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Titolo Data di pubblicazione Autore(i) File
Mutation Profiling of Key Cancer Genes in Primary Breast Cancers and Their Distant Metastases 1-gen-2018 Schrijver Willemijne, A. M. E.; Selenica, Pier; Lee Ju, Youn; Ng, KIU YAN CHARLOTTE; Burke Kathleen, A.; Piscuoglio, Salvatore; Berman Samuel, H.; Reis-Filho Jorge, S.; Weigelt, Britta; van Diest Paul, J.; Moelans Cathy, B.
Mutation tracking in circulating tumor DNA predicts relapse in early breast cancer 1-gen-2015 Garcia-Murillas, Isaac; Schiavon, Gaia; Weigelt, Britta; Ng, KIU YAN CHARLOTTE; Hrebien, Sarah; Cutts Rosalind, J.; Cheang, Maggie; Osin, Peter; Nerurkar, Ashutosh; Kozarewa, Iwanka; Garrido Javier, Armisen; Dowsett, Mitch; Reis-Filho Jorge, S.; Smith Ian, E.; Turner Nicholas, C.
Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy 1-gen-2002 Duga, S; Asselta, R; Bonati, Mt; Malcovati, M; Dalpra, L; Oldani, A; Zucconi, M; Ferinistrambi, L; Tenchini, Ml
Mutational analysis of PRKAR1A and Gs alpha in sporadic adrenocortical tumors 1-gen-2005 Libe, R; Mantovani, G; Bondioni, S; Lania, A; Pedroni, C; Beck-Peccoz, P; Spada, A
A mutational chip to detect TP53, CDKN2A and FAT1 mutations in circulating cell free-DNA of head and neck squamous cell carcinoma patients:a pilot study 1-gen-2019 Ganci, F.; Spinella, F.; Cottone, G.; Cotroneo, E.; Nuccitelli, A.; Biroccio, A.; Sacconi, A.; Manciocco, V.; Pallocca, M.; Rollo, F.; Covello, R.; Benevolo, M.; Spriano, G; Fiorentino, F.; Blandino, G.
Mutational Diversity of Lung Cancer and Associated Lymph Nodes. An Exploratory Prospective Study of 4 Resected cIIIA-N2 1-gen-2019 Legras, Antoine; Roussel, Hélène; Mangiameli, Giuseppe; Arame, Alex; Grand, Bertrand; Pricopi, Ciprian; Badia, Alain; Gibault, Laure; Badoual, Cécile; Fabre, Elizabeth; Laurent-Puig, Pierre; Blons, Hélène; Le Pimpec-Barthes, Françoise
Mutational profile of epithelial, non-glandular sinonasal cancers into 2 prospective clinical trials 1-gen-2019 De, Cecco; Serafini, ; M., S.; Canevari, ; Penso, ; Nicolai, ; Castelnuovo, ; Benazzo, ; Sponghini, ; Orlandi, ; Vischioni, ; Piazza, ; Resteghini, C; Licitra, ; Bossi,
Mutational Profile of Malignant Pleural Mesothelioma (MPM) in the Phase II RAMES Study 1-gen-2020 Pagano, Maria; Ceresoli, Luca Giovanni; Zucali, Paolo Andrea; Pasello, Giulia; Garassino, Marina; Grosso, Federica; Tiseo, Marcello; Soto Parra, Hector; Zanelli, Francesca; Cappuzzo, Federico; Grossi, Francesco; De Marinis, Filippo; Pedrazzoli, Paolo; Gnoni, Roberta; Bonelli, Candida; Torricelli, Federica; Ciarrocchi, Alessia; Normanno, Nicola; Pinto, Carmine
Mutational profile of ZBTB16-RARA-positive acute myeloid leukemia 1-gen-2021 Fabiani, Emiliano; Cicconi, Laura; Nardozza, Anna Maria; Cristiano, Antonio; Rossi, Marianna; Ottone, Tiziana; Falconi, Giulia; Divona, Mariadomenica; Testi, Anna Maria; Annibali, Ombretta; Castelli, Roberto; Lazarevic, Vladimir; Rego, Eduardo; Montesinos, Pau; Esteve, Jordi; Venditti, Adriano; Della Porta, Matteo; Arcese, William; Lo-Coco, Francesco; Voso, Maria Teresa
Mutational screening and functional analyses in the zebrafish model of GIGYF2 as a candidate gene for Parkinson disease 1-gen-2011 Guella, I; Pistocchi, A; Asselta, R; Rimoldi, V; Ghilardi, A; Sironi, F; Trotta, L; Primignani, P; Zini, M; Zecchinelli, A; Coviello, D; Pezzoli, G; Del Giacco, L; Duga, S; Goldwurm, S.
Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene 1-gen-2009 Guella, I; Pistocchi, A; Asselta, R; Rimoldi, V; Ghilardi, A; Sironi, F; Trotta, L; Primignani, P; Zini, M; Zecchinelli, A; Coviello, D; Pezzoli, G; Del Giacco, L; Duga, S; Goldwurm, S
Mutational screening of 25 unrelated FV-deficient patients from six countries 1-gen-2009 Guella, I.; Paraboschi, E.; Duga, S.; Peyvandi, F.; Gemmati, D.; Ciavarella, N.; Mannucci, P. M.; Asselta, R.
Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects 1-gen-2007 Monaldini, L; Asselta, R; Duga, S; Peyvandi, F; Karimi, M; Malcovati, M; Tenchini, Ml
Mutational screening to improve the transplantation decision-making process in MDS 1-gen-2023 Campagna, Alessia; Della Porta, Matteo G.
Mutations causing premature termination codons in the Von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decay 1-gen-2009 Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R
Mutations in disguise 1-gen-2011 Duga, S; Asselta, R
Mutations in the splicing factor SF3B1 are linked to frequent emergence of HLA-DRlow/neg monocytes in lower-risk myelodysplastic neoplasms 1-gen-2024 Winter, Susann; Schneider, Marie; Oelschlaegel, Uta; Maggioni, Giulia; Riva, Elena; Raddi, Marco Gabriele; Bencini, Sara; Peruzzi, Benedetta; Choy, Desmond; Antunes Dos Reis, Rita; Güse, Esther; Lischer, Christopher; Vera, Julio; Timms, Jessica A.; Sompairac, Nicolas; Sockel, Katja; Poloni, Antonella; Tunger, Antje; Della Porta, Matteo Giovanni; Santini, Valeria; Schmitz, Marc; Platzbecker, Uwe; Kordasti, Shahram
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis 1-gen-2017 Smith, Bn; Topp, Sd; Fallini, C; Shibata, H; Chen, Hj; Troakes, C; King, A; Ticozzi, N; Kenna, Kp; Soragia-Gkazi, A; Miller, Jw; Sato, A; Dias, Dm; Jeon, M; Vance, C; Wong, Ch; de Majo, M; Kattuah, W; Mitchell, Jc; Scotter, El; Parkin, Nw; Sapp, Pc; Nolan, M; Nestor, Pj; Simpson, M; Weale, M; Lek, M; Baas, F; de Jong, Jmv; ten Asbroek, Alma; Redondo, Ag; Esteban-Perez, J; Tiloca, C; Verde, F; Duga, S; Leigh, N; Pall, H; Morrison, Ke; Al-Chalabi, A; Shaw, Pj; Kirby, J; Turner, Mr; Talbot, K; Hardiman, O; Glass, Jd; de Belleroche, J; Maki, M; Moss, Se; Miller, C; Gellera, C; Ratti, A; Al-Sarraj, S; Brown, Rh; Silani, V; Landers, Je; Shaw, Ce
Mutations leading to premature termination codons in the Von Willebrand factor gene are associated with allele-specific mRNAs decay 1-gen-2008 Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R
Mutations leading to premature termination codons in the Von Willebrand factor gene are associated with the decay of the mutant mRNAs 1-gen-2008 Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R
Mostrati risultati da 18.856 a 18.875 di 31.782
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