Sfoglia per Rivista FAMILIAL CANCER
An intronic mutation in MLH1 associated with familial colon and breast cancer
2011 F. Bianchi, M. Raponi, F. Piva, A. Viel, I. Bearzi, E. Galizia, R. Bracci, L. Belvederesi, C. Loretelli, C. Brugiati, F. Corradini, D. Baralle, R. Cellerino
A missense germline mutation in exon 7 of the MSH2 gene in a HNPCC family from center-Italy
2007 F. Bianchi, E. Galizia, E. Porfiri, L. Belvederesi, R. Catalani, C. Loretelli, R. Bracci, I. Bearzi, C. Turchi, A. Viel, R. Cellerino
Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family
2022 K.M. Brown, M. Xu, M. Sargen, H. Jang, M. Zhang, T. Zhang, B. Zhu, K. Jones, J. Kim, L. Mendoza, N.K. Hayward, M.A. Tucker, A.M. Goldstein, X.R. Yang, D.R. Stewart, B. Hicks, D. Consonni, A.C. Pesatori, M.C. Fargnoli, K. Peris, A. Stratigos, C. Menin, P. Ghiorzo, S. Puig, E. Nagore, T. Andresson, R. Nussinov, D. Calista, M.T. Landi
Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment
2012 L. Belvederesi, F. Bianchi, C. Loretelli, R. Bracci, S. Cascinu, R. Cellerino
| Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
|---|---|---|---|---|---|
| An intronic mutation in MLH1 associated with familial colon and breast cancer | 2011 | C. Loretelli + | Article (author) | - | |
| A missense germline mutation in exon 7 of the MSH2 gene in a HNPCC family from center-Italy | 2007 | Loretelli, Cristian + | Article (author) | - | |
| Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family | 2022 | Pesatori A. C. + | Article (author) | - | |
| Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment | 2012 | Loretelli, Cristian + | Article (author) | - |
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