IRIS Institutional Research Information System - OPENBS Open Archive UniBS

ZOPPI, NICOLETTA
 Distribuzione geografica
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Continente #
EU - Europa 4.690
NA - Nord America 4.374
AS - Asia 1.272
OC - Oceania 12
SA - Sud America 8
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 4
AN - Antartide 1
Totale 10.366
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Nazione #
US - Stati Uniti d'America 4.358
PL - Polonia 2.692
CN - Cina 634
UA - Ucraina 517
IT - Italia 429
DE - Germania 265
GB - Regno Unito 249
FR - Francia 222
SG - Singapore 207
HK - Hong Kong 152
FI - Finlandia 142
TR - Turchia 90
IE - Irlanda 89
VN - Vietnam 80
IN - India 40
ID - Indonesia 29
BE - Belgio 25
KR - Corea 17
CA - Canada 16
NL - Olanda 16
SE - Svezia 15
AU - Australia 11
RU - Federazione Russa 10
CZ - Repubblica Ceca 7
TW - Taiwan 7
CL - Cile 4
EU - Europa 4
MU - Mauritius 4
SA - Arabia Saudita 4
ES - Italia 3
JP - Giappone 3
AE - Emirati Arabi Uniti 2
AT - Austria 2
BR - Brasile 2
GR - Grecia 2
IL - Israele 2
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
GS - Georgia del Sud e Isole Sandwich Australi 1
IR - Iran 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
NZ - Nuova Zelanda 1
PE - Perù 1
PH - Filippine 1
PT - Portogallo 1
RO - Romania 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
VE - Venezuela 1
Totale 10.366
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Città #
Warsaw 2.691
Fairfield 631
Woodbridge 517
Jacksonville 401
Ashburn 369
Houston 353
Cambridge 252
Seattle 244
Wilmington 243
Brescia 235
Ann Arbor 207
Singapore 170
Chandler 162
Princeton 161
Hong Kong 150
Nanjing 137
Lancaster 134
Beijing 108
New York 91
Dublin 89
Dearborn 85
Helsinki 83
Dong Ket 80
Istanbul 75
Nanchang 45
Changsha 40
Des Moines 37
Shenyang 36
San Diego 34
Hebei 29
Jakarta 29
Jinan 28
Los Angeles 24
Milan 24
Tianjin 24
Kunming 23
Brussels 18
London 18
Jiaxing 17
Munich 17
Shanghai 17
Ningbo 16
Rome 16
Hangzhou 15
Zhengzhou 14
Phoenix 13
Taizhou 12
Verona 12
Seongnam 11
Boardman 10
Lanzhou 10
Falls Church 9
San Francisco 7
Taipei 7
Toronto 7
Washington 7
Auburn Hills 6
Augusta 6
Fuzhou 6
Guangzhou 6
Haikou 6
Norwalk 6
Ottawa 6
Waanrode 6
Council Bluffs 5
Kilburn 5
Kocaeli 5
Leawood 5
Orange 5
San Mateo 5
Changchun 4
Florence 4
Lappeenranta 4
Olomouc 4
Taiyuan 4
Talcahuano 4
Bergamo 3
Canberra 3
Cremona 3
Hefei 3
Honolulu 3
Liverpool 3
Melbourne 3
Nürnberg 3
Palo Del Colle 3
Pune 3
Riyadh 3
Simone 3
Torino 3
Albinea 2
Altamura 2
Berlin 2
Brno 2
Castenedolo 2
Corridonia 2
Falkenstein 2
Fisciano 2
Heraklion 2
Indiana 2
Islington 2
Totale 8.457
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Nome #
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type 303
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 296
Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome 261
GLUT10-Lacking in Arterial Tortuosity Syndrome-Is Localized to the Endoplasmic Reticulum of Human Fibroblasts 252
Bruch's membrane abnormalities in PRDM5-related brittle cornea syndrome 247
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 245
Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport 245
Multifaced Roles of the αvβ3 Integrin in Ehlers–Danlos and Arterial Tortuosity Syndromes’ Dermal Fibroblasts 242
The phenotype of the musculocontractural type of Ehlers-Danlos syndrome due to CHST14 mutations. 240
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 233
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. 225
Arterial Tortuosity Syndrome: a vitamin C compartmentation disease? 221
Clinical and molecular characterization of 40 patients with classic Ehlers--Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations. 216
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations 206
Characterization and expression of slc2a10, the zebrafish ortholog of the human gene involved in arterial tortuosity syndrome. 204
Report on a patient with extremely fragile skin, dermatosparaxis, joint hypermobility, short stature, skeletal deformities, and lipomas: a new syndrome? 193
Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients' skin fibroblasts 193
A cellular test for Ehlers-Danlos syndromes diagnosis. 188
Molecular characterization and transcriptome-wide expression profiling of two patients affected with spondyloepimetaphyseal dysplasia with joint laxity type 185
Classic Ehlers-danlos syndrome: clinical and molecular characterisation of 37 patients 182
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 177
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 171
Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients 160
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant 150
Cellular and molecular mechanisms in the pathogenesis of classical, vascular, and hypermobile ehlers‒danlos syndromes 144
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 143
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 135
Study of conformational properties of a biologically active peptide of Fibronectin by circular dichroism, NMR and molecular dynamics simulation 133
Wound repair capability in EDS fibroblasts can be retrieved by exogenous type V collagen 133
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 130
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 127
Recurrence of the p.R156X TNNI2 mutation in distal arthrogryposis type 2B 125
Angiokeratoma Corporis Diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders. 124
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 124
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type 123
Type III and V collagens modulate the expression and assembly of EDA+ fibronectin in the extracellular matrix of defective Ehlers-Danlos syndrome fibroblasts 113
COL6A5 variants in familial neuropathic chronic itch 109
Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio 106
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations. 103
Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss 103
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β 102
Genotype-phenotype correlation in Italian patients with epidermolysis bullosa dystrophica 101
Exclusion of candidate genes in a family with arterial tortuosity syndrome 99
Effect of dexamethasone on the assembly of the matrix of fibronectin and its receptors organization in Ehlers-Danlos syndrome skin fibroblasts. 98
TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasis 98
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization 97
L’integrina avb3 inibisce il potenziale invasivo e metastatico di cellule tumorali umane esprimenti stabilmente il peptide FN13, attraverso la disattivazione di ILK. 95
Correction of the defective extracellular matrix of Ehlers-Danlos syndrome skin fibroblasts by dexamethasone. 94
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide 92
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 92
Mutations in PRDM5 in brittle cornea syndrome identify a pathway regulating extracellular matrix development and maintenance. 92
Caratterizzazione ed espressione di slc2a10, l’ortologo in Danio rerio del gene umano coinvolto nella sindrome delle arterie tortuose. 92
Dexamethasone-induced healing of chronic leg ulcers in a patient with defective organization of the extracellular matrix of fibronectin. 91
Rescue of migratory defects of Ehlers-Danlos syndrome fibroblasts in vitro by type V collagen but not insulin-like binding protein-1. 91
Altered fibronectin RNA splicing in skin fibroblasts from Ehlers-Danlos syndrome patients: in situ hybridization analysis. 89
Compound heterozygosity for a novel and a recurrent ABCC6 gene mutation in an Italian family with pseudoxanthoma elasticum 88
Does miR-338, a putative negative regulator of the facilitative glucose transporter 10 (GLUT10), play a role in arterial tortuosity syndrome? 88
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 87
Quantitative in situ hybridization for the evaluation of cell – cycle related gene expression. 86
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 86
Alternative splicing of mGluR6 gene generates a truncated glutamate receptor in rat retina. 84
Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients 83
COL1-related overlap disorder: a novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap 83
Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts 83
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 77
Modulation of the facilitative glucose transporters (SLC2A) gene family expression in arterial tortuosity syndrome skin fibroblasts and aortic vascular smooth muscle cells. 73
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 70
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in COL7A1. 68
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome 68
BIOLOGIA E GENETICA DEL MUSCOLO 68
Quantitative evaluation of mRNAs by in situ hybridization and image analysis: principles and applications. 66
Genetic heterogeneity in the Brittle Cornea Syndrome (BCS) –New evidences that ZNF469 and PRDM5 regulate extracellular matrix development and maintenance within the same pathway 64
Quantitative in situ hybridization for the evaluation of gene expression in asynchronous and synchronized cell cultures and in tissue sections 62
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. 60
L’organizzazione della matrice di collagene III nei fibroblasti dermici regola l’espressione di geni coinvolti nell’elastogenesi. 58
The FN13 peptide inhibits human tumor cells invasion through the modulation of alphavbeta3 integrins organization and the inactivation of ILK pathway 57
In search of the SLC2A10 gene role in the etiopathogenesis of arterial tortuosity syndrome by transcriptomic and biochemical approaches 57
Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A>G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy 53
Il collagene III ripristina la migrazione e il riparo delle ferite in vitro in fibroblasti di pazienti affetti da Sindrome di Ehlers-Danlos vascolare. 50
FAK-independent alphavbeta3 integrin-EGFR complexes rescue from anoikis matrix-defective fibroblasts 50
null 49
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 47
Collageni purificati inducono in fibroblasti umani difettivi la sintesi di fibronectina EDA+ e la sua organizzazione nella matrice extracellulare. 46
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? 23
Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts 21
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 19
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 16
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 16
Loeys- Dietz Sindrome and Vascular Ehlers- Danlos Sindrome: differential diagnosis by clinical and molecular approaches 7
Totale 10.646
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Categoria #
all - tutte 41.886
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 41.886
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.130 0 0 0 0 216 353 290 358 259 340 156 158
2020/20211.804 69 211 119 238 85 185 92 177 220 144 144 120
2021/2022789 46 169 21 18 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
2024/2025419 14 8 20 236 141 0 0 0 0 0 0 0
Totale 10.646