IRIS Institutional Research Information System - OPENBS Open Archive UniBS

ZOPPI, NICOLETTA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 7.112
EU - Europa 5.501
AS - Asia 3.032
SA - Sud America 482
Continente sconosciuto - Info sul continente non disponibili 292
AF - Africa 65
OC - Oceania 34
AN - Antartide 1
Totale 16.519
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 6.942
PL - Polonia 2.712
CN - Cina 1.065
SG - Singapore 985
IT - Italia 673
UA - Ucraina 531
BR - Brasile 376
DE - Germania 351
GB - Regno Unito 340
FR - Francia 318
HK - Hong Kong 315
VN - Vietnam 213
FI - Finlandia 212
TR - Turchia 104
RU - Federazione Russa 100
IE - Irlanda 91
IN - India 90
CA - Canada 89
BD - Bangladesh 45
ID - Indonesia 43
NL - Olanda 42
AR - Argentina 33
AU - Australia 32
MX - Messico 26
BE - Belgio 25
IQ - Iraq 23
SE - Svezia 23
SA - Arabia Saudita 21
ZA - Sudafrica 21
PK - Pakistan 20
KR - Corea 19
AT - Austria 18
CL - Cile 16
ES - Italia 16
JP - Giappone 16
VE - Venezuela 14
JM - Giamaica 13
LT - Lituania 13
CR - Costa Rica 12
EC - Ecuador 12
TW - Taiwan 11
PH - Filippine 9
CO - Colombia 8
CZ - Repubblica Ceca 8
IL - Israele 8
MA - Marocco 8
PE - Perù 8
PY - Paraguay 7
TN - Tunisia 7
AE - Emirati Arabi Uniti 6
CH - Svizzera 6
HN - Honduras 6
MY - Malesia 6
TT - Trinidad e Tobago 6
UZ - Uzbekistan 6
MU - Mauritius 5
UY - Uruguay 5
EG - Egitto 4
EU - Europa 4
NP - Nepal 4
PT - Portogallo 4
SC - Seychelles 4
TH - Thailandia 4
BB - Barbados 3
BO - Bolivia 3
CG - Congo 3
ET - Etiopia 3
JO - Giordania 3
KE - Kenya 3
PR - Porto Rico 3
AL - Albania 2
AM - Armenia 2
BA - Bosnia-Erzegovina 2
DO - Repubblica Dominicana 2
GP - Guadalupe 2
GR - Grecia 2
GT - Guatemala 2
HU - Ungheria 2
KG - Kirghizistan 2
LK - Sri Lanka 2
NG - Nigeria 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
OM - Oman 2
SK - Slovacchia (Repubblica Slovacca) 2
AZ - Azerbaigian 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
DZ - Algeria 1
EE - Estonia 1
GA - Gabon 1
GD - Grenada 1
GS - Georgia del Sud e Isole Sandwich Australi 1
HR - Croazia 1
HT - Haiti 1
IR - Iran 1
IS - Islanda 1
KZ - Kazakistan 1
Totale 16.220
Salva come PNG Salva come JPEG
Città #
Warsaw 2.708
Ashburn 652
Fairfield 633
Singapore 555
Woodbridge 517
Jacksonville 404
Houston 367
San Jose 353
Hong Kong 313
Brescia 254
Cambridge 252
Seattle 251
Wilmington 244
Council Bluffs 242
Beijing 236
Ann Arbor 207
The Dalles 189
Princeton 164
Chandler 162
New York 158
Nanjing 137
Lancaster 135
Helsinki 131
Los Angeles 123
Dublin 91
Dearborn 86
Dong Ket 80
Lauterbourg 78
Istanbul 77
Columbus 65
Munich 62
Dallas 51
Milan 50
Rome 48
Nanchang 46
Santa Clara 46
London 45
Des Moines 44
Ho Chi Minh City 42
Changsha 41
San Francisco 41
North Bergen 40
Shenyang 38
Buffalo 37
San Diego 37
Chicago 34
Jakarta 33
Jinan 32
São Paulo 31
North Charleston 30
Redondo Beach 30
Tianjin 30
Hebei 29
Hanoi 27
Phoenix 27
Shanghai 26
Denver 23
Kunming 23
Orem 22
Atlanta 20
Moscow 20
Hangzhou 19
Nuremberg 19
Toronto 19
Turku 19
Boardman 18
Brussels 18
Jiaxing 17
Zhengzhou 17
Frankfurt am Main 16
Ningbo 16
Brooklyn 15
Montreal 14
Johannesburg 13
Mexico City 13
Rio de Janeiro 13
Taizhou 13
Tokyo 13
Verona 13
Baghdad 12
Naples 12
Florence 11
Guangzhou 11
Seongnam 11
Boston 10
Chennai 10
Lanzhou 10
Manchester 10
Porto Alegre 10
Riyadh 10
Washington 10
Belo Horizonte 9
Falls Church 9
Omaha 9
Taipei 9
Vienna 9
Amsterdam 8
Augusta 8
Fuzhou 8
Haiphong 8
Totale 11.458
Salva come PNG Salva come JPEG
Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 440
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type 354
Arterial Tortuosity Syndrome: a vitamin C compartmentation disease? 349
Bruch's membrane abnormalities in PRDM5-related brittle cornea syndrome 341
Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome 339
Multifaced Roles of the αvβ3 Integrin in Ehlers–Danlos and Arterial Tortuosity Syndromes’ Dermal Fibroblasts 313
GLUT10-Lacking in Arterial Tortuosity Syndrome-Is Localized to the Endoplasmic Reticulum of Human Fibroblasts 308
Clinical and molecular characterization of 40 patients with classic Ehlers--Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations. 303
Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport 302
GLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts 299
The phenotype of the musculocontractural type of Ehlers-Danlos syndrome due to CHST14 mutations. 293
Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel B3GALT6 mutations 289
GLUT10 deficiency leads to oxidative stress and non-canonical avb3 integrin-mediated TGF signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts. 288
Characterization and expression of slc2a10, the zebrafish ortholog of the human gene involved in arterial tortuosity syndrome. 282
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations 278
Molecular characterization and transcriptome-wide expression profiling of two patients affected with spondyloepimetaphyseal dysplasia with joint laxity type 278
A cellular test for Ehlers-Danlos syndromes diagnosis. 277
Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients' skin fibroblasts 263
Classic Ehlers-danlos syndrome: clinical and molecular characterisation of 37 patients 262
Type V and type III collagen modulate the expression and assembly of fibronectin extracellar matrix in classic and vascular Ehlers-Danlos syndrome fibroblasts, affecting cell survival and migration 259
Report on a patient with extremely fragile skin, dermatosparaxis, joint hypermobility, short stature, skeletal deformities, and lipomas: a new syndrome? 259
Dermal fibroblast-to-myofibroblast transition sustained by αvβ3 integrin-ILK-Snail1/Slug signaling is a common feature for hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders 244
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 234
Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients 232
COL6A5 variants in familial neuropathic chronic itch 218
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant 212
Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene 211
Cellular and molecular mechanisms in the pathogenesis of classical, vascular, and hypermobile ehlers‒danlos syndromes 211
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 200
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 198
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 196
Study of conformational properties of a biologically active peptide of Fibronectin by circular dichroism, NMR and molecular dynamics simulation 191
Angiokeratoma Corporis Diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders. 190
L’integrina avb3 inibisce il potenziale invasivo e metastatico di cellule tumorali umane esprimenti stabilmente il peptide FN13, attraverso la disattivazione di ILK. 187
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 179
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β 179
Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio 177
Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A>G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy 175
Wound repair capability in EDS fibroblasts can be retrieved by exogenous type V collagen 174
Does miR-338, a putative negative regulator of the facilitative glucose transporter 10 (GLUT10), play a role in arterial tortuosity syndrome? 172
Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts 172
Type III and V collagens modulate the expression and assembly of EDA+ fibronectin in the extracellular matrix of defective Ehlers-Danlos syndrome fibroblasts 170
Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss 165
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type 161
Matrix metalloproteinases inhibition by doxycycline rescues extracellular matrix organization and partly reverts myofibroblast differentiation in hypermobile ehlers-danlos syndrome dermal fibroblasts: A potential therapeutic target? 160
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 158
Caratterizzazione ed espressione di slc2a10, l’ortologo in Danio rerio del gene umano coinvolto nella sindrome delle arterie tortuose. 158
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 157
Recurrence of the p.R156X TNNI2 mutation in distal arthrogryposis type 2B 156
Bridging the Diagnostic Gap for Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders: Evidence of a Common Extracellular Matrix Fragmentation Pattern in Patient Plasma as a Potential Biomarker 154
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations. 153
Altered fibronectin RNA splicing in skin fibroblasts from Ehlers-Danlos syndrome patients: in situ hybridization analysis. 150
Mutations in PRDM5 in brittle cornea syndrome identify a pathway regulating extracellular matrix development and maintenance. 150
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide 149
Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts 146
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization 146
Alternative splicing of mGluR6 gene generates a truncated glutamate receptor in rat retina. 146
TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasis 146
COL1-related overlap disorder: a novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap 146
The novel p.G150R missense mutation in the cartilage matrix protein subdomain of type VII collagen in compound heterozigosity with the c.682+1G>A COL7A1 splicing mutation leads to mild dystrophic epidermolysis bullosa 143
Exclusion of candidate genes in a family with arterial tortuosity syndrome 142
Dexamethasone-induced healing of chronic leg ulcers in a patient with defective organization of the extracellular matrix of fibronectin. 142
Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients 139
Correction of the defective extracellular matrix of Ehlers-Danlos syndrome skin fibroblasts by dexamethasone. 138
Effect of dexamethasone on the assembly of the matrix of fibronectin and its receptors organization in Ehlers-Danlos syndrome skin fibroblasts. 136
Identification of two splicing mutations in the collagen type VII gene (COL7A1) of a patient affected by the localisata variant of recessive dystrophic epidermolysis bullosa 136
Rescue of migratory defects of Ehlers-Danlos syndrome fibroblasts in vitro by type V collagen but not insulin-like binding protein-1. 136
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in COL7A1. 133
Genotype-phenotype correlation in Italian patients with epidermolysis bullosa dystrophica 131
BIOLOGIA E GENETICA DEL MUSCOLO 131
Quantitative in situ hybridization for the evaluation of cell – cycle related gene expression. 125
Compound heterozygosity for a novel and a recurrent ABCC6 gene mutation in an Italian family with pseudoxanthoma elasticum 124
Modulation of the facilitative glucose transporters (SLC2A) gene family expression in arterial tortuosity syndrome skin fibroblasts and aortic vascular smooth muscle cells. 123
Congenital myopathy Ehlers-Danlos overlap syndrome caused by the deficiency of an enzyme involved in protein folding in the endoplasmic reticulum: identification and characterization of a novel disorder. 121
Quantitative evaluation of mRNAs by in situ hybridization and image analysis: principles and applications. 110
Integrative Multi-Omics Approach in Vascular Ehlers–Danlos Syndrome: Further Insights into the Disease Mechanisms by Proteomic Analysis of Patient Dermal Fibroblasts 105
RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading and Proinflammatory Pathomechanisms 105
Genetic heterogeneity in the Brittle Cornea Syndrome (BCS) –New evidences that ZNF469 and PRDM5 regulate extracellular matrix development and maintenance within the same pathway 104
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome 104
Quantitative in situ hybridization for the evaluation of gene expression in asynchronous and synchronized cell cultures and in tissue sections 97
L’organizzazione della matrice di collagene III nei fibroblasti dermici regola l’espressione di geni coinvolti nell’elastogenesi. 96
FAK-independent alphavbeta3 integrin-EGFR complexes rescue from anoikis matrix-defective fibroblasts 91
The FN13 peptide inhibits human tumor cells invasion through the modulation of alphavbeta3 integrins organization and the inactivation of ILK pathway 90
Human fibroblasts with mutations in COL5A1 and COL3A1 genes do not organize collagens and fibronectin in the extracellular matrix, down-regulate alpha2beta1 integrin and recruit alphavbeta3 instead of alpha5beta1 integrin 87
In search of the SLC2A10 gene role in the etiopathogenesis of arterial tortuosity syndrome by transcriptomic and biochemical approaches 87
Il collagene III ripristina la migrazione e il riparo delle ferite in vitro in fibroblasti di pazienti affetti da Sindrome di Ehlers-Danlos vascolare. 83
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 79
Collageni purificati inducono in fibroblasti umani difettivi la sintesi di fibronectina EDA+ e la sua organizzazione nella matrice extracellulare. 79
Loeys- Dietz Sindrome and Vascular Ehlers- Danlos Sindrome: differential diagnosis by clinical and molecular approaches 54
null 49
Totale 16.519
Salva come PNG Salva come JPEG
Categoria #
all - tutte 67.423
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 67.423
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022535 0 0 0 0 21 38 47 45 60 82 66 176
2022/2023563 101 9 11 35 34 164 11 55 75 12 22 34
2023/2024720 41 15 45 64 47 150 42 15 155 27 18 101
2024/20251.553 14 8 20 236 156 133 164 48 166 66 327 215
2025/20263.335 300 398 216 394 299 282 571 142 228 268 159 78
2026/20271.404 221 260 332 531 60 0 0 0 0 0 0 0
Totale 16.519