Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy.
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Genetics of Brugada syndromeIncidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1.Alternative Isoform Analysis of Ttc8 Expression in the Rat Pineal Gland Using a Multi-Platform Sequencing Approach Reveals Neural RegulationA flow cytometry-based screen identifies MBNL1 modulators that rescue splicing defects in myotonic dystrophy type I.Dysregulation of mRNA Localization and Translation in Genetic DiseaseImaging cardiac SCN5A using the novel F-18 radiotracer radiocaine.Playing hide and seek with repeats in local and global de novo transcriptome assembly of short RNA-seq reads.Gene Expression Networks in the Murine Pulmonary Myocardium Provide Insight into the Pathobiology of Atrial Fibrillation.Conservation of alternative splicing in sodium channels reveals evolutionary focus on release from inactivation and structural insights into gating.Emerging roles for RNA-binding proteins as effectors and regulators of cardiovascular disease.Alternative splicing as a regulator of development and tissue identity.Optical Mapping Approaches on Muscleblind-Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy.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.Alternative Splicing of Four Trafficking Genes Regulates Myofiber Structure and Skeletal Muscle PhysiologyExpression of voltage-gated sodium channel Nav1.5 in non-metastatic colon cancer and its associations with estrogen receptor (ER)-β expression and clinical outcomes.Syncope and the risk of sudden cardiac death: Evaluation, management, and prevention.Developmentally regulated alternative splicing is perturbed in type 1 diabetic skeletal muscle.Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome.Misregulation of calcium-handling proteins promotes hyperactivation of calcineurin-NFAT signaling in skeletal muscle of DM1 mice.Complementarity of assembly-first and mapping-first approaches for alternative splicing annotation and differential analysis from RNAseq data.Daunorubicin reduces MBNL1 sequestration caused by CUG-repeat expansion and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy.rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences.Cells of Matter-In Vitro Models for Myotonic Dystrophy.
P2860
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P2860
Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Splicing misregulation of SCN5 ...... hythmia in myotonic dystrophy.
@en
type
label
Splicing misregulation of SCN5 ...... hythmia in myotonic dystrophy.
@en
prefLabel
Splicing misregulation of SCN5 ...... hythmia in myotonic dystrophy.
@en
P2093
P2860
P50
P356
P1476
Splicing misregulation of SCN5 ...... rhythmia in myotonic dystrophy
@en
P2093
Amandine Campan-Fournier
Arnaud Jollet
Bernard Jost
Bjarne Udd
Chantal Sellier
Denis Duboc
Fernande Freyermuth
François Deryckere
Harutoshi Fujimura
P2860
P2888
P356
10.1038/NCOMMS11067
P407
P50
P577
2016-04-11T00:00:00Z