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

Illuminating Cardiac Remodeling: Insights From [18F]-Fluorodeoxyglucose Positron Emission Tomography Imaging in Plakoglobin-Associated Arrhythmogenic Cardiomyopathy

揭示心脏重塑:来自[18F]-氟代脱氧葡萄糖正电子发射断层扫描成像在斑珠蛋白相关致心律失常性心肌病中的启示

Tatjana Williams ,Regina Groß ,Anahi-Paula Arias-Loza ,Peter Nordbeck ,Mike Noerpel ,Alexandra Cirnu ,Laura Kimmel ,DiyaaEldin Ashour ,Gustavo Ramos ,Jens Waschke ,Takahiro Higuchi ,Brenda Gerull

EGFR inhibition leads to enhanced desmosome assembly and cardiomyocyte cohesion via ROCK activation

EGFR 抑制通过激活 ROCK 导致桥粒组装和心肌细胞凝聚力增强

Maria Shoykhet, Orsela Dervishi, Philipp Menauer, Matthias Hiermaier, Sina Moztarzadeh, Colin Osterloh, Ralf J Ludwig, Tatjana Williams, Brenda Gerull, Stefan Kääb, Sebastian Clauss, Dominik Schüttler, Jens Waschke, Sunil Yeruva

Plakophilin 2 regulates intestinal barrier function by modulating protein kinase C activity in vitro

Plakophilin 2 通过体外调节蛋白激酶 C 活性来调节肠道屏障功能

Simon Nagler, Yalda Ghoreishi, Catherine Kollmann, Matthias Kelm, Brenda Gerull, Jens Waschke, Natalie Burkard, Nicolas Schlegel

Altered Expression of TMEM43 Causes Abnormal Cardiac Structure and Function in Zebrafish

TMEM43 表达改变导致斑马鱼心脏结构和功能异常

Miriam Zink, Anne Seewald, Mareike Rohrbach, Andreas Brodehl, Daniel Liedtke, Tatjana Williams, Sarah J Childs, Brenda Gerull

CRISPR/Cas9-edited PKP2 knock-out (JMUi001-A-2) and DSG2 knock-out (JMUi001-A-3) iPSC lines as an isogenic human model system for arrhythmogenic cardiomyopathy (ACM)

CRISPR/Cas9 编辑的 PKP2 敲除 (JMUi001-A-2) 和 DSG2 敲除 (JMUi001-A-3) iPSC 系作为心律失常性心肌病 (ACM) 的同源人类模型系统

Anna Janz, Miriam Zink, Alexandra Cirnu, Annika Hartleb, Christina Albrecht, Simone Rost, Eva Klopocki, Katharina Günther, Frank Edenhofer, Süleyman Ergün, Brenda Gerull

Investigating LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes

利用人诱导多能干细胞衍生的心肌细胞研究LMNA相关扩张型心肌病

Yuval Shemer ,Lucy N Mekies ,Ronen Ben Jehuda ,Polina Baskin ,Rita Shulman ,Binyamin Eisen ,Danielle Regev ,Eloisa Arbustini ,Brenda Gerull ,Mihaela Gherghiceanu ,Eyal Gottlieb ,Michael Arad ,Ofer Binah

A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy

与心律失常性心肌病相关的纯合 DSC2 缺失是由单亲同源性引起的

Andreas Brodehl, Jürgen Weiss, Jana Davina Debus, Caroline Stanasiuk, Bärbel Klauke, Marcus André Deutsch, Henrik Fox, Jördis Bax, Hans Ebbinghaus, Anna Gärtner, Jens Tiesmeier, Thorsten Laser, Andreas Peterschröder, Brenda Gerull, Jan Gummert, Lech Paluszkiewicz, Hendrik Milting

Generation of two patient-derived iPSC lines from siblings (LIBUCi001-A and LIBUCi002-A) and a genetically modified iPSC line (JMUi001-A-1) to mimic dilated cardiomyopathy with ataxia (DCMA) caused by a homozygous DNAJC19 mutation

从兄弟姐妹中生成两个患者来源的 iPSC 系(LIBUCi001-A 和 LIBUCi002-A)和一个转基因 iPSC 系(JMUi001-A-1),以模拟由纯合 DNAJC19 突变引起的扩张型心肌病伴共济失调 (DCMA)

Anna Janz, Ruping Chen, Martina Regensburger, Yuichiro Ueda, Simone Rost, Eva Klopocki, Katharina Günther, Frank Edenhofer, Henry J Duff, Süleyman Ergün, Brenda Gerull

Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype

MYH7 和 MYBPC3 的双等位基因突变导致具有左心室心肌致密化不全表型的严重心肌病

Konstantinos Kolokotronis, Jirko Kühnisch, Eva Klopocki, Josephine Dartsch, Simone Rost, Cathleen Huculak, Giulia Mearini, Stefan Störk, Lucie Carrier, Sabine Klaassen, Brenda Gerull

Mitofusin 2 Is Essential for IP3-Mediated SR/Mitochondria Metabolic Feedback in Ventricular Myocytes

线粒体融合蛋白 2 对心室肌细胞中 IP3 介导的 SR/线粒体代谢反馈至关重要

Lea K Seidlmayer, Christine Mages, Annette Berbner, Petra Eder-Negrin, Paula Anahi Arias-Loza, Mathias Kaspar, Moshi Song, Gerald W Dorn II, Michael Kohlhaas, Stefan Frantz, Christoph Maack, Brenda Gerull, Elena N Dedkova