SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

SELVATICI, Rita
 Distribuzione geografica
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Continente #
NA - Nord America 6.727
EU - Europa 2.800
AS - Asia 1.540
AF - Africa 8
SA - Sud America 8
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 1
Totale 11.089
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Nazione #
US - Stati Uniti d'America 6.690
IT - Italia 779
CN - Cina 684
PL - Polonia 547
SG - Singapore 483
DE - Germania 427
UA - Ucraina 385
GB - Regno Unito 229
TR - Turchia 211
FI - Finlandia 120
SE - Svezia 115
ID - Indonesia 60
FR - Francia 43
RU - Federazione Russa 38
BE - Belgio 36
CA - Canada 35
VN - Vietnam 22
CZ - Repubblica Ceca 17
IN - India 17
HK - Hong Kong 14
IR - Iran 12
AT - Austria 10
LT - Lituania 10
KR - Corea 9
NL - Olanda 9
CH - Svizzera 6
BR - Brasile 5
MY - Malesia 5
RO - Romania 5
DZ - Algeria 4
IE - Irlanda 4
AU - Australia 3
ES - Italia 3
JP - Giappone 3
PT - Portogallo 3
SI - Slovenia 3
TW - Taiwan 3
AE - Emirati Arabi Uniti 2
BD - Bangladesh 2
BG - Bulgaria 2
GH - Ghana 2
GR - Grecia 2
IQ - Iraq 2
LU - Lussemburgo 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
PH - Filippine 2
PK - Pakistan 2
AR - Argentina 1
CL - Cile 1
CO - Colombia 1
EU - Europa 1
GT - Guatemala 1
HR - Croazia 1
HU - Ungheria 1
IL - Israele 1
IS - Islanda 1
KZ - Kazakistan 1
LI - Liechtenstein 1
MK - Macedonia 1
MM - Myanmar 1
MX - Messico 1
QA - Qatar 1
SA - Arabia Saudita 1
TH - Thailandia 1
UZ - Uzbekistan 1
Totale 11.089
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Città #
Fairfield 814
Woodbridge 686
Chandler 619
Warsaw 546
Houston 539
Jacksonville 455
Ann Arbor 392
Ashburn 390
Singapore 360
Wilmington 287
Seattle 280
Santa Clara 261
Cambridge 226
Ferrara 179
Beijing 154
Izmir 142
Nanjing 126
Princeton 118
New York 115
Boardman 110
Milan 108
Shanghai 87
San Diego 78
Jakarta 60
Bremen 57
Addison 50
Shenyang 44
Munich 41
Rome 40
Los Angeles 39
London 38
Helsinki 36
Nanchang 34
Brussels 32
Changsha 30
San Mateo 26
Tianjin 24
Jinan 23
Jiaxing 21
Norwalk 21
Dearborn 20
Frankfurt am Main 20
Hebei 19
Falls Church 18
Redwood City 18
Bologna 16
Brno 16
Ottawa 15
Hong Kong 14
Kunming 13
Mountain View 13
Trebaseleghe 13
Washington 13
Verona 12
Guangzhou 11
Zhengzhou 11
Auburn Hills 10
Dong Ket 10
Florence 10
Lanzhou 10
Toronto 10
Augusta 9
Caserta 9
Ningbo 8
Taizhou 8
Des Moines 7
Indiana 7
Leawood 7
Orange 7
Turin 7
Padova 6
Vienna 6
Ardabil 5
Changchun 5
Chicago 5
Columbus 5
Ferrara di Monte Baldo 5
Kilburn 5
Las Vegas 5
Mumbai 5
Phoenix 5
Bari 4
Council Bluffs 4
Dublin 4
Gothenburg 4
Haikou 4
Kuala Lumpur 4
Monmouth Junction 4
Montréal 4
Philadelphia 4
Queens 4
Redmond 4
Argenta 3
Barton Under Needwood 3
Catania 3
Cuttack 3
Fano 3
Fuzhou 3
Guarda Veneta 3
Lappeenranta 3
Totale 8.174
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Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 333
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking 311
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 303
Meccanismi del danno neuronale indotto dalla tossina mitocondriale sodio azide in colture primarie di corteccia di ratto. Effetti sulle Protein Kinasi C. 298
High Human Papillomavirus DNA loads in Inflammatory Middle Ear Diseases 194
Hypermethylation-induced inactivation of the IRF6 gene as a possible early event in progression of vulvar squamous cell carcinoma associated with lichen sclerosus 190
Merkel cell carcinomas arising in autoimmune disease affected patients treated with biologic drugs including anti-TNF 180
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Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 161
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 151
Tracing Males From Different Continents by Genotyping JC Polyomavirus in DNA From Semen Samples 148
Paternal germline mosaicism in collagen VI related myopathies 141
Sodium Azide Induced Neuronal Damage In Vitro: Evidence for Non-Apoptotic Cell Death 136
Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors 136
SERPINA1 Gene Promoter Is Differentially Methylated in Peripheral Blood Mononuclear Cells of Pregnant Women 136
MTHFR gene promoter hypermethylation correlates with semen samples of infertile couples with recurrence spontaneous abortion 133
N-Aryl-2-phenyl-2,3-dihydro-imidazo[1,2-b]pyrazole-1-carboxamides 7-substituted strongly inhibiting both fMLP-OMe- and IL-8-induced human neutrophil chemotaxis 127
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 127
Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor 121
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 121
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report 121
Differential activation of protein kinase C isoforms following chemical ischemia in rat cerebral cortex slices. 118
In vitro mitochondrial failure and oxidative stress mimic biochemical features of Alzheimer disease 118
A Family with γ-Thalassemia and High Hb A2 Levels 115
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Study of synthetic peptides derived from the PKI55 protein, a protein kinase C modulator, in human neutrophils stimulated by the methyl ester derivative of the hydrophobic N-formyl tripeptide for-Met-Leu-Phe-OH. 111
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 111
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 108
Mice genetic immunization with plasmid DNA encoding a secreted form of HSV-1 gB induces a protective immune response against herpes simplex virus type 1 infection 106
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 103
Association of retinoic acid receptor ß gene with onset and progression of lichen sclerosus-associated vulvar squamous cell carcinoma 102
Structural characterization of promoter sequences of the gene coding human PKI55 protein, a protein kinase C inhibitor 100
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Sodium azide: a useful tool for in vitro studying neurodegenerative diseases. 99
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family 98
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Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice 95
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Uso di oligoribonucleotidi antisenso per il ripristino dell'espressione della distrofina 92
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RNAseq in urine-derived stem cells identified the expression of 308 neuromuscular gene transcripts [NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.384] 91
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Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes 87
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DMD gene molecular genetic characterization in Eastern Europe and non European countries 82
SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain 82
FUNCTIONALITY AND DRUG METABOLISM OF FRESHLY AND CRYOPRESERVED CULTURED HUMAN HEPATOCYTES 81
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Un anno di attività diagnostica del laboratorio di Genetica molecolare di Ferrara 80
Report of a novel ATP7A mutation causing distal motor neuropathy 80
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries 75
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Differential involvement of kinase pathways is required for human neutrophil function triggered by formylpeptides 73
Studio di CNVs nel locus HLA (6p21.32) mediante Array CGH in pazienti con Sclerosi Multipla e malformazioni venose 73
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Protective effect of a peptide derived from the endogenous PKC inhibitor PKI55 on the neurosecretory function in ischemic brain slices 72
NMD CHIP: Un Progetto Europeo per la diagnosi delle patologie neuromuscolari 71
Activation of signal tranduction pathway leading to chemotaxis in human neutrophils by a pure chemoattractant. 71
chemotactic formylpeptides activation of protein kinase C and mitogen-activated protein kinases in human neutrophils 70
Study of synthetic peptides derived from PKI55, a PKC modulator, in stimulated human neutrophils. 70
Physical and transcriptional characterization of human urinary stem cell populations 69
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 69
Genetica molecolare dell’inattivazione della via PKC-dipendente da parte della proteina PKI55 e peptidi sintetici da essa derivati nella trasduzione del segnale in condizioni normali e patologiche 67
Protein kinase C isoforms changes induced by chemical ischemia-reperfusion in rat cerebral cortex slices 65
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 65
Specific activation of mitogen-activated protein kinases and protein kinase C isoforms in formylpeptides-induced human neutrophils chemotaxis. 64
Uso di oligoribonucleotidi antisenso (AONs) per il ripristino dell'espressione della distrofina 64
Involvement of specific PKC isoforms in atopic asthma patients 64
Effects of Synthetic Peptides on the Inflammatory Response and Their Therapeutic Potential. 62
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Genetica molecolare dell’inattivazione della via PKC-dipendente da parte della proteina PKI55 e peptidi sintetici da essa derivati nella trasduzione del segnale in condizioni normali e patologiche 59
activation of signal transduction pathway leading to chemotaxis human neutrophils by a pure chemoattractant 59
Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4 59
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing 57
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Studio di nanoparticelle biocompatibili per il ripristino della distrofina in topi mdx 56
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy 56
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The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 55
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Hypermethylation-induced inactivation of IRF6 and RARΒ genes as potential prognostic biomarker in vulvar squamous cell carcinoma 53
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Studio genotipo-fenotipo in casi familiari di CCSVI-MS mediante tecnologie high through put 51
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Diagnosi molecolare delle eredoatassie: recenti risultati del nostro laboratorio. 48
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Solving unsolved rare neurological diseases—a Solve-RD viewpoint 43
Totale 9.924
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Categoria #
all - tutte 52.041
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 298
Totale 52.339
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.384 0 0 0 0 126 218 190 191 221 268 105 65
2020/20211.607 124 175 81 237 63 164 62 178 42 199 202 80
2021/20221.238 45 146 93 60 45 35 92 59 49 87 123 404
2022/20231.455 130 123 54 160 273 174 75 137 158 24 101 46
2023/2024966 67 77 53 32 52 169 60 58 71 33 38 256
2024/20251.111 84 104 280 210 433 0 0 0 0 0 0 0
Totale 11.287