IRIS Institutional Research Information System - OPENBS Open Archive UniBS

ZOPPI, NICOLETTA
 Distribuzione geografica
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Continente #
NA - Nord America 5.723
EU - Europa 5.294
AS - Asia 2.934
SA - Sud America 467
AF - Africa 60
OC - Oceania 32
Continente sconosciuto - Info sul continente non disponibili 4
AN - Antartide 1
Totale 14.515
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Nazione #
US - Stati Uniti d'America 5.641
PL - Polonia 2.710
CN - Cina 1.035
SG - Singapore 956
IT - Italia 531
UA - Ucraina 531
BR - Brasile 369
DE - Germania 348
FR - Francia 318
GB - Regno Unito 313
HK - Hong Kong 309
FI - Finlandia 212
VN - Vietnam 210
TR - Turchia 104
RU - Federazione Russa 93
IE - Irlanda 90
IN - India 89
CA - Canada 50
BD - Bangladesh 41
ID - Indonesia 40
NL - Olanda 37
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
AT - Austria 18
KR - Corea 18
PK - Pakistan 15
CL - Cile 14
JP - Giappone 13
VE - Venezuela 13
ES - Italia 11
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
MU - Mauritius 5
PH - Filippine 5
UY - Uruguay 5
EG - Egitto 4
EU - Europa 4
IL - Israele 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
CH - Svizzera 2
GR - Grecia 2
HU - Ungheria 2
JM - Giamaica 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
CR - Costa Rica 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
NO - Norvegia 1
RO - Romania 1
SC - Seychelles 1
SN - Senegal 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
Totale 14.515
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Città #
Warsaw 2.707
Fairfield 631
Ashburn 565
Singapore 544
Woodbridge 517
Jacksonville 403
Houston 364
Hong Kong 307
Cambridge 252
Seattle 250
Brescia 247
Wilmington 244
Beijing 226
Ann Arbor 207
San Jose 184
The Dalles 168
Chandler 162
Princeton 161
Nanjing 137
Lancaster 135
New York 133
Helsinki 131
Los Angeles 100
Dublin 90
Dearborn 85
Dong Ket 80
Lauterbourg 78
Istanbul 77
Council Bluffs 75
Munich 62
Nanchang 46
Des Moines 43
Ho Chi Minh City 42
Changsha 41
London 40
Shenyang 38
Buffalo 35
Milan 34
San Diego 34
Jakarta 32
Jinan 32
Redondo Beach 30
São Paulo 30
Tianjin 30
Hebei 29
San Francisco 29
Rome 28
Chicago 27
Hanoi 26
Santa Clara 25
Shanghai 24
Dallas 23
Kunming 23
Phoenix 22
Moscow 20
Orem 20
Hangzhou 19
Nuremberg 19
Turku 19
Brussels 18
Jiaxing 17
Zhengzhou 17
Ningbo 16
Boardman 14
Frankfurt am Main 14
Mexico City 13
Rio de Janeiro 13
Taizhou 13
Toronto 13
Verona 13
Baghdad 12
Brooklyn 12
Johannesburg 12
Guangzhou 11
Seongnam 11
Atlanta 10
Chennai 10
Lanzhou 10
Montreal 10
Porto Alegre 10
Tokyo 10
Belo Horizonte 9
Denver 9
Falls Church 9
Riyadh 9
Vienna 9
Washington 9
Amsterdam 8
Fuzhou 8
Haiphong 8
Manchester 8
New Delhi 8
Paris 8
Taipei 8
Augusta 7
Boston 7
Dhaka 7
Poplar 7
Turin 7
Auburn Hills 6
Totale 10.612
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Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 383
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type 336
Bruch's membrane abnormalities in PRDM5-related brittle cornea syndrome 315
Arterial Tortuosity Syndrome: a vitamin C compartmentation disease? 315
Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome 309
GLUT10-Lacking in Arterial Tortuosity Syndrome-Is Localized to the Endoplasmic Reticulum of Human Fibroblasts 295
Multifaced Roles of the αvβ3 Integrin in Ehlers–Danlos and Arterial Tortuosity Syndromes’ Dermal Fibroblasts 292
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 288
Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport 288
Clinical and molecular characterization of 40 patients with classic Ehlers--Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations. 280
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 279
The phenotype of the musculocontractural type of Ehlers-Danlos syndrome due to CHST14 mutations. 274
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. 272
Characterization and expression of slc2a10, the zebrafish ortholog of the human gene involved in arterial tortuosity syndrome. 265
A cellular test for Ehlers-Danlos syndromes diagnosis. 262
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations 261
Molecular characterization and transcriptome-wide expression profiling of two patients affected with spondyloepimetaphyseal dysplasia with joint laxity type 255
Classic Ehlers-danlos syndrome: clinical and molecular characterisation of 37 patients 240
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 235
Report on a patient with extremely fragile skin, dermatosparaxis, joint hypermobility, short stature, skeletal deformities, and lipomas: a new syndrome? 233
Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients' skin fibroblasts 231
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 218
Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients 214
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant 199
Cellular and molecular mechanisms in the pathogenesis of classical, vascular, and hypermobile ehlers‒danlos syndromes 194
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 194
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 186
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 184
Angiokeratoma Corporis Diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders. 181
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 181
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 179
Study of conformational properties of a biologically active peptide of Fibronectin by circular dichroism, NMR and molecular dynamics simulation 178
Wound repair capability in EDS fibroblasts can be retrieved by exogenous type V collagen 170
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β 166
COL6A5 variants in familial neuropathic chronic itch 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 161
Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio 158
Does miR-338, a putative negative regulator of the facilitative glucose transporter 10 (GLUT10), play a role in arterial tortuosity syndrome? 156
Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts 155
Type III and V collagens modulate the expression and assembly of EDA+ fibronectin in the extracellular matrix of defective Ehlers-Danlos syndrome fibroblasts 153
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type 150
L’integrina avb3 inibisce il potenziale invasivo e metastatico di cellule tumorali umane esprimenti stabilmente il peptide FN13, attraverso la disattivazione di ILK. 149
Recurrence of the p.R156X TNNI2 mutation in distal arthrogryposis type 2B 149
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 148
Caratterizzazione ed espressione di slc2a10, l’ortologo in Danio rerio del gene umano coinvolto nella sindrome delle arterie tortuose. 147
Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss 147
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 146
Altered fibronectin RNA splicing in skin fibroblasts from Ehlers-Danlos syndrome patients: in situ hybridization analysis. 140
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations. 139
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization 135
TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasis 135
Exclusion of candidate genes in a family with arterial tortuosity syndrome 133
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 133
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide 131
Correction of the defective extracellular matrix of Ehlers-Danlos syndrome skin fibroblasts by dexamethasone. 127
Mutations in PRDM5 in brittle cornea syndrome identify a pathway regulating extracellular matrix development and maintenance. 127
Effect of dexamethasone on the assembly of the matrix of fibronectin and its receptors organization in Ehlers-Danlos syndrome skin fibroblasts. 125
Genotype-phenotype correlation in Italian patients with epidermolysis bullosa dystrophica 125
Dexamethasone-induced healing of chronic leg ulcers in a patient with defective organization of the extracellular matrix of fibronectin. 125
Rescue of migratory defects of Ehlers-Danlos syndrome fibroblasts in vitro by type V collagen but not insulin-like binding protein-1. 125
Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients 124
Alternative splicing of mGluR6 gene generates a truncated glutamate receptor in rat retina. 124
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in COL7A1. 120
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 119
COL1-related overlap disorder: a novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap 119
Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts 116
Compound heterozygosity for a novel and a recurrent ABCC6 gene mutation in an Italian family with pseudoxanthoma elasticum 116
Quantitative in situ hybridization for the evaluation of cell – cycle related gene expression. 115
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 115
Modulation of the facilitative glucose transporters (SLC2A) gene family expression in arterial tortuosity syndrome skin fibroblasts and aortic vascular smooth muscle cells. 113
BIOLOGIA E GENETICA DEL MUSCOLO 105
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. 100
Genetic heterogeneity in the Brittle Cornea Syndrome (BCS) –New evidences that ZNF469 and PRDM5 regulate extracellular matrix development and maintenance within the same pathway 98
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome 98
Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A>G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy 94
Quantitative evaluation of mRNAs by in situ hybridization and image analysis: principles and applications. 92
Quantitative in situ hybridization for the evaluation of gene expression in asynchronous and synchronized cell cultures and in tissue sections 89
L’organizzazione della matrice di collagene III nei fibroblasti dermici regola l’espressione di geni coinvolti nell’elastogenesi. 88
Integrative Multi-Omics Approach in Vascular Ehlers–Danlos Syndrome: Further Insights into the Disease Mechanisms by Proteomic Analysis of Patient Dermal Fibroblasts 84
FAK-independent alphavbeta3 integrin-EGFR complexes rescue from anoikis matrix-defective fibroblasts 81
In search of the SLC2A10 gene role in the etiopathogenesis of arterial tortuosity syndrome by transcriptomic and biochemical approaches 80
The FN13 peptide inhibits human tumor cells invasion through the modulation of alphavbeta3 integrins organization and the inactivation of ILK pathway 75
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 75
Il collagene III ripristina la migrazione e il riparo delle ferite in vitro in fibroblasti di pazienti affetti da Sindrome di Ehlers-Danlos vascolare. 75
Collageni purificati inducono in fibroblasti umani difettivi la sintesi di fibronectina EDA+ e la sua organizzazione nella matrice extracellulare. 71
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 69
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 61
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? 58
null 49
Loeys- Dietz Sindrome and Vascular Ehlers- Danlos Sindrome: differential diagnosis by clinical and molecular approaches 44
Totale 14.803
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Categoria #
all - tutte 58.286
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 58.286
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021408 0 0 0 0 0 0 0 0 0 144 144 120
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
2024/20251.553 14 8 20 236 156 133 164 48 166 66 327 215
2025/20263.023 300 398 216 394 299 282 571 142 228 193 0 0
Totale 14.803