IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BARLATI, Sergio
 Distribuzione geografica
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Continente #
NA - Nord America 19.295
EU - Europa 10.120
AS - Asia 9.334
SA - Sud America 1.625
Continente sconosciuto - Info sul continente non disponibili 745
AF - Africa 189
OC - Oceania 57
AN - Antartide 2
Totale 41.367
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Nazione #
US - Stati Uniti d'America 18.813
CN - Cina 3.618
SG - Singapore 2.900
PL - Polonia 2.347
UA - Ucraina 1.927
DE - Germania 1.551
BR - Brasile 1.334
IT - Italia 1.021
HK - Hong Kong 918
FR - Francia 812
FI - Finlandia 707
GB - Regno Unito 619
VN - Vietnam 549
IN - India 406
RU - Federazione Russa 392
TR - Turchia 316
IE - Irlanda 286
CA - Canada 241
BD - Bangladesh 167
SE - Svezia 110
AR - Argentina 98
MX - Messico 76
NL - Olanda 70
ID - Indonesia 69
BE - Belgio 63
ZA - Sudafrica 62
IQ - Iraq 56
EC - Ecuador 54
AU - Australia 46
JP - Giappone 45
ES - Italia 41
PK - Pakistan 36
AT - Austria 33
CO - Colombia 33
JM - Giamaica 32
SA - Arabia Saudita 32
CZ - Repubblica Ceca 31
NG - Nigeria 31
VE - Venezuela 30
EU - Europa 28
IR - Iran 25
KR - Corea 22
PY - Paraguay 21
TT - Trinidad e Tobago 21
KE - Kenya 20
LU - Lussemburgo 20
UZ - Uzbekistan 20
CR - Costa Rica 19
LT - Lituania 18
HN - Honduras 17
MA - Marocco 17
PE - Perù 17
JO - Giordania 16
CL - Cile 15
GT - Guatemala 14
UY - Uruguay 14
AE - Emirati Arabi Uniti 13
IL - Israele 12
MU - Mauritius 12
MY - Malesia 12
KZ - Kazakistan 11
NZ - Nuova Zelanda 11
TN - Tunisia 11
CH - Svizzera 10
PH - Filippine 10
TH - Thailandia 10
GP - Guadalupe 9
NI - Nicaragua 9
PR - Porto Rico 9
BO - Bolivia 8
DZ - Algeria 8
EG - Egitto 8
PA - Panama 8
RO - Romania 8
AZ - Azerbaigian 7
NP - Nepal 7
TW - Taiwan 7
AL - Albania 6
AM - Armenia 6
BG - Bulgaria 6
ET - Etiopia 6
KG - Kirghizistan 6
LK - Sri Lanka 6
SD - Sudan 6
SV - El Salvador 6
BB - Barbados 5
CW - ???statistics.table.value.countryCode.CW??? 5
DO - Repubblica Dominicana 5
HU - Ungheria 5
OM - Oman 5
PS - Palestinian Territory 5
SI - Slovenia 5
SK - Slovacchia (Repubblica Slovacca) 5
BH - Bahrain 4
DK - Danimarca 4
RS - Serbia 4
BA - Bosnia-Erzegovina 3
EE - Estonia 3
GE - Georgia 3
LA - Repubblica Popolare Democratica del Laos 3
Totale 40.608
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Città #
Warsaw 2.343
Fairfield 1.757
Ashburn 1.747
Singapore 1.614
Woodbridge 1.533
Jacksonville 1.369
Houston 1.005
San Jose 954
Hong Kong 912
Beijing 755
Cambridge 717
Seattle 697
Ann Arbor 694
Wilmington 662
Chandler 608
Nanjing 544
Princeton 537
The Dalles 499
Council Bluffs 455
New York 408
Helsinki 401
Dublin 285
Dearborn 283
Los Angeles 278
Brescia 271
Columbus 270
Lauterbourg 237
Istanbul 235
Nanchang 188
Des Moines 175
Shenyang 161
Ho Chi Minh City 159
Buffalo 139
Munich 134
Hebei 131
Lancaster 131
São Paulo 127
Jinan 123
Milan 117
Changsha 116
Moscow 113
Chicago 106
San Francisco 106
Hanoi 105
Tianjin 105
San Diego 102
Dallas 98
Shanghai 98
Santa Clara 91
Jiaxing 87
Orem 87
Kunming 79
Redondo Beach 72
Dong Ket 71
London 71
Hangzhou 62
Toronto 58
Phoenix 56
Montreal 52
Zhengzhou 52
Verona 49
Brussels 47
Chennai 47
Ningbo 47
Turku 44
Rio de Janeiro 43
Guangzhou 42
Atlanta 40
Brooklyn 40
Frankfurt am Main 37
Kocaeli 37
Charlotte 36
Johannesburg 35
Tokyo 35
Belo Horizonte 34
Denver 34
Abuja 31
Pune 31
Nuremberg 30
Rome 30
Boston 29
Paris 29
San Mateo 29
Boardman 28
Jakarta 28
Lanzhou 28
Taizhou 27
Augusta 26
Haikou 26
Washington 26
Mumbai 25
Norwalk 25
Dhaka 23
Baghdad 22
Mexico City 22
Naples 22
Curitiba 21
Da Nang 21
Guayaquil 21
Melbourne 21
Totale 26.710
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Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 438
Effects of neuroinflammation on the regenerative capacity of brain stem cells 351
"GenotypeColour": colour visualisation of SNPs and CNVs 344
3,6'-Dithiothalidomide, a new TNF-α synthesis inhibitor, attenuates the effect of Aβ1-42 intracerebroventricular injection on hippocampal neurogenesis and memory deficit 336
New Copy Number Variations in Schizophrenia 329
Glutamatergic Reinnervation and Assembly of Glutamatergic Synapses in Adult Rat Skeletal Muscle Occurs at Cholinergic Endplates 326
Glutamatergic reinnervation through peripheral nerve graft dictates assembly of glutamatergic synapses at rat skeletal muscle 326
ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency 323
Mutations in TGFBR2 gene cause spontaneous cervical artery dissection 316
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 313
Gene expression profile in fibroblasts of Huntington's disease patients and controls 293
Cyclooxygenase-1 is involved in the inhibition of hippocampal neurogenesis after lipopolysaccharide-induced neuroinflammation 293
Linee guida. Diagnosi delle epidermolisi bollose ereditarie. 284
A cellular test for Ehlers-Danlos syndromes diagnosis. 274
Proteomic identification of LASP-1 down-regulation after RNAi urokinase silencing in human hepatocellular carcinoma cells. 271
AMPA receptor regulation at the mRNA and protein level in rat primary cortical cultures 269
Altered mRNA editing and expression of ionotropic glutamate receptors after kainic acid exposure in cyclooxygenase-2 deficient mice. 261
Analysis of triplet repeats of the FRAXA locus using a novel sequencing procedure 248
miR-193a sensitizes hepatocellular carcinoma cells to sorafenib and impairs their aggressive properties. 242
Effects of miR-193a and sorafenib on hepatocellular carcinoma cells. 236
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 234
Gene expression profile in fibroblasts of Huntington's disease patients and controls. 226
Clinical and genetic characteristics of late-onset Huntington's disease 217
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay. 215
Differential expression of miR-24 and miR27a in cirrhotic/non cirrhotic HCC 214
-G308A tumor necrosis factor alpha functional polymorphism and schizophrenia risk: Meta-analysis plus association study 210
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 207
AMPA receptor regulation at the mRNA and protein level in rat primary cortical cultures 206
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 204
miR103 e miR-107 sono coinvolti nella regolazione dell'espressione di CDK5R1/p35 implicato nella migrazione neuronale. 201
Human hepatocellular carcinoma cell-specific miRNAs reveal the differential expression of miR-24 and miR-27a in cirrhotic/non-cirrhotic HCC 200
Differential expression of miR-24 and miR27a in cirrhotic/non cirrhotic HCC. 197
Cytogenetic and molecular characterization of a de-novo t(2p;7p) translocation involving TNS3 and EXOC6B genes in a boy with a complex syndromic phenotype 196
Preparazione di colture primarie di fibroblasti di embrione di pollo . 196
Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: analysis of transcript levels in dermal fibroblasts 194
Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia 193
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 193
A Taq RFLP for the human fibronectin (FN1) gene 193
Acute spinal cord injury persistently reduces R/G RNA editing of AMPA receptors 193
-G308A tumor necrosis factor alpha functional polymorphism and schizophrenia risk: Meta-analysis plus association study 193
Analysis of Copy Number Variations in Schizophrenia Italian Patients 192
The type III-9 repeat of human fibronectin is encoded by a single exon which is not alternatively spliced. 191
MicroRNAs as Biomarkers of hepatocellular carcinoma and molecular targeted therapeutics with sorafenib 191
Kainate Receptor RNA Editing is Markedly Altered by Acute Spinal Cord Injury. 189
LASP1 directly interacts with vimentin and its expression stratifies patients affected by human hepatocellular carcinoma 188
Study of conformational properties of a biologically active peptide of Fibronectin by circular dichroism, NMR and molecular dynamics simulation 187
A frequent HaeIII RFLP of the human fibronectin gene 186
microRNAs and human hepatocellular carcinoma 186
L’integrina avb3 inibisce il potenziale invasivo e metastatico di cellule tumorali umane esprimenti stabilmente il peptide FN13, attraverso la disattivazione di ILK. 184
AMPA RECEPTOR PROPERTIES ARE MODULATED IN THE EARLY STAGES FOLLOWING PILOCARPINE-INDUCED STATUS EPILEPTICUS 184
A common MspI RFLP of the human fibronectin gene (FN1) 182
Mesenchymal cells from human amniotic fluid survive and migrate after transplantation into adult rat brain 179
Activity Regulation of Adenosine Deaminases Acting on RNA (ADARs) 179
Association of partial AZFc region deletions with spermatogenic impairment and male infertility. 178
Molecular and cytogenetic characterization of extra-structurally abnormal chromosomes (ESACs) found prenatally: outcome and follow-up 178
The study of HCC cell specific miRNas reveals one novel human miR and miR-21, miR24 and miR-27a differential expression in HCC 177
A -96C-T mutation in the promoter of the collagen type VII gene (COL7A1) abolishing transcription in a patient affected by recessive dystrophic epidermolys bullosa 176
"Degradation of human plasma and extracellular matrix fibronectin by tissue type plasminogen activator and urokinase" 175
Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio 175
Wound repair capability in EDS fibroblasts can be retrieved by exogenous type V collagen 174
Arterial tortuosity syndrome in two Italian paediatric patients. 173
miR24, MiR 27a e miR193a nell'HCC: potenzialità prognostiche e terapeutiche. 173
Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype 172
The study of HCC-cell specific miRs reveals one novel human miR and miR-21, miR-24 and miR-27a differential expression in HCC. 172
BRCA1 and BRCA2 genetic test in high risk patients and families : counselling and management 172
MicroRNA 193a negatively regulates urokinase and in combination with sorafenib impairs the aggressive properties of HCC cells 171
Chronic phencyclidine administration reduces the expression and editing of specific glutamate receptors in rat prefrontal cortex 170
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13 170
Gallus gallus NEU3 sialidase as model to study protein evolution mechanism based on rapid evolving loops 169
RT-PCR detection of fibronectin EDA+ and EDB+ mRNA isoforms: molecular markers for hepatocellular carcinoma 168
Assignment of the human metabotropic glutamate receptor gene GRM4 to chromosome 6 band p21.3 by radiation hybrid mapping. 167
Psychopathologic, neuropsychological and functional outcome measures during cognitive rehabilitation in schizophrenia: A prospective controlled study in a real-world setting. 166
Chromosome Abnormalities and Yq microdeletions in Infertile italian couples referred for assisted reproductive tecnique 163
Antidepressant treatments change 5-HT2C receptor mRNA expression in rat prefrontal/frontal cortex and hippocampus 163
De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia 163
FSH receptor polymorphisms in a population of infertile women and controls 163
The analysis of HCC-cell specific miRs reveals one novel human miR and miR-21, miR-24, and miR-27a differential expression in cirrhotic/non- cirrhotic HCC. 161
Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy. 160
Overexpression of wild type and mutant mucolipin proteins in mammalian cells: effects on the late endocytic compartment organization 160
One-lane chemical sequencing of 3'-fluorescent-labeled DNA 160
Branch point and donor splice-site COL7A1 mutations in mild recessive dystrophic epidermolysis bullosa. 159
Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient. 159
miR-193a sensitizes hepatocellular carcinoma cells to sorafenib and impairs their aggressive properties. 159
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 158
Chronic antidepressant treatments induce a time-dependent up-regulation of AMPA receptor subunit protein levels 158
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 157
In vitro c-met inhibition by antisense RNA and plasmid -based RNAi down modulates migration and invasion of hepatocellular carcinoma cells. 157
Caratterizzazione ed espressione di slc2a10, l’ortologo in Danio rerio del gene umano coinvolto nella sindrome delle arterie tortuose. 157
Antisense u-PA mRNA strategy inhibits the proliferation and invasion of human hepatocellular carcinoma cells. 156
Identification of novel alternatively-spliced mRNA isoforms of metabotropic glutamate receptor 6 gene in rat and human retina. 156
Recurrence of the p.R156X TNNI2 mutation in distal arthrogryposis type 2B 156
Sequential analysis of multistage hepatocarcinogenesis reveals that miR100 and PLK1 dysregulation is an early event maintained along tumor progression. 156
Glutamate receptor RNA editing: a molecular analysis of GluR2, GluR5 and GluR6 in human brain tissues and in NT2 cells following in vitro neural differentiation. 155
Cellular expression and alternative splicing of SLC25A23, a member of the mitochondrial Ca2+ dependent solute carrier protein family 155
Chemical method for DNA sequence determination from the 5'-extremity on PCR amplified fragments. 155
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 154
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations. 153
A rapid and highly sensitive solid phase enzyme immunoassay specific for human fibronectin using a characterized monoclonal antibody 153
De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma. 152
Ischemic stroke in an adolescent with arterial tortuosity syndrome. 150
Totale 20.257
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Categoria #
all - tutte 180.990
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 180.990
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.672 0 0 0 90 23 75 156 104 121 309 253 541
2022/20231.815 296 34 56 134 177 490 12 165 274 9 79 89
2023/20242.022 129 51 153 148 109 387 127 60 493 49 25 291
2024/20254.476 24 40 29 610 533 423 446 73 540 198 925 635
2025/20268.906 911 1.218 620 1.339 902 636 1.405 303 475 729 251 117
2026/20272.576 458 407 821 890 0 0 0 0 0 0 0 0
Totale 41.367