Viola Calabrò

Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.

Tom Vulliamy, Michele D’Urso, G. Battistuzzi et al. · Proceedings of the National Academy of Sciences · 1988 · 252 citations · Full text

Genetics, Human Polymorphism, Molecular Biology +16

Repression of transcriptional activity at a distance by the evolutionary conserved KRAB domain present in a subfamily of zinc finger proteins

Gina Pengue, Viola Calabrò, Paola Cannada Bartoli et al. · Nucleic Acids Research · 1994 · 132 citations · Full text

MDM2 and Fbw7 cooperate to induce p63 protein degradation following DNA damage and cell differentiation

Francesco Galli, Mariangela Rossi, Yuri D’Alessandra et al. · Journal of Cell Science · 2010 · 96 citations · Full text

Dna Damage, Molecular Regulation, Apoptosis +18

The Human MDM2 Oncoprotein Increases the Transcriptional Activity and the Protein Level of the p53 Homolog p63

Viola Calabrò, Gelsomina Mansueto, Tiziana Parisi et al. · Journal of Biological Chemistry · 2002 · 92 citations · Full text

Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis.

Viola Calabrò, Philip J. Mason, Stefania Filosa et al. · PubMed · 1993 · 84 citations