NASTI, SABINA

NASTI, SABINA  

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A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL) 1-gen-2008 Harland, M; Goldstein, Am; Kukalizch, K; Taylor, C; Hogg, D; Puig, S; Badenas, C; Gruis, N; TER HUURNE, J; Bergman, W; Hayward, Nk; Stark, M; Tsao, H; Tucker, Ma; Landi, Mt; Bianchi, Giovanna; Ghiorzo, Paola; Kanetsky, Pa; Elder, D; Mann, Gj; Holland, Ea; Bishop, Dt; NEWTON BISHOP, J; J., Malvehy; C., Badenas; R., Cervera; Francisco, Cuellar; Rosa, Marti; JOAN BRUNET, Vidal; Guang, Yang; Nicholas, Martin; David, Whiteman; Adele, Green; Joanne, Aitken; Paola, Minghetti; Michela, Mantelli; Pastorino, Lorenza; Nasti, Sabina; Gargiulo, Sara; Sara, Gliori; Sushila, Mistry; JULIETTE RERSON, Moor; Wilma, Bergman; JEANET A. C., TER HUURNE; CLASINE VAN DER, Drift; LENY VAN, Mourik; COBY OUT, Luiting; FRANS VAN, Nieuwpoort; Valerie, Chaudru; Agnes, Chompret; Caroline, Kanengiesser; J. L., Michel; F., Grange; B., Sassolas; J. M., Limacher; D., Couillet; F., Truchetet; J. P., Cesarini; F., Boitier; J., CHEVRANT BRETON; C., Lasset; M., Longy; P., Joly; N., BASSET SEGUIN; T., Lesimple; C., Dugast; Michael, Ming; PATRICIA VAN, Belle; Anton, Platz; Suzanne, Egyhazi; Rainer, Tuominen; Diana, Linden; Helen, Schmid; Alon, Scope; Felix, Pavlotsky; Eitan, Friedman; Mark, Eliason
ANALISI GENOME-WIDE PER LA SUSCETTIBILITÀ AL MELANOMA: NUOVI LOCICHE CONFERMANO IL RUOLO DEI GENI DELLA PIGMENTAZIONE 1-gen-2009 Ghiorzo, Paola; Pastorino, Lorenza; Battistuzzi, Linda; Bruno, William; Gargiulo, Sara; Nasti, Sabina; Queirolo, P.; Bianchi, Giovanna
Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study 1-gen-2010 Demenais, F; Mohamdi, H; Chaudru, V; Goldstein, Am; NEWTON BISHOP JA, ; Bishop, Dt; Kanetsky, Pa; Hayward, Nk; Gillanders, E; Elder, De; Avril, Mf; Azizi, E; VAN BELLE, P; Bergman, W; BIANCHI-SCARRÀ, G; BRESSAC-DE PAILLERETS, B; Calista, D; Carrera, C; Hansson, J; Harland, M; Hogg, D; Höiom, V; Holland, Ea; Ingvar, C; Landi, Mt; Lang, Jm; Mackie, Rm; Mann, Gj; Ming, Me; Njauw, Cj; Olsson, H; Palmer, J; Pastorino, L; Puig, S; RANDERSON-MOOR, J; Stark, M; Tsao, H; Tucker, Ma; VAN DER VELDEN, P; Yang, Xr; Gruis, N; Melanoma Genetics Consortium: Demenais, F; Mohamdi, H; Chaudru, V; Corda, E; Jeannin, P; Maubec, E; Avril, Mf; Bressac-de Paillerets, B; Lesueur, F; de Lichy, M; Landi, Mt; Calista, D; Landi, G; Minghetti, P; Capirossi, D; Bertazzi, Pa; Arcangeli, F; Bianhi-Scarrà, G; Pastorino, L; Battistuzzi, L; Bruno, W; Gargiulo, S; Ghiorzo, P; Gliori, S; Nasti, S; Origone, P; Queirolo, P; Gruis, Na; van Nieuwpport FA, ; Bergman, W; van der Velden, P; van Mourik, L; Aguilera, P; Badenas, C; Carrera, C; Cervera, R; Cuellar, F; Gabriel, D; Gonzalez, M; Iglesias, P; Malvehy, J; Marti-Laborda, R; Mila, M; Ogbah, Z; Butille, Ja; Puig, S; Alós, L; Ancero, A; Arguís, P; Campo, A; Castel, T; Conill, C; Palou, J; Rull, R; Sánchez, M; Vidal-Sicart, S; Vilalta, A; Vilella, R; Olsson, H; Ingvar, C; Nielsen, K; Måsbäck, A; Harbst, K; Jönsson, G; Borg, Å; Höiom, V; Hansson, J; Tuominen, R; Lindén, D; Mackie, R; Lang, J; Newton Bishop JA, ; Affleck, P; Barrett, Jh; Bishop, Dt; Harrison, J; Iles, Mm; Randerson-Moor, J; Harland, M; Taylor, Jc; Whittaker, L; Kukalizch, K; Leake, S; Karpavicius, B; Haynes, S; Mack, T; Chan, M; Taylor, Y; Tsao, H; Njauw, Cn; Goldstein, Am; Tucker, Ma; Yang, Xr; Kanetsky, P; Elder, D; Van Belle, P; Ming, M; Mitra, N; Ruffin, A; Tesema, L; Parossian, S; Hogg, D; Loo, Jc; Martin, Ng; Montgomery, Gw; Duffy, Dl; Whiteman, Dc; Macgregor, S; Hayward, Nk; Mann, Gj; Kefford, Rf; Schmid, H; Holland, Ea.; Ghiorzo, P.; Bruno, W.
Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLDmutation in Brenner tumor 1-gen-2014 Giovanni, Ponti; Cristel, Ruini; Giampiero, Girolomoni; Giovanni, Pellacani; Francesca, Farnetani; Pastorino, Lorenza; Ghiorzo, Paola; Alexander Michal, Witkowski; Bianchi, Giovanna; Aldo, Tomasi; Pietro, Loschi; Nasti, Sabina
C242T polymorphism in CYBA gene (p22phox) and risk of coronary artery disease in a population of Caucasian Italians 1-gen-2006 Nasti, Sabina; Spallarossa, P; Altieri, Paola; Garibaldi, Silvano; Fabbi, Patrizia; Polito, L; Bacino, L; Brunelli, M; Brunelli, Claudio; Barsotti, Antonio; Ghigliotti, Giorgio
Carvedilol prevents doxorubicin-induced free radical release and apoptosis in cardiomyocytes in vitro. 1-gen-2004 Spallarossa, P; Garibaldi, Silvano; Altieri, Paola; Fabbi, Patrizia; Manca, V; Nasti, Sabina; Rossettin, P; Ghigliotti, Giorgio; Ballestrero, Alberto; Patrone, Franco; Barsotti, Antonio; Brunelli, Claudio
CDKN2A and MC1R analysis in amelanotic and pigmented melanoma. 1-gen-2009 Ghiorzo, Paola; Pastorino, Lorenza; Pizzichetta, Ma; Bono, R; Queirolo, P; Talamini, R; Annessi, G; Bruno, William; Nasti, Sabina; Gargiulo, Sara; Battistuzzi, Linda; Sini, Mc; Palmieri, G; Bianchi, Giovanna; Italian Melanoma, Intergroup
CDKN2A is the main susceptibility gene in Italian pancreatic cancer families. 1-gen-2012 Ghiorzo, Paola; Fornarini, G; Sciallero, S; Battistuzzi, Linda; Belli, F; Bernard, L; Bonelli, L; Borgonovo, Giacomo; Bruno, William; DE CIAN, Franco; Decensi, A; Filauro, M; Faravelli, F; Gozza, A; Gargiulo, Sara; Mariette, F; Nasti, Sabina; Pastorino, Lorenza; Queirolo, P; Savarino, Vincenzo; Varesco, L; Bianchi, Giovanna; Belli, F.; Dulbecco, Pietro; Mastracci, Luca; Grillo, Federica; Papadia, FRANCESCO SAVERIO; Queirolo, P.; Parodi, C.; Sacchi, G.
CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma 1-gen-2008 Pastorino, Lorenza; Bonelli, L; Ghiorzo, Paola; Queirolo, P; Battistuzzi, Linda; Balleari, E; Nasti, Sabina; Gargiulo, Sara; Gliori, S; Savoia, P; ABATE OSELLA, S; Bernengo, Mg; Bianchi, Giovanna
CDKN2A/p16INK4a 5’UTR variants in melanoma and pancreatic cancer predisposition: lost in translation, somewhere 1-gen-2011 Ghiorzo, Paola; Andreotti, Virginia; A., Bisio; F., Alessandrini; A., Provenzani; A., Quattrone; Nasti, Sabina; Gargiulo, Sara; M. A., Denti; A., Inga; Bianchi, Giovanna
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy. 1-gen-2012 Ghiorzo, P; Pensotti, V; Fornarini, G; Sciallero, S; Battistuzzi, L; Belli, F; Bonelli, L; Borgonovo, G; Bruno, W; Gozza, A; Gargiulo, S; Mastracci, L; Nasti, S; Palmieri, G; Papadia, F; Pastorino, L; Russo, A; Savarino, V; Varesco, L; Bernard, L; Scarra, Gb
Features associated with germline CDKN2A mutations: A GenoMEL study of melanoma-prone families from three continents 1-gen-2007 Goldstein, A. M.; Chan, M.; Harland, M.; Hayward, N. K.; Demenais, F.; Bishop, D. T.; Azizi, E.; Bergman, W.; Bianchi, Giovanna; Bruno, William; Calista, D.; CANNON ALBRIGHT, L. A.; Chaudru, V.; Chompret, A.; Cuellar, F.; Elder, D. E.; Ghiorzo, Paola; Gillanders, E. M.; Gruis, N. A.; Jhansson, Dhogg; Holland, E. A.; Kanetsky, PETER A.; Kefford, R. F.; Landi, Mt; Lang, Ju; Leachman, S. A.; Mackie, R. M.; Magnusson, V.; Mann, G. J.; NEWTON BISHOP, J.; Palmer, J. M.; Spuig, ; PUIG BUTILLE, J. A.; Stark, M.; Tsao, H.; Tucker, M. A.; Whitaker, L.; Yakobson, E.; Malvehy, J.; Badenas, C.; Cervera, R.; Francisco, Cuellar; Rosa, Marti´; JOAN BRUNET VIDAL, ; Guang, Yang; Nicholas, Martin; David, Whiteman; Adele, Green; Joanne, Aitken; Paola, Minghetti; Mantelli, Michela; Pastorino, Lorenza; Nasti, Sabina; Gargiulo, Sara; Sara, Gliori; Sushila, Mistry; JULIETTE RANDERSON MOOR, ; Wilma, Bergman; TER HUURNE, JEANET A. C.; CLASINE VAN DER DRIFT, ; LENY VAN MOURIK, ; COBY OUT LUITING, ; FRANS VAN NIEUWPOORT, ; Valerie, Chaudru; Agnes, Chompret; Caroline, Kanengiesser; Michel, J. L.; Grange, F.; Sassolas, B.; Limacher, J. M.; Couillet, D.; Truchetet, F.; Cesarini, J. P.; Boitier, F.; CHEVRANT BRETON, J.; Lasset, C.; Longy, M.; Joly, P.; BASSET SEGUIN, N.; Lesimple, T.; Dugast, C.; Arupa, Ganguly; Michael, Ming; PATRICIA VAN BELLE, ; Anton, Platz; Suzanne, Egyhazi; Rainer, Tuominen; Diana, Linden; Helen, Schmid; Alon, Scope; Felix, Pavlotsky; Eitan, Friedman; Mark, Eliason
Five novel germline function-impairing mutations of CYLD in Italian patients with multiple cylindromas 1-gen-2009 Nasti, Sabina; Pastorino, Lorenza; Bruno, William; Gargiulo, Sara; Battistuzzi, Linda; E., Zavattaro; G., Leigheb; V., DE FRANCESCO; A., Tulli; F., Mari; Bianchi, Giovanna; Ghiorzo, Paola
Functional analysis of CDKN2A/p16INK4a 5'-UTR variants predisposing to melanoma 1-gen-2010 Bisio, A; Nasti, Sabina; Jordan, Jj; Gargiulo, Sara; Pastorino, Lorenza; Provenzani, A; Quattrone, A; Queirolo, P; Bianchi, Giovanna; Ghiorzo, Paola; Inga, A.
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. 1-gen-2011 Amos, Ci; Wang, Le; Lee, Je; Gershenwald, Je; Chen, Wv; Fang, S; Kosoy, R; Zhang, M; Qureshi, Aa; Vattathil, S; Schacherer, Cw; Gardner, Jm; Wang, Y; Bishop, Dt; Barrett, Jh; Macgregor, S; Hayward, Nk; Martin, Ng; Duffy, Dl; Mann, Gj; Cust, A; Hopper, J; Brown, Km; Grimm, Ea; Xu, Y; Han, Y; Jing, K; Mchugh, C; Laurie, Cc; Doheny, Kf; Pugh, Ew; Seldin, Mf; Han, J; Wei, Q; Genomel, Investigators; Q., Mega Investigators; AMFS Investigators Mann, Gj; Hopper, Jl; Aitken, Jf; Armstrong, Bk; Giles, Gg; Kefford, Rf; Cust, Ae; Jenkins, Ma; Schmid, H; Aguilera, P; Badenas, C; Carrera, C; Cuellar, F; Gabriel, D; Martinez, E; Gonzalez, M; Iglesias, P; Malvehy, J; Marti Laborda, R; Mila, M; Ogbah, Z; Butille, Ja; Puig, S; Alós, L; Arance, A; Arguís, P; Campo, A; Castel, T; Conill, C; Palou, J; Rull, R; Sánchez, M; Vidal Sicart, S; Vilalta, A; Vilella, R; Martin, Ng; Montgomery, Gw; Duffy, Dl; Whiteman, Dc; Macgregor, S; Hayward, Nk; Whiteman, D; Webb, P; Green, A; Parsons, P; Purdie, D; Hayward, N; Landi, Mt; Calista, D; Landi, G; Minghetti, P; Arcangeli, F; Bertazzi, Pa; Bianchi, Giovanna; Ghiorzo, Paola; Pastorino, Lorenza; Bruno, William; Battistuzzi, Linda; Gargiulo, Sara; Nasti, Sabina; Gliori, S; Origone, Paola; Andreotti, V; Queirolo, P; Mackie, R; Lang, J; Bishop, Ja; Affleck, P; Barrett, Jh; Bishop, Dt; Harrison, J; Iles, Mm; Randerson Moor, J; Harland, M; Taylor, Jc; Whittaker, L; Kukalizch, K; Leake, S; Karpavicius, B; Haynes, S; Mack, T; Chan, M; Taylor, Y; Davies, J; King, P; Gruis, Na; van Nieuwpoort, Fa; Out, C; van der Drift, C; Bergman, W; Kukutsch, N; Bavinck, Jn; Bakker, B; van der Stoep, N; ter Huurne, J; van der Rhee, H; Bekkenk, M; Snels, D; van Praag, M; Brochez, L; Gerritsen, R; Crijns, M; Vasen, H; Olsson, H; Ingvar, C; Jönsson, G; Borg, Å; Måsbäck, A; Lundgren, L; Baeckenhorn, K; Nielsen, K; Casslén, As; Helsing, P; Andresen, Pa; Rootwelt, H; Akslen, La; Molven, A; Avril, Mf; Bressac de Paillerets, B; Chaudru, V; Chateigner, N; Corda, E; Jeannin, P; Lesueur, F; de Lichy, M; Maubec, E; Mohamdi, H; Demenais, F; Andry Benzaquen, P; Bachollet, B; Bérard, F; Berthet, P; Boitier, F; Bonadona, V; Bonafé, Jl; Bonnetblanc, Jm; Cambazard, F; Caron, O; Caux, F; Chevrant Breton, J; Chompret, A; Dalle, S; Demange, L; Dereure, O; Doré, Mx; Doutre, Ms; Dugast, C; Faivre, L; Grange, F; Humbert, P; Joly, P; Kerob, D; Lasset, C; Leccia, Mt; Lenoir, G; Leroux, D; Levang, J; Lipsker, D; Mansard, S; Martin, L; Martin Denavit, T; Mateus, C; Michel, Jl; Morel, P; Olivier Faivre, L; Perrot, Jl; Robert, C; Ronger Savle, S; Sassolas, B; Souteyrand, P; Stoppa Lyonnet, D; Thomas, L; Vabres, P; Wierzbicka, E; Elder, D; Kanetsky, P; Knorr, J; Ming, M; Mitra, N; Ruffin, A; Van Belle, P; Debniak, T; Lubiński, J; Mirecka, A; Ertmański, S; Novakovic, S; Hocevar, M; Peric, B; Cerkovnik, P; Höiom, V; Hansson, J; Mann, Gj; Kefford, Rf; Schmid, H; Holland, Ea; Azizi, E; Galore Haskel, G; Friedman, E; Baron Epel, O; Scope, A; Pavlotsky, F; Yakobson, E; Cohen Manheim, I; Laitman, Y; Milgrom, R; Shimoni, I; Kozlovaa, E.
Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome. 1-gen-2009 Gargiulo, Sara; Torrini, M; Ollila, S; Nasti, Sabina; Pastorino, Lorenza; Savarino, Vincenzo; Bonelli, L; Battistuzzi, L; Mastracci, Luca; Bruno, William; Savarino, V; Sciallero, S; Borgonovo, Giacomo; Nyström, M; Bianchi, Giovanna; Mareni, Cristina; Ghiorzo, Paola
Hereditary trichilemmal cysts: A proposal for the assessment of diagnostic clinical criteria 1-gen-2013 Seidenari, S.; Pellacani, G.; Nasti, Sabina; Tomasi, Andrea; Pastorino, Lorenza; Ghiorzo, Paola; Ruini, C.; Bianchi, Giovanna; Pollio, A.; Mandel, Vd; Ponti, G.
Identification of a SUFU germline mutation in a family with Gorlin syndrome 1-gen-2009 Pastorino, L; Ghiorzo, P; Nasti, S; Battistuzzi, L; Cusano, R; Marzocchi, C; Garrè, Ml; Clementi, M; BIANCHI SCARRA', G.
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. 1-gen-2006 Ghiorzo, Paola; Gargiulo, Sara; Pastorino, Lorenza; Nasti, Sabina; Savarino, Vincenzo; Bruno, William; Gliori, S; Sertoli, MARIO ROBERTO; Burroni, A; Savarino, V; Gensini, F; Sestini, R; Queirolo, P; Goldstein, Am; Bianchi, Giovanna
Increased Risk of Colorectal Adenomas in Italian Subjects Carrying the p53 PIN3 A2-Pro72 Haplotype. 1-gen-2007 Perfumo, C; Bonelli, L; Menichini, P; Inga, A; Gismondi, V; Ciferri, E; Percivale, P; Bianchi, Giovanna; Nasti, Sabina; Fronza, G; Varesco, L.