2021
DOI: 10.1109/access.2021.3082174
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In Silico Investigation of CACNA2D1 S755T Mutation Associated With Short QT Syndrome

Abstract: Short QT syndrome (SQTS) is a genetic disease characterized by constantly short QT intervals and high risks of sudden death. SQTS6 is one of the identified SQTS genotype variants associated with the CACNA2D1 S755T mutation. However, the pathogenesis of SQTS induced arrhythmias remains unclear. To identify the underlying mechanisms of SQTS6 induced arrhythmias, a multi-scale human ventricle model comprising cell to organ levels was built. Cellular data was fitted at the cell level to reproduce the electrophysio… Show more

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“…This approach is similar to the approaches outlined in Feng ( 2021 ), Liu et al ( 2020 ), Frésard ( 2020 ), Meneghetti et al ( 2020 ) and Xia ( 2022 ). Recent years have seen a rise in the use of CNN-transformer hybrid models for the segmentation of multimodal brain tumors as well as other 2D and 3D medical images (Vukicevic 2020 ; Zhang et al 2021 ).…”
Section: Review Of Existing Multiorgan Disease Detection Techniquesmentioning
confidence: 99%
“…This approach is similar to the approaches outlined in Feng ( 2021 ), Liu et al ( 2020 ), Frésard ( 2020 ), Meneghetti et al ( 2020 ) and Xia ( 2022 ). Recent years have seen a rise in the use of CNN-transformer hybrid models for the segmentation of multimodal brain tumors as well as other 2D and 3D medical images (Vukicevic 2020 ; Zhang et al 2021 ).…”
Section: Review Of Existing Multiorgan Disease Detection Techniquesmentioning
confidence: 99%