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Lipo-Glc-1,6-P2: A Bioprecursor Prodrug for Phosphomannomutase-2 Congenital Disorder of Glycosylation Lipo-Glc-1,6-P2:一种用于糖基化先天性磷甘露糖互变酶-2障碍的生物前体前药 Sodano, Federica; Monticelli, Maria; Mele, Bruno Hay; Rolando, Barbara; Lazzarato, Loretta; De Simone, Angela; Andrisano, Vincenza; Paris, Debora; Rimoli, Maria Grazia; Cubellis, Maria Vittoria; Andreotti, Giuseppina 分享 收藏
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Beneficial effects of Glc-1,6-P2 modulation on mutant phosphomannomutase-2 Glc-1,6-P2调控对突变磷甘露糖变位酶-2的有益作用 Monticelli, Maria; Paris, Debora; Monti, Maria Chiara; Morretta, Elva; Pakanova, Zuzana; Nemcovic, Marek; Kodrikova, Rebeka; Cubellis, Maria Vittoria; Andreotti, Giuseppina 分享 收藏
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Oxidoreductases and metal cofactors in the functioning of the earth 地球功能中的氧化还原酶和金属辅因子 Mele, Bruno Hay; Monticelli, Maria; Leone, Serena; Bastoni, Deborah; Barosa, Bernardo; Cascone, Martina; Migliaccio, Flavia; Montemagno, Francesco; Ricciardelli, Annarita; Tonietti, Luca; Rotundi, Alessandra; Cordone, Angelina; Giovannelli, Donato 分享 收藏
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Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances Pignata, Laura; Cecere, Francesco; Verma, Ankit; Mele, Bruno Hay; Monticelli, Maria; Acurzio, Basilia; Giaccari, Carlo; Sparago, Angela; Hernandez Mora, Jose Ramon; Monteagudo-Sanchez, Ana; Esteller, Manel; Pereda, Arrate; Tenorio-Castano, Jair; Palumbo, Orazio; Carella, Massimo; Prontera, Paolo; Piscopo, Carmelo; Accadia, Maria; Lapunzina, Pablo; Cubellis, Maria Vittoria; Perez de Nanclares, Guiomar; Monk, David; Riccio, Andrea; Cerrato, Flavia 分享 收藏
Human Cryptic Host Defence Peptide GVF27 Exhibits Anti-Infective Properties against Biofilm Forming Members of the Burkholderia cepacia Complex Bosso, Andrea; Gaglione, Rosa; Di Girolamo, Rocco; Veldhuizen, Edwin J. A.; Garcia-Vello, Pilar; Fusco, Salvatore; Cafaro, Valeria; Monticelli, Maria; Culurciello, Rosanna; Notomista, Eugenio; Arciello, Angela; Pizzo, Elio 分享 收藏
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance Cubellis, Maria Vittoria; Pignata, Laura; Verma, Ankit; Sparago, Angela; Del Prete, Rosita; Monticelli, Maria; Calzari, Luciano; Antona, Vincenzo; Melis, Daniela; Tenconi, Romano; Russo, Silvia; Cerrato, Flavia; Riccio, Andrea 分享 收藏