IRIS
VIAGGI, SILVIA
 Distribuzione geografica
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Continente #
EU - Europa 6.571
AS - Asia 300
NA - Nord America 35
SA - Sud America 33
AF - Africa 3
Totale 6.942
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Nazione #
IT - Italia 6.563
SG - Singapore 124
CN - Cina 83
VN - Vietnam 67
US - Stati Uniti d'America 29
BR - Brasile 25
HK - Hong Kong 12
AR - Argentina 5
MX - Messico 5
GB - Regno Unito 3
ID - Indonesia 3
BD - Bangladesh 2
BY - Bielorussia 2
IR - Iran 2
AZ - Azerbaigian 1
BG - Bulgaria 1
CA - Canada 1
CL - Cile 1
CM - Camerun 1
DE - Germania 1
IN - India 1
IQ - Iraq 1
JO - Giordania 1
JP - Giappone 1
KE - Kenya 1
NG - Nigeria 1
NL - Olanda 1
PE - Perù 1
PK - Pakistan 1
TR - Turchia 1
UY - Uruguay 1
Totale 6.942
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Città #
Genova 3.825
Genoa 1.670
Rapallo 609
Vado Ligure 440
Singapore 53
Ho Chi Minh City 25
Beijing 22
Bordighera 18
Ashburn 13
Hanoi 12
Hong Kong 12
Mexico City 5
São Paulo 5
Haiphong 4
New York 3
Biên Hòa 2
Bắc Giang 2
Da Nang 2
Goiânia 2
Guangzhou 2
Uberaba 2
Amman 1
Ananindeua 1
Ankara 1
Aracaju 1
Araguaína 1
Baghdad 1
Baku 1
Boston 1
Brest 1
Brooklyn 1
Buenos Aires 1
Bình Dương 1
Bắc Ninh 1
Chennai 1
Chicago 1
Curitiba 1
Dallas 1
Denver 1
Freiburg im Breisgau 1
Godoy Cruz 1
Guaratinguetá 1
Hải Dương 1
Iguatu 1
Itapevi 1
Ituzaingó 1
Jakarta 1
Jhelum 1
Jinan 1
Lagos 1
Liaoyuan 1
Lima 1
London 1
Los Angeles 1
Manchester 1
Mariana 1
Mauá 1
Minsk 1
Montevideo 1
Montreal 1
Nairobi 1
Nha Trang 1
Ninh Bình 1
Nova Esperança 1
Orem 1
Passo Fundo 1
Pelotas 1
Phoenix 1
Poplar 1
Quảng Ngãi 1
Quận Chín 1
Recife 1
San Miguel de Tucumán 1
Santa Clara 1
Santa Luzia 1
Santiago 1
Santiago del Estero 1
Santos 1
Sofia 1
São José dos Campos 1
Sóc Trăng 1
Tehran 1
Thái Bình 1
Tianjin 1
Tokyo 1
Tây Ninh 1
Yaoundé 1
Totale 6.794
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Nome #
5-methylcytosine at HpaII sites in p53 is not hypermutable after UVC irradiation 248
Analisi di espressione dei geni GNAQ e GNA11 frequentemente mutati nel melanoma uveale Analisi di espressione dei geni GNAQ e GNA11 frequentemente mutati nel melanoma uveale. 230
Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma 218
A gene trap approach to isolate mammalian genes involved in the cellular response to genotoxic stress 208
The analysis of 10 potential spindle poisons for their ability to induce CREST-positive micronuclei in human diploid fibroblasts. 201
Uncommon cytogenetic findings in a case of splenic marginal zone lymphoma with aggressive clinical course 193
Malignant pleural mesothelioma: time for translational research 178
Effects of simulated microgravity on metabolic activities related to DNA damage and repair in lymphoblastoid cells 176
Differential behaviour of normal, transformed and Fanconi's anemia lymphoblastoid cells to modeled microgravity 175
Analysis of the Expression and Single-Nucleotide Variant Frequencies of the Butyrophilin-like 2 Gene in Patients With Uveal Melanoma 174
The yeast p53 functional assay: a new tool for molecular epidemiology. Hopes and facts 172
N-(2-Chloroethyl)-N-Nitrosourea tethered to lexitropsin induces minor groove lesions at the p53 cDNA which are more cytotoxic than mutagenic 168
P53 mutations experimetally induced by 8-methoxypsoralene plus UVA (PUVA) differ from those found in human skin cancer developed in PUVA treated patients 157
Secondary Somatic Mutations in G-Protein-Related Pathways and Mutation Signatures in Uveal Melanoma 156
Partial characterization of SUVi, a new mammalian gene induced by UV-C and expressed during the S phase of the cell cycle 148
Chromosome rearrangements associated with CAD gene amplification. Experiments with cell hybrids. 145
Analysis of the DNA contant distribution of micronuclei using flow sorting and fluorescent in situ hybridization with a centromeric DNA probe. 144
Flow cytometric analysis of bromodeoxyuridine-induced micronuclei. 143
New insights into red-ox response modulation in Fanconi's anemia cells by hydrogen peroxide and glutathione depletors. 141
Chromosome aberrations evaluated by CGH in B-cell chronic lymphocytic leukemia: correlation with CD38 expression. 136
Identification of a novel set of genes reflecting different in vivo invasive patterns of human GBM cells 136
Stable formation of mutated p53 multimers in a Chinese hamster cell line causes defective p53 nuclear localization and abrogates its residual function. 135
Centrosomal and mitotic abnormalities in cell lines derived from papillary thyroid cancer harboring specific gene alterations 134
Flow cytometric analysis of micronuclei in the CD2+ subpopulation of human lymphocytes enriched by magnetic separation. 130
Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in case of AIDS related Burkitt ‘s lymphoma. 130
MICRORNA EXPRESSION PROFILES IN HIGH-GRADE PROSTATIC INTRAEPITHELIAL NEOPLASIA (HGPIN): RE-DEFINING THE PROSTATE CANCER PRECURSOR LESION ACCORDING TO THE GENETIC SIGNATURE 128
Chromosome aberrations evaluated by comparative genomic hybridization in B cell chronic lymphocytic leukemia: correlation with CD38 expression 127
How many mutations does it take to make a uveal melanoma? 125
Mutation frequencies of GNAQ, GNA11, BAP1, SF3B1, EIF1AX and TERT in uveal melanoma: detection of an activating mutation in theTERT gene promoter in a single case of uveal melanoma. 124
Exposure of human lymphocytes and lymphoblastoid cells to simulated microgravity strongly affects energy metabolism and DNA repair 121
The presence of high-risk chromosome aberrations in chronic lymphocytic leukaemia does not correlate with centrosome aberrations. 117
ALFA-COBRATOXIN, A NATURAL ALFA-7-NICOTINIC RECEPTOR ANTAGONIST, AS PUTATIVE ANTICANCER DRUG IN NON SMALL CELL LUNG CANCER AND MESOTHELIOMA 116
Analisi di varianti genetiche del gene Butyrophilin-like 2 (BTNL2), un membro della famiglia B7 di immunomodulatori nel melanoma della coroide. 112
Radiation-induced structural modification in dsDNA analysed by FT-Raman spectroscopy. 105
GNA11 mutations are associated with increased metastatic risk of uveal melanoma in two independent datasets with information on mutations and gene expression 105
The role of nucleotide pool alkylation in the induction of numerical chromosome aberrations. 100
Alterazioni del genoma nelle cellule somatiche e il processo di cancerogenesi 100
Multicenter External Validation of the Liverpool Uveal Melanoma Prognosticator Online: An OOG Collaborative Study 100
Measurement of micronuclei by flow cytometry. 98
Micronuclei: a biological indicator of radiation damage. 97
The induction of numerical aberrations in human lymphocyte cultures and V79 Chinese hamster cells by diethylsulphate. 97
Centrosome aberrations and spindle defects in thyroid carcinoma cells harboring specific oncogene activation. 97
Cycle Analysis of Three Human Colon Adenocarcinoma Cell Lines: Comparison Between Two- and Three-Dimensional Cell Culture Systems. 95
In uveal melanoma Gα-protein GNA11 mutations convey a shorter disease-specific survival and are more strongly associated with loss of BAP1 and chromosomal alterations than Gα-protein GNAQ mutations 87
INDUCED PLURIPOTENT STEM CELL FACILITY: PRODUZIONE DI CELLULE STAMINALI ADULTE PER STUDI FUNZIONALI PER LA RICERCA DI NUOVI PRINCIPI TERAPEUTICI 84
Induction of kinetochore containing micronuclei by exogenous O6-methylguanine requires conversion of the methylated base to a nucleotide. 82
Identification and fate of a marker chromosome in metotrexate resistant V79,B7 cells by flow karyotyping and sorting, metaphase analysis and in situ hybridation. 82
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome 82
New evidence for the presence of chromosomes in micronuclei. 78
Antikinetochore antibodiesand flow karyotyping: new techniques to detect aneuploidy in mammalian cellsinduced by ionizing radiation and chemicals 78
Kinetics of radiation-Cytochrome C-induced modifications in liposomes analysed by FT-Raman Spectroscopy. 73
La mutazione nelle cellule somatiche 69
Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness 64
Induction of kinetochore positive and negative micronuclei in V79 cells by the alkylating agent diethylsulfate 56
Chromosomal Deletion Involving ANKRD26 Leads to Expression of a Fusion Protein Responsible for ANKRD26-Related Thrombocytopenia 22
Totale 6.997
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Categoria #
all - tutte 21.624
article - articoli 18.907
book - libri 0
conference - conferenze 1.537
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.180
Totale 43.248
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021190 0 0 0 0 0 31 27 25 27 32 31 17
2021/2022701 42 58 48 104 22 22 45 154 28 51 44 83
2022/2023730 66 41 14 65 143 117 3 67 131 4 70 9
2023/2024443 24 40 7 48 37 55 66 18 30 18 33 67
2024/20251.027 13 80 29 56 194 86 102 167 36 49 106 109
2025/2026924 228 90 84 202 264 56 0 0 0 0 0 0
Totale 6.997