SELVATICI, Rita
 Distribuzione geografica
Continente #
NA - Nord America 6.313
EU - Europa 2.588
AS - Asia 1.127
AF - Africa 6
OC - Oceania 5
SA - Sud America 4
Continente sconosciuto - Info sul continente non disponibili 1
Totale 10.044
Nazione #
US - Stati Uniti d'America 6.295
IT - Italia 704
CN - Cina 649
PL - Polonia 547
UA - Ucraina 385
DE - Germania 375
TR - Turchia 211
GB - Regno Unito 208
SG - Singapore 157
SE - Svezia 113
FI - Finlandia 98
FR - Francia 42
RU - Federazione Russa 38
ID - Indonesia 29
BE - Belgio 17
CZ - Repubblica Ceca 17
IN - India 17
CA - Canada 16
HK - Hong Kong 14
VN - Vietnam 14
IR - Iran 12
AT - Austria 9
NL - Olanda 7
CH - Svizzera 5
RO - Romania 5
DZ - Algeria 4
IE - Irlanda 4
MY - Malesia 4
AU - Australia 3
ES - Italia 3
SI - Slovenia 3
TW - Taiwan 3
AE - Emirati Arabi Uniti 2
BD - Bangladesh 2
BG - Bulgaria 2
GH - Ghana 2
GR - Grecia 2
JP - Giappone 2
KR - Corea 2
NZ - Nuova Zelanda 2
PH - Filippine 2
AR - Argentina 1
BR - Brasile 1
CL - Cile 1
CO - Colombia 1
EU - Europa 1
GT - Guatemala 1
HR - Croazia 1
IQ - Iraq 1
IS - Islanda 1
KZ - Kazakistan 1
LI - Liechtenstein 1
MK - Macedonia 1
MM - Myanmar 1
MX - Messico 1
PK - Pakistan 1
SA - Arabia Saudita 1
TH - Thailandia 1
UZ - Uzbekistan 1
Totale 10.044
Città #
Fairfield 814
Woodbridge 686
Chandler 619
Warsaw 546
Houston 539
Jacksonville 455
Ann Arbor 392
Ashburn 389
Wilmington 287
Seattle 280
Cambridge 226
Ferrara 176
Beijing 154
Izmir 142
Nanjing 126
Princeton 118
New York 115
Boardman 110
Milan 99
Singapore 86
Shanghai 83
San Diego 78
Bremen 57
Addison 50
Shenyang 44
Nanchang 34
Rome 34
Changsha 30
Jakarta 29
San Mateo 26
London 25
Tianjin 24
Jinan 23
Jiaxing 21
Norwalk 21
Dearborn 20
Hebei 19
Falls Church 18
Redwood City 18
Brno 16
Bologna 15
Helsinki 15
Hong Kong 14
Brussels 13
Kunming 13
Mountain View 13
Trebaseleghe 13
Los Angeles 11
Verona 11
Zhengzhou 11
Auburn Hills 10
Dong Ket 10
Guangzhou 10
Lanzhou 10
Munich 10
Washington 10
Augusta 9
Caserta 9
Florence 8
Ningbo 8
Taizhou 8
Des Moines 7
Indiana 7
Leawood 7
Orange 7
Turin 7
Vienna 6
Ardabil 5
Changchun 5
Chicago 5
Columbus 5
Ferrara di Monte Baldo 5
Frankfurt am Main 5
Kilburn 5
Mumbai 5
Phoenix 5
Bari 4
Council Bluffs 4
Dublin 4
Gothenburg 4
Haikou 4
Monmouth Junction 4
Montréal 4
Philadelphia 4
Queens 4
Redmond 4
Argenta 3
Barton Under Needwood 3
Cuttack 3
Guarda Veneta 3
Kuala Lumpur 3
Lappeenranta 3
Mcallen 3
Melfi 3
Naperville 3
Oberwil 3
Ottawa 3
Parma 3
Poggio Renatico 3
Tappahannock 3
Totale 7.428
Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 322
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking 303
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 296
Meccanismi del danno neuronale indotto dalla tossina mitocondriale sodio azide in colture primarie di corteccia di ratto. Effetti sulle Protein Kinasi C. 273
High Human Papillomavirus DNA loads in Inflammatory Middle Ear Diseases 182
null 172
Merkel cell carcinomas arising in autoimmune disease affected patients treated with biologic drugs including anti-TNF 168
Hypermethylation-induced inactivation of the IRF6 gene as a possible early event in progression of vulvar squamous cell carcinoma associated with lichen sclerosus 147
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 143
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 140
Paternal germline mosaicism in collagen VI related myopathies 134
Sodium Azide Induced Neuronal Damage In Vitro: Evidence for Non-Apoptotic Cell Death 130
Tracing Males From Different Continents by Genotyping JC Polyomavirus in DNA From Semen Samples 128
Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors 128
SERPINA1 Gene Promoter Is Differentially Methylated in Peripheral Blood Mononuclear Cells of Pregnant Women 127
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 123
MTHFR gene promoter hypermethylation correlates with semen samples of infertile couples with recurrence spontaneous abortion 114
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Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor 113
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report 113
In vitro mitochondrial failure and oxidative stress mimic biochemical features of Alzheimer disease 112
Differential activation of protein kinase C isoforms following chemical ischemia in rat cerebral cortex slices. 110
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 108
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 105
A Family with γ-Thalassemia and High Hb A2 Levels 105
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. 104
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 103
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 102
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 101
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Structural characterization of promoter sequences of the gene coding human PKI55 protein, a protein kinase C inhibitor 95
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Association of retinoic acid receptor ß gene with onset and progression of lichen sclerosus-associated vulvar squamous cell carcinoma 93
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International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 92
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Uso di oligoribonucleotidi antisenso per il ripristino dell'espressione della distrofina 88
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Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice 87
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Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family 86
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Sodium azide: a useful tool for in vitro studying neurodegenerative diseases. 84
RNAseq in urine-derived stem cells identified the expression of 308 neuromuscular gene transcripts [NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.384] 83
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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 77
DMD gene molecular genetic characterization in Eastern Europe and non European countries 75
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FUNCTIONALITY AND DRUG METABOLISM OF FRESHLY AND CRYOPRESERVED CULTURED HUMAN HEPATOCYTES 74
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Report of a novel ATP7A mutation causing distal motor neuropathy 72
Un anno di attività diagnostica del laboratorio di Genetica molecolare di Ferrara 71
Differential involvement of kinase pathways is required for human neutrophil function triggered by formylpeptides 69
Studio di CNVs nel locus HLA (6p21.32) mediante Array CGH in pazienti con Sclerosi Multipla e malformazioni venose 68
Protective effect of a peptide derived from the endogenous PKC inhibitor PKI55 on the neurosecretory function in ischemic brain slices 67
chemotactic formylpeptides activation of protein kinase C and mitogen-activated protein kinases in human neutrophils 66
Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes 65
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries 65
NMD CHIP: Un Progetto Europeo per la diagnosi delle patologie neuromuscolari 63
Activation of signal tranduction pathway leading to chemotaxis in human neutrophils by a pure chemoattractant. 62
Specific activation of mitogen-activated protein kinases and protein kinase C isoforms in formylpeptides-induced human neutrophils chemotaxis. 61
Uso di oligoribonucleotidi antisenso (AONs) per il ripristino dell'espressione della distrofina 61
Study of synthetic peptides derived from PKI55, a PKC modulator, in stimulated human neutrophils. 61
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Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 60
Effects of Synthetic Peptides on the Inflammatory Response and Their Therapeutic Potential. 59
Physical and transcriptional characterization of human urinary stem cell populations 58
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 57
Protein kinase C isoforms changes induced by chemical ischemia-reperfusion in rat cerebral cortex slices 57
Involvement of specific PKC isoforms in atopic asthma patients 57
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Studio di nanoparticelle biocompatibili per il ripristino della distrofina in topi mdx 53
Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4 53
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activation of signal transduction pathway leading to chemotaxis human neutrophils by a pure chemoattractant 51
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Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy 48
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Studio genotipo-fenotipo in casi familiari di CCSVI-MS mediante tecnologie high through put 47
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 46
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing 46
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 45
Hypermethylation-induced inactivation of IRF6 and RARΒ genes as potential prognostic biomarker in vulvar squamous cell carcinoma 42
Diagnosi molecolare delle eredoatassie: recenti risultati del nostro laboratorio. 42
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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 39
Totale 9.256
Categoria #
all - tutte 40.723
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 224
Totale 40.947


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.098 299 67 74 274 126 218 190 191 221 268 105 65
2020/20211.607 124 175 81 237 63 164 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
2024/202566 66 0 0 0 0 0 0 0 0 0 0 0
Totale 10.242