SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

SELVATICI, Rita
 Distribuzione geografica
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Continente #
NA - Nord America 9.681
AS - Asia 4.773
EU - Europa 4.287
SA - Sud America 1.014
AF - Africa 117
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 2
AN - Antartide 1
Totale 19.886
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Nazione #
US - Stati Uniti d'America 9.410
SG - Singapore 2.025
CN - Cina 1.333
IT - Italia 1.092
BR - Brasile 879
DE - Germania 814
PL - Polonia 600
HK - Hong Kong 472
UA - Ucraina 414
GB - Regno Unito 341
VN - Vietnam 261
FI - Finlandia 259
TR - Turchia 242
RU - Federazione Russa 164
SE - Svezia 145
CA - Canada 137
NL - Olanda 123
MX - Messico 111
IN - India 103
FR - Francia 89
ID - Indonesia 78
AR - Argentina 58
BD - Bangladesh 55
ZA - Sudafrica 54
JP - Giappone 49
AT - Austria 44
BE - Belgio 42
ES - Italia 39
CZ - Repubblica Ceca 26
LT - Lituania 26
MA - Marocco 24
IQ - Iraq 21
PK - Pakistan 20
EC - Ecuador 18
CH - Svizzera 13
CO - Colombia 13
IE - Irlanda 13
IR - Iran 13
KR - Corea 13
VE - Venezuela 11
IL - Israele 10
MY - Malesia 10
PY - Paraguay 10
AE - Emirati Arabi Uniti 9
CL - Cile 9
PE - Perù 9
KE - Kenya 8
RO - Romania 8
AU - Australia 7
AZ - Azerbaigian 7
TN - Tunisia 7
UZ - Uzbekistan 7
DZ - Algeria 6
JM - Giamaica 6
PT - Portogallo 6
UY - Uruguay 6
EG - Egitto 5
JO - Giordania 5
SA - Arabia Saudita 5
KG - Kirghizistan 4
KZ - Kazakistan 4
NG - Nigeria 4
NZ - Nuova Zelanda 4
TH - Thailandia 4
TW - Taiwan 4
BG - Bulgaria 3
CR - Costa Rica 3
HN - Honduras 3
LV - Lettonia 3
NP - Nepal 3
PH - Filippine 3
SI - Slovenia 3
TJ - Tagikistan 3
AL - Albania 2
AO - Angola 2
BY - Bielorussia 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
GH - Ghana 2
GR - Grecia 2
GT - Guatemala 2
HU - Ungheria 2
LB - Libano 2
LU - Lussemburgo 2
NI - Nicaragua 2
OM - Oman 2
QA - Qatar 2
SC - Seychelles 2
SV - El Salvador 2
AQ - Antartide 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BO - Bolivia 1
CI - Costa d'Avorio 1
CM - Camerun 1
CY - Cipro 1
EE - Estonia 1
ET - Etiopia 1
EU - Europa 1
GD - Grenada 1
Totale 19.875
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Città #
Singapore 1.138
Ashburn 1.014
Fairfield 814
Woodbridge 686
Chandler 619
Warsaw 595
Houston 552
Beijing 508
Hong Kong 469
Jacksonville 459
Santa Clara 449
Ann Arbor 392
Dallas 311
Munich 303
Seattle 295
Wilmington 288
Cambridge 227
Los Angeles 213
Ferrara 207
New York 207
Izmir 142
Milan 138
Nanjing 127
Princeton 118
Boardman 116
Helsinki 108
São Paulo 105
Buffalo 99
Ho Chi Minh City 90
Shanghai 87
San Diego 78
Mexico City 73
Jakarta 67
The Dalles 63
Brooklyn 61
London 61
Rome 58
Bremen 57
Turku 55
Addison 50
Hanoi 47
Tokyo 46
Shenyang 45
Amsterdam 44
Frankfurt am Main 44
Chicago 42
Phoenix 41
Hefei 40
Johannesburg 40
Montreal 40
Denver 38
Orem 36
Brussels 35
Tianjin 35
Chennai 34
Nanchang 34
Changsha 33
Bologna 32
Toronto 32
Moscow 31
Rio de Janeiro 30
Poplar 29
Stockholm 29
Atlanta 28
Jinan 26
San Mateo 26
Mumbai 23
Nuremberg 23
Jiaxing 22
Ottawa 22
Brasília 21
Falkenstein 21
Norwalk 21
San Francisco 21
Dearborn 20
Vienna 20
Hebei 19
Falls Church 18
Redwood City 18
Columbus 17
Manchester 17
Brno 16
Florence 16
Boston 15
Guangzhou 15
Augusta 14
Haiphong 14
Zhengzhou 14
Belo Horizonte 13
Charlotte 13
Kunming 13
Mountain View 13
Querétaro 13
Trebaseleghe 13
Verona 13
Washington 13
Ankara 12
Curitiba 12
North Bergen 12
Salvador 12
Totale 12.995
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Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 421
Meccanismi del danno neuronale indotto dalla tossina mitocondriale sodio azide in colture primarie di corteccia di ratto. Effetti sulle Protein Kinasi C. 420
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking 383
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 378
Merkel cell carcinomas arising in autoimmune disease affected patients treated with biologic drugs including anti-TNF 369
Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor 350
Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes 307
Hypermethylation-induced inactivation of the IRF6 gene as a possible early event in progression of vulvar squamous cell carcinoma associated with lichen sclerosus 286
MTHFR gene promoter hypermethylation correlates with semen samples of infertile couples with recurrence spontaneous abortion 279
High Human Papillomavirus DNA loads in Inflammatory Middle Ear Diseases 277
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 245
A Family with γ-Thalassemia and High Hb A2 Levels 231
Paternal germline mosaicism in collagen VI related myopathies 230
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 222
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 219
Association of retinoic acid receptor ß gene with onset and progression of lichen sclerosus-associated vulvar squamous cell carcinoma 216
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report 205
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 203
Sodium Azide Induced Neuronal Damage In Vitro: Evidence for Non-Apoptotic Cell Death 201
Tracing Males From Different Continents by Genotyping JC Polyomavirus in DNA From Semen Samples 199
SERPINA1 Gene Promoter Is Differentially Methylated in Peripheral Blood Mononuclear Cells of Pregnant Women 195
Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors 192
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 191
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 185
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 185
Sodium azide: a useful tool for in vitro studying neurodegenerative diseases. 182
In vitro mitochondrial failure and oxidative stress mimic biochemical features of Alzheimer disease 178
Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice 178
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Differential activation of protein kinase C isoforms following chemical ischemia in rat cerebral cortex slices 172
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family 169
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 163
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 163
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries 163
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 162
Activation of signal tranduction pathway leading to chemotaxis in human neutrophils by a pure chemoattractant. 154
RNAseq in urine-derived stem cells identified the expression of 308 neuromuscular gene transcripts [NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.384] 153
Physical and transcriptional characterization of human urinary stem cell populations 151
An interconnected data infrastructure to support large-scale rare disease research 146
DMD gene molecular genetic characterization in Eastern Europe and non European countries 145
Un anno di attività diagnostica del laboratorio di Genetica molecolare di Ferrara 144
Structural characterization of promoter sequences of the gene coding human PKI55 protein, a protein kinase C inhibitor 144
Differential involvement of kinase pathways is required for human neutrophil function triggered by formylpeptides 143
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing 140
FUNCTIONALITY AND DRUG METABOLISM OF FRESHLY AND CRYOPRESERVED CULTURED HUMAN HEPATOCYTES 138
Protective effect of a peptide derived from the endogenous PKC inhibitor PKI55 on the neurosecretory function in ischemic brain slices 138
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 136
Report of a novel ATP7A mutation causing distal motor neuropathy 136
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 133
Silenziamento allele-specifico del pre-mRNA del gene PTPN11 in pazienti con Sindrome di Noonan (NS1) 133
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 133
Protein kinase C isoforms changes induced by chemical ischemia-reperfusion in rat cerebral cortex slices 131
Altered proliferative kinetics in PHA-activated human T-lymphocytes treated with the anti-HLA class I monoclonal antibody 01.65 131
activation of signal transduction pathway leading to chemotaxis human neutrophils by a pure chemoattractant 131
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 131
Uso di oligoribonucleotidi antisenso per il ripristino dell'espressione della distrofina 129
NMD CHIP: Un Progetto Europeo per la diagnosi delle patologie neuromuscolari 128
Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4 127
Study of synthetic peptides derived from PKI55, a PKC modulator, in stimulated human neutrophils. 125
chemotactic formylpeptides activation of protein kinase C and mitogen-activated protein kinases in human neutrophils 124
Involvement of specific PKC isoforms in atopic asthma patients 124
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 121
Anchored anti-HLA class I monoclonal antibody fails to induce inhibition of PHA-activated lymphocytes proliferation 120
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy 119
Anti HLA class I monoclonal antibody effect on PKC kinetics in PHA activated human peripheral blood mononuclear and E+ cells 118
An anti-HLA class I monoclonal antibody alters the progression in the cell cycle of phytohemagglutinin-activated human T lymphocytes 117
A 'pure' chemoattractant formylpeptide analogue triggers a specific signalling pathway in human neutrophil chemotaxis 115
Adaptative value of a PKC-PKI55 feedback loop of inhibition that prevents the kinase's deregulation. 114
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Studio di CNVs nel locus HLA (6p21.32) mediante Array CGH in pazienti con Sclerosi Multipla e malformazioni venose 113
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 113
Brugada ECG pattern in hypertrophic cardiomyopathy: Brugada phenocopy or overlapping syndrome? 112
Brugada Syndrome: More than a Monogenic Channelopathy 111
Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project 110
Co-operation in cell transformation between BK virus and the human c-Harvey-ras oncogene 109
Hypermethylation-induced inactivation of IRF6 and RARΒ genes as potential prognostic biomarker in vulvar squamous cell carcinoma 107
Serological and molecular HLA typing in Italian Behcet's patients: significant association to B51-DR5-DQw3 haplotype 103
Solving unsolved rare neurological diseases—a Solve-RD viewpoint 103
Cardiac conduction disorders in young adults: clinical characteristics and genetic background of an underestimated population 102
Effects of Synthetic Peptides on the Inflammatory Response and Their Therapeutic Potential. 102
Uso di oligoribonucleotidi antisenso (AONs) per il ripristino dell'espressione della distrofina 101
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A window on the lab: one year of diagnostic activity in the molecular genetics laboratory of Ferrara – Italy 100
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing 99
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Specific activation of mitogen-activated protein kinases and protein kinase C isoforms in formylpeptides-induced human neutrophils chemotaxis. 99
Identification of a novel protein kinase C inhibitor in microsomes from phytohaemagglutinin activated human peripheral blood mononuclear cells 98
Identification of a new mutation in RSK2, the gene for coffin–lowry syndrome (CLS), in two related patients with mild and atypical phenotypes 98
C-fos, c-myc and IL-2R mRNA expression in PHA activated T lymphocytes treated with a monoclonal anti-HLA class I antibody (MAb 01.65) 97
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic Diseases 97
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Induction of malignant subcutaneous sarcomas in hamsters by a recombinant DNA containing BK virus early region and the activated human c-Harvey-ras oncogene 96
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Protein kinase C activity, translocation, and selective isoform subcellular redistribution in the rat cerebral cortex after in vitro ischemia 93
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Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 92
Totale 15.882
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Categoria #
all - tutte 86.839
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 547
Totale 87.386
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021927 0 0 0 0 0 164 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
2024/20254.340 84 104 280 210 486 439 274 247 648 469 653 446
2025/20265.592 1.052 534 843 1.339 1.596 228 0 0 0 0 0 0
Totale 20.108