Sfoglia per Rivista FAMILIAL CANCER
CDH1 germline mutations and hereditary lobular breast cancer
2016 G. Corso, M. Intra, C. Trentin, P. Veronesi, V. Galimberti
CDH1 mutations recurrence and global clustering in genetically tested families with hereditary diffuse gastric cancer syndrome: results from a systematic study
2022 G. Corso, V. Tagliaferri, G. Massari, A. Cioffi, E. Maria Cristina Rossi, P. Veronesi, F. Magnoni
Evidence of tumor microsatellite instability in gastric cancer with familial aggregation
2009 C. Pedrazzani, G. Corso, S. Velho, M. Leite, V. Pascale, F. Bettarini, D. Marrelli, R. Seruca, F. Roviello
Familial gastric cancer: update for practice management
2011 G. Corso, D. Marrelli, F. Roviello
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
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile