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

Signal Override: Precision Editing of Protein Kinase Cα in Heart Failure

信号覆盖:心力衰竭中蛋白激酶Cα的精确编辑

Ratnavadivel, Sandra; Zhang, Jing; Sheikh, Farah

Connexin-43 Restoration Alleviates Desmosomal Arrhythmogenic Cardiomyopathy

连接蛋白-43的恢复可缓解桥粒性致心律失常性心肌病

Zhang, Jing; Zanella, Fabian; Ellis, Matthew W; Bradford, William H; Gutierrez-Lara, Erika Joana; Wang, Tsui-Min; Fujita, Kyohei; Duron, Charlize; Karakikes, Ioannis; Lyon, Robert C; Mezzano, Valeria; Roberts, Jason D; Carromeu, Cassiano; Gu, Yusu; Martin, Jody L; Muotri, Alysson R; Scheinman, Melvin M; Peterson, Kirk L; Sheikh, Farah

RhoGEF Ect2 supports RhoA activity at cell-cell junctions through desmoplakin

RhoGEF Ect2 通过桥粒斑蛋白在细胞间连接处支持 RhoA 的活性。

Zarkoob, Hoda; Kam, Chen Y; Koetsier, Jennifer L; McCarthy, Erin; Jaiganesh, Avinash; Kelsell, David P; Sheikh, Farah; Godsel, Lisa M; Green, Kathleen J

Taxing Hearts: TAX1BP3 Loss Stirs Up TRPV4 Channels in Arrhythmogenic Cardiomyopathy

心脏负担:TAX1BP3 缺失激活致心律失常性心肌病中的 TRPV4 通道

Ratnavadivel, Sandra; Jreije, Afaf; Sheikh, Farah

TMEM-ing the Tide: Gene Therapy Holds Promise for ARVC5

TMEM 引领潮流:基因疗法有望治愈 ARVC5

Ratnavadivel, Sandra; Ellis, Matthew W; Sheikh, Farah

Combined Loss of Obsc and Obsl1 in Murine Hearts Results in Diastolic Dysfunction, Altered Metabolism, and Deregulated Mitophagy

小鼠心脏中 Obsc 和 Obsl1 的联合缺失会导致舒张功能障碍、代谢改变和线粒体自噬失调

Fujita, Kyohei; Desmond, Patrick; Blondelle, Jordan; Soták, Matúš; Rajan, Meenu Rohini; Clark, Madison; Estève, Éric; Chan, Yunghang; Gu, Yusu; Actis Dato, Virginia; Marrocco, Valeria; Dalton, Nancy D; Ghassemian, Majid; Do, Aryanne; Klos, Matthew; Peterson, Kirk L; Sheikh, Farah; Cho, Yoshitake; Börgeson, Emma; Lange, Stephan

Preclinical efficacy and safety of AAVrh10-based plakophilin-2 gene therapy (LX2020) as a treatment for arrhythmogenic cardiomyopathy.

基于 AAVrh10 的 plakophilin-2 基因疗法 (LX2020) 治疗致心律失常性心肌病的临床前疗效和安全性

Zhang Jing, Gutierrez-Lara Erika Joana, Do Aryanne, Nguyen Lena, Nair Anju, Selvan Nithya, Fenn Tim, Adler Eric, Khanna Richie, Sheikh Farah

Disease penetrance and phenotypic spectrum of desmoplakin variant carriers in the population

人群中桥粒斑蛋白变异携带者的疾病外显率和表型谱

Gurumoorthi, Manasa; Dabbagh, Ghaith Sharaf; Wolfe, Rachel; Hesse, Kerrick; Shah, Ravi; Kurzlechner, Leonie; Yadav, Kanishk; Balint, Brittany; Asatryan, Babken; Sheikh, Farah; Chahal, C Anwar A; Landstrom, Andrew P

Association of RhoGEF Ect2 with Desmoplakin Supports RhoA Activity at Intercellular Junctions: Implications for Carvajal Disease

RhoGEF Ect2 与桥粒蛋白的结合支持细胞间连接处的 RhoA 活性:对卡瓦哈尔病的影响

Zarkoob, Hoda; Kam, Chen Yuan; Koetsier, Jennifer; Jaiganesh, Avinash; McCarthy, Erin; Kelsell, David; Sheikh, Farah; Godsel, Lisa M; Green, Kathleen J

Massive middle cerebral artery stroke in a young patient with a large Chiari network and possible patent foramen ovale: A case report

一例年轻患者发生大面积大脑中动脉卒中,伴有大面积Chiari畸形网和可能的卵圆孔未闭:病例报告

Ahmed, Said Abdirahman; Adam, Bakar Ali; Abdi, Ahmed Elmi; Waberi, Mohamud Mire; Abdi, Ishak Ahmed; Mohamud, Mohamed Abdullahi; Hassan, Mohamed Sheikh; Farah, Osman Dahir; Aadan, Shafici Ahmed; Mohamed, Yahye Garad; Hassan, Mohamed Omar