IRIS Institutional Research Information System - OPENBS Open Archive UniBS

ZOPPI, NICOLETTA
 Distribuzione geografica
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Continente #
NA - Nord America 5.952
EU - Europa 5.330
AS - Asia 2.974
SA - Sud America 467
AF - Africa 60
OC - Oceania 32
Continente sconosciuto - Info sul continente non disponibili 4
AN - Antartide 1
Totale 14.820
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Nazione #
US - Stati Uniti d'America 5.852
PL - Polonia 2.710
CN - Cina 1.054
SG - Singapore 973
IT - Italia 555
UA - Ucraina 531
BR - Brasile 369
DE - Germania 351
FR - Francia 318
GB - Regno Unito 316
HK - Hong Kong 310
FI - Finlandia 212
VN - Vietnam 210
TR - Turchia 104
RU - Federazione Russa 93
IE - Irlanda 90
IN - India 90
CA - Canada 61
BD - Bangladesh 41
ID - Indonesia 40
NL - Olanda 39
AR - Argentina 32
AU - Australia 30
BE - Belgio 25
MX - Messico 25
IQ - Iraq 23
SE - Svezia 21
SA - Arabia Saudita 20
ZA - Sudafrica 20
KR - Corea 19
AT - Austria 18
PK - Pakistan 15
CL - Cile 14
ES - Italia 13
JP - Giappone 13
VE - Venezuela 13
EC - Ecuador 10
TW - Taiwan 10
CZ - Repubblica Ceca 8
MA - Marocco 8
PE - Perù 8
CO - Colombia 7
PY - Paraguay 7
TN - Tunisia 7
AE - Emirati Arabi Uniti 6
LT - Lituania 6
MY - Malesia 6
UZ - Uzbekistan 6
IL - Israele 5
MU - Mauritius 5
PH - Filippine 5
UY - Uruguay 5
CH - Svizzera 4
CR - Costa Rica 4
EG - Egitto 4
EU - Europa 4
JM - Giamaica 4
NP - Nepal 4
PT - Portogallo 4
CG - Congo 3
ET - Etiopia 3
JO - Giordania 3
KE - Kenya 3
AL - Albania 2
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
GR - Grecia 2
HU - Ungheria 2
LK - Sri Lanka 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
OM - Oman 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
AZ - Azerbaigian 1
BB - Barbados 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GA - Gabon 1
GS - Georgia del Sud e Isole Sandwich Australi 1
HN - Honduras 1
IR - Iran 1
IS - Islanda 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LV - Lettonia 1
MT - Malta 1
NI - Nicaragua 1
NO - Norvegia 1
RO - Romania 1
SC - Seychelles 1
SN - Senegal 1
SV - El Salvador 1
Totale 14.818
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Città #
Warsaw 2.707
Fairfield 632
Ashburn 574
Singapore 548
Woodbridge 517
Jacksonville 403
Houston 364
Hong Kong 308
Cambridge 252
Seattle 250
Brescia 248
Wilmington 244
San Jose 234
Beijing 229
Ann Arbor 207
The Dalles 168
Chandler 162
Princeton 161
New York 143
Nanjing 137
Lancaster 135
Helsinki 131
Los Angeles 104
Dublin 90
Dearborn 86
Council Bluffs 84
Dong Ket 80
Lauterbourg 78
Istanbul 77
Munich 62
Nanchang 46
Des Moines 43
Ho Chi Minh City 42
London 42
Changsha 41
Shenyang 38
Buffalo 36
Milan 34
San Diego 34
Jakarta 32
Jinan 32
San Francisco 31
Dallas 30
Redondo Beach 30
Rome 30
Santa Clara 30
São Paulo 30
Tianjin 30
Hebei 29
Chicago 27
Hanoi 26
Shanghai 24
Kunming 23
Phoenix 23
Moscow 20
Orem 20
Hangzhou 19
Nuremberg 19
Turku 19
Brussels 18
Jiaxing 17
Zhengzhou 17
Frankfurt am Main 16
Ningbo 16
Toronto 16
Boardman 14
Mexico City 13
Rio de Janeiro 13
Taizhou 13
Verona 13
Baghdad 12
Brooklyn 12
Denver 12
Johannesburg 12
Guangzhou 11
Montreal 11
Seongnam 11
Atlanta 10
Chennai 10
Lanzhou 10
Porto Alegre 10
Tokyo 10
Belo Horizonte 9
Boston 9
Falls Church 9
Riyadh 9
Vienna 9
Washington 9
Amsterdam 8
Augusta 8
Fuzhou 8
Haiphong 8
Manchester 8
New Delhi 8
Paris 8
Taipei 8
Dhaka 7
Poplar 7
Turin 7
Auburn Hills 6
Totale 10.737
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Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 397
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type 338
Bruch's membrane abnormalities in PRDM5-related brittle cornea syndrome 322
Arterial Tortuosity Syndrome: a vitamin C compartmentation disease? 321
Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome 317
Multifaced Roles of the αvβ3 Integrin in Ehlers–Danlos and Arterial Tortuosity Syndromes’ Dermal Fibroblasts 299
GLUT10-Lacking in Arterial Tortuosity Syndrome-Is Localized to the Endoplasmic Reticulum of Human Fibroblasts 298
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 289
Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport 289
Clinical and molecular characterization of 40 patients with classic Ehlers--Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations. 285
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 283
The phenotype of the musculocontractural type of Ehlers-Danlos syndrome due to CHST14 mutations. 279
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. 278
Characterization and expression of slc2a10, the zebrafish ortholog of the human gene involved in arterial tortuosity syndrome. 268
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations 264
A cellular test for Ehlers-Danlos syndromes diagnosis. 263
Molecular characterization and transcriptome-wide expression profiling of two patients affected with spondyloepimetaphyseal dysplasia with joint laxity type 258
Classic Ehlers-danlos syndrome: clinical and molecular characterisation of 37 patients 252
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 240
Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients' skin fibroblasts 240
Report on a patient with extremely fragile skin, dermatosparaxis, joint hypermobility, short stature, skeletal deformities, and lipomas: a new syndrome? 239
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 221
Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients 219
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 207
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant 203
Cellular and molecular mechanisms in the pathogenesis of classical, vascular, and hypermobile ehlers‒danlos syndromes 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 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
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 187
Angiokeratoma Corporis Diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders. 183
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
Study of conformational properties of a biologically active peptide of Fibronectin by circular dichroism, NMR and molecular dynamics simulation 178
COL6A5 variants in familial neuropathic chronic itch 172
Wound repair capability in EDS fibroblasts can be retrieved by exogenous type V collagen 171
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β 167
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
Does miR-338, a putative negative regulator of the facilitative glucose transporter 10 (GLUT10), play a role in arterial tortuosity syndrome? 160
Type III and V collagens modulate the expression and assembly of EDA+ fibronectin in the extracellular matrix of defective Ehlers-Danlos syndrome fibroblasts 156
Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts 156
Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss 156
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type 155
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
Caratterizzazione ed espressione di slc2a10, l’ortologo in Danio rerio del gene umano coinvolto nella sindrome delle arterie tortuose. 149
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 148
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations. 142
Altered fibronectin RNA splicing in skin fibroblasts from Ehlers-Danlos syndrome patients: in situ hybridization analysis. 141
TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasis 137
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization 136
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide 134
Exclusion of candidate genes in a family with arterial tortuosity syndrome 134
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 134
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 130
Correction of the defective extracellular matrix of Ehlers-Danlos syndrome skin fibroblasts by dexamethasone. 130
Mutations in PRDM5 in brittle cornea syndrome identify a pathway regulating extracellular matrix development and maintenance. 130
Dexamethasone-induced healing of chronic leg ulcers in a patient with defective organization of the extracellular matrix of fibronectin. 129
COL1-related overlap disorder: a novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap 127
Effect of dexamethasone on the assembly of the matrix of fibronectin and its receptors organization in Ehlers-Danlos syndrome skin fibroblasts. 126
Genotype-phenotype correlation in Italian patients with epidermolysis bullosa dystrophica 126
Alternative splicing of mGluR6 gene generates a truncated glutamate receptor in rat retina. 126
Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients 125
Rescue of migratory defects of Ehlers-Danlos syndrome fibroblasts in vitro by type V collagen but not insulin-like binding protein-1. 125
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in COL7A1. 123
Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts 119
Compound heterozygosity for a novel and a recurrent ABCC6 gene mutation in an Italian family with pseudoxanthoma elasticum 118
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 117
Quantitative in situ hybridization for the evaluation of cell – cycle related gene expression. 115
Modulation of the facilitative glucose transporters (SLC2A) gene family expression in arterial tortuosity syndrome skin fibroblasts and aortic vascular smooth muscle cells. 114
BIOLOGIA E GENETICA DEL MUSCOLO 106
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. 101
Genetic heterogeneity in the Brittle Cornea Syndrome (BCS) –New evidences that ZNF469 and PRDM5 regulate extracellular matrix development and maintenance within the same pathway 99
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome 99
Quantitative evaluation of mRNAs by in situ hybridization and image analysis: principles and applications. 96
Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A>G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy 96
Integrative Multi-Omics Approach in Vascular Ehlers–Danlos Syndrome: Further Insights into the Disease Mechanisms by Proteomic Analysis of Patient Dermal Fibroblasts 91
Quantitative in situ hybridization for the evaluation of gene expression in asynchronous and synchronized cell cultures and in tissue sections 90
L’organizzazione della matrice di collagene III nei fibroblasti dermici regola l’espressione di geni coinvolti nell’elastogenesi. 89
FAK-independent alphavbeta3 integrin-EGFR complexes rescue from anoikis matrix-defective fibroblasts 85
In search of the SLC2A10 gene role in the etiopathogenesis of arterial tortuosity syndrome by transcriptomic and biochemical approaches 82
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 76
The FN13 peptide inhibits human tumor cells invasion through the modulation of alphavbeta3 integrins organization and the inactivation of ILK pathway 76
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 76
Il collagene III ripristina la migrazione e il riparo delle ferite in vitro in fibroblasti di pazienti affetti da Sindrome di Ehlers-Danlos vascolare. 76
Collageni purificati inducono in fibroblasti umani difettivi la sintesi di fibronectina EDA+ e la sua organizzazione nella matrice extracellulare. 73
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 63
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? 59
null 49
Loeys- Dietz Sindrome and Vascular Ehlers- Danlos Sindrome: differential diagnosis by clinical and molecular approaches 44
Totale 15.108
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Categoria #
all - tutte 61.355
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 61.355
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021120 0 0 0 0 0 0 0 0 0 0 0 120
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
2024/20251.553 14 8 20 236 156 133 164 48 166 66 327 215
2025/20263.328 300 398 216 394 299 282 571 142 228 268 159 71
Totale 15.108