Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Zhenxing Liao"'
Autor:
Yingrui Li, Hendrik Dinkel, Dalia Pakalniskyte, Alexandra Viktoria Busley, Lukas Cyganek, Rujia Zhong, Feng Zhang, Qiang Xu, Lasse Maywald, Assem Aweimer, Mengying Huang, Zhenxing Liao, Zenghui Meng, Chen Yan, Timo Prädel, Lena Rose, Alexander Moscu‐Gregor, Alyssa Hohn, Zhen Yang, Lin Qiao, Andreas Mügge, Xiaobo Zhou, Ibrahim Akin, Ibrahim El‐Battrawy
Publikováno v:
Clinical and Translational Medicine, Vol 13, Iss 3, Pp n/a-n/a (2023)
Abstract Background Brugada syndrome (BrS) is causing sudden cardiac death (SCD) mainly at young age. Studying the underlying mechanisms associated with BrS type I electrocardiogram (ECG) changes in the presence of fever and roles of autophagy for Br
Externí odkaz:
https://doaj.org/article/c96503a7f7184eef92bef287fc6cc881
Autor:
Mengying Huang, Zhenxing Liao, Xin Li, Zhen Yang, Xuehui Fan, Yingrui Li, Zhihan Zhao, Siegfried Lang, Lukas Cyganek, Xiaobo Zhou, Ibrahim Akin, Martin Borggrefe, Ibrahim El-Battrawy
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Aims: The short QT syndrome type 1 (SQT1) is linked to hERG channel mutations (e.g., N588K). Drug effects on hERG channel gating kinetics in SQT1-cells have not been investigated.Methods: This study used hiPSC-CMs of a healthy donor and a SQT1-patien
Externí odkaz:
https://doaj.org/article/2f5fe5842def4a55bdbdf25d5c1e9677
Autor:
Rujia Zhong, Theresa Schimanski, Feng Zhang, Huan Lan, Alyssa Hohn, Qiang Xu, Mengying Huang, Zhenxing Liao, Lin Qiao, Zhen Yang, Yingrui Li, Zhihan Zhao, Xin Li, Lena Rose, Sebastian Albers, Lasse Maywald, Jonas Müller, Hendrik Dinkel, Ardan Saguner, Johannes W. G. Janssen, Narasimha Swamy, Yannick Xi, Siegfried Lang, Mandy Kleinsorge, Firat Duru, Xiaobo Zhou, Sebastian Diecke, Lukas Cyganek, Ibrahim Akin, Ibrahim El-Battrawy
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 15, p 8313 (2022)
Aims: Some gene variants in the sodium channels, as well as calcium channels, have been associated with Brugada syndrome (BrS). However, the investigation of the human cellular phenotype and the use of drugs for BrS in presence of variant in the calc
Externí odkaz:
https://doaj.org/article/0fc5cabdcf3c4f0d9c2e49983942d643
Autor:
Zhenxing Liao, Yingrui Li, Xuehui Fan, Zhen Yang, Ibrahim El-Battrawy, Xiaobo Zhou, Ibrahim Akin
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 4, p 119 (2022)
Studies have suggested a connection between inflammation and arrhythmogenesis of Brugada syndrome (BrS). However, experimental studies regarding the roles of inflammation in the arrhythmogenesis of BrS and its underlying mechanism are still lacking.
Externí odkaz:
https://doaj.org/article/dff0f1cd0bb6462ebab5f42c0d5f2328
Autor:
Ibrahim El-Battrawy, Jonas Müller, Zhihan Zhao, Lukas Cyganek, Rujia Zhong, Feng Zhang, Mandy Kleinsorge, Huan Lan, Xin Li, Qiang Xu, Mengying Huang, Zhenxing Liao, Alexander Moscu-Gregor, Sebastian Albers, Hendrik Dinkel, Siegfried Lang, Sebastian Diecke, Wolfram-Hubertus Zimmermann, Jochen Utikal, Thomas Wieland, Martin Borggrefe, Xiaobo Zhou, Ibrahim Akin
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
BackgroundAmong rare channelopathies BrS patients are at high risk of sudden cardiac death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations including SCN1B have been implicated to BrS. Studying the human cellular p
Externí odkaz:
https://doaj.org/article/e4d847f1203f41bca3784f5844070f87
Autor:
Farbod Sedaghat-Hamedani, Sabine Rebs, Ibrahim El-Battrawy, Safak Chasan, Tobias Krause, Jan Haas, Rujia Zhong, Zhenxing Liao, Qiang Xu, Xiaobo Zhou, Ibrahim Akin, Edgar Zitron, Norbert Frey, Katrin Streckfuss-Bömeke, Elham Kayvanpour
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 23, p 12990 (2021)
Introduction: Familial dilated cardiomyopathy (DCM) is clinically variable and has been associated with mutations in more than 50 genes. Rapid improvements in DNA sequencing have led to the identification of diverse rare variants with unknown signifi
Externí odkaz:
https://doaj.org/article/378146170755471f826219b3da298792
Autor:
Xiaoxi Zhang, Yunbin Hu, Carlos R. Lien-Medrano, Juan Li, Jinping Shi, Xinshun Qin, Zhenxing Liao, Yan Wang, Zishu Wang, Jiawei Li, Jianing Chen, Guangyu Zhang, Johannes V. Barth, Thomas Frauenheim, Willi Auwärter, Akimitsu Narita, Klaus Müllen, Carlos-Andres Palma
Publikováno v:
Journal of the American Chemical Society. 145:8757-8763
Autor:
Yingrui Li, Lena Rose, Timo Prädel, Mandy Kleinsorge, Xuehui Fan, Zhenxing Liao, Hendrik Dinkel, Alexandra Viktoria Busley, Rujia Zhong, Feng Zhang, Qiang Xu, Lasse Maywald, Assem Aweimer, Mengying Huang, Alexander Moscu-Gregor, Nazha Hamdani, Alyssa Hohn, Zhen Yang, Lin Qiao, Andreas Mügge, Lukas Cyganek, Xiaobo Zhou, Ibrahim Akin, Ibrahim PD. Dr. El-Battrawy
Publikováno v:
SSRN Electronic Journal.
Autor:
Ibrahim El‐Battrawy, Huan Lan, Lukas Cyganek, Lasse Maywald, Rujia Zhong, Feng Zhang, Qiang Xu, Jihyun Lee, Eliane Duperrex, Andreas Hierlemann, Ardan M. Saguner, Firat Duru, Boldizsar Kovacs, Mengying Huang, Zhenxing Liao, Sebastian Albers, Jonas Müller, Hendrik Dinkel, Lena Rose, Alyssa Hohn, Zhen Yang, Lin Qiao, Yingrui Li, Siegfried Lang, Mandy Kleinsorge, Andreas Mügge, Assem Aweimer, Xuehui Fan, Sebastian Diecke, Ibrahim Akin, Guang Li, Xiaobo Zhou
Publikováno v:
Clinical and Translational Medicine, 11 (12)
Clinical and Translational Medicine
Clinical and Translational Medicine
Clinical and Translational Medicine, 11 (12)
ISSN:2001-1326
ISSN:2001-1326
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cdacc094f9e5669c1b113fdc898aae5
https://hdl.handle.net/20.500.11850/528688
https://hdl.handle.net/20.500.11850/528688
Autor:
Xiaobo Zhou, Zhihan Zhao, Sebastian Diecke, Martin Borggrefe, Huan Lan, Qiang Xu, Xin Li, Mengying Huang, Siegfried Lang, Jochen Utikal, Wolfram-Hubertus Zimmermann, Ibrahim El-Battrawy, Thomas Wieland, Sebastian Albers, Rujia Zhong, Hendrik Dinkel, Zhenxing Liao, Mandy Kleinsorge, Boris Rudic, Ibrahim Akin, Lukas Cyganek, Jonas Müller
Publikováno v:
EP Europace. 21:1410-1421
Aims Brugada syndrome (BrS) is associated with a pronounced risk to develop sudden cardiac death (SCD). Up to 21% of patients are related to mutations in SCN5A. Studies identified SCN10A as a contributor of BrS. However, the investigation of the huma