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

Restoring brain wiring, mobility, sleep, and lifespan with a novel repurposed modulator of voltage-gated K(+) channels: an emerging perspective for channelopathies

利用新型电压门控钾离子通道调节剂恢复大脑连接、活动能力、睡眠和寿命：通道病治疗的新视角

期刊:Journal of Translational Medicine
影响因子:7.5
doi:10.1186/s12967-025-07609-6
Setzu, Maria Dolores; Casu, Maria Antonietta; Mocci, Ignazia; Talani, Giuseppe; Haidar, Fatemah M; Sanna, Fabrizio; Manis, Cristina; Caboni, Pierluigi; Bru-Mercier, Gilles; Biggio, Francesca; Krishnan, Manigandan; Muroni, Patrizia; Maria Baroli, Bianca; Frau, Roberto; Concas, Luca; Puligheddu, Monica; Subramanya, Sandeep B; Imbrici, Paola; D'Adamo, Maria Cristina; Pessia, Mauro
神经科学
发表日期：2026
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Therapeutic Potentials of Phytochemicals in Pancreatitis: Targeting Calcium Signaling, Ferroptosis, microRNAs, and Inflammation with Drug-Likeness Evaluation

植物化学物质在胰腺炎治疗中的应用潜力：靶向钙信号传导、铁死亡、microRNA和炎症的药物相似性评价

期刊:Nutrients
影响因子:5
doi:10.3390/nu17243841
Farhat, Fatma; Venkataraman, Balaji; Bhongade, Bhoomendra A; Pessia, Mauro; Ojha, Shreesh; Subramanya, Sandeep B
炎症
胰腺炎
信号转导
炎症/感染
Immunology/Inflammation
铁死亡
发表日期：2025
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Phytochemical Compounds as Promising Therapeutics for Intestinal Fibrosis in Inflammatory Bowel Disease: A Critical Review

植物化学化合物作为炎症性肠病肠纤维化的潜在治疗药物：一项重要综述

期刊:Nutrients
影响因子:5
doi:10.3390/nu16213633
Touny, Aya A; Venkataraman, Balaji; Ojha, Shreesh; Pessia, Mauro; Subramanian, Veedamali S; Hariharagowdru, Shamanth Neralagundi; Subramanya, Sandeep B
炎症
炎症/感染
发表日期：2024
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An activator of voltage-gated K(+) channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1

电压门控钾离子通道Kv1.1激活剂作为1型发作性共济失调的候选治疗药物

期刊:Proceedings of the National Academy of Sciences of the United States of America
影响因子:9.1
doi:10.1073/pnas.2207978120
Servettini, Ilenio; Talani, Giuseppe; Megaro, Alfredo; Setzu, Maria Dolores; Biggio, Francesca; Briffa, Michelle; Guglielmi, Luca; Savalli, Nicoletta; Binda, Francesca; Delicata, Francis; Bru-Mercier, Gilles; Vassallo, Neville; Maglione, Vittorio; Cauchi, Ruben J; Di Pardo, Alba; Collu, Maria; Imbrici, Paola; Catacuzzeno, Luigi; D'Adamo, Maria Cristina; Olcese, Riccardo; Pessia, Mauro
发表日期：2023
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KCNK18 Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel Activity

与智力障碍和神经发育障碍相关的KCNK18双等位基因变异会改变TRESK通道活性

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms22116064
Pavinato, Lisa; Nematian-Ardestani, Ehsan; Zonta, Andrea; De Rubeis, Silvia; Buxbaum, Joseph; Mancini, Cecilia; Bruselles, Alessandro; Tartaglia, Marco; Pessia, Mauro; Tucker, Stephen J; D'Adamo, Maria Cristina; Brusco, Alfredo
发育与干细胞
NK1
神经科学
KCNK1
发表日期：2021
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Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches

Kv1.1通道病：病理生理机制和治疗方法

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms21082935
D'Adamo, Maria Cristina; Liantonio, Antonella; Rolland, Jean-Francois; Pessia, Mauro; Imbrici, Paola
发表日期：2020
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Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies

地塞米松在多形性胶质母细胞瘤治疗中的应用：机制与争议

期刊:Frontiers in Molecular Neuroscience
影响因子:3.8
doi:10.3389/fnmol.2019.00065
Cenciarini, Marta; Valentino, Mario; Belia, Silvia; Sforna, Luigi; Rosa, Paolo; Ronchetti, Simona; D'Adamo, Maria Cristina; Pessia, Mauro
细胞生物学
发表日期：2019
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Structure, Gating and Basic Functions of the Ca2+-activated K Channel of Intermediate Conductance

中等电导钙激活钾通道的结构、门控和基本功能

期刊:Current Neuropharmacology
影响因子:5.3
doi:10.2174/1570159X15666170830122402
Sforna, Luigi; Megaro, Alfredo; Pessia, Mauro; Franciolini, Fabio; Catacuzzeno, Luigi
发表日期：2018
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Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia

评论：电压传感器中的一种通道病突变揭示了保守的苯丙氨酸对Kv1.1通道门控特性和共济失调的影响。

期刊:Frontiers in Cellular Neuroscience
影响因子:4
doi:10.3389/fncel.2018.00174
Hasan, Sonia; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D'Adamo, Maria Cristina
发表日期：2018
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Lethal digenic mutations in the K(+) channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay.

K(+)通道Kir4.1 (KCNJ10)和SLACK (KCNT1)的致命双基因突变与严重的致残性癫痫和神经发育迟缓有关

期刊:Journal of Neurophysiology
影响因子:2.1
doi:10.1152/jn.00284.2017
Hasan Sonia, Balobaid Ameera, Grottesi Alessandro, Dabbagh Omar, Cenciarini Marta, Rawashdeh Rifaat, Al-Sagheir Afaf, Bove Cecilia, Macchioni Lara, Pessia Mauro, Al-Owain Mohammed, D'Adamo Maria Cristina
发育与干细胞
神经科学
发表日期：2017
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