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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Antonio Musio

Istituto di Tecnologie Biomediche

Consiglio Nazionale delle Ricerche

Via Fratelli Cervi

93, 20090 Segrate

Italy

[email]@itb.cnr.it

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Affiliation

Istituto di Tecnologie Biomediche, Consiglio Nazionale delle Ricerche, Via Fratelli Cervi, 93, 20090 Segrate, Italy. 2003 - 2006

References

X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations. Musio, A., Selicorni, A., Focarelli, M.L., Gervasini, C., Milani, D., Russo, S., Vezzoni, P., Larizza, L. Nat. Genet. (2006) [Pubmed]
SMC1 involvement in fragile site expression. Musio, A., Montagna, C., Mariani, T., Tilenni, M., Focarelli, M.L., Brait, L., Indino, E., Benedetti, P.A., Chessa, L., Albertini, A., Ried, T., Vezzoni, P. Hum. Mol. Genet. (2005) [Pubmed]
Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes. Musio, A., Mariani, T., Montagna, C., Zambroni, D., Ascoli, C., Ried, T., Vezzoni, P. Gene (2004) [Pubmed]
Inhibition of BUB1 results in genomic instability and anchorage-independent growth of normal human fibroblasts. Musio, A., Montagna, C., Zambroni, D., Indino, E., Barbieri, O., Citti, L., Villa, A., Ried, T., Vezzoni, P. Cancer Res. (2003) [Pubmed]