SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

RIMESSI, Paola
 Distribuzione geografica
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Continente #
NA - Nord America 6.772
AS - Asia 3.437
EU - Europa 2.353
SA - Sud America 485
Continente sconosciuto - Info sul continente non disponibili 100
AF - Africa 84
OC - Oceania 19
Totale 13.250
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Nazione #
US - Stati Uniti d'America 6.591
SG - Singapore 1.364
CN - Cina 826
DE - Germania 513
IT - Italia 456
VN - Vietnam 393
BR - Brasile 372
UA - Ucraina 273
PL - Polonia 240
GB - Regno Unito 230
HK - Hong Kong 229
FI - Finlandia 173
TR - Turchia 171
SE - Svezia 113
CA - Canada 97
IN - India 89
BD - Bangladesh 86
FR - Francia 86
JP - Giappone 78
RU - Federazione Russa 77
MX - Messico 51
ID - Indonesia 44
AR - Argentina 40
NL - Olanda 39
ZA - Sudafrica 32
IQ - Iraq 30
ES - Italia 29
CO - Colombia 20
LT - Lituania 20
VE - Venezuela 20
AT - Austria 19
BE - Belgio 18
PH - Filippine 18
CZ - Repubblica Ceca 16
PK - Pakistan 16
AU - Australia 15
TN - Tunisia 13
UZ - Uzbekistan 13
SA - Arabia Saudita 12
CL - Cile 10
CH - Svizzera 9
EC - Ecuador 9
MA - Marocco 9
MY - Malesia 9
CR - Costa Rica 8
EG - Egitto 8
JO - Giordania 8
AE - Emirati Arabi Uniti 7
DZ - Algeria 7
IE - Irlanda 7
IR - Iran 7
PY - Paraguay 7
JM - Giamaica 6
KE - Kenya 6
NP - Nepal 6
LB - Libano 5
AZ - Azerbaigian 4
HN - Honduras 4
RO - Romania 4
BB - Barbados 3
BO - Bolivia 3
HU - Ungheria 3
MK - Macedonia 3
NZ - Nuova Zelanda 3
PS - Palestinian Territory 3
PT - Portogallo 3
QA - Qatar 3
SI - Slovenia 3
TW - Taiwan 3
AO - Angola 2
BG - Bulgaria 2
BS - Bahamas 2
BY - Bielorussia 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
GR - Grecia 2
KH - Cambogia 2
KZ - Kazakistan 2
MD - Moldavia 2
OM - Oman 2
PA - Panama 2
PR - Porto Rico 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
UY - Uruguay 2
BH - Bahrain 1
CD - Congo 1
CM - Camerun 1
EE - Estonia 1
ET - Etiopia 1
GE - Georgia 1
GT - Guatemala 1
IL - Israele 1
KG - Kirghizistan 1
LI - Liechtenstein 1
LK - Sri Lanka 1
LV - Lettonia 1
ME - Montenegro 1
ML - Mali 1
MR - Mauritania 1
Totale 13.139
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Città #
Singapore 841
Ashburn 752
San Jose 592
Fairfield 460
Woodbridge 437
Chandler 378
Houston 352
Beijing 317
Jacksonville 273
Santa Clara 269
Munich 262
Warsaw 235
Ann Arbor 231
Hong Kong 223
Council Bluffs 195
Seattle 175
Wilmington 153
Los Angeles 148
New York 137
Cambridge 134
Ho Chi Minh City 121
Izmir 92
Nanjing 81
Dallas 76
Hanoi 76
Helsinki 76
Tokyo 74
Princeton 68
Milan 65
Shanghai 54
Lauterbourg 52
Buffalo 51
London 51
Ferrara 49
São Paulo 47
San Diego 44
Boardman 41
Orem 38
Turku 37
Montreal 34
Bremen 32
Mexico City 32
Bologna 30
Da Nang 30
Tianjin 30
Brooklyn 29
Jakarta 29
Hefei 28
Chicago 27
Dearborn 27
Denver 26
Falkenstein 26
Toronto 25
Stockholm 24
Atlanta 23
Phoenix 23
Frankfurt am Main 22
Johannesburg 22
San Mateo 22
The Dalles 21
Poplar 20
Chennai 19
Brussels 18
Falls Church 18
Haiphong 18
Changsha 17
Washington 17
Hebei 15
Jiaxing 15
Nanchang 15
Naples 14
San Francisco 14
Shenyang 13
Amsterdam 12
Mumbai 12
Rio de Janeiro 12
Rome 12
Tashkent 12
Brasília 11
Brno 11
Guangzhou 11
Moscow 11
Philadelphia 11
Reggio Emilia 11
Auburn Hills 10
Baghdad 10
Charlotte 10
Norwalk 10
Boston 9
Hangzhou 9
Istanbul 9
Ningbo 9
Nuremberg 9
Ottawa 9
Des Moines 8
Haikou 8
Hải Dương 8
Jinan 8
Kunming 8
Mountain View 8
Totale 8.800
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Nome #
HIV-1 Tat protein modulates the generation of cytotoxic T cell epitopes by modifying proteasome composition and enzymatic activity 423
Un'ipotonia sospetta 395
Persistent Dystrophin Protein Restoration 90 Days after a Course of Intraperitoneally Administered Naked 2′OMePS AON and ZM2 NP-AON Complexes in mdx Mice 324
A Family with γ-Thalassemia and High Hb A2 Levels 302
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse 284
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 277
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies 271
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 267
A BK virus episomal vector for constitutive high expression of exogenous cDNAs in human cells 264
Exon skipping-mediated dystrophin reading frame restoration for small mutations 257
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 252
Antisense modulation of both exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon responsible for X-linked dilated cardiomyopathy 249
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 242
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point 236
Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice 231
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 223
Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective 220
Identification of cytotoxic T lymphocyte epitopes of human herpesvirus 8 219
Exon Skipping Quantification by Real-Time PCR 217
Transcriptional behavior of DMD gene duplications in DMD/BMD males 216
The DMD Locus Harbours Multiple Long Non-Coding RNAs Which Orchestrate and Control Transcription of Muscle Dystrophin mRNA Isoforms 215
Antisense oligonucleotides conjugated with lipophilic compounds: synthesis and in vitro evaluation of exon skipping in duchenne muscular dystrophy 213
Antisense oligonucleotides capable of inducing exon skipping in dystrophin gene and their use in treatment of duchenne muscular dystrophy 212
Characterization of a 4-Mb region at chromosome 6q21 harboring a replicative senescence gene 211
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human 208
Generation of a human induced pluripotent stem cell line (UNIFEi001-A) from a patient with Spinocerebellar ataxia type 1 (SCA1) 207
T.P.2.07 The systemic administration of a low dose of 2OMePS-AON combined with novel cationic polymethylmethacrylate nanoparticles induces the rescue of dystrophin expression in the mdx murine model 197
High expression of exogenous cDNAs directed by HIV-1 long terminal repeat in human cells constitutively producing HIV-1 tat and adenovirus E1A/E1B 195
Can paranasal sinus computed tomography screen for cystic fibrosis heterozygotes? 195
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing 195
Characterization of BKV variants rescued from human tumors and tumor cell lines 192
DMD gene molecular genetic characterization in Eastern Europe and non European countries 192
Systemic Expression of HIV-1 tat Gene in Transgenic Mice Induces Endothelial Proliferation and Ibmors of Different Histotypes 191
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 185
Preclinical PK and PD studies on 2′-O-methyl-phosphorothioate RNA antisense oligonucleotides in the mdx mouse model 183
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: In vitro mimicking and antisense modulation of the splicing abnormality 181
Phenotypic and genotypic heterogeneity in transthyretin-related cardiac amyloidosis: towards tailoring of therapeutic strategies? 180
In vivo study of an aberrant dystrophin exon inclusion in X-linked dilated cardiomyopathy 180
Transformation of human cells by recombinant DNA molecules containing BK virus early region and the human activated c-Hras or c-myc oncogenes 176
Farmacogenetica dei taxani nel trattamento del carcinoma mammario: possibile ruolo nell’identificazione del rischio di tossicità. 175
Carpal tunnel syndrome in cardiac amyloidosis: implications for early diagnosis and prognostic role across the spectrum of aetiologies 172
Uso di modelli di trasformazione virale nello studio dei geni oncosoppressori tramite trasferimento monocromosomico. 170
La consulenza oncogenetica per il carcinoma mammario ed ovarico con ricorrenza familiare come parte di un Percorso integrato multidisciplinare. 170
Tempo and mode of evolution of a primate-specific retrotransposon belonging to the LINE 1 family. 168
Workload measurement for molecular genetics laboratory: A survey study 166
Prenatal diagnosis of Duchenne muscular dystrophy by comparative genomic hybridization 165
Tumorigenicity and anchorage-independent growth suppression of BK virus transformed mouse cells by human chromosome 11 157
Localizzazione preliminare di tumor suppressor genes mediante chromosome transfer. 155
Nanoparticle-Mediated Delivery of Antisense Oligoribonucleotides Allows Restoration of Dystrophin Expression in the mdx Mouse 153
Genetic analysis of a 6q21 region harboring a senescence gene: construction of a 4 megabase yeast artificial chromosome contig 152
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 149
ncRNAs originating from the dystrophin gene as biomarker for assessing antisense therapy 149
Conjugates of oligonucleotides and bile acids and their derivatives for pharmaceutical active molecules delivery 145
Brody disease: Insights into biochemical features of SERCA1 and identification of a novel mutation 140
Nanoparticle of the core-​shell type suitable for delivering therapeutic oligonucleotides to target tissues and the use thereof for the preparation of a medicament for treating duchenne muscular dystrophy 138
Nanoparticle of the core-shell type suitable for delivering therapeutic oligonucleotides to target tissues and the use thereof for the preparation of a medicament for treating duchenne muscular distrophy 137
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Tumor suppressor genes. New perspectives for clinical investigations in cancer 126
Presence of HHV-8 DNA in semen of immunocompetent HIV-negative individuals from different geographical areas in Italy. 123
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. 123
Nanoparticles are effective vehicles for systemic delivery of 2 ' OMePS antisense oligonucleotides in exon skipping-mediated dystrophin restoration 119
Pre-trial antisense screening of myogenic cells from boys with Duchenne muscular dystrophy and genomic and transcriptomic biomarkers discovery for treatment monitoring 116
Dystrophin restoration in skeletal, heart and skin arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexes. 110
Association of CYP1B1 with hypersensitivity induced by Taxane therapy in breast cancer patients 103
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Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 76
Protection from herpes simplex virus type 1 lethal and latent infections by secreted recombinant glycoprotein B costitutively expressed in human cells with a BK virus episomal vector 72
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Totale 13.250
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Categoria #
all - tutte 57.578
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.536
Totale 59.114
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022685 0 0 90 22 50 27 38 34 27 42 79 276
2022/2023801 72 81 20 111 167 100 40 66 87 8 35 14
2023/2024478 37 66 29 8 33 123 20 38 9 13 8 94
2024/20252.004 44 30 139 85 242 179 113 102 410 158 266 236
2025/20265.038 533 185 386 654 771 351 688 236 406 514 194 120
2026/2027554 134 248 172 0 0 0 0 0 0 0 0 0
Totale 13.250