SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

SELVATICI, Rita
 Distribuzione geografica
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Continente #
NA - Nord America 11.690
AS - Asia 6.462
EU - Europa 4.950
SA - Sud America 1.224
AF - Africa 186
OC - Oceania 22
Continente sconosciuto - Info sul continente non disponibili 4
AN - Antartide 1
Totale 24.539
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Nazione #
US - Stati Uniti d'America 11.356
SG - Singapore 2.475
CN - Cina 1.478
IT - Italia 1.381
BR - Brasile 983
DE - Germania 847
VN - Vietnam 781
PL - Polonia 615
HK - Hong Kong 528
UA - Ucraina 422
GB - Regno Unito 373
FI - Finlandia 308
TR - Turchia 261
BD - Bangladesh 222
FR - Francia 210
RU - Federazione Russa 173
IN - India 169
CA - Canada 166
SE - Svezia 155
NL - Olanda 154
JP - Giappone 152
MX - Messico 124
ID - Indonesia 90
AR - Argentina 85
ZA - Sudafrica 75
ES - Italia 53
IQ - Iraq 53
AT - Austria 48
BE - Belgio 45
PK - Pakistan 41
EC - Ecuador 35
CO - Colombia 34
MA - Marocco 31
LT - Lituania 30
CZ - Repubblica Ceca 28
VE - Venezuela 25
MY - Malesia 24
PH - Filippine 24
SA - Arabia Saudita 22
CL - Cile 21
AU - Australia 18
IE - Irlanda 18
CH - Svizzera 17
RO - Romania 17
TN - Tunisia 17
KE - Kenya 16
KR - Corea 15
UZ - Uzbekistan 15
JM - Giamaica 14
PY - Paraguay 14
IL - Israele 13
IR - Iran 13
AE - Emirati Arabi Uniti 12
JO - Giordania 11
PE - Perù 11
DZ - Algeria 9
EG - Egitto 9
BO - Bolivia 8
CR - Costa Rica 8
PT - Portogallo 8
AZ - Azerbaigian 7
ET - Etiopia 7
KZ - Kazakistan 7
TH - Thailandia 7
UY - Uruguay 7
NP - Nepal 6
HU - Ungheria 5
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 24.511
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Città #
Singapore 1.532
Ashburn 1.397
Fairfield 814
San Jose 768
Woodbridge 686
Chandler 619
Warsaw 609
Houston 558
Beijing 530
Hong Kong 513
Santa Clara 481
Jacksonville 461
Ann Arbor 392
Dallas 331
Munich 305
Seattle 298
New York 289
Wilmington 289
Los Angeles 262
Ho Chi Minh City 256
Cambridge 228
Ferrara 214
Hanoi 177
Helsinki 156
Milan 154
Tokyo 146
Izmir 142
Nanjing 128
Buffalo 121
Boardman 118
Princeton 118
São Paulo 113
Council Bluffs 110
Lauterbourg 103
Shanghai 89
Orem 82
The Dalles 82
San Diego 79
Mexico City 78
Rome 74
Brooklyn 71
Jakarta 69
London 66
Frankfurt am Main 62
Bremen 61
Johannesburg 57
Amsterdam 55
Turku 55
Montreal 53
Chicago 52
Addison 50
Denver 49
Phoenix 47
Bologna 45
Shenyang 45
Chennai 43
Toronto 41
Hefei 40
Da Nang 37
Haiphong 36
Tianjin 36
Atlanta 35
Brussels 35
Changsha 35
Nanchang 34
Stockholm 34
Moscow 32
Rio de Janeiro 30
Manchester 29
Mumbai 29
Poplar 29
Jinan 26
Nuremberg 26
San Mateo 26
Naples 24
Columbus 23
Ottawa 23
Brasília 22
Jiaxing 22
Norwalk 22
San Francisco 22
Vienna 22
Baghdad 21
Falkenstein 21
Dearborn 20
Dhaka 20
Florence 20
Falls Church 19
Hebei 19
Boston 18
Redwood City 18
Brno 16
Charlotte 16
Verona 16
Curitiba 15
Dublin 15
Guangzhou 15
Hải Dương 15
Medellín 15
Santiago 15
Totale 15.866
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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. 488
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 472
Merkel cell carcinomas arising in autoimmune disease affected patients treated with biologic drugs including anti-TNF 439
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 411
Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor 403
Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes 361
MTHFR gene promoter hypermethylation correlates with semen samples of infertile couples with recurrence spontaneous abortion 338
High Human Papillomavirus DNA loads in Inflammatory Middle Ear Diseases 325
Hypermethylation-induced inactivation of the IRF6 gene as a possible early event in progression of vulvar squamous cell carcinoma associated with lichen sclerosus 318
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 276
Association of retinoic acid receptor ß gene with onset and progression of lichen sclerosus-associated vulvar squamous cell carcinoma 275
A Family with γ-Thalassemia and High Hb A2 Levels 274
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 272
Paternal germline mosaicism in collagen VI related myopathies 272
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
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 251
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 248
Sodium Azide Induced Neuronal Damage In Vitro: Evidence for Non-Apoptotic Cell Death 234
Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors 230
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 228
Tracing Males From Different Continents by Genotyping JC Polyomavirus in DNA From Semen Samples 227
SERPINA1 Gene Promoter Is Differentially Methylated in Peripheral Blood Mononuclear Cells of Pregnant Women 227
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 225
Silenziamento allele-specifico del pre-mRNA del gene PTPN11 in pazienti con Sindrome di Noonan (NS1) 220
Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice 220
Sodium azide: a useful tool for in vitro studying neurodegenerative diseases. 219
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family 214
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 213
In vitro mitochondrial failure and oxidative stress mimic biochemical features of Alzheimer disease 208
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries 205
Differential activation of protein kinase C isoforms following chemical ischemia in rat cerebral cortex slices 204
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 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
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 194
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 190
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing 188
An interconnected data infrastructure to support large-scale rare disease research 187
Physical and transcriptional characterization of human urinary stem cell populations 187
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 187
Activation of signal tranduction pathway leading to chemotaxis in human neutrophils by a pure chemoattractant. 185
DMD gene molecular genetic characterization in Eastern Europe and non European countries 184
RNAseq in urine-derived stem cells identified the expression of 308 neuromuscular gene transcripts [NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.384] 181
Protective effect of a peptide derived from the endogenous PKC inhibitor PKI55 on the neurosecretory function in ischemic brain slices 179
Anti HLA class I monoclonal antibody effect on PKC kinetics in PHA activated human peripheral blood mononuclear and E+ cells 179
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 175
Structural characterization of promoter sequences of the gene coding human PKI55 protein, a protein kinase C inhibitor 174
Differential involvement of kinase pathways is required for human neutrophil function triggered by formylpeptides 174
Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project 173
null 172
Un anno di attività diagnostica del laboratorio di Genetica molecolare di Ferrara 171
Report of a novel ATP7A mutation causing distal motor neuropathy 169
FUNCTIONALITY AND DRUG METABOLISM OF FRESHLY AND CRYOPRESERVED CULTURED HUMAN HEPATOCYTES 168
NMD CHIP: Un Progetto Europeo per la diagnosi delle patologie neuromuscolari 168
activation of signal transduction pathway leading to chemotaxis human neutrophils by a pure chemoattractant 166
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy 166
Study of synthetic peptides derived from PKI55, a PKC modulator, in stimulated human neutrophils. 165
An anti-HLA class I monoclonal antibody alters the progression in the cell cycle of phytohemagglutinin-activated human T lymphocytes 164
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 164
Generation of a human induced pluripotent stem cell line (UNIFEi001-A) from a patient with Spinocerebellar ataxia type 1 (SCA1) 161
Cardiac conduction disorders in young adults: clinical characteristics and genetic background of an underestimated population 161
MECP2 mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA Mapping 160
Altered proliferative kinetics in PHA-activated human T-lymphocytes treated with the anti-HLA class I monoclonal antibody 01.65 160
Protein kinase C isoforms changes induced by chemical ischemia-reperfusion in rat cerebral cortex slices 159
chemotactic formylpeptides activation of protein kinase C and mitogen-activated protein kinases in human neutrophils 157
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 157
Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4 157
Solving unsolved rare neurological diseases—a Solve-RD viewpoint 152
A 'pure' chemoattractant formylpeptide analogue triggers a specific signalling pathway in human neutrophil chemotaxis 151
mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies 151
Uso di oligoribonucleotidi antisenso per il ripristino dell'espressione della distrofina 150
Anchored anti-HLA class I monoclonal antibody fails to induce inhibition of PHA-activated lymphocytes proliferation 150
Hypermethylation-induced inactivation of IRF6 and RARΒ genes as potential prognostic biomarker in vulvar squamous cell carcinoma 149
Adaptative value of a PKC-PKI55 feedback loop of inhibition that prevents the kinase's deregulation. 147
Brugada Syndrome: More than a Monogenic Channelopathy 145
Involvement of specific PKC isoforms in atopic asthma patients 144
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 142
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing 139
SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern 139
Identification of a new mutation in RSK2, the gene for coffin–lowry syndrome (CLS), in two related patients with mild and atypical phenotypes 139
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 135
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) 135
Brugada ECG pattern in hypertrophic cardiomyopathy: Brugada phenocopy or overlapping syndrome? 134
DMD deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis 131
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14 130
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 130
Serological and molecular HLA typing in Italian Behcet's patients: significant association to B51-DR5-DQw3 haplotype 128
Diagnosi molecolare delle eredoatassie: recenti risultati del nostro laboratorio. 128
Induction of malignant subcutaneous sarcomas in hamsters by a recombinant DNA containing BK virus early region and the activated human c-Harvey-ras oncogene 127
Effects of Synthetic Peptides on the Inflammatory Response and Their Therapeutic Potential. 126
Relevance of Next-Generation Sequencing in the Diagnosis of Thalassemia and Hemoglobinopathies: The Experience of Four Italian Diagnostic Hubs 125
Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe 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
Identification of a novel protein kinase C inhibitor in microsomes from phytohaemagglutinin activated human peripheral blood mononuclear cells 124
Protein kinase C activity, translocation, and selective isoform subcellular redistribution in the rat cerebral cortex after in vitro ischemia 124
A window on the lab: one year of diagnostic activity in the molecular genetics laboratory of Ferrara – Italy 124
Uso di oligoribonucleotidi antisenso (AONs) per il ripristino dell'espressione della distrofina 123
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 122
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases 121
Totale 19.705
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Categoria #
all - tutte 98.186
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 640
Totale 98.826
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202180 0 0 0 0 0 0 0 0 0 0 0 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
2025/202610.247 1.052 534 843 1.339 1.596 655 1.202 537 765 995 647 82
Totale 24.763