SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

SELVATICI, Rita
 Distribuzione geografica
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Continente #
NA - Nord America 9.793
AS - Asia 4.946
EU - Europa 4.309
SA - Sud America 1.046
AF - Africa 124
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 4
AN - Antartide 1
Totale 20.234
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Nazione #
US - Stati Uniti d'America 9.518
SG - Singapore 2.101
CN - Cina 1.338
IT - Italia 1.101
BR - Brasile 905
DE - Germania 815
PL - Polonia 601
HK - Hong Kong 474
UA - Ucraina 414
GB - Regno Unito 344
VN - Vietnam 325
FI - Finlandia 260
TR - Turchia 242
RU - Federazione Russa 164
SE - Svezia 147
CA - Canada 140
NL - Olanda 124
MX - Messico 112
IN - India 105
FR - Francia 89
ID - Indonesia 78
BD - Bangladesh 61
AR - Argentina 59
ZA - Sudafrica 58
JP - Giappone 52
AT - Austria 44
BE - Belgio 42
ES - Italia 41
IQ - Iraq 28
CZ - Repubblica Ceca 26
LT - Lituania 26
MA - Marocco 24
PK - Pakistan 23
EC - Ecuador 18
VE - Venezuela 15
CH - Svizzera 13
CO - Colombia 13
IE - Irlanda 13
IR - Iran 13
KR - Corea 13
IL - Israele 11
KE - Kenya 10
MY - Malesia 10
PY - Paraguay 10
AE - Emirati Arabi Uniti 9
CL - Cile 9
PE - Perù 9
UZ - Uzbekistan 9
RO - Romania 8
AU - Australia 7
AZ - Azerbaigian 7
TN - Tunisia 7
UY - Uruguay 7
DZ - Algeria 6
JM - Giamaica 6
PT - Portogallo 6
EG - Egitto 5
JO - Giordania 5
SA - Arabia Saudita 5
BG - Bulgaria 4
KG - Kirghizistan 4
KZ - Kazakistan 4
NG - Nigeria 4
NZ - Nuova Zelanda 4
TH - Thailandia 4
TW - Taiwan 4
CR - Costa Rica 3
HN - Honduras 3
LV - Lettonia 3
NP - Nepal 3
OM - Oman 3
PH - Filippine 3
SI - Slovenia 3
TJ - Tagikistan 3
XK - ???statistics.table.value.countryCode.XK??? 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
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
Totale 20.220
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Città #
Singapore 1.209
Ashburn 1.037
Fairfield 814
Woodbridge 686
Chandler 619
Warsaw 596
Houston 554
Beijing 508
Hong Kong 471
Jacksonville 459
Santa Clara 451
Ann Arbor 392
Dallas 312
Munich 303
Seattle 295
Wilmington 288
Cambridge 227
Los Angeles 225
New York 213
Ferrara 207
Izmir 142
Milan 138
Nanjing 127
Princeton 118
Boardman 116
Ho Chi Minh City 111
Helsinki 108
São Paulo 108
Buffalo 99
Shanghai 87
San Diego 78
Mexico City 74
Jakarta 67
The Dalles 65
Brooklyn 64
London 62
Rome 58
Bremen 57
Hanoi 57
Turku 55
Addison 50
Tokyo 49
Orem 46
Amsterdam 45
Denver 45
Shenyang 45
Frankfurt am Main 44
Johannesburg 44
Chicago 43
Montreal 43
Phoenix 43
Hefei 40
Brussels 35
Chennai 35
Tianjin 35
Nanchang 34
Bologna 33
Changsha 33
Toronto 32
Moscow 31
Stockholm 31
Rio de Janeiro 30
Poplar 29
Atlanta 28
Jinan 26
San Mateo 26
Mumbai 24
Nuremberg 23
Jiaxing 22
Ottawa 22
Brasília 21
Falkenstein 21
Norwalk 21
San Francisco 21
Dearborn 20
Vienna 20
Hebei 19
Falls Church 18
Manchester 18
Redwood City 18
Boston 17
Columbus 17
Haiphong 17
Brno 16
Florence 16
Da Nang 15
Guangzhou 15
San Jose 15
Augusta 14
Zhengzhou 14
Belo Horizonte 13
Charlotte 13
Council Bluffs 13
Kunming 13
Mountain View 13
Querétaro 13
Trebaseleghe 13
Verona 13
Washington 13
Ankara 12
Totale 13.205
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Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 426
Meccanismi del danno neuronale indotto dalla tossina mitocondriale sodio azide in colture primarie di corteccia di ratto. Effetti sulle Protein Kinasi C. 424
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking 385
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 382
Merkel cell carcinomas arising in autoimmune disease affected patients treated with biologic drugs including anti-TNF 373
Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor 353
Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes 312
Hypermethylation-induced inactivation of the IRF6 gene as a possible early event in progression of vulvar squamous cell carcinoma associated with lichen sclerosus 289
MTHFR gene promoter hypermethylation correlates with semen samples of infertile couples with recurrence spontaneous abortion 284
High Human Papillomavirus DNA loads in Inflammatory Middle Ear Diseases 282
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 248
A Family with γ-Thalassemia and High Hb A2 Levels 235
Paternal germline mosaicism in collagen VI related myopathies 233
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 227
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 223
Association of retinoic acid receptor ß gene with onset and progression of lichen sclerosus-associated vulvar squamous cell carcinoma 222
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report 211
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 206
Sodium Azide Induced Neuronal Damage In Vitro: Evidence for Non-Apoptotic Cell Death 204
Tracing Males From Different Continents by Genotyping JC Polyomavirus in DNA From Semen Samples 201
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 196
SERPINA1 Gene Promoter Is Differentially Methylated in Peripheral Blood Mononuclear Cells of Pregnant Women 196
Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors 194
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 190
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 187
Sodium azide: a useful tool for in vitro studying neurodegenerative diseases. 187
Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice 182
In vitro mitochondrial failure and oxidative stress mimic biochemical features of Alzheimer disease 180
Differential activation of protein kinase C isoforms following chemical ischemia in rat cerebral cortex slices 174
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family 173
null 172
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 167
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries 167
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 164
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 163
Activation of signal tranduction pathway leading to chemotaxis in human neutrophils by a pure chemoattractant. 159
RNAseq in urine-derived stem cells identified the expression of 308 neuromuscular gene transcripts [NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.384] 155
Physical and transcriptional characterization of human urinary stem cell populations 154
An interconnected data infrastructure to support large-scale rare disease research 151
DMD gene molecular genetic characterization in Eastern Europe and non European countries 148
Un anno di attività diagnostica del laboratorio di Genetica molecolare di Ferrara 147
Structural characterization of promoter sequences of the gene coding human PKI55 protein, a protein kinase C inhibitor 147
Differential involvement of kinase pathways is required for human neutrophil function triggered by formylpeptides 146
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing 145
FUNCTIONALITY AND DRUG METABOLISM OF FRESHLY AND CRYOPRESERVED CULTURED HUMAN HEPATOCYTES 140
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 139
Protective effect of a peptide derived from the endogenous PKC inhibitor PKI55 on the neurosecretory function in ischemic brain slices 139
Report of a novel ATP7A mutation causing distal motor neuropathy 137
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 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 135
Silenziamento allele-specifico del pre-mRNA del gene PTPN11 in pazienti con Sindrome di Noonan (NS1) 135
activation of signal transduction pathway leading to chemotaxis human neutrophils by a pure chemoattractant 135
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 135
Altered proliferative kinetics in PHA-activated human T-lymphocytes treated with the anti-HLA class I monoclonal antibody 01.65 134
NMD CHIP: Un Progetto Europeo per la diagnosi delle patologie neuromuscolari 133
Protein kinase C isoforms changes induced by chemical ischemia-reperfusion in rat cerebral cortex slices 133
Uso di oligoribonucleotidi antisenso per il ripristino dell'espressione della distrofina 132
Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4 130
chemotactic formylpeptides activation of protein kinase C and mitogen-activated protein kinases in human neutrophils 129
Study of synthetic peptides derived from PKI55, a PKC modulator, in stimulated human neutrophils. 127
Anti HLA class I monoclonal antibody effect on PKC kinetics in PHA activated human peripheral blood mononuclear and E+ cells 126
Involvement of specific PKC isoforms in atopic asthma patients 126
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 125
Anchored anti-HLA class I monoclonal antibody fails to induce inhibition of PHA-activated lymphocytes proliferation 123
An anti-HLA class I monoclonal antibody alters the progression in the cell cycle of phytohemagglutinin-activated human T lymphocytes 122
A 'pure' chemoattractant formylpeptide analogue triggers a specific signalling pathway in human neutrophil chemotaxis 121
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy 121
Adaptative value of a PKC-PKI55 feedback loop of inhibition that prevents the kinase's deregulation. 118
Brugada Syndrome: More than a Monogenic Channelopathy 114
Studio di CNVs nel locus HLA (6p21.32) mediante Array CGH in pazienti con Sclerosi Multipla e malformazioni venose 114
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 114
Brugada ECG pattern in hypertrophic cardiomyopathy: Brugada phenocopy or overlapping syndrome? 114
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Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project 111
Co-operation in cell transformation between BK virus and the human c-Harvey-ras oncogene 111
Hypermethylation-induced inactivation of IRF6 and RARΒ genes as potential prognostic biomarker in vulvar squamous cell carcinoma 111
Solving unsolved rare neurological diseases—a Solve-RD viewpoint 106
Cardiac conduction disorders in young adults: clinical characteristics and genetic background of an underestimated population 105
Uso di oligoribonucleotidi antisenso (AONs) per il ripristino dell'espressione della distrofina 104
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing 103
Effects of Synthetic Peptides on the Inflammatory Response and Their Therapeutic Potential. 103
Serological and molecular HLA typing in Italian Behcet's patients: significant association to B51-DR5-DQw3 haplotype 103
A window on the lab: one year of diagnostic activity in the molecular genetics laboratory of Ferrara – Italy 103
Specific activation of mitogen-activated protein kinases and protein kinase C isoforms in formylpeptides-induced human neutrophils chemotaxis. 101
Identification of a new mutation in RSK2, the gene for coffin–lowry syndrome (CLS), in two related patients with mild and atypical phenotypes 101
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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) 100
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Identification of a novel protein kinase C inhibitor in microsomes from phytohaemagglutinin activated human peripheral blood mononuclear cells 99
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic Diseases 98
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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
Protein kinase C activity, translocation, and selective isoform subcellular redistribution in the rat cerebral cortex after in vitro ischemia 96
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Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 94
Generation of a human induced pluripotent stem cell line (UNIFEi001-A) from a patient with Spinocerebellar ataxia type 1 (SCA1) 93
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Totale 16.161
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Categoria #
all - tutte 87.766
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 557
Totale 88.323
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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
2025/20265.940 1.052 534 843 1.339 1.596 576 0 0 0 0 0 0
Totale 20.456