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

Targeting miRNA-1a and miRNA-15b: A Novel Combinatorial Strategy to Drive Adult Cardiac Regeneration.

靶向 miRNA-1a 和 miRNA-15b:一种促进成人心脏再生的新型组合策略

Yuan Ting, Wu Meiqian, Zhu Chaonan, Yu Hao, Pham Minh Duc, Bottermann Katharina, Mao Yijie, Wang Yue, Langner Mathias, Peitzsch Mirko, Das Arka Provo, Kauferstein Silke, Ward Jonathan, Mirtschink Peter, Zeiher Andreas Michael, Dimmeler Stefanie, Krishnan Jaya

From rare events to systematic data collection: the RESCUED registry for sudden cardiac death in the young in Germany

从罕见事件到系统性数据收集:德国青年猝死登记研究(RESCUED)

Barkauskas, Renaldas; Jenewein, Tina; Scheiper-Welling, Stefanie; Wilmes, Verena; Niess, Constanze; Petzel-Witt, Silvana; Reitz, Alexandra; Gradhand, Elise; Falagkari, Anastasia; Papathanasiou, Maria; Wakili, Reza; Leistner, David M; Vasseur, Jessica; Göbel, Jens; Storf, Holger; Toennes, Stefan W; Kettner, Matthias; Verhoff, Marcel A; Beckmann, Britt-Maria; Kauferstein, Silke; Corvest, Eva

Cardiac dysfunction related to cardiac mRNA and protein traffic impairment due to reduced unconventional motor protein myosin-5b expression

心脏功能障碍与心脏mRNA和蛋白质运输受损有关,这是由于非常规运动蛋白肌球蛋白-5b表达降低所致。

Heimerl, Maren; Erschow, Sergej; Müller-Olling, Mirco; Manstein, Dietmar J; Decher, Niels; Kauferstein, Silke; Jenewein, Tina; Pich, Andreas; Ricke-Hoch, Melanie; Hilfiker-Kleiner, Denise

Correction: "Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders"

更正:“对遗传性心律失常患者中意义不明的变异进行重新评估”

Martin, Sarah; Jenewein, Tina; Geisen, Christof; Scheiper-Welling, Stefanie; Kauferstein, Silke

"Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders"

“对遗传性心律失常患者中意义不明的变异进行重新评估”

Martin, Sarah; Jenewein, Tina; Geisen, Christof; Scheiper-Welling, Stefanie; Kauferstein, Silke

Can wearables outscore general practitioners? Congenital long QT syndrome diagnosis initiated by a smartwatch

可穿戴设备能否超越全科医生?智能手表促成了先天性长QT间期综合征的诊断

Rudic, Boris; Kauferstein, Silke; Akin, Ibrahim; Borggrefe, Martin

Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome KCNQ1 Variants

对一系列新型Romano-Ward综合征KCNQ1变异体进行功能表征

Rinné, Susanne; Oertli, Annemarie; Nagel, Claudia; Tomsits, Philipp; Jenewein, Tina; Kääb, Stefan; Kauferstein, Silke; Loewe, Axel; Beckmann, Britt Maria; Decher, Niels

Telemedical monitoring in patients with inborn cardiac disease - experience of a tertiary care centre

远程医疗监测在先天性心脏病患者中的应用——一家三级医疗中心的经验

Westphal, Dominik S; Federle, David; Steger, Alexander; Vodermeier, Tanja; Scheiper-Welling, Stefanie; Jenewein, Tina; Beckmann, Britt-Maria; Kauferstein, Silke; Martens, Eimo; Hahn, Franziska

Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by Involving an Integrin-αVβ6/TGF-β Signaling Cascade

桥粒黏附缺陷通过整合素-αVβ6/TGF-β信号级联反应导致致心律失常性心肌病

Schinner, Camilla; Xu, Lifen; Franz, Henriette; Zimmermann, Aude; Wanuske, Marie-Therès; Rathod, Maitreyi; Hanns, Pauline; Geier, Florian; Pelczar, Pawel; Liang, Yan; Lorenz, Vera; Stüdle, Chiara; Maly, Piotr I; Kauferstein, Silke; Beckmann, Britt M; Sheikh, Farah; Kuster, Gabriela M; Spindler, Volker

Variant interpretation in molecular autopsy: a useful dilemma

分子尸检中的变异解读:一个有用的难题

Scheiper-Welling, Stefanie; Tabunscik, Monika; Gross, Theresa E; Jenewein, Tina; Beckmann, Britt M; Niess, Constanze; Gradhand, Elise; Wunder, Cora; Schneider, Peter M; Rothschild, Markus A; Verhoff, Marcel A; Kauferstein, Silke