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

A Holistic Approach to Identifying a Positron Emission Tomography (PET) Tracer Candidate for In Vivo Imaging of Purinergic P2X7 Receptor in Neuroinflammation

采用整体方法识别用于神经炎症中嘌呤能P2X7受体体内成像的正电子发射断层扫描（PET）示踪剂候选物

期刊:ACS Pharmacology and Translational Science
影响因子:3.7
doi:10.1021/acsptsci.5c00820
Ghafir El Idrissi, Imane; Spinaci, Andrea; Vitone, Daniele; Intranuovo, Francesca; Niso, Mauro; Brunetti, Leonardo; Francucci, Beatrice; Pazarlar, Burcu A; Magnusdottir, Kristin H; Paradies, Eleonora; Marobbio, Carlo Marya Thomas; Ricci, Ludovica; Grignolo, Marianna; Iacobazzi, Rosa Maria; Marucci, Gabriella; Dal Ben, Diego; Lambertucci, Catia; Volpini, Rosaria; Denora, Nunzio; Adinolfi, Elena; Mikkelsen, Jens D; Buccioni, Michela; Lacivita, Enza; Leopoldo, Marcello
炎症
炎症/感染
信号转导
神经科学
神经炎症
发表日期：2026
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Therapeutic combination of L-ascorbic acid, N-acetylcysteine, and dimethyl fumarate in Friedreich's ataxia: insights from in vitro models.

L-抗坏血酸、N-乙酰半胱氨酸和富马酸二甲酯联合治疗弗里德赖希共济失调：来自体外模型的见解

期刊:Redox Report
影响因子:7.4
doi:10.1080/13510002.2025.2505303
Edzeamey Fred Jonathan, Ramchunder Zenouska, Valle Gómez Adamo, Ge Haobo, Marobbio Carlo Marya Thomas, Pourzand Charareh, Virmouni Sara Anjomani
其它
发表日期：2025
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P2 Receptor Antagonists Rescue Defective Heme Content in an In Vitro SLC25A38-Associated Congenital Sideroblastic Anemia Cell Model.

P2 受体拮抗剂可挽救体外 SLC25A38 相关先天性铁粒幼细胞性贫血细胞模型中缺陷的血红素含量

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms252413314
Santoro Antonella, De Santis Silvia, Palmieri Ferdinando, Vozza Angelo, Agrimi Gennaro, Andolfo Immacolata, Russo Roberta, Palazzo Antonio, Storlazzi Clelia Tiziana, Ferrucci Arianna, Jun Yong Woong, Kool Eric T, Fiermonte Giuseppe, Iolascon Achille, Paradies Eleonora, Marobbio Carlo Marya Thomas, Palmieri Luigi
细胞生物学
发表日期：2024
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Citrate Regulates the Saccharomyces cerevisiae Mitochondrial GDP/GTP Carrier (Ggc1p) by Triggering Unidirectional Transport of GTP

柠檬酸盐通过触发GTP的单向运输来调节酿酒酵母线粒体GDP/GTP载体（Ggc1p）。

期刊:Journal of Fungi
影响因子:4
doi:10.3390/jof8080795
Seccia, Roberta; De Santis, Silvia; Di Noia, Maria A; Palmieri, Ferdinando; Miniero, Daniela V; Marmo, Raffaele; Paradies, Eleonora; Santoro, Antonella; Pierri, Ciro L; Palmieri, Luigi; Marobbio, Carlo M T; Vozza, Angelo
线粒体
发表日期：2022
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Transcriptionally promiscuous "blurry" promoters in Tc1/mariner transposons allow transcription in distantly related genomes

Tc1/mariner转座子中转录活性广泛的“模糊”启动子允许远亲基因组中的转录。

期刊:Mobile DNA
影响因子:3.1
doi:10.1186/s13100-019-0155-6
Palazzo, Antonio; Lorusso, Patrizio; Miskey, Csaba; Walisko, Oliver; Gerbino, Andrea; Marobbio, Carlo Marya Thomas; Ivics, Zoltán; Marsano, René Massimiliano
发表日期：2019
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SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency

SLC25A10双等位基因突变与难治性癫痫性脑病伴复合物I缺陷相关

期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddx419
Punzi, Giuseppe; Porcelli, Vito; Ruggiu, Matteo; Hossain, Md F; Menga, Alessio; Scarcia, Pasquale; Castegna, Alessandra; Gorgoglione, Ruggiero; Pierri, Ciro L; Laera, Luna; Lasorsa, Francesco M; Paradies, Eleonora; Pisano, Isabella; Marobbio, Carlo M T; Lamantea, Eleonora; Ghezzi, Daniele; Tiranti, Valeria; Giannattasio, Sergio; Donati, Maria A; Guerrini, Renzo; Palmieri, Luigi; Palmieri, Ferdinando; De Grassi, Anna
癫痫
神经科学
发表日期：2018
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Characterization of Human and Yeast Mitochondrial Glycine Carriers with Implications for Heme Biosynthesis and Anemia

人类和酵母线粒体甘氨酸载体的特性及其对血红素生物合成和贫血的影响

期刊:Journal of Biological Chemistry
影响因子:3.9
doi:10.1074/jbc.M116.736876
Lunetti, Paola; Damiano, Fabrizio; De Benedetto, Giuseppe; Siculella, Luisa; Pennetta, Antonio; Muto, Luigina; Paradies, Eleonora; Marobbio, Carlo Marya Thomas; Dolce, Vincenza; Capobianco, Loredana
代谢
Human
线粒体
Yeast
贫血
发表日期：2016
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Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26

SLC25A26基因突变导致的线粒体内甲基化缺陷

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2015.09.013
Kishita, Yoshihito; Pajak, Aleksandra; Bolar, Nikhita Ajit; Marobbio, Carlo M T; Maffezzini, Camilla; Miniero, Daniela V; Monné, Magnus; Kohda, Masakazu; Stranneheim, Henrik; Murayama, Kei; Naess, Karin; Lesko, Nicole; Bruhn, Helene; Mourier, Arnaud; Wibom, Rolf; Nennesmo, Inger; Jespers, Ann; Govaert, Paul; Ohtake, Akira; Van Laer, Lut; Loeys, Bart L; Freyer, Christoph; Palmieri, Ferdinando; Wredenberg, Anna; Okazaki, Yasushi; Wedell, Anna
线粒体
表观遗传
DNA甲基化
发表日期：2015
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A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: functional analysis of the mutant protein

一名土耳其HHH综合征患者的SLC25A15基因发生新型突变：突变蛋白的功能分析

期刊:Molecular Genetics and Metabolism
影响因子:3.5
doi:10.1016/j.ymgme.2014.03.002
Ersoy Tunalı, Nagehan; Marobbio, Carlo M T; Tiryakioğlu, N Ozan; Punzi, Giuseppe; Saygılı, Seha K; Onal, Hasan; Palmieri, Ferdinando
发表日期：2014
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The ARL2 GTPase is required for mitochondrial morphology, motility, and maintenance of ATP levels

ARL2 GTPase 是线粒体形态、运动能力和 ATP 水平维持所必需的

期刊:PLoS One
影响因子:2.9
doi:10.1371/journal.pone.0099270
Laura E Newman, Cheng-jing Zhou, Samatha Mudigonda, Alexa L Mattheyses, Eleonora Paradies, Carlo Marya Thomas Marobbio, Richard A Kahn
信号转导
发表日期：2014
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