - Repubblica Dominicana 6
KZ - Kazakistan 6
MY - Malesia 6
LK - Sri Lanka 5
NO - Norvegia 5
RS - Serbia 5
SV - El Salvador 5
AL - Albania 4
AO - Angola 4
BO - Bolivia 4
MK - Macedonia 4
NI - Nicaragua 4
PR - Porto Rico 4
SY - Repubblica araba siriana 4
BB - Barbados 3
EE - Estonia 3
GE - Georgia 3
GR - Grecia 3
GT - Guatemala 3
HN - Honduras 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
BH - Bahrain 2
Totale 35.091
Città #
Singapore 2.145
San Jose 1.461
Chandler 949
Moscow 857
Hong Kong 755
Ashburn 747
Beijing 614
Ho Chi Minh City 555
Jacksonville 540
Hanoi 465
Amsterdam 434
Naples 433
Santa Clara 427
Los Angeles 311
Millbury 280
Princeton 279
The Dalles 265
Napoli 263
Lauterbourg 259
Boston 223
Munich 223
Nanjing 216
Rome 214
Stockholm 190
Milan 171
New York 161
Houston 156
Tokyo 146
Wilmington 144
Buffalo 142
Dallas 131
Ottawa 114
São Paulo 105
Dong Ket 94
Da Nang 87
Palermo 83
Haiphong 82
Council Bluffs 80
Des Moines 75
Woodbridge 75
Brooklyn 72
Helsinki 67
Nanchang 67
Redondo Beach 64
Warsaw 63
Mcallen 62
Montreal 62
Montréal 62
Denver 61
Hefei 58
Seattle 58
Orem 57
Chicago 55
Chennai 54
Atlanta 53
Turku 51
Turin 49
Frankfurt am Main 46
London 46
Johannesburg 45
Shenyang 42
Catania 41
Tianjin 38
Boardman 37
Rio de Janeiro 37
Bologna 36
Mexico City 36
Biên Hòa 35
Falls Church 35
Norwalk 35
Phoenix 35
San Francisco 35
Bari 34
Hebei 34
Poplar 34
Augusta 30
Manchester 30
Cagliari 29
Falkenstein 27
Paris 27
Toronto 27
Changsha 26
Jiaxing 26
Redwood City 26
Dublin 25
Salerno 25
Ann Arbor 24
Florence 24
Kronberg 24
Mumbai 23
Nuremberg 23
Belo Horizonte 22
Bangkok 21
Can Tho 21
Hải Dương 21
Washington 21
Shanghai 20
Caserta 19
Dearborn 19
Genoa 19
Totale 17.246
Nome #
Newborn screening: uno strumento per la diagnosi di difetti metabolici materni non diagnosticati 3.310
"Classical organic acidurias": diagnosis and pathogenesis. 550
Tools and Avenues for Nanotechnology-based Vectors Exploitation for Biomarker Signature and Therapeutical Drug Delivery 359
Diagnosi di malattie metaboliche su sospetto clinico a confronto con dati di screening metabolico allargato 353
Mutation screening of dynein genes in patients affected by primary ciliary diskinesia or Kartagener syndrome 214
Meccanismi epigenetici nella patogenesi dell'allergia al latte vaccino 208
A novel mutation in RP1 is a major cause of autosomal dominant retinitis pigmentosa in Southern Italy. 195
Detection of colonic dysplasia in patients with ulcerative colitis using a targeted fluorescent peptide and confocal laser endomicroscopy: A pilot study 191
Distribution of human beta-defensin polymorphisms in various control and cystic fibrosis populations. 185
Ischemic Neoangiogenesis Enhanced by {beta}2-Adrenergic Receptor Overexpression. A Novel Role for the Endothelial Adrenergic System. 177
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 175
Epigenetic features of FoxP3 in children with cow’s milk allergy 173
A child cohort study from South Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy 171
Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies 167
A First Look at an Automated Pipeline for NGS-Based Breast-Cancer Diagnosis: The CArDIGAN Approach 167
14-3-3 theta, a direct interactor of AF4, influences HOXA9 expression in RS4;11 leukemia cell line. 166
Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with rab geranylgeranyl transferase. 164
The Cause of Death of a Child in the 18th Century Solved by Bone Microbiome Typing Using Laser Microdissection and Next Generation Sequencing 164
A role for D-aspartate oxidase in schizophrenia and in schizophrenia-related symptoms induced by phencyclidine in mice 163
Metastatic group 3 medulloblastoma is driven by PRUNE1 targeting NME1-TGF-β-OTX2-SNAIL via PTEN inhibition. 163
Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case Report. 161
Altered miR-193a-5p expression in children with cow's milk allergy 160
De novo sequencing and assembly of the whole genome of Novosphingobium Puteolanum PP1Y: a putative biotechnology engine 159
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 159
Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and Perspectives 157
Yield and clinical significance of genetic screening in elite and amateur athletes 156
A paraoxonase gene polymorphism pon 1 (55) as an independent factor for increased carotid imt in women 155
Unraveling the structural and functional features of an aldolase A mutant involved in the hemolytic anemia and severe rhabdomyolysis reported in a child 154
Adenoviral mediated gene transfer of the beta 2 adrenergic receptor (beta 2AR) corrects impaired angiogenesis in the ischemic hinlimb of hypertensive SHR rats 154
Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing 153
Genotype-phenotype correlation: A triple DNA mutational event in a boy entering sport conveys an additional pathogenicity risk 153
Isolation of microRNAs from floral bud and leaf tissue of Orchis italica (Orchidaceae) 152
De novo sequencing and assembly of the whole genome of Novosphingobium sp. PP1Y 151
The role of the gut microbiome in the healthy adult status 148
Cardiac ion channel genes analysis in LQTS or Brugada families of Southern Italy revealed nineteen mutations, including nine novel ones 148
Argomenti di biochimica 148
Mutation screening in sarcomeric genes in Italian HCM paediatric population 146
A novel pathogenic BRCA1 splicing variant produces partial intron retention in the mature messenger RNA 146
A case of discordance between phenotype and genotype in malignant hyperthermia in the presence of the arg614cys mutation in the RYR1 gene 145
Digenic heterozygosity in KCNQ1 and KCNH2 genes causes severe long QT phenotype 144
A deep sequencing approach to uncover the inflorescence miRNome of the orchid Orchis italica. 144
A rare case of sterol-C4-methyl oxidase deficiency in a young Italian male: Biochemical and molecular characterization 144
A Novel DHPLC-Based Procedure for the Analysis of COL1A1 and COL1A2 Mutations in Osteogenesis Imperfecta. 143
PEGylated helper-dependent adenoviral vector expressing human Apo A-I for gene therapy in LDLR-deficient mice 143
Adenosylmethionine as a precursor for nucleic acids modification 142
Basi molecolari delle emoglobinopatie ed approcci diagnostici attraverso le metodologie del DNA ricombinante 141
The analysis of the inflorescence miRNome of the orchid Orchis italica reveals a DEF-like MADS-box gene as a new miRNA target 141
New insights into the Bcr-Abl activity-independent mechanisms of resistance to imatinib mesylate in KCL22 cells: the role of Shp1 and Shp2 140
DNA sequence capture and high-throughput sequencing technology: a novel approach to identify a large number of hypertrophic cardiomyopathy-causing genes 138
14-3-3 θ over-expression increases both the cytosolic amount of AF4 and the expression levels of its target genes. 138
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 138
Serum pseudouridine in the diagnosis of acute leukaemias and as a novel prognostic indicator in acute lymphoblastic leukaemia 138
Pseudouridine determination in blood serum as tumor marker 137
Novel mutations and structural implications in R-type pyruvate kinase-deficient patients from southern Italy. 137
Coexistence of two distinct cell populations (CD56(+)TcRgammadelta(+) and CD56(+)TcRgammadelta(-)) in a case of aggressive CD56(+) lymphoma/leukemia. 137
Complete phenotypic and genotypic lineage switch in a Philadelphia chromosome-positive acute lymphoblastic leukemia. 137
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss 136
The molecular analysis of BRCA1 and BRCA2: Next-generation sequencing supersedes conventional approaches 135
Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing 135
Cyclic beta defensins analogs fot the treatment of infections 134
Cyclic beta defensisns analogs for the tratment of infections 134
Partial purification and MALDI-TOF MS analysis of UN1, a tumor antigen membrane glycoprotein. 133
JURL-MK1 (c-kit(high)/CD30-/CD40-) and JURL-MK2 (c-kit(low)/CD30+/CD40+) cell lines: 'two-sided' model for investigating leukemic megakaryocytopoiesis. 133
An Altered Gut Microbiome Profile in a Child Affected by Crohn's Disease Normalized After Nutritional Therapy 133
Natural phenylalanine hydroxylase variants that confer a mild phenotype affect the enzyme's conformational stability and oligomerization equilibrium 131
Characterization of cholesterol biosynthesis defects: a new case of sterol-C4-methyl oxidase deficiency in Italy 131
Nano-bio interface between human plasma and niosomes with different formulations indicates protein corona patterns for nanoparticle cell targeting and uptake 131
Clinical Efficacy of Isatuximab Plus Carfilzomib and Dexamethasone in Relapsed/Refractory Multiple Myeloma Patients 130
MLL-AF4 oncoprotein up-regulates fibroblast growth factor receptor 2 (FGFR2) gene expression in hematopoietic progenitor cells 130
Red blood cells affect the margination of microparticles in synthetic microcapillaries and intravital microcirculation as a function of their size and shape 130
Holt-Oram syndrome associated with anomalies of the feet 129
La pseudouridina come marcatore delle neoplasie di origine retrovirale 129
Biochemical and genetic characterization of a cholesterol biosynthesis defect: a new case of sterol-C4-methyl oxidase defect in a young Italian male 129
Molecular diagnosis of Brugada syndrome via next-generation sequencing of a multigene panel in a young athlete 129
The abundance of the long intergenic non-coding RNA 01087 differentiates between luminal and triple-negative breast cancers and predicts patient outcome 129
An ancestral host defence peptide within human β-defensin 3 recapitulates the antibacterial and antiviral activity of the full-length molecule 128
Sex-comparative analysis of the miRNome of human amniotic stem cells during obesity 127
DIVERSE HUMAN ALDOLASE C GENE PROMOTER REGIONS ARE REQUIRED TO DIRECT SPECIFIC LACZ EXPRESSION IN THE HIPPOCAMPUS AND PURKINJE CELLS OF TRANSGENIC MICE. 126
Prenatal diagnosis of cystic fibrosis: a case of twin pregnancy diagnosis and a review of 5 yeras experience. 126
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function 126
BBS1, BBS10 and BBS2 are major causative genes for Bardet-Biedl syndrome in Italian patients. 126
Haemophilia A: molecular insights. 125
Diagnostic value of various serum antibodies detected by diverse methods in childhood celiac disease. 125
IgA antibodies to tissue transglutaminase: An effective diagnostic test for celiac disease. 124
Identification of two mutation within the transglutaminase 1 gene patients with lamellar ichthyosis. 124
No change in the mucosal gut microbiome is associated with celiac disease-specific microbiome alteration in adult patients 124
Phenotypic expression of genotype-phenotype correlation in cystic fibrosis patients carrying the 852del22 mutation. 123
BCR/ABL genes and leukemic phenotype: from molecular mechanisms to clinical relation. 123
Interaction with 14-3-3 θ reduces AF4 transactivation function by inhibiting its nuclear translocation 123
Comparative metagenomic analysis of human gut microbiome composition using two different bioinformatic pipelines 123
Characterization of deletion breakpoints within intron 50 and 51 of the dystrophin gene 122
Detection of new mutations in hMLH1 gene in five out of ten Italian Hereditary Non Polyposis Colorectal Cancer (HNPCC) families 121
All-trans-retinoic acid (ATRA) responsive skin relapses of acute promyelocytic leukaemia followed by ATRA-induced pseudotumour cerebri 121
Carcinoembryonic antigen mRNA analysis detects micrometsatatic cells in blood from lung cancer patients. 120
Hereditary fructose intolerance and celiac disease: a novel genetic association 120
Diagnosi prenatale della sindrome nude-SCID. 120
Host defense peptide-derived privileged scaffolds for anti-infective drug discovery 120
Transcription factor TBX1 overexpression induces downregulation of proteins involved in retinoic acid metabolism: a comparative proteomic analysis. 118
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 118
Association of H558R Polymorphism In SCN5A Gene With Familial Dilated Cardiomyopathy 118
Totale 18.274
Categoria #
all - tutte 103.492
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 103.492


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021136 0 0 0 0 0 0 0 0 0 0 0 136
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
2025/202614.700 1.738 923 1.384 1.584 2.820 614 1.579 854 1.763 1.048 314 79
Totale 35.626