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

A genome-wide CRISPR screen identifies the TNRC18 gene locus as a regulator of inflammatory signaling

全基因组 CRISPR 筛选发现 TNRC18 基因位点是炎症信号传导的调节因子。

Fedik Rahimov # ,Sujana Ghosh # ,Sakina Petiwala ,Mary Schmidt ,Eugene Nyamugenda ,Manman Shi ,Jason Tam ,Daniel Verduzco ,Sanjana Singh ,Victor Avram ,Apexa Modi ,Celso A Espinoza ,Charles Lu ,Jing Wang ,Ashleigh Keller ,Michael Macoritto ,Naim Al Mahi ,Tifani Anton ,Namjin Chung ,Michael J Flister ,Kanstantsin V Katlinski ,Amlan Biswas ,Anneke I den Hollander ,Jeffrey F Waring ,Joshua D Stender

Maintenance therapy with a P2Y12 receptor inhibitor after cangrelor in patients with acute coronary syndrome. The ELECTRA-SIRIO 2 investigators' viewpoint

急性冠脉综合征患者在接受坎格瑞洛治疗后,使用P2Y12受体抑制剂进行维持治疗。ELECTRA-SIRIO 2研究者的观点

Kubica, Jacek; Adamski, Piotr; Gajda, Robert; Kubica, Aldona; Ostrowska, Małgorzata; Casu, Gavino; Gorog, Diana A; Gurbel, Paul A; Hajdukiewicz, Tomasz; Jaguszewski, Miłosz; Jeong, Young-Hoon; Kosobucka-Ozdoba, Agata; Motovska, Zuzana; Niezgoda, Piotr; Piasecki, Maciej; Podhajski, Przemysław; Raggi, Paolo; Rahimov, Uzeyir; Siller-Matula, Jolanta M; Skonieczny, Grzegorz; Szarpak, Łukasz; Szymański, Paweł; Tantry, Udaya; Navarese, Eliano P

Early treatment with inhibitors of P2Y12 receptor in patients with ST-segment elevation myocardial infarction - 2023 ESC recommendations and scientific evidence. Is clinical evidence sufficient to suggest a move towards precision medicine? The ELECTRA-SIRIO 2 investigators' viewpoint

对ST段抬高型心肌梗死患者早期应用P2Y12受体抑制剂治疗——2023年ESC指南及科学证据。临床证据是否足以支持精准医疗的推进?ELECTRA-SIRIO 2研究者的观点

Kubica, Jacek; Adamski, Piotr; Badariene, Jolita; Bonaca, Marc; Buszman, Piotr; Gabulova, Rahima; Gajda, Robert; Geisler, Tobias; Gil, Robert; Gorog, Diana A; Gurbel, Paul A; Hajdukiewicz, Tomasz; Hudzik, Bartosz; James, Stefan; Jeong, Young-Hoon; Kern, Adam; Kochman, Wacław; Kubica, Aldona; Kuliczkowski, Wiktor; Magielski, Przemysław; Niezgoda, Piotr; Ostrowska, Małgorzata; Raggi, Paolo; Rahimov, Uzeyir; Skonieczny, Grzegorz; Siller-Matula, Jolanta M; Specchia, Giuseppe; Szarpak, Łukasz; Szymański, Paweł; Tantry, Udaya; Umińska, Julia; Navarese, Eliano Pio

High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene

芬兰腭裂的高发病率和地理分布与 IRF6 基因有关

Fedik Rahimov #, Pekka Nieminen #, Priyanka Kumari #, Emma Juuri, Tiit Nikopensius, Kitt Paraiso, Jakob German, Antti Karvanen, Mart Kals, Abdelrahman G Elnahas, Juha Karjalainen, Mitja Kurki, Aarno Palotie; FinnGen; Estonian Biobank Research Team; Arja Heliövaara, Tõnu Esko, Sakari Jukarainen, Prii

Functional characterization of a single nucleotide polymorphism associated with Alzheimer's disease in a hiPSC-based neuron model

基于 hiPSC 的神经元模型中与阿尔茨海默病相关的单核苷酸多态性的功能表征

Lindsay R Stolzenburg, Sahar Esmaeeli, Ameya S Kulkarni, Erin Murphy, Taekyung Kwon, Christina Preiss, Lamiaa Bahnassawy, Joshua D Stender, Justine D Manos, Peter Reinhardt, Fedik Rahimov, Jeffrey F Waring, Cyril Y Ramathal

Risk factors in cardiovascular patients: Challenges and opportunities to improve secondary prevention

心血管疾病患者的危险因素:改善二级预防的挑战与机遇

Gabulova, Rahima; Marzà-Florensa, Anna; Rahimov, Uzeyir; Isayeva, Mahluga; Alasgarli, Shahana; Musayeva, Afag; Gahramanova, Sona; Ibrahimov, Firdovsi; Aliyev, Farid; Imanov, Galib; Rasulova, Rahmana; Vaartjes, Ilonca; Klipstein-Grobusch, Kerstin; Graham, Ian; Grobbee, Diederick E

Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesis

DUX4 错误表达的转基因斑马鱼模型揭示了其在 FSHD 发病机制中的发育作用

Anna Pakula, Angela Lek, Jeffrey Widrick, Hiroaki Mitsuhashi, Katlynn M Bugda Gwilt, Vandana A Gupta, Fedik Rahimov, June Criscione, Yuanfan Zhang, Devin Gibbs, Quinn Murphy, Anusha Manglik, Lillian Mead, Louis Kunkel

A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency

TFRC基因(编码转铁蛋白受体1)的错义突变会导致联合免疫缺陷。

Jabara, Haifa H; Boyden, Steven E; Chou, Janet; Ramesh, Narayanaswamy; Massaad, Michel J; Benson, Halli; Bainter, Wayne; Fraulino, David; Rahimov, Fedik; Sieff, Colin; Liu, Zhi-Jian; Alshemmari, Salem H; Al-Ramadi, Basel K; Al-Dhekri, Hasan; Arnaout, Rand; Abu-Shukair, Mohammad; Vatsayan, Anant; Silver, Eli; Ahuja, Sanjay; Davies, E Graham; Sola-Visner, Martha; Ohsumi, Toshiro K; Andrews, Nancy C; Notarangelo, Luigi D; Fleming, Mark D; Al-Herz, Waleed; Kunkel, Louis M; Geha, Raif S

CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies.

CD82 是人类肌肉卫星细胞的预期分离标志物,与肌营养不良症有关

Alexander Matthew S, Rozkalne Anete, Colletta Alessandro, Spinazzola Janelle M, Johnson Samuel, Rahimov Fedik, Meng Hui, Lawlor Michael W, Estrella Elicia, Kunkel Louis M, Gussoni Emanuela

MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms

MicroRNA-486 依赖的 DOCK3/PTEN/AKT 信号通路调节可改善肌营养不良症相关症状

Matthew S Alexander, Juan Carlos Casar, Norio Motohashi, Natássia M Vieira, Iris Eisenberg, Jamie L Marshall, Molly J Gasperini, Angela Lek, Jennifer A Myers, Elicia A Estrella, Peter B Kang, Frederic Shapiro, Fedik Rahimov, Genri Kawahara, Jeffrey J Widrick, Louis M Kunkel