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Maria Monticelli

institute of biomolecular chemistry (icb)

17H指数
61论文数
1.0K被引数
收录论文 12
发表时间
Proteo-Metabolomic Profiling of PMM2-CDG Reveals Dysregulation of Retinoic Acid Synthesis, Myo-Inositol, and the Hexosamine PathwayPMM2-CDG的蛋白质-代谢组学分析揭示了视黄酸合成、肌醇和己糖胺通路的功能失调
err2026-08-21
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errOAAI
errDiana Gallego; Giuseppina Andreotti; Maria Monticelli; Debora Paris; Arturo Martín-Martínez; Alejandra Gámez; Mercedes Serrano; José Córdoba-Caballero; Pedro Seoane; Juan A. G. Ranea; Belén Pérez
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Lipo-Glc-1,6-P2: A Bioprecursor Prodrug for Phosphomannomutase-2 Congenital Disorder of GlycosylationLipo-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
err2026-04-01
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errSodano, 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
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Beneficial effects of Glc-1,6-P2 modulation on mutant phosphomannomutase-2Glc-1,6-P2调控对突变磷甘露糖变位酶-2的有益作用
err2025-06-01
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PREAI
errMonticelli, Maria; Paris, Debora; Monti, Maria Chiara; Morretta, Elva; Pakanova, Zuzana; Nemcovic, Marek; Kodrikova, Rebeka; Cubellis, Maria Vittoria; Andreotti, Giuseppina
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Exploring ligand interactions with human phosphomannomutases using recombinant bacterial thermal shift assay and biochemical validation
err2024-07-01
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errMonticelli, Maria; Mele, Bruno Hay; Wright, Demi Marie; Guerriero, Simone; Andreotti, Giuseppina; Cubellis, Maria Vittoria
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Congenital disorders of glycosylation: narration of a story through its patents先天性糖基化障碍: 通过其专利讲述一个故事
err2023-08-29
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errMonticelli, Maria; D'Onofrio, Tania; Jaeken, Jaak; Morava, Eva; Andreotti, Giuseppina; Cubellis, Maria Vittoria
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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
err2023-08-11
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errMele, 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
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Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease
err2022-10-10
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errVignogna, Ryan C.; Allocca, Mariateresa; Monticelli, Maria; Norris, Joy W.; Steet, Richard; Perlstein, Ethan O.; Andreotti, Giuseppina; Lang, Gregory, I
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Stakeholders' views on drug development: the congenital disorders of glycosylation community perspective利益相关者对药物开发的看法: 糖基化社区的先天性疾病观点
err2022-07-30
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errMonticelli, Maria; Francisco, Rita; Brasil, Sandra; Marques-da-Silva, Dorinda; Rijoff, Tatiana; Pascoal, Carlota; Jaeken, Jaak; Videira, Paula A.; Ferreira, Vanessa dos Reis
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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
err2022-05-28
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errPignata, 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
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Human Cryptic Host Defence Peptide GVF27 Exhibits Anti-Infective Properties against Biofilm Forming Members of the Burkholderia cepacia Complex
err2022-02-21
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errBosso, 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
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Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
err2020-09-14
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errCubellis, 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
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