scholarly article | Q13442814 |
P819 | ADS bibcode | 2012PLoSO...735353S |
P356 | DOI | 10.1371/JOURNAL.PONE.0035353 |
P932 | PMC publication ID | 3325934 |
P698 | PubMed publication ID | 22514734 |
P5875 | ResearchGate publication ID | 224709297 |
P50 | author | Sachio Morimoto | Q40010169 |
P2093 | author name string | Nagomi Kurebayashi | |
Takashi Murayama | |||
Takashi Sakurai | |||
Takao Shioya | |||
Fuminori Odagiri | |||
Hiroyuki Daida | |||
Takeshi Suzuki | |||
Yuji Nakazato | |||
Hiroto Nishizawa | |||
Akihito Chugun | |||
Masami Sugihara | |||
P2860 | cites work | Large-scale analysis of ion channel gene expression in the mouse heart during perinatal development. | Q52006604 |
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Molecular basis of transient outward K+ current diversity in mouse ventricular myocytes. | Q52132199 | ||
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Relationship between K+ channel down-regulation and [Ca2+]i in rat ventricular myocytes following myocardial infarction | Q77393695 | ||
Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation | Q80447572 | ||
Postnatal development has a marked effect on ventricular repolarization in mice | Q80736288 | ||
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 | Q81492019 | ||
A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy. | Q24301857 | ||
NRSF regulates the fetal cardiac gene program and maintains normal cardiac structure and function | Q24634087 | ||
Causes of abnormal Ca2+ transients in Guinea pig pathophysiological ventricular muscle revealed by Ca2+ and action potential imaging at cellular level | Q27342134 | ||
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy | Q28139470 | ||
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Cellular basis of triggered arrhythmias in heart failure | Q28251279 | ||
The homeodomain transcription factor Irx5 establishes the mouse cardiac ventricular repolarization gradient | Q28587676 | ||
Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice | Q28591672 | ||
The Genetic Basis for Cardiomyopathy | Q29300961 | ||
Behavior of Ca(2+) waves in multicellular preparations from guinea pig ventricle | Q33205833 | ||
Aberrant cell-to-cell coupling in Ca2+-overloaded guinea pig ventricular muscles | Q33326801 | ||
Electrophysiological remodeling in hypertrophy and heart failure | Q33758963 | ||
Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy. | Q33894656 | ||
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Specific pattern of ionic channel gene expression associated with pacemaker activity in the mouse heart | Q34361080 | ||
Mechanical effects on arrhythmogenesis: from pipette to patient. | Q35121854 | ||
Electrophysiological changes in heart failure and their relationship to arrhythmogenesis | Q35635094 | ||
Long QT syndrome: reduced repolarization reserve and the genetic link | Q36335258 | ||
Sarcomeric protein mutations in dilated cardiomyopathy | Q36369921 | ||
Arrhythmogenic ion-channel remodeling in the heart: heart failure, myocardial infarction, and atrial fibrillation. | Q36788875 | ||
Sarcomeric proteins and inherited cardiomyopathies. | Q37023249 | ||
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What explains black-white differences in survival in idiopathic dilated cardiomyopathy? The Washington, DC, Dilated Cardiomyopathy Study | Q38954596 | ||
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. | Q40804479 | ||
The natural history of idiopathic dilated cardiomyopathy | Q40854386 | ||
The contribution of refractoriness to arrhythmic substrate in hypokalemic Langendorff-perfused murine hearts. | Q41947515 | ||
Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease. | Q42160059 | ||
Up-regulation of type 2 iodothyronine deiodinase in dilated cardiomyopathy | Q43068905 | ||
Functional roles of cardiac and vascular ATP-sensitive potassium channels clarified by Kir6.2-knockout mice | Q43562608 | ||
Arrhythmogenesis and contractile dysfunction in heart failure: Roles of sodium-calcium exchange, inward rectifier potassium current, and residual beta-adrenergic responsiveness | Q43633756 | ||
SR calcium handling and calcium after-transients in a rabbit model of heart failure | Q44385086 | ||
Regional, age-dependent, and genotype-dependent differences in ventricular action potential duration and activation time in 410 Langendorff-perfused mouse hearts | Q44767110 | ||
Functional properties of K+ currents in adult mouse ventricular myocytes | Q44991716 | ||
Characteristics of wave fronts during ventricular fibrillation in human hearts with dilated cardiomyopathy: role of increased fibrosis in the generation of reentry | Q45307190 | ||
Electrical remodeling in a transgenic mouse model of alpha1B-adrenergic receptor overexpression. | Q45968267 | ||
Therapeutic effect of {beta}-adrenoceptor blockers using a mouse model of dilated cardiomyopathy with a troponin mutation. | Q45991846 | ||
A simple technique for isolating healthy heart cells from mouse models | Q46916697 | ||
Heterogeneous expression of repolarizing, voltage-gated K+ currents in adult mouse ventricles | Q47350584 | ||
Hallmarks of ion channel gene expression in end-stage heart failure | Q48206560 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | heart failure | Q181754 |
P304 | page(s) | e35353 | |
P577 | publication date | 2012-04-13 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Multistep ion channel remodeling and lethal arrhythmia precede heart failure in a mouse model of inherited dilated cardiomyopathy | |
P478 | volume | 7 |
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Q34388593 | Pioglitazone improves potassium channel remodeling induced by angiotensin II in atrial myocytes |
Q91885085 | Reduced hybrid/complex N-glycosylation disrupts cardiac electrical signaling and calcium handling in a model of dilated cardiomyopathy |
Q36730574 | The link between abnormal calcium handling and electrical instability in acquired long QT syndrome--Does calcium precipitate arrhythmic storms? |
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Q34576662 | Usefulness of running wheel for detection of congestive heart failure in dilated cardiomyopathy mouse model |
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