IRIS Institutional Research Information System - OPENBS Open Archive UniBS

ZOPPI, NICOLETTA
 Distribuzione geografica
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Continente #
EU - Europa 2.125
NA - Nord America 1.829
AS - Asia 507
AF - Africa 41
SA - Sud America 40
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 3
Totale 4.572
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Nazione #
US - Stati Uniti d'America 1.764
DE - Germania 635
FR - Francia 387
IT - Italia 272
RU - Federazione Russa 199
CN - Cina 147
CZ - Repubblica Ceca 142
GB - Regno Unito 92
NL - Olanda 77
UA - Ucraina 75
IN - India 68
KR - Corea 64
PL - Polonia 59
CA - Canada 55
VN - Vietnam 55
JP - Giappone 39
SE - Svezia 35
IE - Irlanda 26
AU - Australia 24
TW - Taiwan 23
ZA - Sudafrica 22
HK - Hong Kong 20
BR - Brasile 19
ES - Italia 15
FI - Finlandia 15
ID - Indonesia 15
CH - Svizzera 14
GR - Grecia 13
BE - Belgio 12
IR - Iran 11
SG - Singapore 11
TH - Thailandia 11
CL - Cile 10
RO - Romania 10
MX - Messico 9
TR - Turchia 8
DK - Danimarca 7
PT - Portogallo 7
AT - Austria 6
NO - Norvegia 6
IL - Israele 5
QA - Qatar 5
AE - Emirati Arabi Uniti 4
ET - Etiopia 4
HU - Ungheria 4
MT - Malta 4
PH - Filippine 4
PK - Pakistan 4
BD - Bangladesh 3
EC - Ecuador 3
EU - Europa 3
NZ - Nuova Zelanda 3
SD - Sudan 3
AR - Argentina 2
CO - Colombia 2
DZ - Algeria 2
GH - Ghana 2
JO - Giordania 2
MO - Macao, regione amministrativa speciale della Cina 2
NG - Nigeria 2
OM - Oman 2
PE - Perù 2
RS - Serbia 2
SI - Slovenia 2
VE - Venezuela 2
AZ - Azerbaigian 1
BY - Bielorussia 1
CM - Camerun 1
CU - Cuba 1
EG - Egitto 1
FO - Isole Faroe 1
GE - Georgia 1
HR - Croazia 1
KE - Kenya 1
LB - Libano 1
LI - Liechtenstein 1
LT - Lituania 1
LV - Lettonia 1
LY - Libia 1
MD - Moldavia 1
MK - Macedonia 1
NP - Nepal 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TN - Tunisia 1
Totale 4.572
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Città #
Fairfield 202
Houston 133
Woodbridge 116
Ashburn 115
Buffalo 109
Seattle 85
Frankfurt am Main 72
Brescia 71
Wilmington 70
Cambridge 68
Nürnberg 67
Ann Arbor 59
Dong Ket 51
Warsaw 49
Leawood 35
Beijing 34
Saint Petersburg 31
Seongnam 28
Paris 27
Dublin 21
Amsterdam 19
Ottawa 18
Rome 18
Stockholm 17
Clearwater 16
Council Bluffs 16
Phoenix 16
Boardman 15
Taipei 15
Wuhan 15
Chicago 14
Guangzhou 13
Las Vegas 13
Los Angeles 13
Milan 13
Dearborn 12
Helsinki 12
Muizenberg 12
San Diego 12
Shanghai 12
Lenoir 10
Nanjing 10
Nuremberg 10
Samara 10
Seoul 9
Toronto 9
Bangkok 8
Hartford 8
New York 8
Singapore 8
São Paulo 8
Bengaluru 7
Brisbane 7
Hangzhou 7
Jakarta 7
Padova 7
Saint Louis 7
University Park 7
Berlin 6
London 6
Moscow 6
Mumbai 6
Parsippany 6
Provo 6
Riva 6
San Jose 6
Tokyo 6
Andover 5
Austin 5
Bethesda 5
Catanzaro 5
Chongqing 5
Doha 5
Elizabeth City 5
Farnborough 5
Henderson 5
Irvine 5
Istanbul 5
Portland 5
Rennes 5
San Francisco 5
Suri 5
Sydney 5
Athens 4
Aurora 4
Bangalore 4
Boston 4
Chennai 4
Falkenstein 4
Florence 4
Krimpen Aan Den Ijssel 4
New Taipei 4
Philadelphia 4
Santa Barbara 4
Shenyang 4
Sunnyvale 4
Albuquerque 3
Atlanta 3
Bologna 3
Bondeno 3
Totale 2.079
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Nome #
A cellular test for Ehlers-Danlos syndromes diagnosis., file ddc633e3-a946-4e2e-e053-3705fe0a4c80 793
Characterization and expression of slc2a10, the zebrafish ortholog of the human gene involved in arterial tortuosity syndrome., file ddc633e3-a947-4e2e-e053-3705fe0a4c80 611
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome, file ddc633e2-aaeb-4e2e-e053-3705fe0a4c80 608
The phenotype of the musculocontractural type of Ehlers-Danlos syndrome due to CHST14 mutations., file ddc633e2-db53-4e2e-e053-3705fe0a4c80 559
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations, file ddc633e3-a94d-4e2e-e053-3705fe0a4c80 233
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type, file ddc633e3-2064-4e2e-e053-3705fe0a4c80 179
Report on a patient with extremely fragile skin, dermatosparaxis, joint hypermobility, short stature, skeletal deformities, and lipomas: a new syndrome?, file ddc633e3-aae4-4e2e-e053-3705fe0a4c80 169
Cellular and molecular mechanisms in the pathogenesis of classical, vascular, and hypermobile ehlers‒danlos syndromes, file ddc633e3-f65d-4e2e-e053-3705fe0a4c80 165
Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome, file ddc633e3-8b7d-4e2e-e053-3705fe0a4c80 147
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, file ddc633e3-9bb1-4e2e-e053-3705fe0a4c80 146
Clinical and molecular characterization of 40 patients with classic Ehlers--Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations., file ddc633e2-b9bf-4e2e-e053-3705fe0a4c80 121
Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport, file ddc633e3-1769-4e2e-e053-3705fe0a4c80 112
GLUT10-Lacking in Arterial Tortuosity Syndrome-Is Localized to the Endoplasmic Reticulum of Human Fibroblasts, file ddc633e3-6806-4e2e-e053-3705fe0a4c80 112
Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients' skin fibroblasts, file ddc633e3-c866-4e2e-e053-3705fe0a4c80 112
Bruch's membrane abnormalities in PRDM5-related brittle cornea syndrome, file ddc633e2-db2a-4e2e-e053-3705fe0a4c80 100
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant, file ddc633e4-01b5-4e2e-e053-3705fe0a4c80 100
Molecular characterization and transcriptome-wide expression profiling of two patients affected with spondyloepimetaphyseal dysplasia with joint laxity type, file ddc633e3-aae2-4e2e-e053-3705fe0a4c80 74
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, file ddc633e3-8a8d-4e2e-e053-3705fe0a4c80 72
Classic Ehlers-danlos syndrome: clinical and molecular characterisation of 37 patients, file ddc633e3-a94b-4e2e-e053-3705fe0a4c80 68
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, file ddc633e3-46ca-4e2e-e053-3705fe0a4c80 55
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, file ddc633e3-a949-4e2e-e053-3705fe0a4c80 51
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?, file ddc633e4-5ca1-4e2e-e053-3705fe0a4c80 47
Arterial Tortuosity Syndrome: a vitamin C compartmentation disease?, file ddc633e3-57f4-4e2e-e053-3705fe0a4c80 27
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., file ddc633e3-5a2c-4e2e-e053-3705fe0a4c80 25
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, file 3847cbe7-c451-4027-b9e4-950b2fa13d30 19
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects, file ddc633e3-a514-4e2e-e053-3705fe0a4c80 19
Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts, file c14474ff-8c2d-4394-8858-b23e60ffe754 12
Multifaced Roles of the αvβ3 Integrin in Ehlers–Danlos and Arterial Tortuosity Syndromes’ Dermal Fibroblasts, file ddc633e3-9ff5-4e2e-e053-3705fe0a4c80 10
Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio, file ddc633e2-afe5-4e2e-e053-3705fe0a4c80 4
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β, file ddc633e4-0367-4e2e-e053-3705fe0a4c80 4
Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts, file ddc633e4-365d-4e2e-e053-3705fe0a4c80 3
Genetic heterogeneity in the Brittle Cornea Syndrome (BCS) –New evidences that ZNF469 and PRDM5 regulate extracellular matrix development and maintenance within the same pathway, file ddc633e2-a24a-4e2e-e053-3705fe0a4c80 2
COL6A5 variants in familial neuropathic chronic itch, file ddc633e3-4b98-4e2e-e053-3705fe0a4c80 2
Exclusion of candidate genes in a family with arterial tortuosity syndrome, file ddc633e2-a9e6-4e2e-e053-3705fe0a4c80 1
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome, file ddc633e2-aa6e-4e2e-e053-3705fe0a4c80 1
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, file ddc633e2-abaf-4e2e-e053-3705fe0a4c80 1
Mutations in PRDM5 in brittle cornea syndrome identify a pathway regulating extracellular matrix development and maintenance., file ddc633e2-afe6-4e2e-e053-3705fe0a4c80 1
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations., file ddc633e2-b022-4e2e-e053-3705fe0a4c80 1
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., file ddc633e2-b063-4e2e-e053-3705fe0a4c80 1
Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss, file ddc633e2-b8b3-4e2e-e053-3705fe0a4c80 1
Type III and V collagens modulate the expression and assembly of EDA+ fibronectin in the extracellular matrix of defective Ehlers-Danlos syndrome fibroblasts, file ddc633e2-bc62-4e2e-e053-3705fe0a4c80 1
Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients, file ddc633e3-8c61-4e2e-e053-3705fe0a4c80 1
Totale 4.770
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Categoria #
all - tutte 10.443
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 10.443
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019227 0 0 0 0 0 0 0 0 0 58 87 82
2019/2020863 75 52 44 89 79 89 84 73 83 48 75 72
2020/2021834 50 84 54 71 75 80 67 60 75 60 63 95
2021/2022867 46 74 68 83 82 84 59 58 74 53 125 61
2022/2023574 43 42 115 79 39 74 33 29 22 21 36 41
2023/2024803 46 47 101 41 45 58 101 252 73 39 0 0
Totale 4.770