Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
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Published in Genetics in medicine (01.01.2021)
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Published in Circulation (New York, N.Y.) (28.07.2020)
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Neonatal Wnt-dependent Lgr5 positive stem cells are essential for uterine gland development
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A computational analysis of the effect of sevoflurane in a human ventricular cell model of long QT syndrome: Importance of repolarization reserve in the QT-prolonging effect of sevoflurane
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Bradycardia Is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations
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Published in Internal Medicine (01.07.2018)
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Published in Circulation Journal (25.10.2022)
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Novel CACNA1C R511Q mutation, located in domain Ⅰ-Ⅱ linker, causes non-syndromic type-8 long QT syndrome
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Published in Journal of the American College of Cardiology (25.08.2009)
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Published in Heart rhythm (01.05.2010)
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Published in Frontiers in physiology (19.07.2024)
Published in Frontiers in physiology (19.07.2024)
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Oyama, Kotaro, Zeeb, Vadim, Kawamura, Yuki, Arai, Tomomi, Gotoh, Mizuho, Itoh, Hideki, Itabashi, Takeshi, Suzuki, Madoka, Ishiwata, Shin'ichi
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