S. Viaggi

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5-methylcytosine at HpaII sites in p53 is not hypermutable after UVC irradiation.

A. Inga, P. Monti, G. Fronza, 1999, Mutation research.

Multicenter External Validation of the Liverpool Uveal Melanoma Prognosticator Online: An OOG Collaborative Study

N. Bornfeld, A. Eleuteri, S. Viaggi, 2020, Cancers.

Secondary Somatic Mutations in G-Protein-Related Pathways and Mutation Signatures in Uveal Melanoma

A. Barla, S. Viaggi, P. A. van der Velden, 2019, Cancers.

p53 mutations experimentally induced by 8-methoxypsoralen plus UVA (PUVA) differ from those found in human skin cancers in PUVA-treated patients.

A. Inga, P. Monti, G. Fronza, 2000, Mutagenesis.

Exposure of human lymphocytes and lymphoblastoid cells to simulated microgravity strongly affects energy metabolism and DNA repair

P. Degan, L. Ottaggio, S. Viaggi, 2005, Journal of cellular biochemistry.

Centrosomal and mitotic abnormalities in cell lines derived from papillary thyroid cancer harboring specific gene alterations

P. Degan, S. Viaggi, R. Vanni, 2011, Molecular Cytogenetics.

A gene trap approach to isolate mammalian genes involved in the cellular response to genotoxic stress.

G. Fronza, P. Menichini, L. Ottaggio, 1997, Nucleic acids research.

Measurement of micronuclei by flow cytometry.

M. Nüsse, S. Viaggi, E. Weller, 1994, Methods in cell biology.

Analysis of the Expression and Single-Nucleotide Variant Frequencies of the Butyrophilin-like 2 Gene in Patients With Uveal Melanoma.

M. Pistillo, P. Queirolo, M. Mandalà, 2016, JAMA ophthalmology.

Chromosome rearrangements associated with CAD gene amplification. Experiments with cell hybrids.

M. Nüsse, L. Ottaggio, S. Viaggi, 1992, Mutation research.

The yeast p53 functional assay: a new tool for molecular epidemiology. Hopes and facts.

A. Inga, P. Monti, G. Fronza, 2000, Mutation research.

Stable formation of mutated p53 multimers in a Chinese hamster cell line causes defective p53 nuclear localization and abrogates its residual function

G. Fronza, P. Campomenosi, P. Menichini, 2006, Journal of cellular biochemistry.

Mutation frequencies of GNAQ, GNA11, BAP1, SF3B1, EIF1AX and TERT in uveal melanoma: detection of an activating mutation in the TERT gene promoter in a single case of uveal melanoma

S. Zupo, S. Viaggi, M. Gualco, 2014, British Journal of Cancer.

Partial characterization of SUVi, a new mammalian gene induced by UV‐c and expressed during the S phase of the cell cycle

G. Fronza, P. Campomenosi, P. Menichini, 2001, Environmental and molecular mutagenesis.

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.

P. Monti, S. Viaggi, R. Jockers, 2022, European journal of cancer.

Chromosome aberrations evaluated by comparative genomic hybridization in B-cell chronic lymphocytic leukemia: correlation with CD38 expression.

S. Zupo, M. Ferrarini, L. Ottaggio, 2003, Haematologica.

Uncommon cytogenetic findings in a case of splenic marginal zone lymphoma with aggressive clinical course.

S. Zupo, L. Ottaggio, S. Viaggi, 2004, Cancer genetics and cytogenetics.

Radiation-induced structural modifications in dsDNA analysed by FT-Raman spectroscopy.

M. Nüsse, S. Viaggi, K. Sailer, 1996, International journal of radiation biology.

The presence of high‐risk chromosome aberrations in chronic lymphocytic leukaemia does not correlate with centrosome aberrations

L. Ottaggio, S. Viaggi, A. Zunino, 2008, Hematological oncology.

New evidence for the presence of chromosomes in micronuclei of human and Chinese hamster cells.

S. Viaggi, A. Abbondandolo, S. Bonatti, 1987, Mutagenesis.

Kinetics of radiation- and cytochrome c-induced modifications in liposomes analysed by FT-Raman spectroscopy.

M. Nüsse, S. Viaggi, K. Sailer, 1997, Biochimica et biophysica acta.

Analysis of the DNA content distribution of micronuclei using flow sorting and fluorescent in situ hybridization with a centromeric DNA probe.

M. Nüsse, S. Viaggi, J. Grawé, 1996, Mutagenesis.

Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness

G. Gimelli, L. Ramenghi, S. Viaggi, 2022, Cytogenetic and Genome Research.

Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.

G. Fronza, L. Ottaggio, S. Viaggi, 2000, Haematologica.

Micronuclei: a biological indicator of radiation damage.

C. Streffer, W. Müller, M. Nüsse, 1996, Mutation research.

Antikinetochore antibodies and flow karyotyping: new techniques to detect aneuploidy in mammalian cells induced by ionizing radiation and chemicals.

M. Nüsse, S. Viaggi, S. Bonatti, 1987, Molecular toxicology.

Chapter 9 Measurement of Micronuclei by Flow Cytometry

M. Nüsse, S. Viaggi, E. Weller, 1994 .

New insights into redox response modulation in Fanconi’s anemia cells by hydrogen peroxide and glutathione depletors

P. Degan, S. Viaggi, P. Cuccarolo, 2012, The FEBS journal.

Cytogenetic Characterization and Cell Cycle Analysis of Three Human Colon Adenocarcinoma Cell Lines: Comparison Between Two- and Three-Dimensional Cell Culture Systems

M. Bardella, S. Viaggi, E. Erba, 2009, Cancer investigation.

Induction of kinetochore positive and negative micronuclei in V79 cells by the alkylating agent diethylsulphate.

M. Nüsse, S. Viaggi, S. Bonatti, 1989, Mutagenesis.

The analysis of 10 potential spindle poisons for their ability to induce CREST-positive micronuclei in human diploid fibroblasts.

S. Viaggi, A. Abbondandolo, S. Bonatti, 1992, Mutagenesis.

Flow cytometric analysis of micronuclei in the CD2+/- subpopulation of human lymphocytes enriched by magnetic separation.

H. Braselmann, M. Nüsse, S. Viaggi, 1995, International journal of radiation biology.

Induction of kinetochore‐containing micronuclei by exogenous 06‐methylguanine requires conversion of the methylated base to a nucleotide

A. Aprile, S. Viaggi, A. Abbondandolo, 1995, Environmental and molecular mutagenesis.

Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome

A. Covone, S. Viaggi, V. Capra, 2023, Genes.

Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma

S. Viaggi, A. Amaro, D. Coviello, 2018, Genes, chromosomes & cancer.

Identification of a novel set of genes reflecting different in vivo invasive patterns of human GBM cells

S. Viaggi, Ulrich Pfeffer, S. Candiani, 2012, BMC Cancer.

Differential behaviour of normal, transformed and Fanconi's anemia lymphoblastoid cells to modeled microgravity

P. Degan, S. Viaggi, F. Barbieri, 2010, Journal of Biomedical Science.

The induction of numerical chromosome aberrations in human lymphocyte cultures and V79 Chinese hamster cells by diethyl sulfate.

S. Viaggi, A. Abbondandolo, S. Bonatti, 1988, Mutation research.