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Citation: S. Cairo et al., WBSCR14, a gene mapping to the Williams-Beuren syndrome deleted region, isa new member of the Mlx transcription factor network, HUM MOL GEN, 10(6), 2001, pp. 617-627

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Authors: Reymond, A Meroni, G Fantozzi, A Merla, G Cairo, S Luzi, L Riganelli, D Zanaria, E Messali, S Cainarca, S Guffanti, A Minucci, S Pelicci, PG Ballabio, A

Citation: A. Reymond et al., The tripartite motif family identifies cell compartments, EMBO J, 20(9), 2001, pp. 2140-2151

Authors: Meroni, G Cairo, S Merla, G Messali, S Brent, R Ballabio, A Reymond, A

Citation: G. Meroni et al., Mlx, a new Max-Like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway?, ONCOGENE, 19(29), 2000, pp. 3266-3277

Authors: Reymond, A Volorio, S Merla, G Al-Maghtheh, M Zuffardi, O Bulfone, A Ballabio, A Zollo, M

Citation: A. Reymond et al., Evidence for interaction between human PRUNE and nm23-H1 NDPKinase, ONCOGENE, 18(51), 1999, pp. 7244-7252

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Citation: D. Seripa et al., Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinemia patients and in the general population from Southern Italy, J INH MET D, 22(5), 1999, pp. 670-671