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

Rational design, synthesis, and evaluation of novel polypharmacological compounds targeting Na(V)1.5, K(V)1.5, and K(2)P channels for atrial fibrillation.

针对 Na(V)1.5、K(V)1.5 和 K(2)P 通道治疗心房颤动的新型多药理化合物的合理设计、合成和评价

Camargo-Ayala Lorena, Bedoya Mauricio, Dasí Albert, Prüser Merten, Schütte Sven, Prent-Peñaloza Luis, Adasme-Carreño Francisco, Kiper Aytug K, Rinné Susanne, Camargo-Ayala Paola Andrea, Peña-Martínez Paula A, Bueno-Orovio Alfonso, Varela Diego, Wiedmann Felix, Márquez Montesinos José C E, Mazola Yuliet, Venturini Whitney, Zúñiga Rafael, Zúñiga Leandro, Schmidt Constanze, Rodriguez Blanca, Ravens Ursula, Decher Niels, Gutiérrez Margarita, González Wendy

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

Ion occupancy of the selectivity filter controls opening of a cytoplasmic gate in the K(2P) channel TALK-2

选择性过滤器的离子占据控制着K(2P)通道TALK-2中胞质门的开放。

Neelsen, Lea C; Riel, Elena B; Rinné, Susanne; Schmid, Freya-Rebecca; Jürs, Björn C; Bedoya, Mauricio; Langer, Jan P; Eymsh, Bisher; Kiper, Aytug K; Cordeiro, Sönke; Decher, Niels; Baukrowitz, Thomas; Schewe, Marcus

A novel KCNC3 gene variant in the voltage-dependent Kv3.3 channel in an atypical form of SCA13 with dominant central vertigo

一种新型的KCNC3基因变异,存在于电压依赖性Kv3.3通道中,与一种非典型SCA13型疾病(以中枢性眩晕为主)相关

Bernhard, Felix P; Schütte, Sven; Heidenblut, Moritz; Oehme, Moritz; Rinné, Susanne; Decher, Niels

Correction: Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking

更正:POPDC蛋白突变对异源相互作用和膜转运的不同影响

Swan, Alexander H; Schindler, Roland F R; Savarese, Marco; Mayer, Isabelle; Rinné, Susanne; Bleser, Felix; Schänzer, Anne; Hahn, Andreas; Sabatelli, Mario; Perna, Francesco; Chapman, Kathryn; Pfuhl, Mark; Spivey, Alan C; Decher, Niels; Udd, Bjarne; Tasca, Giorgio; Brand, Thomas

Cloxyquin activates hTRESK by allosteric modulation of the selectivity filter

氯喹通过变构调节选择性过滤器来激活hTRESK。

Schreiber, Julian Alexander; Derksen, Anastasia; Goerges, Gunnar; Schütte, Sven; Sörgel, Jasmin; Kiper, Aytug K; Strutz-Seebohm, Nathalie; Ruck, Tobias; Meuth, Sven G; Decher, Niels; Seebohm, Guiscard

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

Calcium Handling Remodeling Underlies Impaired Sympathetic Stress Response in Ventricular Myocardium from Cacna1c Haploinsufficient Rats

Cacna1c单倍体不足大鼠心室肌交感神经应激反应受损的根本原因是钙处理重塑

Fender, Hauke; Walter, Kim; Kiper, Aytug K; Plačkić, Jelena; Kisko, Theresa M; Braun, Moria D; Schwarting, Rainer K W; Rohrbach, Susanne; Wöhr, Markus; Decher, Niels; Kockskämper, Jens

Common Structural Pattern for Flecainide Binding in Atrial-Selective K(v)1.5 and Na(v)1.5 Channels: A Computational Approach

心房选择性K(v)1.5和Na(v)1.5通道中氟卡尼结合的常见结构模式:一种计算方法

Mazola, Yuliet; Márquez Montesinos, José C E; Ramírez, David; Zúñiga, Leandro; Decher, Niels; Ravens, Ursula; Yarov-Yarovoy, Vladimir; González, Wendy

Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy

全外显子组测序发现Cav1.3基因CACNA1D中的杂合变异与家族性窦房结功能障碍和局灶性特发性癫痫相关

Rinné, Susanne; Stallmeyer, Birgit; Pinggera, Alexandra; Netter, Michael F; Matschke, Lina A; Dittmann, Sven; Kirchhefer, Uwe; Neudorf, Ulrich; Opp, Joachim; Striessnig, Jörg; Decher, Niels; Schulze-Bahr, Eric