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

AI-Driven Polypharmacology in Small-Molecule Drug Discovery

人工智能驱动的小分子药物发现中的多药理学

Abdelsayed, Mena

Drug Repurposing for AML: Structure-Based Virtual Screening and Molecular Simulations of FDA-Approved Compounds with Polypharmacological Potential

药物再利用治疗急性髓系白血病:基于结构的虚拟筛选和具有多药理活性的FDA批准化合物的分子模拟

Abdelsayed, Mena; Boulaamane, Yassir

Mechanisms underlying the antiarrhythmic effect of ARumenamide-787 in experimental models of the J wave syndromes and hypothermia.

ARumenamide-787 在 J 波综合征和低温症实验模型中抗心律失常作用的机制

Di Diego José M, Barajas-Martinez Hector, Cox Robert, Robinson Victoria M, Jung Joseph, Fouda Mohamed, Patocskai Bence, Abdelsayed Mena, Ruben Peter C, Antzelevitch Charles

Repurposing drugs to treat cardiovascular disease in the era of precision medicine

在精准医疗时代,重新利用现有药物治疗心血管疾病

Abdelsayed, Mena; Kort, Eric J; Jovinge, Stefan; Mercola, Mark

Exome Sequencing and the Management of Neurometabolic Disorders

外显子组测序与神经代谢疾病的管理

Tarailo-Graovac, Maja; Shyr, Casper; Ross, Colin J; Horvath, Gabriella A; Salvarinova, Ramona; Ye, Xin C; Zhang, Lin-Hua; Bhavsar, Amit P; Lee, Jessica J Y; Drögemöller, Britt I; Abdelsayed, Mena; Alfadhel, Majid; Armstrong, Linlea; Baumgartner, Matthias R; Burda, Patricie; Connolly, Mary B; Cameron, Jessie; Demos, Michelle; Dewan, Tammie; Dionne, Janis; Evans, A Mark; Friedman, Jan M; Garber, Ian; Lewis, Suzanne; Ling, Jiqiang; Mandal, Rupasri; Mattman, Andre; McKinnon, Margaret; Michoulas, Aspasia; Metzger, Daniel; Ogunbayo, Oluseye A; Rakic, Bojana; Rozmus, Jacob; Ruben, Peter; Sayson, Bryan; Santra, Saikat; Schultz, Kirk R; Selby, Kathryn; Shekel, Paul; Sirrs, Sandra; Skrypnyk, Cristina; Superti-Furga, Andrea; Turvey, Stuart E; Van Allen, Margot I; Wishart, David; Wu, Jiang; Wu, John; Zafeiriou, Dimitrios; Kluijtmans, Leo; Wevers, Ron A; Eydoux, Patrice; Lehman, Anna M; Vallance, Hilary; Stockler-Ipsiroglu, Sylvia; Sinclair, Graham; Wasserman, Wyeth W; van Karnebeek, Clara D

Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy

SCN4A基因功能缺失突变会导致严重的胎儿运动减少症或“经典”先天性肌病。

Zaharieva, Irina T; Thor, Michael G; Oates, Emily C; van Karnebeek, Clara; Hendson, Glenda; Blom, Eveline; Witting, Nanna; Rasmussen, Magnhild; Gabbett, Michael T; Ravenscroft, Gianina; Sframeli, Maria; Suetterlin, Karen; Sarkozy, Anna; D'Argenzio, Luigi; Hartley, Louise; Matthews, Emma; Pitt, Matthew; Vissing, John; Ballegaard, Martin; Krarup, Christian; Slørdahl, Andreas; Halvorsen, Hanne; Ye, Xin Cynthia; Zhang, Lin-Hua; Løkken, Nicoline; Werlauff, Ulla; Abdelsayed, Mena; Davis, Mark R; Feng, Lucy; Phadke, Rahul; Sewry, Caroline A; Morgan, Jennifer E; Laing, Nigel G; Vallance, Hilary; Ruben, Peter; Hanna, Michael G; Lewis, Suzanne; Kamsteeg, Erik-Jan; Männikkö, Roope; Muntoni, Francesco

Voltage-gated sodium channels: pharmaceutical targets via anticonvulsants to treat epileptic syndromes

电压门控钠通道:通过抗惊厥药物治疗癫痫综合征的药物靶点

Abdelsayed, Mena; Sokolov, Stanislav