| Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndrome T Aizawa, Y Wada, K Hasegawa, H Huang, T Imamura, J Gao, A Kashiwa, ... Europace 25 (4), 1491-1499, 2023 | 17 | 2023 |
| Novel Calmodulin Variant p. E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent … J Gao, T Makiyama, Y Yamamoto, T Kobayashi, H Aoki, TL Maurissen, ... Circulation: Arrhythmia and Electrophysiology 16 (3), e011387, 2023 | 11 | 2023 |
| Disrupted CaV1. 2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model A Kashiwa, T Makiyama, H Kohjitani, TL Maurissen, T Ishikawa, ... Heart rhythm 20 (1), 89-99, 2023 | 6 | 2023 |
| KCNQ1 Channel Dysfunction in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Carrying a CALM2-N98S Mutation Associated With Long QT … Y Yamamoto, TM Makiyama, Y Wuriyanghai, H Kohjitani, S Hirose, J Gao, ... Circulation 140 (Suppl_1), A13222-A13222, 2019 | | 2019 |
| P5025 Structural insights into catecholaminergic polymorphic ventricular tachycardia-associated RyR2 mutant channels using a three-dimensional in silico model J Gao, T Makiyama, S Ohno, Y Yamamoto, Y Wuriyanghai, H Kohjitani, ... European Heart Journal 40 (Supplement_1), ehz746. 0203, 2019 | | 2019 |
