Multistep ion channel remodeling and lethal arrhythmia precede heart failure in a mouse model of inherited dilated cardiomyopathy (Q34238976)

31 July 2017

Multistep ion channel remodeling and lethal arrhythmia precede heart failure in a mouse model of inherited dilated cardiomyopathy (English)

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31 July 2017

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Sachio Morimoto

11

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author name string

Takeshi Suzuki

1

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31 July 2017

Takao Shioya

2

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31 July 2017

Takashi Murayama

3

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31 July 2017

Masami Sugihara

4

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31 July 2017

Fuminori Odagiri

5

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31 July 2017

Yuji Nakazato

6

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31 July 2017

Hiroto Nishizawa

7

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31 July 2017

Akihito Chugun

8

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31 July 2017

Takashi Sakurai

9

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31 July 2017

Hiroyuki Daida

10

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31 July 2017

Nagomi Kurebayashi

12

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31 July 2017

language of work or name

English

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publication date

13 April 2012

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31 July 2017

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31 July 2017

7

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31 July 2017

4

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31 July 2017

e35353

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Creative Commons Attribution 4.0 International

31 July 2017

start time

13 April 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes.

6 July 2018

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6 July 2018

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Causes of abnormal Ca2+ transients in Guinea pig pathophysiological ventricular muscle revealed by Ca2+ and action potential imaging at cellular level

6 July 2018

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Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease.

6 July 2018

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Aberrant cell-to-cell coupling in Ca2+-overloaded guinea pig ventricular muscles

6 July 2018

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6 July 2018

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Arrhythmogenic ion-channel remodeling in the heart: heart failure, myocardial infarction, and atrial fibrillation.

6 July 2018

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The contribution of refractoriness to arrhythmic substrate in hypokalemic Langendorff-perfused murine hearts.

6 July 2018

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Large-scale analysis of ion channel gene expression in the mouse heart during perinatal development.

6 July 2018

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A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy.

6 July 2018

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Sarcomeric protein mutations in dilated cardiomyopathy

6 July 2018

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Long QT syndrome: reduced repolarization reserve and the genetic link

6 July 2018

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The homeodomain transcription factor Irx5 establishes the mouse cardiac ventricular repolarization gradient

6 July 2018

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Specific pattern of ionic channel gene expression associated with pacemaker activity in the mouse heart

6 July 2018

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Behavior of Ca(2+) waves in multicellular preparations from guinea pig ventricle

6 July 2018

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Cellular basis of triggered arrhythmias in heart failure

6 July 2018

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Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice

6 July 2018

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Electrophysiological changes in heart failure and their relationship to arrhythmogenesis

6 July 2018

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NRSF regulates the fetal cardiac gene program and maintains normal cardiac structure and function

6 July 2018

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Mechanical effects on arrhythmogenesis: from pipette to patient.

6 July 2018

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Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.

6 July 2018

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Targeted replacement of KV1.5 in the mouse leads to loss of the 4-aminopyridine-sensitive component of I(K,slow) and resistance to drug-induced qt prolongation.

6 July 2018

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The Genetic Basis for Cardiomyopathy

6 July 2018

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Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

6 July 2018

1 reference

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Electrophysiological remodeling in hypertrophy and heart failure

6 July 2018

1 reference

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Characteristics of wave fronts during ventricular fibrillation in human hearts with dilated cardiomyopathy: role of increased fibrosis in the generation of reentry

6 July 2018

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What explains black-white differences in survival in idiopathic dilated cardiomyopathy? The Washington, DC, Dilated Cardiomyopathy Study

6 July 2018

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The natural history of idiopathic dilated cardiomyopathy

6 July 2018

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Electrical remodeling in a transgenic mouse model of alpha1B-adrenergic receptor overexpression.

6 July 2018

1 reference

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Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Up-regulation of type 2 iodothyronine deiodinase in dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Heterogeneous expression of repolarizing, voltage-gated K+ currents in adult mouse ventricles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Regional, age-dependent, and genotype-dependent differences in ventricular action potential duration and activation time in 410 Langendorff-perfused mouse hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Functional properties of K+ currents in adult mouse ventricular myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Molecular basis of transient outward K+ current diversity in mouse ventricular myocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Functional roles of cardiac and vascular ATP-sensitive potassium channels clarified by Kir6.2-knockout mice

21 January 2018

1 reference

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SR calcium handling and calcium after-transients in a rabbit model of heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Arrhythmogenesis and contractile dysfunction in heart failure: Roles of sodium-calcium exchange, inward rectifier potassium current, and residual beta-adrenergic responsiveness

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Therapeutic effect of {beta}-adrenoceptor blockers using a mouse model of dilated cardiomyopathy with a troponin mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Hallmarks of ion channel gene expression in end-stage heart failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

A simple technique for isolating healthy heart cells from mouse models

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3325934

Idiopathic Dilated Cardiomyopathy

28 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035353

Targeted deletion of Kv4.2 eliminates I(to,f) and results in electrical and molecular remodeling, with no evidence of ventricular hypertrophy or myocardial dysfunction

21 January 2018

1 reference

12 December 2020

Postnatal development has a marked effect on ventricular repolarization in mice

1 reference

12 December 2020

Remodelling of ionic currents in hypertrophied and failing hearts of transgenic mice overexpressing calsequestrin

1 reference

12 December 2020

Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation

1 reference

12 December 2020

Relationship between K+ channel down-regulation and [Ca2+]i in rat ventricular myocytes following myocardial infarction

1 reference

12 December 2020

Enhanced dispersion of repolarization and refractoriness in transgenic mouse hearts promotes reentrant ventricular tachycardia

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0035353

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DOI

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31 July 2017

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31 July 2017

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