IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BARLATI, Sergio
 Distribuzione geografica
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Continente #
NA - Nord America 17.613
EU - Europa 10.039
AS - Asia 9.288
SA - Sud America 1.583
Continente sconosciuto - Info sul continente non disponibili 740
AF - Africa 188
OC - Oceania 54
AN - Antartide 2
Totale 39.507
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Nazione #
US - Stati Uniti d'America 17.273
CN - Cina 3.615
SG - Singapore 2.895
PL - Polonia 2.346
UA - Ucraina 1.927
DE - Germania 1.550
BR - Brasile 1.312
IT - Italia 970
HK - Hong Kong 916
FR - Francia 811
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 189
BD - Bangladesh 164
SE - Svezia 110
AR - Argentina 96
MX - Messico 74
NL - Olanda 70
ID - Indonesia 66
BE - Belgio 63
ZA - Sudafrica 61
IQ - Iraq 56
EC - Ecuador 49
JP - Giappone 45
AU - Australia 43
ES - Italia 40
PK - Pakistan 35
AT - Austria 33
SA - Arabia Saudita 32
CZ - Repubblica Ceca 31
NG - Nigeria 31
EU - Europa 28
VE - Venezuela 26
CO - Colombia 25
IR - Iran 25
JM - Giamaica 23
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
CL - Cile 15
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
CR - Costa Rica 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
BG - Bulgaria 6
ET - Etiopia 6
HN - Honduras 6
LK - Sri Lanka 6
PH - Filippine 6
SD - Sudan 6
TH - Thailandia 6
TT - Trinidad e Tobago 6
AL - Albania 5
DO - Repubblica Dominicana 5
OM - Oman 5
PS - Palestinian Territory 5
SI - Slovenia 5
SK - Slovacchia (Repubblica Slovacca) 5
BB - Barbados 4
BH - Bahrain 4
GT - Guatemala 4
HU - Ungheria 4
KG - Kirghizistan 4
RS - Serbia 4
BA - Bosnia-Erzegovina 3
GE - Georgia 3
AO - Angola 2
CU - Cuba 2
CY - Cipro 2
DK - Danimarca 2
DM - Dominica 2
GR - Grecia 2
KH - Cambogia 2
LA - Repubblica Popolare Democratica del Laos 2
Totale 38.761
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Città #
Warsaw 2.342
Fairfield 1.757
Singapore 1.613
Woodbridge 1.532
Ashburn 1.453
Jacksonville 1.368
Houston 1.005
Hong Kong 910
Beijing 753
Cambridge 716
Seattle 697
Ann Arbor 694
San Jose 684
Wilmington 660
Chandler 608
Nanjing 544
Princeton 537
The Dalles 498
Helsinki 401
New York 396
Dublin 285
Dearborn 283
Brescia 268
Columbus 265
Los Angeles 265
Lauterbourg 237
Istanbul 234
Council Bluffs 217
Nanchang 188
Des Moines 174
Shenyang 161
Ho Chi Minh City 157
Buffalo 137
Munich 134
Hebei 131
Lancaster 131
Jinan 123
Changsha 116
São Paulo 114
Milan 113
Moscow 113
Tianjin 105
Hanoi 103
San Diego 98
San Francisco 98
Shanghai 98
Jiaxing 87
Orem 87
Dallas 83
Chicago 80
Kunming 79
Redondo Beach 72
Dong Ket 71
Santa Clara 71
London 69
Hangzhou 62
Zhengzhou 52
Verona 49
Montreal 48
Toronto 48
Brussels 47
Chennai 47
Ningbo 47
Turku 44
Phoenix 43
Rio de Janeiro 43
Guangzhou 42
Frankfurt am Main 37
Kocaeli 37
Brooklyn 36
Tokyo 35
Belo Horizonte 34
Johannesburg 34
Atlanta 32
Denver 32
Abuja 31
Pune 31
Nuremberg 30
Boston 29
Paris 29
Jakarta 28
Lanzhou 28
San Mateo 28
Boardman 27
Charlotte 27
Taizhou 27
Augusta 26
Haikou 26
Rome 26
Norwalk 25
Mumbai 24
Dhaka 23
Washington 23
Baghdad 22
Mexico City 22
Da Nang 21
Melbourne 21
Amsterdam 20
Curitiba 20
Fuzhou 20
Totale 25.698
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Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 405
"GenotypeColour": colour visualisation of SNPs and CNVs 341
Effects of neuroinflammation on the regenerative capacity of brain stem cells 340
3,6'-Dithiothalidomide, a new TNF-α synthesis inhibitor, attenuates the effect of Aβ1-42 intracerebroventricular injection on hippocampal neurogenesis and memory deficit 327
New Copy Number Variations in Schizophrenia 322
Glutamatergic reinnervation through peripheral nerve graft dictates assembly of glutamatergic synapses at rat skeletal muscle 321
Glutamatergic Reinnervation and Assembly of Glutamatergic Synapses in Adult Rat Skeletal Muscle Occurs at Cholinergic Endplates 320
ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency 314
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 308
Mutations in TGFBR2 gene cause spontaneous cervical artery dissection 303
Gene expression profile in fibroblasts of Huntington's disease patients and controls 283
Cyclooxygenase-1 is involved in the inhibition of hippocampal neurogenesis after lipopolysaccharide-induced neuroinflammation 282
Linee guida. Diagnosi delle epidermolisi bollose ereditarie. 278
A cellular test for Ehlers-Danlos syndromes diagnosis. 267
Proteomic identification of LASP-1 down-regulation after RNAi urokinase silencing in human hepatocellular carcinoma cells. 266
AMPA receptor regulation at the mRNA and protein level in rat primary cortical cultures 264
Altered mRNA editing and expression of ionotropic glutamate receptors after kainic acid exposure in cyclooxygenase-2 deficient mice. 253
Analysis of triplet repeats of the FRAXA locus using a novel sequencing procedure 243
Effects of miR-193a and sorafenib on hepatocellular carcinoma cells. 232
miR-193a sensitizes hepatocellular carcinoma cells to sorafenib and impairs their aggressive properties. 228
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 226
Gene expression profile in fibroblasts of Huntington's disease patients and controls. 219
Differential expression of miR-24 and miR27a in cirrhotic/non cirrhotic HCC 212
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay. 208
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 202
AMPA receptor regulation at the mRNA and protein level in rat primary cortical cultures 201
-G308A tumor necrosis factor alpha functional polymorphism and schizophrenia risk: Meta-analysis plus association study 201
Clinical and genetic characteristics of late-onset Huntington's disease 201
miR103 e miR-107 sono coinvolti nella regolazione dell'espressione di CDK5R1/p35 implicato nella migrazione neuronale. 194
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 193
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 190
Human hepatocellular carcinoma cell-specific miRNAs reveal the differential expression of miR-24 and miR-27a in cirrhotic/non-cirrhotic HCC 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 189
Differential expression of miR-24 and miR27a in cirrhotic/non cirrhotic HCC. 189
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 187
MicroRNAs as Biomarkers of hepatocellular carcinoma and molecular targeted therapeutics with sorafenib 186
Kainate Receptor RNA Editing is Markedly Altered by Acute Spinal Cord Injury. 186
-G308A tumor necrosis factor alpha functional polymorphism and schizophrenia risk: Meta-analysis plus association study 185
Preparazione di colture primarie di fibroblasti di embrione di pollo . 185
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 184
A Taq RFLP for the human fibronectin (FN1) gene 184
The type III-9 repeat of human fibronectin is encoded by a single exon which is not alternatively spliced. 184
Study of conformational properties of a biologically active peptide of Fibronectin by circular dichroism, NMR and molecular dynamics simulation 183
Acute spinal cord injury persistently reduces R/G RNA editing of AMPA receptors 183
microRNAs and human hepatocellular carcinoma 181
A frequent HaeIII RFLP of the human fibronectin gene 180
AMPA RECEPTOR PROPERTIES ARE MODULATED IN THE EARLY STAGES FOLLOWING PILOCARPINE-INDUCED STATUS EPILEPTICUS 179
Analysis of Copy Number Variations in Schizophrenia Italian Patients 177
Activity Regulation of Adenosine Deaminases Acting on RNA (ADARs) 176
A common MspI RFLP of the human fibronectin gene (FN1) 175
LASP1 directly interacts with vimentin and its expression stratifies patients affected by human hepatocellular carcinoma 174
Wound repair capability in EDS fibroblasts can be retrieved by exogenous type V collagen 174
Association of partial AZFc region deletions with spermatogenic impairment and male infertility. 173
Molecular and cytogenetic characterization of extra-structurally abnormal chromosomes (ESACs) found prenatally: outcome and follow-up 173
The study of HCC cell specific miRNas reveals one novel human miR and miR-21, miR24 and miR-27a differential expression in HCC 172
L’integrina avb3 inibisce il potenziale invasivo e metastatico di cellule tumorali umane esprimenti stabilmente il peptide FN13, attraverso la disattivazione di ILK. 171
"Degradation of human plasma and extracellular matrix fibronectin by tissue type plasminogen activator and urokinase" 169
miR24, MiR 27a e miR193a nell'HCC: potenzialità prognostiche e terapeutiche. 168
MicroRNA 193a negatively regulates urokinase and in combination with sorafenib impairs the aggressive properties of HCC cells 167
Chronic phencyclidine administration reduces the expression and editing of specific glutamate receptors in rat prefrontal cortex 166
BRCA1 and BRCA2 genetic test in high risk patients and families : counselling and management 166
Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype 165
The study of HCC-cell specific miRs reveals one novel human miR and miR-21, miR-24 and miR-27a differential expression in HCC. 165
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13 165
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 164
Assignment of the human metabotropic glutamate receptor gene GRM4 to chromosome 6 band p21.3 by radiation hybrid mapping. 164
Mesenchymal cells from human amniotic fluid survive and migrate after transplantation into adult rat brain 162
Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio 162
Gallus gallus NEU3 sialidase as model to study protein evolution mechanism based on rapid evolving loops 162
RT-PCR detection of fibronectin EDA+ and EDB+ mRNA isoforms: molecular markers for hepatocellular carcinoma 161
Arterial tortuosity syndrome in two Italian paediatric patients. 161
Psychopathologic, neuropsychological and functional outcome measures during cognitive rehabilitation in schizophrenia: A prospective controlled study in a real-world setting. 160
De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia 160
Chromosome Abnormalities and Yq microdeletions in Infertile italian couples referred for assisted reproductive tecnique 158
Antidepressant treatments change 5-HT2C receptor mRNA expression in rat prefrontal/frontal cortex and hippocampus 157
Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy. 155
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. 155
Overexpression of wild type and mutant mucolipin proteins in mammalian cells: effects on the late endocytic compartment organization 154
Chronic antidepressant treatments induce a time-dependent up-regulation of AMPA receptor subunit protein levels 154
Recurrence of the p.R156X TNNI2 mutation in distal arthrogryposis type 2B 153
miR-193a sensitizes hepatocellular carcinoma cells to sorafenib and impairs their aggressive properties. 153
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 152
In vitro c-met inhibition by antisense RNA and plasmid -based RNAi down modulates migration and invasion of hepatocellular carcinoma cells. 152
Branch point and donor splice-site COL7A1 mutations in mild recessive dystrophic epidermolysis bullosa. 152
Caratterizzazione ed espressione di slc2a10, l’ortologo in Danio rerio del gene umano coinvolto nella sindrome delle arterie tortuose. 151
FSH receptor polymorphisms in a population of infertile women and controls 151
One-lane chemical sequencing of 3'-fluorescent-labeled DNA 150
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. 149
De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma. 149
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 149
Antisense u-PA mRNA strategy inhibits the proliferation and invasion of human hepatocellular carcinoma cells. 148
Identification of novel alternatively-spliced mRNA isoforms of metabotropic glutamate receptor 6 gene in rat and human retina. 147
Chemical method for DNA sequence determination from the 5'-extremity on PCR amplified fragments. 147
Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient. 147
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 146
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations. 146
Sequential analysis of multistage hepatocarcinogenesis reveals that miR100 and PLK1 dysregulation is an early event maintained along tumor progression. 146
Altered fibronectin RNA splicing in skin fibroblasts from Ehlers-Danlos syndrome patients: in situ hybridization analysis. 145
Cellular expression and alternative splicing of SLC25A23, a member of the mitochondrial Ca2+ dependent solute carrier protein family 144
Ischemic stroke in an adolescent with arterial tortuosity syndrome. 143
Totale 19.504
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Categoria #
all - tutte 172.839
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 172.839
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.262 0 556 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
2025/20268.906 911 1.218 620 1.339 902 636 1.405 303 475 729 251 117
2026/2027716 458 258 0 0 0 0 0 0 0 0 0 0
Totale 39.507