日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy

影响 NQO1 蛋白水平的基因变异会影响艾地苯醌治疗莱伯遗传性视神经病变的疗效。

Serena Jasmine Aleo ,Valentina Del Dotto ,Martina Romagnoli ,Claudio Fiorini ,Giada Capirossi ,Camille Peron ,Alessandra Maresca ,Leonardo Caporali ,Mariantonietta Capristo ,Concetta Valentina Tropeano ,Claudia Zanna ,Fred N Ross-Cisneros ,Alfredo A Sadun ,Maria Gemma Pignataro ,Carla Giordano ,Chiara Fasano ,Andrea Cavaliere ,Anna Maria Porcelli ,Gaia Tioli ,Francesco Musiani ,Alessia Catania ,Costanza Lamperti ,Stefania Bianchi Marzoli ,Annamaria De Negri ,Maria Lucia Cascavilla ,Marco Battista ,Piero Barboni ,Michele Carbonelli ,Giulia Amore ,Chiara La Morgia ,Dmitrii Smirnov ,Catalina Vasilescu ,Aiman Farzeen ,Beryll Blickhaeuser ,Holger Prokisch ,Claudia Priglinger ,Bettina Livonius ,Claudia B Catarino ,Thomas Klopstock ,Valeria Tiranti ,Valerio Carelli ,Anna Maria Ghelli

Lipidomics reveals the reshaping of the mitochondrial phospholipid profile in cells lacking OPA1 and mitofusins

脂质组学揭示缺乏 OPA1 和线粒体融合蛋白的细胞中线粒体磷脂谱的重塑

Andrea Castellaneta, Ilario Losito, Vito Porcelli, Serena Barile, Alessandra Maresca, Valentina Del Dotto, Valentina Losacco, Ludovica Sofia Guadalupi, Cosima Damiana Calvano, David C Chan, Valerio Carelli, Luigi Palmieri, Tommaso R I Cataldi

Methyl carbamates of phosphatidylethanolamines and phosphatidylserines reveal bacterial contamination in mitochondrial lipid extracts of mouse embryonic fibroblasts

磷脂酰乙醇胺和磷脂酰丝氨酸的甲基氨基甲酸酯揭示了小鼠胚胎成纤维细胞线粒体脂质提取物中的细菌污染

Andrea Castellaneta, Vito Porcelli, Ilario Losito, Serena Barile, Alessandra Maresca, Valentina Del Dotto, Ludovica Sofia Guadalupi, Cosima Damiana Calvano, Valerio Carelli, Luigi Palmieri, Tommaso R I Cataldi

Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy

病理性线粒体自噬破坏了莱伯氏遗传性视神经病变中的线粒体稳态

Alberto Danese, Simone Patergnani, Alessandra Maresca, Camille Peron, Andrea Raimondi, Leonardo Caporali, Saverio Marchi, Chiara La Morgia, Valentina Del Dotto, Claudia Zanna, Angelo Iannielli, Alice Segnali, Ivano Di Meo, Andrea Cavaliere, Magdalena Lebiedzinska-Arciszewska, Mariusz R Wieckowski, A

Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys

雷帕霉素可挽救携带线粒体 tRNALys m.8344A > G 突变的细胞的线粒体功能障碍

Mariantonietta Capristo, Valentina Del Dotto, Concetta Valentina Tropeano, Claudio Fiorini, Leonardo Caporali, Chiara La Morgia, Maria Lucia Valentino, Monica Montopoli, Valerio Carelli, Alessandra Maresca

Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy

LIG3 中的双等位基因变异导致一种新型线粒体神经胃肠脑肌病

Elena Bonora, Sanjiban Chakrabarty, Georgios Kellaris, Makiko Tsutsumi, Francesca Bianco, Christian Bergamini, Farid Ullah, Federica Isidori, Irene Liparulo, Chiara Diquigiovanni, Luca Masin, Nicola Rizzardi, Mariapia Giuditta Cratere, Elisa Boschetti, Valentina Papa, Alessandra Maresca, Giovanna Ce

Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations

药物重新定位作为与 OPA1 突变相关的神经退行性疾病的治疗策略

Serena J Aleo, Valentina Del Dotto, Mario Fogazza, Alessandra Maresca, Tiziana Lodi, Paola Goffrini, Anna Ghelli, Michela Rugolo, Valerio Carelli, Enrico Baruffini, Claudia Zanna

Exploring Metabolic Adaptations to the Acidic Microenvironment of Osteosarcoma Cells Unveils Sphingosine 1-Phosphate as a Valuable Therapeutic Target

探索骨肉瘤细胞对酸性微环境的代谢适应性揭示鞘氨醇 1-磷酸酯是一种有价值的治疗靶点

Margherita Cortini, Andrea Armirotti, Marta Columbaro, Dario Livio Longo, Gemma Di Pompo, Elena Cannas, Alessandra Maresca, Costantino Errani, Alessandra Longhi, Alberto Righi, Valerio Carelli, Nicola Baldini, Sofia Avnet

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

SSBP1 突变导致线粒体 DNA 耗竭,从而引发复杂的视神经萎缩症

Valentina Del Dotto, Farid Ullah, Ivano Di Meo, Pamela Magini, Mirjana Gusic, Alessandra Maresca, Leonardo Caporali, Flavia Palombo, Francesca Tagliavini, Evan Harris Baugh, Bertil Macao, Zsolt Szilagyi, Camille Peron, Margaret A Gustafson, Kamal Khan, Chiara La Morgia, Piero Barboni, Michele Carbon

Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome

在没有原发性线粒体功能障碍的情况下,钙处理不当会导致 Wolfram 综合征的细胞病理

Chiara La Morgia #, Alessandra Maresca #, Giulia Amore, Laura Ludovica Gramegna, Michele Carbonelli, Emanuela Scimonelli, Alberto Danese, Simone Patergnani, Leonardo Caporali, Francesca Tagliavini, Valentina Del Dotto, Mariantonietta Capristo, Federico Sadun, Piero Barboni, Giacomo Savini, Stefania