IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BARLATI, Sergio
 Distribuzione geografica
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Continente #
NA - Nord America 16.953
EU - Europa 10.013
AS - Asia 9.244
SA - Sud America 1.571
AF - Africa 188
OC - Oceania 54
Continente sconosciuto - Info sul continente non disponibili 28
AN - Antartide 2
Totale 38.053
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Nazione #
US - Stati Uniti d'America 16.652
CN - Cina 3.608
SG - Singapore 2.886
PL - Polonia 2.345
UA - Ucraina 1.927
DE - Germania 1.550
BR - Brasile 1.304
IT - Italia 952
HK - Hong Kong 910
FR - Francia 809
FI - Finlandia 707
GB - Regno Unito 601
VN - Vietnam 541
IN - India 405
RU - Federazione Russa 392
TR - Turchia 314
IE - Irlanda 286
CA - Canada 174
BD - Bangladesh 143
SE - Svezia 110
AR - Argentina 94
MX - Messico 70
NL - Olanda 68
ID - Indonesia 66
BE - Belgio 63
ZA - Sudafrica 61
IQ - Iraq 56
EC - Ecuador 49
JP - Giappone 44
AU - Australia 43
ES - Italia 39
PK - Pakistan 35
AT - Austria 33
SA - Arabia Saudita 32
CZ - Repubblica Ceca 31
NG - Nigeria 31
EU - Europa 28
CO - Colombia 25
IR - Iran 25
VE - Venezuela 25
KR - Corea 21
PY - Paraguay 21
KE - Kenya 20
LU - Lussemburgo 20
UZ - Uzbekistan 19
LT - Lituania 17
MA - Marocco 17
PE - Perù 17
JO - Giordania 16
JM - Giamaica 15
CL - Cile 14
UY - Uruguay 14
AE - Emirati Arabi Uniti 13
IL - Israele 12
MU - Mauritius 12
KZ - Kazakistan 11
NZ - Nuova Zelanda 11
TN - Tunisia 11
CH - Svizzera 10
DZ - Algeria 8
EG - Egitto 8
MY - Malesia 8
PA - Panama 8
RO - Romania 8
AZ - Azerbaigian 7
BO - Bolivia 7
NP - Nepal 7
TW - Taiwan 7
AM - Armenia 6
CR - Costa Rica 6
ET - Etiopia 6
LK - Sri Lanka 6
PH - Filippine 6
SD - Sudan 6
TH - Thailandia 6
TT - Trinidad e Tobago 6
AL - Albania 5
BG - Bulgaria 5
HN - Honduras 5
OM - Oman 5
PS - Palestinian Territory 5
SI - Slovenia 5
SK - Slovacchia (Repubblica Slovacca) 5
BB - Barbados 4
BH - Bahrain 4
DO - Repubblica Dominicana 4
HU - Ungheria 4
KG - Kirghizistan 4
RS - Serbia 4
BA - Bosnia-Erzegovina 3
GE - Georgia 3
AO - Angola 2
CY - Cipro 2
DK - Danimarca 2
DM - Dominica 2
GR - Grecia 2
GT - Guatemala 2
KH - Cambogia 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
Totale 38.024
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Città #
Warsaw 2.341
Fairfield 1.756
Singapore 1.607
Woodbridge 1.532
Ashburn 1.427
Jacksonville 1.367
Houston 1.004
Hong Kong 905
Beijing 750
Cambridge 716
Seattle 696
Ann Arbor 694
San Jose 661
Wilmington 660
Chandler 608
Nanjing 544
Princeton 537
The Dalles 497
Helsinki 401
New York 394
Dublin 285
Dearborn 283
Brescia 268
Los Angeles 262
Lauterbourg 237
Istanbul 234
Nanchang 188
Des Moines 173
Shenyang 161
Ho Chi Minh City 157
Buffalo 137
Munich 134
Hebei 131
Lancaster 131
Jinan 123
Changsha 116
Moscow 113
São Paulo 112
Milan 110
Tianjin 105
Hanoi 103
San Diego 98
San Francisco 98
Shanghai 96
Jiaxing 87
Orem 87
Kunming 79
Dallas 78
Chicago 77
Redondo Beach 72
Dong Ket 71
London 69
Hangzhou 62
Santa Clara 60
Council Bluffs 53
Zhengzhou 52
Verona 49
Brussels 47
Chennai 47
Montreal 47
Ningbo 47
Toronto 47
Turku 44
Guangzhou 42
Rio de Janeiro 42
Frankfurt am Main 37
Kocaeli 37
Phoenix 36
Belo Horizonte 34
Brooklyn 34
Johannesburg 34
Tokyo 34
Atlanta 32
Abuja 31
Denver 31
Pune 31
Nuremberg 30
Boston 29
Paris 29
Jakarta 28
Lanzhou 28
San Mateo 28
Taizhou 27
Augusta 26
Boardman 26
Charlotte 26
Haikou 26
Norwalk 25
Mumbai 24
Rome 24
Dhaka 23
Washington 23
Baghdad 22
Mexico City 22
Da Nang 21
Melbourne 21
Amsterdam 20
Curitiba 20
Fuzhou 20
Guayaquil 20
Totale 25.170
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Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 397
"GenotypeColour": colour visualisation of SNPs and CNVs 337
Effects of neuroinflammation on the regenerative capacity of brain stem cells 329
3,6'-Dithiothalidomide, a new TNF-α synthesis inhibitor, attenuates the effect of Aβ1-42 intracerebroventricular injection on hippocampal neurogenesis and memory deficit 326
New Copy Number Variations in Schizophrenia 318
Glutamatergic Reinnervation and Assembly of Glutamatergic Synapses in Adult Rat Skeletal Muscle Occurs at Cholinergic Endplates 313
Glutamatergic reinnervation through peripheral nerve graft dictates assembly of glutamatergic synapses at rat skeletal muscle 313
ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency 311
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 301
Mutations in TGFBR2 gene cause spontaneous cervical artery dissection 298
Gene expression profile in fibroblasts of Huntington's disease patients and controls 282
Cyclooxygenase-1 is involved in the inhibition of hippocampal neurogenesis after lipopolysaccharide-induced neuroinflammation 277
Linee guida. Diagnosi delle epidermolisi bollose ereditarie. 271
Proteomic identification of LASP-1 down-regulation after RNAi urokinase silencing in human hepatocellular carcinoma cells. 263
A cellular test for Ehlers-Danlos syndromes diagnosis. 263
AMPA receptor regulation at the mRNA and protein level in rat primary cortical cultures 260
Altered mRNA editing and expression of ionotropic glutamate receptors after kainic acid exposure in cyclooxygenase-2 deficient mice. 250
Analysis of triplet repeats of the FRAXA locus using a novel sequencing procedure 241
Effects of miR-193a and sorafenib on hepatocellular carcinoma cells. 228
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 221
miR-193a sensitizes hepatocellular carcinoma cells to sorafenib and impairs their aggressive properties. 221
Gene expression profile in fibroblasts of Huntington's disease patients and controls. 217
Differential expression of miR-24 and miR27a in cirrhotic/non cirrhotic HCC 209
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay. 206
Clinical and genetic characteristics of late-onset Huntington's disease 200
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 199
AMPA receptor regulation at the mRNA and protein level in rat primary cortical cultures 199
-G308A tumor necrosis factor alpha functional polymorphism and schizophrenia risk: Meta-analysis plus association study 198
miR103 e miR-107 sono coinvolti nella regolazione dell'espressione di CDK5R1/p35 implicato nella migrazione neuronale. 190
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 188
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 187
Differential expression of miR-24 and miR27a in cirrhotic/non cirrhotic HCC. 187
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 186
Human hepatocellular carcinoma cell-specific miRNAs reveal the differential expression of miR-24 and miR-27a in cirrhotic/non-cirrhotic HCC 186
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 185
-G308A tumor necrosis factor alpha functional polymorphism and schizophrenia risk: Meta-analysis plus association study 183
The type III-9 repeat of human fibronectin is encoded by a single exon which is not alternatively spliced. 182
Preparazione di colture primarie di fibroblasti di embrione di pollo . 182
MicroRNAs as Biomarkers of hepatocellular carcinoma and molecular targeted therapeutics with sorafenib 182
Kainate Receptor RNA Editing is Markedly Altered by Acute Spinal Cord Injury. 182
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 181
Acute spinal cord injury persistently reduces R/G RNA editing of AMPA receptors 180
Study of conformational properties of a biologically active peptide of Fibronectin by circular dichroism, NMR and molecular dynamics simulation 178
microRNAs and human hepatocellular carcinoma 178
AMPA RECEPTOR PROPERTIES ARE MODULATED IN THE EARLY STAGES FOLLOWING PILOCARPINE-INDUCED STATUS EPILEPTICUS 176
A frequent HaeIII RFLP of the human fibronectin gene 175
Analysis of Copy Number Variations in Schizophrenia Italian Patients 173
Activity Regulation of Adenosine Deaminases Acting on RNA (ADARs) 173
A Taq RFLP for the human fibronectin (FN1) gene 172
LASP1 directly interacts with vimentin and its expression stratifies patients affected by human hepatocellular carcinoma 172
Wound repair capability in EDS fibroblasts can be retrieved by exogenous type V collagen 171
A common MspI RFLP of the human fibronectin gene (FN1) 170
Association of partial AZFc region deletions with spermatogenic impairment and male infertility. 170
Molecular and cytogenetic characterization of extra-structurally abnormal chromosomes (ESACs) found prenatally: outcome and follow-up 170
The study of HCC cell specific miRNas reveals one novel human miR and miR-21, miR24 and miR-27a differential expression in HCC 170
miR24, MiR 27a e miR193a nell'HCC: potenzialità prognostiche e terapeutiche. 166
"Degradation of human plasma and extracellular matrix fibronectin by tissue type plasminogen activator and urokinase" 165
Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype 164
Chronic phencyclidine administration reduces the expression and editing of specific glutamate receptors in rat prefrontal cortex 164
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13 164
BRCA1 and BRCA2 genetic test in high risk patients and families : counselling and management 164
Assignment of the human metabotropic glutamate receptor gene GRM4 to chromosome 6 band p21.3 by radiation hybrid mapping. 163
The study of HCC-cell specific miRs reveals one novel human miR and miR-21, miR-24 and miR-27a differential expression in HCC. 163
MicroRNA 193a negatively regulates urokinase and in combination with sorafenib impairs the aggressive properties of HCC cells 163
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 162
Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio 161
L’integrina avb3 inibisce il potenziale invasivo e metastatico di cellule tumorali umane esprimenti stabilmente il peptide FN13, attraverso la disattivazione di ILK. 160
Arterial tortuosity syndrome in two Italian paediatric patients. 160
Gallus gallus NEU3 sialidase as model to study protein evolution mechanism based on rapid evolving loops 160
RT-PCR detection of fibronectin EDA+ and EDB+ mRNA isoforms: molecular markers for hepatocellular carcinoma 158
De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia 158
Chromosome Abnormalities and Yq microdeletions in Infertile italian couples referred for assisted reproductive tecnique 157
Psychopathologic, neuropsychological and functional outcome measures during cognitive rehabilitation in schizophrenia: A prospective controlled study in a real-world setting. 156
Antidepressant treatments change 5-HT2C receptor mRNA expression in rat prefrontal/frontal cortex and hippocampus 154
Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy. 152
Chronic antidepressant treatments induce a time-dependent up-regulation of AMPA receptor subunit protein levels 152
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. 152
miR-193a sensitizes hepatocellular carcinoma cells to sorafenib and impairs their aggressive properties. 152
Overexpression of wild type and mutant mucolipin proteins in mammalian cells: effects on the late endocytic compartment organization 151
Recurrence of the p.R156X TNNI2 mutation in distal arthrogryposis type 2B 151
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 150
Branch point and donor splice-site COL7A1 mutations in mild recessive dystrophic epidermolysis bullosa. 150
In vitro c-met inhibition by antisense RNA and plasmid -based RNAi down modulates migration and invasion of hepatocellular carcinoma cells. 149
Mesenchymal cells from human amniotic fluid survive and migrate after transplantation into adult rat brain 149
Caratterizzazione ed espressione di slc2a10, l’ortologo in Danio rerio del gene umano coinvolto nella sindrome delle arterie tortuose. 149
FSH receptor polymorphisms in a population of infertile women and controls 149
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 148
One-lane chemical sequencing of 3'-fluorescent-labeled DNA 148
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. 147
Identification of novel alternatively-spliced mRNA isoforms of metabotropic glutamate receptor 6 gene in rat and human retina. 146
De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma. 146
Chemical method for DNA sequence determination from the 5'-extremity on PCR amplified fragments. 146
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 145
Antisense u-PA mRNA strategy inhibits the proliferation and invasion of human hepatocellular carcinoma cells. 145
Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient. 145
Sequential analysis of multistage hepatocarcinogenesis reveals that miR100 and PLK1 dysregulation is an early event maintained along tumor progression. 145
Cellular expression and alternative splicing of SLC25A23, a member of the mitochondrial Ca2+ dependent solute carrier protein family 143
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations. 142
Ischemic stroke in an adolescent with arterial tortuosity syndrome. 141
Altered fibronectin RNA splicing in skin fibroblasts from Ehlers-Danlos syndrome patients: in situ hybridization analysis. 141
Totale 19.173
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Categoria #
all - tutte 166.528
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 166.528
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021154 0 0 0 0 0 0 0 0 0 0 0 154
2021/20222.336 74 556 34 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
2025/20268.879 911 1.218 620 1.339 902 636 1.405 303 475 729 251 90
Totale 38.764