SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

BOVOLENTA, Matteo
 Distribuzione geografica
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Continente #
NA - Nord America 830
EU - Europa 384
AS - Asia 117
AF - Africa 13
OC - Oceania 9
SA - Sud America 7
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.361
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Nazione #
US - Stati Uniti d'America 806
IT - Italia 81
CH - Svizzera 78
FR - Francia 75
CN - Cina 64
DE - Germania 53
VN - Vietnam 21
GB - Regno Unito 18
PL - Polonia 14
RU - Federazione Russa 14
HN - Honduras 12
SE - Svezia 10
CA - Canada 9
IN - India 9
AU - Australia 8
JP - Giappone 7
NL - Olanda 7
CZ - Repubblica Ceca 6
FI - Finlandia 5
ZA - Sudafrica 5
AE - Emirati Arabi Uniti 4
AT - Austria 4
CL - Cile 4
ES - Italia 4
SC - Seychelles 4
HK - Hong Kong 3
PK - Pakistan 3
RS - Serbia 3
BR - Brasile 2
BZ - Belize 2
DK - Danimarca 2
EG - Egitto 2
GR - Grecia 2
IE - Irlanda 2
NP - Nepal 2
RO - Romania 2
UA - Ucraina 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BE - Belgio 1
CO - Colombia 1
HU - Ungheria 1
MO - Macao, regione amministrativa speciale della Cina 1
MU - Mauritius 1
MX - Messico 1
NZ - Nuova Zelanda 1
SG - Singapore 1
TN - Tunisia 1
TR - Turchia 1
TW - Taiwan 1
Totale 1.361
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Città #
Fairfield 89
Santa Cruz 74
Ashburn 61
Houston 51
Centre Hall 44
Buffalo 43
Seattle 38
Woodbridge 37
Lausanne 35
Geneva 32
Ann Arbor 26
Albignasego 23
Cambridge 22
Des Moines 22
Wilmington 22
Ferrara 21
Dong Ket 20
Chicago 15
Warsaw 14
Shanghai 13
Centro 12
Paris 11
Columbus 10
New York 10
San Diego 10
Henderson 9
Stockholm 8
Las Vegas 7
Wuhan 7
Beijing 6
Boardman 6
Cedar Knolls 6
Chandler 6
Lincoln 6
Stuttgart 6
Bengaluru 5
Dallas 5
Ferrara di Monte Baldo 5
Los Angeles 5
Ottawa 5
Bremen 4
Guangzhou 4
Hangzhou 4
Helsinki 4
Milan 4
Muizenberg 4
Phoenix 4
San Francisco 4
Tokyo 4
Bologna 3
Brooklyn 3
Creazzo 3
Frankfurt am Main 3
Lahore 3
Le Mont-sur-lausanne 3
London 3
Manassas 3
Melbourne 3
Provo 3
Pully 3
San Jose 3
Auburn 2
Basel 2
Belize City 2
Brookline 2
Cairo 2
Changsha 2
Chions 2
Chios 2
Clearwater 2
Copenhagen 2
Dublin 2
Easton 2
Grenoble 2
Herndon 2
Kathmandu 2
Keyport 2
Kraljevo 2
Lake Forest 2
Leawood 2
Leiden 2
Nanjing 2
New Albany 2
Orléans 2
Providence 2
Shenyang 2
Shenzhen 2
Sydney 2
Tianjin 2
Toronto 2
Walpole 2
A Coruña 1
Atlanta 1
Austin 1
Barcelona 1
Biel/Bienne 1
Bristol 1
Büdelsdorf 1
Camponogara 1
Carbonera 1
Totale 988
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Nome #
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis, file e309ade3-2242-3969-e053-3a05fe0a2c94 289
Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 System, file e309ade1-53ae-3969-e053-3a05fe0a2c94 211
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression, file e309ade1-7717-3969-e053-3a05fe0a2c94 171
Exploring Splicing-Switching Molecules For Seckel Syndrome Therapy, file e309ade1-2444-3969-e053-3a05fe0a2c94 127
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy, file e309ade0-d00c-3969-e053-3a05fe0a2c94 124
An engineered tale-transcription factor rescues transcription of factor VII impaired by promoter mutations and enhances its endogenous expression in hepatocytes, file e309ade0-d8c6-3969-e053-3a05fe0a2c94 57
C6orf10 low-frequency and rare variants in italian multiple sclerosis patients, file e309ade3-2317-3969-e053-3a05fe0a2c94 55
C6orf10 low-frequency and rare variants in italian multiple sclerosis patients, file e309ade2-317b-3969-e053-3a05fe0a2c94 52
Exploiting The CRISPR/CAS9 System to Study Alternative Splicing In Vivo: Application to titin, file e309ade0-e1c4-3969-e053-3a05fe0a2c94 50
Ex Vivo COL7A1 Correction for Recessive Dystrophic Epidermolysis Bullosa Using CRISPR/Cas9 and Homology-Directed Repair, file e309ade1-f260-3969-e053-3a05fe0a2c94 44
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice, file e309ade0-b077-3969-e053-3a05fe0a2c94 37
Fo ATP synthase C subunit serum levels in patients with ST-segment Elevation Myocardial Infarction: Preliminary findings, file e309ade4-2fdf-3969-e053-3a05fe0a2c94 34
Antisense modulation of both exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon responsible for X-linked dilated cardiomyopathy, file e309ade0-3472-3969-e053-3a05fe0a2c94 23
CRISPR activation on coagulation F7 or F8 promoters potentiate trascriptional activity in the normal and mutated gene context, file e309ade4-d57e-3969-e053-3a05fe0a2c94 18
Antisense oligonucleotides conjugated with lipophilic compounds: synthesis and in vitro evaluation of exon skipping in duchenne muscular dystrophy, file e309ade5-84e6-3969-e053-3a05fe0a2c94 12
Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies, file e309ade0-33fe-3969-e053-3a05fe0a2c94 11
A naturally occurring mutation in ATP synthase subunit c is associated with increased damage following hypoxia/reoxygenation in STEMI patients, file 95a7ad4a-44e5-46e9-a8fd-0ced46c0864a 10
The DMD Locus Harbours Multiple Long Non-Coding RNAs Which Orchestrate and Control Transcription of Muscle Dystrophin mRNA Isoforms, file e309ade0-4c73-3969-e053-3a05fe0a2c94 10
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype, file e309ade0-3a91-3969-e053-3a05fe0a2c94 9
Nanoparticle-Mediated Delivery of Antisense Oligoribonucleotides Allows Restoration of Dystrophin Expression in the mdx Mouse, file e031f2bb-a3a4-4f77-83e0-2c65ca6819b9 8
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies, file e309ade0-29cf-3969-e053-3a05fe0a2c94 8
Synthesis and exon‐skipping properties of a 3′‐ursodeoxycholic acid‐conjugated oligonucleotide targeting dmd pre‐mrna: Pre‐synthetic versus post‐ synthetic approach, file eebe9c20-7716-4c40-b332-2d18a464b834 8
The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5 ' X-linked dilated cardiomyopathy, file e309ade0-34b8-3969-e053-3a05fe0a2c94 7
Antisense-Induced Messenger Depletion Corrects a COL6A2 Dominant Mutation in Ullrich Myopathy, file 8880d778-aad1-4dde-80ac-0aa5f6a9b5ab 6
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse, file 9df483b3-a9b9-4ae5-9b5e-66bcf6a55275 5
Rapid, comprehensive analysis of the dystrophin transcript by a custom micro-fluidic exome array, file cd8506b5-5e3d-4c58-a899-0e08c2f7985a 4
Exploiting The CRISPR/CAS9 System to Study Alternative Splicing In Vivo: Application to titin, file e309ade4-c40e-3969-e053-3a05fe0a2c94 4
Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis, file e309ade0-374d-3969-e053-3a05fe0a2c94 3
Macrophages: a minimally invasive tool for monitoring collagen VI myopathies, file e309ade0-2fb3-3969-e053-3a05fe0a2c94 2
Antisense-Induced Messenger Depletion Corrects a COL6A2 Dominant Mutation in Ullrich Myopathy, file e309ade0-446c-3969-e053-3a05fe0a2c94 2
null, file e309ade0-ac1e-3969-e053-3a05fe0a2c94 2
Crispr/Cas9-based COL7A1 editing for recessive dystrophic epidermolysis bullosa, file e309ade0-d157-3969-e053-3a05fe0a2c94 2
Omics approach and novel biostatistic tools identified RPL3L as potential genetic modifier of clinical severity in female carriers of Duchenne muscle dystrophy, file e309ade3-1e2a-3969-e053-3a05fe0a2c94 2
null, file e309ade4-b4bf-3969-e053-3a05fe0a2c94 2
PLC-beta2 monitors the drug-induced release of differentiation blockade in tumoral myeloid precursors, file e309ade0-25b3-3969-e053-3a05fe0a2c94 1
Transcriptional behavior of DMD gene duplications in DMD/BMD males, file e309ade0-29cd-3969-e053-3a05fe0a2c94 1
Autosomal recessive Bethlem myopathy, file e309ade0-3380-3969-e053-3a05fe0a2c94 1
Prenatal diagnosis of Duchenne muscular dystrophy by comparative genomic hybridization, file e309ade0-3381-3969-e053-3a05fe0a2c94 1
Exon skipping-mediated dystrophin reading frame restoration for small mutations, file e309ade0-3387-3969-e053-3a05fe0a2c94 1
Identification and characterization of novel collagen VI non-canonical splicing mutations causing ullrich congenital muscular dystrophy, file e309ade0-3ba5-3969-e053-3a05fe0a2c94 1
Fo ATP synthase C subunit serum levels in patients with ST-segment Elevation Myocardial Infarction: Preliminary findings, file e309ade0-d00b-3969-e053-3a05fe0a2c94 1
Transcriptomics analysis in collagen VI myopathy: Role of circadian genes using novel fluidic card tools, file e309ade0-f00f-3969-e053-3a05fe0a2c94 1
D.P.7 Whole exome sequencing as genetic diagnostic tool in myofibrillar myopathies, file e309ade4-cc36-3969-e053-3a05fe0a2c94 1
A new rat model for Duchenne muscular dystrophy generated by CRISPR-induced deletion of Exon 45, file e309ade5-35c7-3969-e053-3a05fe0a2c94 1
Totale 1.419
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Categoria #
all - tutte 5.134
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 5.134
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201929 0 0 0 0 0 0 0 0 0 0 17 12
2019/2020129 10 11 10 20 10 7 12 9 14 15 5 6
2020/2021289 8 10 5 9 8 10 34 26 51 40 48 40
2021/2022344 30 12 15 43 44 14 11 19 24 14 78 40
2022/2023312 13 25 56 35 43 44 17 26 12 10 24 7
2023/2024251 5 18 24 5 62 32 11 29 31 22 12 0
Totale 1.419