SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

SELVATICI, Rita
 Distribuzione geografica
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Continente #
NA - Nord America 11.964
AS - Asia 6.590
EU - Europa 5.020
SA - Sud America 1.236
AF - Africa 186
OC - Oceania 22
Continente sconosciuto - Info sul continente non disponibili 4
AN - Antartide 1
Totale 25.023
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Nazione #
US - Stati Uniti d'America 11.615
SG - Singapore 2.490
CN - Cina 1.495
IT - Italia 1.437
BR - Brasile 988
DE - Germania 847
VN - Vietnam 781
PL - Polonia 615
HK - Hong Kong 541
UA - Ucraina 422
GB - Regno Unito 375
FI - Finlandia 308
BD - Bangladesh 301
TR - Turchia 261
FR - Francia 212
CA - Canada 175
RU - Federazione Russa 173
IN - India 169
NL - Olanda 156
SE - Svezia 155
JP - Giappone 152
MX - Messico 125
ID - Indonesia 90
AR - Argentina 87
ZA - Sudafrica 75
ES - Italia 53
IQ - Iraq 53
BE - Belgio 49
AT - Austria 48
PK - Pakistan 41
CO - Colombia 37
EC - Ecuador 35
MA - Marocco 31
LT - Lituania 30
CZ - Repubblica Ceca 28
VE - Venezuela 27
MY - Malesia 26
PH - Filippine 24
SA - Arabia Saudita 22
CL - Cile 21
AU - Australia 18
IE - Irlanda 18
CH - Svizzera 17
JM - Giamaica 17
RO - Romania 17
TN - Tunisia 17
KE - Kenya 16
KR - Corea 15
UZ - Uzbekistan 15
PY - Paraguay 14
IL - Israele 13
IR - Iran 13
AE - Emirati Arabi Uniti 12
JO - Giordania 11
PE - Perù 11
PT - Portogallo 11
CR - Costa Rica 9
DZ - Algeria 9
EG - Egitto 9
AZ - Azerbaigian 8
BO - Bolivia 8
ET - Etiopia 7
KZ - Kazakistan 7
TH - Thailandia 7
UY - Uruguay 7
HU - Ungheria 6
NP - Nepal 6
KG - Kirghizistan 5
OM - Oman 5
SI - Slovenia 5
TW - Taiwan 5
AL - Albania 4
BG - Bulgaria 4
GR - Grecia 4
GT - Guatemala 4
KW - Kuwait 4
LV - Lettonia 4
NG - Nigeria 4
NZ - Nuova Zelanda 4
SN - Senegal 4
AO - Angola 3
BY - Bielorussia 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
HN - Honduras 3
LB - Libano 3
QA - Qatar 3
RS - Serbia 3
TJ - Tagikistan 3
XK - ???statistics.table.value.countryCode.XK??? 3
BB - Barbados 2
GH - Ghana 2
HR - Croazia 2
LU - Lussemburgo 2
MD - Moldavia 2
NI - Nicaragua 2
SC - Seychelles 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
AQ - Antartide 1
Totale 24.993
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Città #
Singapore 1.543
Ashburn 1.428
Fairfield 814
San Jose 770
Woodbridge 686
Chandler 619
Warsaw 609
Houston 558
Beijing 537
Hong Kong 526
Santa Clara 523
Jacksonville 461
Ann Arbor 392
Dallas 334
Munich 305
Seattle 298
New York 295
Wilmington 289
Los Angeles 273
Ho Chi Minh City 256
Cambridge 229
Ferrara 214
Hanoi 177
Council Bluffs 169
Milan 157
Helsinki 156
Tokyo 146
Izmir 142
Nanjing 128
Buffalo 127
Boardman 118
Princeton 118
São Paulo 115
Lauterbourg 103
Shanghai 90
The Dalles 83
Orem 82
Rome 79
San Diego 79
Mexico City 78
Brooklyn 72
Jakarta 69
London 68
Frankfurt am Main 62
Bremen 61
Johannesburg 57
Amsterdam 55
Turku 55
Montreal 53
Chicago 52
Addison 50
Denver 49
Phoenix 49
Toronto 49
Bologna 46
Shenyang 45
Chennai 43
Hefei 40
Da Nang 37
Atlanta 36
Haiphong 36
Tianjin 36
Brussels 35
Changsha 35
Nanchang 34
Stockholm 34
Moscow 32
Rio de Janeiro 30
Manchester 29
Mumbai 29
Poplar 29
Jinan 26
Naples 26
Nuremberg 26
San Mateo 26
Columbus 23
Ottawa 23
San Francisco 23
Brasília 22
Jiaxing 22
Norwalk 22
Vienna 22
Baghdad 21
Falkenstein 21
Dearborn 20
Dhaka 20
Florence 20
Boston 19
Falls Church 19
Hebei 19
Redwood City 18
Brno 16
Charlotte 16
Medellín 16
Turin 16
Verona 16
Curitiba 15
Dublin 15
Guangzhou 15
Hải Dương 15
Totale 16.091
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Nome #
Meccanismi del danno neuronale indotto dalla tossina mitocondriale sodio azide in colture primarie di corteccia di ratto. Effetti sulle Protein Kinasi C. 502
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 476
Merkel cell carcinomas arising in autoimmune disease affected patients treated with biologic drugs including anti-TNF 450
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking 429
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 412
Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor 406
Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes 363
MTHFR gene promoter hypermethylation correlates with semen samples of infertile couples with recurrence spontaneous abortion 343
High Human Papillomavirus DNA loads in Inflammatory Middle Ear Diseases 326
Hypermethylation-induced inactivation of the IRF6 gene as a possible early event in progression of vulvar squamous cell carcinoma associated with lichen sclerosus 319
A Family with γ-Thalassemia and High Hb A2 Levels 294
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 284
Paternal germline mosaicism in collagen VI related myopathies 278
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 276
Association of retinoic acid receptor ß gene with onset and progression of lichen sclerosus-associated vulvar squamous cell carcinoma 276
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 254
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 252
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report 252
Sodium Azide Induced Neuronal Damage In Vitro: Evidence for Non-Apoptotic Cell Death 237
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 232
Silenziamento allele-specifico del pre-mRNA del gene PTPN11 in pazienti con Sindrome di Noonan (NS1) 230
Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors 230
SERPINA1 Gene Promoter Is Differentially Methylated in Peripheral Blood Mononuclear Cells of Pregnant Women 229
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 228
Tracing Males From Different Continents by Genotyping JC Polyomavirus in DNA From Semen Samples 228
Sodium azide: a useful tool for in vitro studying neurodegenerative diseases. 222
Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice 222
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 219
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family 214
In vitro mitochondrial failure and oxidative stress mimic biochemical features of Alzheimer disease 210
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries 209
Differential activation of protein kinase C isoforms following chemical ischemia in rat cerebral cortex slices 207
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 200
An interconnected data infrastructure to support large-scale rare disease research 197
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 195
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 194
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 194
Physical and transcriptional characterization of human urinary stem cell populations 189
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing 189
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 188
DMD gene molecular genetic characterization in Eastern Europe and non European countries 187
Activation of signal tranduction pathway leading to chemotaxis in human neutrophils by a pure chemoattractant. 186
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 185
Generation of a human induced pluripotent stem cell line (UNIFEi001-A) from a patient with Spinocerebellar ataxia type 1 (SCA1) 183
Protective effect of a peptide derived from the endogenous PKC inhibitor PKI55 on the neurosecretory function in ischemic brain slices 181
Anti HLA class I monoclonal antibody effect on PKC kinetics in PHA activated human peripheral blood mononuclear and E+ cells 181
RNAseq in urine-derived stem cells identified the expression of 308 neuromuscular gene transcripts [NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.384] 181
Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project 179
Structural characterization of promoter sequences of the gene coding human PKI55 protein, a protein kinase C inhibitor 179
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 177
Differential involvement of kinase pathways is required for human neutrophil function triggered by formylpeptides 176
Un anno di attività diagnostica del laboratorio di Genetica molecolare di Ferrara 173
null 172
NMD CHIP: Un Progetto Europeo per la diagnosi delle patologie neuromuscolari 172
Report of a novel ATP7A mutation causing distal motor neuropathy 171
MECP2 mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA Mapping 170
FUNCTIONALITY AND DRUG METABOLISM OF FRESHLY AND CRYOPRESERVED CULTURED HUMAN HEPATOCYTES 168
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy 168
Study of synthetic peptides derived from PKI55, a PKC modulator, in stimulated human neutrophils. 168
Cardiac conduction disorders in young adults: clinical characteristics and genetic background of an underestimated population 167
activation of signal transduction pathway leading to chemotaxis human neutrophils by a pure chemoattractant 167
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 167
An anti-HLA class I monoclonal antibody alters the progression in the cell cycle of phytohemagglutinin-activated human T lymphocytes 166
Protein kinase C isoforms changes induced by chemical ischemia-reperfusion in rat cerebral cortex slices 163
Altered proliferative kinetics in PHA-activated human T-lymphocytes treated with the anti-HLA class I monoclonal antibody 01.65 163
Relevance of Next-Generation Sequencing in the Diagnosis of Thalassemia and Hemoglobinopathies: The Experience of Four Italian Diagnostic Hubs 161
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 160
Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4 160
chemotactic formylpeptides activation of protein kinase C and mitogen-activated protein kinases in human neutrophils 158
mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies 157
Uso di oligoribonucleotidi antisenso per il ripristino dell'espressione della distrofina 154
Solving unsolved rare neurological diseases—a Solve-RD viewpoint 153
Anchored anti-HLA class I monoclonal antibody fails to induce inhibition of PHA-activated lymphocytes proliferation 152
Hypermethylation-induced inactivation of IRF6 and RARΒ genes as potential prognostic biomarker in vulvar squamous cell carcinoma 152
A 'pure' chemoattractant formylpeptide analogue triggers a specific signalling pathway in human neutrophil chemotaxis 151
Adaptative value of a PKC-PKI55 feedback loop of inhibition that prevents the kinase's deregulation. 149
Involvement of specific PKC isoforms in atopic asthma patients 147
Brugada Syndrome: More than a Monogenic Channelopathy 145
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 143
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing 141
SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern 141
Identification of a new mutation in RSK2, the gene for coffin–lowry syndrome (CLS), in two related patients with mild and atypical phenotypes 141
DMD deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis 140
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) 140
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14 138
Co-operation in cell transformation between BK virus and the human c-Harvey-ras oncogene 138
Studio di CNVs nel locus HLA (6p21.32) mediante Array CGH in pazienti con Sclerosi Multipla e malformazioni venose 137
Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe 135
Brugada ECG pattern in hypertrophic cardiomyopathy: Brugada phenocopy or overlapping syndrome? 134
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 133
Induction of malignant subcutaneous sarcomas in hamsters by a recombinant DNA containing BK virus early region and the activated human c-Harvey-ras oncogene 130
Diagnosi molecolare delle eredoatassie: recenti risultati del nostro laboratorio. 130
Serological and molecular HLA typing in Italian Behcet's patients: significant association to B51-DR5-DQw3 haplotype 129
Effects of Synthetic Peptides on the Inflammatory Response and Their Therapeutic Potential. 128
Uso di oligoribonucleotidi antisenso (AONs) per il ripristino dell'espressione della distrofina 126
Protein kinase C activity, translocation, and selective isoform subcellular redistribution in the rat cerebral cortex after in vitro ischemia 125
Competitive effect of anti-HLA class I monoclonal antibody (01.65) and N-N-staurosporine on prolipherative response of PHA activated T-lymphocytes. 125
A window on the lab: one year of diagnostic activity in the molecular genetics laboratory of Ferrara – Italy 125
Identification of a novel protein kinase C inhibitor in microsomes from phytohaemagglutinin activated human peripheral blood mononuclear cells 124
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases 121
Totale 20.128
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Categoria #
all - tutte 101.415
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 662
Totale 102.077
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/202610.489 1.052 534 843 1.339 1.596 655 1.202 537 765 995 647 324
2026/2027242 242 0 0 0 0 0 0 0 0 0 0 0
Totale 25.247