TRICARICO, ROSSELLA

TRICARICO, ROSSELLA  

DIPARTIMENTO DI BIOLOGIA E BIOTECNOLOGIE "LAZZARO SPALLANZANI"  

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A perspective on diet, epigenetics and complex diseases: where is the field headed next? 1-gen-2022 Coppedè, Fabio; Franzago, Marica; Giardina, Emiliano; Nigro, Cristiana Lo; Matullo, Giuseppe; Moltrasio, Chiara; Nacmias, Benedetta; Pileggi, Silvana; Sirchia, Silvia Maria; Stoccoro, Andrea; Storlazzi, Clelia Tiziana; Stuppia, Liborio; Tricarico, Rossella; Merla, Giuseppe
A population of Nestin-expressing progenitors in the cerebellum exhibits increased tumorigenicity 1-gen-2013 Li, P; Du, F; Yuelling, Lw; Lin, T; Muradimova, Re; Tricarico, R; Wang, J; Enikolopov, G; Bellacosa, A; Wechsler-Reya, Rj; Yang, Zj.
Active DNA Demethylation in Development, Human Disease and Cancer 1-gen-2015 Tricarico, R; Bellacosa, A
Alterazioni somatiche del gene kras in pazienti con mutazioni mono e bialleliche di MUTYH 1-gen-2009 Tricarico, Rossella; Mareni, Cristina; Ciambotti, Benedetta; Nardone, Valeria; Gentile, A.; Lucci Cordisco, E.; Pedroni, M.; Piepoli, A.; Ponz de Leon, M.; Varesco, L.; Viel, A.; Genuardi, Maurizio
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database 1-gen-2014 Thompson, Ba; Spurdle, Ab; Plazzer, Jp; Greenblatt, Ms; Newcomb P, . . .; Sarin, R; Haile, R; Hofstra, R; Ward, R; Tricarico, R; Bacares R et, Al.
Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants 1-gen-2017 Tricarico, Rossella; Kasela, Mariann; Mareni, Cristina; Thompson, Bryony A; Drouet, Aurélie; Staderini, Lucia; Gorelli, Greta; Crucianelli, Francesca; Ingrosso, Valentina; Kantelinen, Jukka; Papi, Laura; De Angioletti, Maria; Berardi, Margherita; Gaildrat, Pascaline; Soukarieh, Omar; Turchetti, Daniela; Martins, Alexandra; Spurdle, Amanda B; Nyström, Minna; Genuardi, Maurizio
BRCA1 Mutation-Specific Responses to 53BP1 Loss-Induced Homologous Recombination and PARP Inhibitor Resistance 1-gen-2018 Nacson, J; Krais, Jj; Bernhardy, Aj; Clausen, E; Feng, W; Wang, Y; Nicolas, E; Cai, Kq; Tricarico, R; Hua, X; Dimarcantonio, D; Martinez, E; Zong, D; Handorf, Ea; Bellacosa, A; Testa, Jr; Nussenzweig, A; Gupta, Gp; Sykes, Sm; Johnson, N
BRCA2 in Ovarian Development and Function 1-gen-2019 Turchetti, D; Zuntini, R; Tricarico, R
Comprehensive characterization of PTEN mutational profile in a series of 34,129 colorectal cancers 1-gen-2022 Serebriiskii, Ilya G; Pavlov, Valery; Tricarico, Rossella; Andrianov, Grigorii; Nicolas, Emmanuelle; Parker, Mitchell I; Newberg, Justin; Frampton, Garrett; Meyer, Joshua E; Golemis, Erica A
Disease-associated genetic variation in human mitochondrial protein 1-gen-2019 Nicolas, E; Tricarico, R; Savage, M; Golemis, Ea; Hall, Mj
Duodenal carcinoma in a 37-year-old man with Cowden/Bannayan syndrome 1-gen-2012 de Leon, Mp; Di Gregorio, C; Giunti, L; Roncucci, L; Pedroni, M; Tinca, Ac; Crucianelli, F; Tricarico, Rossella; Genuardi, Maurizio
Endometrial cancer and somatic G>T KRAS transversion in patients with constitutional MUTYH biallelic mutations 1-gen-2009 Tricarico, Rossella; Paola, Bet; Benedetta, Ciambotti; Carmela Di, Gregorio; Beatrice, Gatteschi; Viviana, Gismondi; Benedetta, Toschi; Tonelli, Francesco; Liliana, Varesco; Genuardi, Maurizio
Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC 1-gen-2007 B., Roncari; M., Pedroni; S., Maffei; C., DI GREGORIO; G., Ponti; A., Scarselli; L., Losi; P., Benatti; L., Roncucci; C., DE GAETANI; L., Camellini; E., LUCCI CORDISCO; Tricarico, Rossella; Genuardi, Maurizio; M., PONZ DE LEON
Haploinsufficiency in tumor predisposition syndromes: altered genomic transcription in morphologically normal cells heterozygous for VHL or TSC mutation 1-gen-2017 Peri, S; Caretti, E; Tricarico, R; Devarajan, K; Cheung, M; Sementino, E; Menges, Cw; Nicolas, E; Vanderveer, La; Howard, S; Conrad, P; Crowell, Ja; Campbell, Ks; Ross, Ea; Godwin, Ak; Yeung, At; Clapper, Ml; Uzzo, Rg; Henske, Ep; Ricketts CJ et, Al.
High resolution melting analysis for a rapididentification of heterozygous and homozygous sequence changes in the MUTYH gene 1-gen-2011 Tricarico, Rossella; F., Crucianelli; A., Alvau; Orlando, Claudio; Sestini, Roberta; Tonelli, Francesco; Valanzano, Rosa; M., Genuardi
Interaction with the DNA Repair Protein Thymine DNA Glycosylase Regulates Histone Acetylation by p300 1-gen-2016 Henry, Ra; Mancuso, P; Kuo, Ym; Tricarico, R; Tini, M; Cole, Pa; Bellacosa, A; Andrews, Aj.
Involvement of MBD4 inactivation in mismatch repair-deficient tumorigenesis 1-gen-2015 Tricarico, R; Cortellino, S; Riccio, A; Jagmohan-Changur, S; Van der Klift, H; Wijnen, J; Turner, D; Ventura, A; Rovella, V; Percesepe, A; Lucci-Cordisco, E; Radice, P; Bertario, L; Pedroni, M; Ponz de Leon, M; Mancuso, P; Devarajan, K; Cai, Kq; Klein-Szanto, Aj; Neri, G; Møller, P; Viel, A; Genuardi, M; Fodde, R; Bellacosa, A
MLH1 constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria 1-gen-2014 Crucianelli, F1; Tricarico, Rossella; Turchetti, D; Gorelli, G; Gensini, Francesca; Sestini, Roberta; Giunti, L; Pedroni, M; Ponz de Leon, M; Civitelli, S; Genuardi, Maurizio
MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH-Associated Polyposis 1-gen-2013 Pin, E; Pastrello, C; Tricarico, R; Papi, L; Quaia, M; Fornasarig, M; Carnevali, I; Oliani, C; Fornasin, A; Agostini, M; Maestro, R; Barana, D; Aretz, S; Genuardi, M; Viel, A.
MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events 1-gen-2014 Tricarico, R; *Aretz, S; Papi, L; Spier, I; Pin, E; Horpaopan, S; Cordisco, El; Pedroni, M; Stienen, D; Gentile, A; Panza, A; Piepoli, A; de Leon, Mp; Friedl, W; Viel, A; Genuardi, M (* co-first author)