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Maturation of hiPSC-derived cardiomyocytes in cardiac microtissues promotes adult alternative splicing of sodium channel revealing mutation effects associated with cardiac arrhythmia.

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Title: Maturation of hiPSC-derived cardiomyocytes in cardiac microtissues promotes adult alternative splicing of sodium channel revealing mutation effects associated with cardiac arrhythmia.
Authors: Campostrini, G1 (AUTHOR), Oostwaard, D Ward-Van1 (AUTHOR), Kosmidis, G1 (AUTHOR), Verkerk, AO2 (AUTHOR), Bezzina, CR2 (AUTHOR), Mummery, CL1 (AUTHOR), Bellin, M1 (AUTHOR)
Source: Cardiovascular Research. 2022 Supplement, Vol. 118, p1-1. 1p.
Database: Academic Search Ultimate
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  Data: Maturation of hiPSC-derived cardiomyocytes in cardiac microtissues promotes adult alternative splicing of sodium channel revealing mutation effects associated with cardiac arrhythmia.
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  Data: <searchLink fieldCode="JN" term="%22Cardiovascular+Research%22">Cardiovascular Research</searchLink>. 2022 Supplement, Vol. 118, p1-1. 1p.
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        Value: 10.1093/cvr/cvac066.020
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      – Code: eng
        Text: English
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      – TitleFull: Maturation of hiPSC-derived cardiomyocytes in cardiac microtissues promotes adult alternative splicing of sodium channel revealing mutation effects associated with cardiac arrhythmia.
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            NameFull: Oostwaard, D Ward-Van
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            NameFull: Kosmidis, G
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            – D: 02
              M: 06
              Text: 2022 Supplement
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              Y: 2022
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              Value: 118
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