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The W101C KCNJ5 Mutation Induces Slower Pacing by Constitutively Active GIRK Channels in hiPSC-Derived Cardiomyocytes.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 20, p. 15290, doi. 10.3390/ijms242015290
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- Publication type:
- Article
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 22, p. 14215, doi. 10.3390/ijms232214215
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- Publication type:
- Article
The Disease-Specific Phenotype in Cardiomyocytes Derived from Induced Pluripotent Stem Cells of Two Long QT Syndrome Type 3 Patients.
- Published in:
- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0083005
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- Publication type:
- Article
Effect of lovastatin on coxsackievirus B3 infection in human endothelial cells.
- Published in:
- Inflammation Research, 2014, v. 63, n. 4, p. 267, doi. 10.1007/s00011-013-0695-z
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- Publication type:
- Article
In vitro Modeling of Ryanodine Receptor 2 Dysfunction Using Human Induced Pluripotent Stem Cells.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2011, v. 28, n. 4, p. 579, doi. 10.1159/000335753
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- Publication type:
- Article
A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations.
- Published in:
- 2021
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- Publication type:
- journal article
Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease–Causing Mutation.
- Published in:
- Journal of the American Heart Association, 2017, v. 6, n. 7, p. 1, doi. 10.1161/JAHA.116.005135
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- Publication type:
- Article
Detection of Patients with Congenital and Often Concealed Long-QT Syndrome by Novel Deep Learning Models.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 7, p. 1135, doi. 10.3390/jpm12071135
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- Publication type:
- Article
An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteins.
- Published in:
- European Heart Journal, 2020, v. 41, n. 30, p. 2878, doi. 10.1093/eurheartj/ehaa383
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- Publication type:
- Article
Case report: cosegregation of a TPM1 in-frame deletion (p.Lys7del) with familial non-compaction cardiomyopathy (NCCM).
- Published in:
- 2024
- By:
- Publication type:
- Letter
Long, longer, long QT syndrome: what makes the difference?
- Published in:
- Cardiovascular Research, 2021, v. 117, n. 3, p. 637, doi. 10.1093/cvr/cvab025
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- Publication type:
- Article