Clinical and genetic characteristics of myotonia congenita in Chinese population by Yuting He, Yusen Qiu, Ying Xiong, Yu Shen, Kaiyan Jiang, Hancun Yi, Pengcheng Huang, Yu Zhu, Min Zhu, Meihong Zhou, Daojun Hong, Dandan Tan

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Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic Diagnostics by Maria Gnazzo, Giovanni Parlapiano, Francesca Di Lorenzo, Daniele Perrino, Silvia Genovese, Valentina Lanari, Daniela Righi, Federica Calì, Massimo Stefano Silvetti, Elena Falcone, Alessia Bauleo, Fabrizio Drago, Antonio Novelli, Anwar Baban

Subjects: “…channelopathies…”
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Characterization of four structurally diverse inhibitors of SUR2-containing KATP channels by Kangjun Li, Vaishali Satpute Janve, Jerod Denton

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Comprehensive Diagnostic Work-Up for Uncovering the Causes of Sudden Cardiac Death: The Role of Family Members by Emanuele Monda, Gaetano Diana, Daniele Bruno, Marta Rubino, Giuseppe Palmiero, Federica Verrillo, Chiara Cirillo, Annapaola Cirillo, Adelaide Fusco, Martina Caiazza, Santo Dellegrottaglie, Diego Colonna, Berardo Sarubbi, Pietro Buono, Maria Giovanna Russo, Giuseppe Limongelli

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Periodic paralysis across the life course: age-related phenotype transition and sarcopenia overlap by Karen Suetterlin, Karen Suetterlin, Sinead Law, William David Arnold, William David Arnold, William David Arnold, William David Arnold

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Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy by Timothy J Abreo, Emma C Thompson, Anuraag Madabushi, Kristen L Park, Heun Soh, Nissi Varghese, Carlos G Vanoye, Kristen Springer, Jim Johnson, Scotty Sims, Zhigang Ji, Ana G Chavez, Miranda J Jankovic, Bereket Habte, Aamir R Zuberi, Cathleen M Lutz, Zhao Wang, Vaishnav Krishnan, Lisa Dudler, Stephanie Einsele-Scholz, Jeffrey L Noebels, Alfred L George, Atul Maheshwari, Anastasios Tzingounis, Edward C Cooper

Subjects: “…channelopathy…”
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Ion channels research in hPSC-RPE cells: bridging benchwork to clinical applications by Ping Xu, Weisheng Zou, Wenjing Yin, Guifu Chen, Guanjie Gao, Xiufeng Zhong

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Fetal bradycardia associated with left ventricle noncompaction diagnosed as HCN4 mutations by Kosuke Yonehara

Subjects: “…cardiac channelopathy…”
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Pin1 promotes human CaV2.1 channel polyubiquitination by RNF138: pathophysiological implication for episodic ataxia type 2 by Ssu-Ju Fu, Kai-Min Cheng, Cheng-Tsung Hsiao, Ya-Ching Fang, Chung-Jiuan Jeng, Chih-Yung Tang

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Evaluation of four KCNMA1 channelopathy variants on BK channel current under CaV1.2 activation by Ria L. Dinsdale, Andrea L. Meredith

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