SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

SELVATICI, Rita
 Distribuzione geografica
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Continente #
NA - Nord America 11.151
AS - Asia 6.278
EU - Europa 4.781
SA - Sud America 1.223
AF - Africa 186
OC - Oceania 22
Continente sconosciuto - Info sul continente non disponibili 4
AN - Antartide 1
Totale 23.646
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Nazione #
US - Stati Uniti d'America 10.843
SG - Singapore 2.448
CN - Cina 1.454
IT - Italia 1.229
BR - Brasile 983
DE - Germania 842
VN - Vietnam 780
PL - Polonia 615
HK - Hong Kong 520
UA - Ucraina 422
GB - Regno Unito 373
FI - Finlandia 308
TR - Turchia 261
FR - Francia 209
RU - Federazione Russa 173
IN - India 169
NL - Olanda 152
CA - Canada 151
SE - Svezia 150
JP - Giappone 149
MX - Messico 124
BD - Bangladesh 104
ID - Indonesia 90
AR - Argentina 85
ZA - Sudafrica 75
ES - Italia 53
IQ - Iraq 53
AT - Austria 47
BE - Belgio 45
PK - Pakistan 41
EC - Ecuador 35
CO - Colombia 34
MA - Marocco 31
CZ - Repubblica Ceca 28
LT - Lituania 28
PH - Filippine 24
VE - Venezuela 24
MY - Malesia 23
SA - Arabia Saudita 22
CL - Cile 21
AU - Australia 18
IE - Irlanda 18
RO - Romania 17
TN - Tunisia 17
CH - Svizzera 16
KE - Kenya 16
UZ - Uzbekistan 15
KR - Corea 14
PY - Paraguay 14
IL - Israele 13
IR - Iran 13
AE - Emirati Arabi Uniti 11
JO - Giordania 11
PE - Perù 11
JM - Giamaica 10
DZ - Algeria 9
EG - Egitto 9
BO - Bolivia 8
PT - Portogallo 8
AZ - Azerbaigian 7
ET - Etiopia 7
KZ - Kazakistan 7
TH - Thailandia 7
UY - Uruguay 7
NP - Nepal 6
CR - Costa Rica 5
HU - Ungheria 5
KG - Kirghizistan 5
OM - Oman 5
SI - Slovenia 5
TW - Taiwan 5
AL - Albania 4
BG - Bulgaria 4
GR - Grecia 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
GT - Guatemala 3
HN - Honduras 3
LB - Libano 3
QA - Qatar 3
RS - Serbia 3
TJ - Tagikistan 3
XK - ???statistics.table.value.countryCode.XK??? 3
GH - Ghana 2
HR - Croazia 2
LU - Lussemburgo 2
MD - Moldavia 2
NI - Nicaragua 2
SC - Seychelles 2
SV - El Salvador 2
AQ - Antartide 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
Totale 23.619
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Città #
Singapore 1.525
Ashburn 1.363
Fairfield 814
Woodbridge 686
Chandler 619
San Jose 609
Warsaw 609
Houston 556
Beijing 527
Hong Kong 505
Santa Clara 469
Jacksonville 460
Ann Arbor 392
Dallas 317
Munich 305
Seattle 297
Wilmington 288
Ho Chi Minh City 255
Los Angeles 243
New York 229
Cambridge 227
Ferrara 211
Hanoi 177
Helsinki 156
Milan 148
Tokyo 146
Izmir 142
Nanjing 127
Princeton 118
Boardman 117
São Paulo 113
Council Bluffs 110
Buffalo 104
Lauterbourg 103
Shanghai 89
The Dalles 82
Orem 80
Mexico City 78
San Diego 78
Jakarta 69
London 66
Brooklyn 65
Rome 63
Frankfurt am Main 62
Bremen 57
Johannesburg 57
Turku 55
Amsterdam 54
Addison 50
Montreal 50
Chicago 49
Denver 46
Shenyang 45
Phoenix 44
Chennai 43
Bologna 42
Hefei 40
Da Nang 37
Haiphong 36
Tianjin 36
Brussels 35
Toronto 35
Atlanta 34
Nanchang 34
Stockholm 34
Changsha 33
Moscow 32
Rio de Janeiro 30
Mumbai 29
Poplar 29
Manchester 27
Jinan 26
Nuremberg 26
San Mateo 26
Ottawa 23
Brasília 22
Jiaxing 22
Vienna 22
Baghdad 21
Falkenstein 21
Norwalk 21
San Francisco 21
Dearborn 20
Dhaka 20
Columbus 19
Hebei 19
Falls Church 18
Redwood City 18
Boston 17
Brno 16
Florence 16
Curitiba 15
Dublin 15
Guangzhou 15
Hải Dương 15
Medellín 15
Santiago 15
Augusta 14
Belo Horizonte 14
Lahore 14
Totale 15.438
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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. 475
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 467
Merkel cell carcinomas arising in autoimmune disease affected patients treated with biologic drugs including anti-TNF 429
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking 425
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 409
Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor 388
Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes 351
MTHFR gene promoter hypermethylation correlates with semen samples of infertile couples with recurrence spontaneous abortion 324
Hypermethylation-induced inactivation of the IRF6 gene as a possible early event in progression of vulvar squamous cell carcinoma associated with lichen sclerosus 317
High Human Papillomavirus DNA loads in Inflammatory Middle Ear Diseases 310
A Family with γ-Thalassemia and High Hb A2 Levels 270
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 268
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 268
Paternal germline mosaicism in collagen VI related myopathies 266
Association of retinoic acid receptor ß gene with onset and progression of lichen sclerosus-associated vulvar squamous cell carcinoma 262
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report 248
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 246
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 245
Sodium Azide Induced Neuronal Damage In Vitro: Evidence for Non-Apoptotic Cell Death 231
Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors 226
Tracing Males From Different Continents by Genotyping JC Polyomavirus in DNA From Semen Samples 224
SERPINA1 Gene Promoter Is Differentially Methylated in Peripheral Blood Mononuclear Cells of Pregnant Women 224
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 223
Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice 219
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 218
Silenziamento allele-specifico del pre-mRNA del gene PTPN11 in pazienti con Sindrome di Noonan (NS1) 211
Sodium azide: a useful tool for in vitro studying neurodegenerative diseases. 210
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family 208
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 206
In vitro mitochondrial failure and oxidative stress mimic biochemical features of Alzheimer disease 205
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries 200
Differential activation of protein kinase C isoforms following chemical ischemia in rat cerebral cortex slices 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 192
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 191
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 188
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing 183
Activation of signal tranduction pathway leading to chemotaxis in human neutrophils by a pure chemoattractant. 181
Physical and transcriptional characterization of human urinary stem cell populations 181
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 181
An interconnected data infrastructure to support large-scale rare disease research 180
DMD gene molecular genetic characterization in Eastern Europe and non European countries 179
RNAseq in urine-derived stem cells identified the expression of 308 neuromuscular gene transcripts [NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.384] 175
null 172
Protective effect of a peptide derived from the endogenous PKC inhibitor PKI55 on the neurosecretory function in ischemic brain slices 172
Differential involvement of kinase pathways is required for human neutrophil function triggered by formylpeptides 170
Un anno di attività diagnostica del laboratorio di Genetica molecolare di Ferrara 168
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 168
FUNCTIONALITY AND DRUG METABOLISM OF FRESHLY AND CRYOPRESERVED CULTURED HUMAN HEPATOCYTES 166
Report of a novel ATP7A mutation causing distal motor neuropathy 165
Anti HLA class I monoclonal antibody effect on PKC kinetics in PHA activated human peripheral blood mononuclear and E+ cells 162
Structural characterization of promoter sequences of the gene coding human PKI55 protein, a protein kinase C inhibitor 161
activation of signal transduction pathway leading to chemotaxis human neutrophils by a pure chemoattractant 161
NMD CHIP: Un Progetto Europeo per la diagnosi delle patologie neuromuscolari 160
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 159
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy 158
chemotactic formylpeptides activation of protein kinase C and mitogen-activated protein kinases in human neutrophils 155
Altered proliferative kinetics in PHA-activated human T-lymphocytes treated with the anti-HLA class I monoclonal antibody 01.65 155
An anti-HLA class I monoclonal antibody alters the progression in the cell cycle of phytohemagglutinin-activated human T lymphocytes 154
Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4 154
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 154
Study of synthetic peptides derived from PKI55, a PKC modulator, in stimulated human neutrophils. 153
Protein kinase C isoforms changes induced by chemical ischemia-reperfusion in rat cerebral cortex slices 152
A 'pure' chemoattractant formylpeptide analogue triggers a specific signalling pathway in human neutrophil chemotaxis 150
Uso di oligoribonucleotidi antisenso per il ripristino dell'espressione della distrofina 149
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 147
Anchored anti-HLA class I monoclonal antibody fails to induce inhibition of PHA-activated lymphocytes proliferation 147
Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project 146
Adaptative value of a PKC-PKI55 feedback loop of inhibition that prevents the kinase's deregulation. 144
Generation of a human induced pluripotent stem cell line (UNIFEi001-A) from a patient with Spinocerebellar ataxia type 1 (SCA1) 142
Brugada Syndrome: More than a Monogenic Channelopathy 139
Cardiac conduction disorders in young adults: clinical characteristics and genetic background of an underestimated population 138
Involvement of specific PKC isoforms in atopic asthma patients 138
Hypermethylation-induced inactivation of IRF6 and RARΒ genes as potential prognostic biomarker in vulvar squamous cell carcinoma 138
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 137
Solving unsolved rare neurological diseases—a Solve-RD viewpoint 136
Identification of a new mutation in RSK2, the gene for coffin–lowry syndrome (CLS), in two related patients with mild and atypical phenotypes 135
Co-operation in cell transformation between BK virus and the human c-Harvey-ras oncogene 133
Studio di CNVs nel locus HLA (6p21.32) mediante Array CGH in pazienti con Sclerosi Multipla e malformazioni venose 131
Brugada ECG pattern in hypertrophic cardiomyopathy: Brugada phenocopy or overlapping syndrome? 131
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing 130
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) 127
DMD deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis 124
Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe 124
Effects of Synthetic Peptides on the Inflammatory Response and Their Therapeutic Potential. 124
Serological and molecular HLA typing in Italian Behcet's patients: significant association to B51-DR5-DQw3 haplotype 124
mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies 124
Induction of malignant subcutaneous sarcomas in hamsters by a recombinant DNA containing BK virus early region and the activated human c-Harvey-ras oncogene 123
Competitive effect of anti-HLA class I monoclonal antibody (01.65) and N-N-staurosporine on prolipherative response of PHA activated T-lymphocytes. 122
SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern 121
MECP2 mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA Mapping 121
Identification of a novel protein kinase C inhibitor in microsomes from phytohaemagglutinin activated human peripheral blood mononuclear cells 121
A window on the lab: one year of diagnostic activity in the molecular genetics laboratory of Ferrara – Italy 121
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 121
Uso di oligoribonucleotidi antisenso (AONs) per il ripristino dell'espressione della distrofina 119
Protein kinase C activity, translocation, and selective isoform subcellular redistribution in the rat cerebral cortex after in vitro ischemia 119
Specific activation of mitogen-activated protein kinases and protein kinase C isoforms in formylpeptides-induced human neutrophils chemotaxis. 118
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic Diseases 118
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases 117
Relevance of Next-Generation Sequencing in the Diagnosis of Thalassemia and Hemoglobinopathies: The Experience of Four Italian Diagnostic Hubs 114
Effects of chemical ischemia in cerebral cortex slices. Focus on nitric oxide. 114
Totale 18.947
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Categoria #
all - tutte 93.493
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 600
Totale 94.093
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021481 0 0 0 0 0 0 0 0 0 199 202 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
2025/20269.354 1.052 534 843 1.339 1.596 655 1.202 537 765 831 0 0
Totale 23.870