Paulina Sander, Michael Feng, Maria K Schweitzer, Fabiola Wilting, Sophie M Gutenthaler, Daniela M Arduino, Sandra Fischbach, Lisa Dreizehnter, Alessandra Moretti, Thomas Gudermann, Fabiana Perocchi, Johann Schredelseker. Br J Pharmacol 2021
Times Cited: 4
Times Cited: 4
Times Cited
Times Co-cited
Similarity
MitoQ improves mitochondrial dysfunction in heart failure induced by pressure overload.
Rogério Faustino Ribeiro Junior, Erinne Rose Dabkowski, Kadambari Chandra Shekar, Kelly A O Connell, Peter A Hecker, Michael P Murphy. Free Radic Biol Med 2018
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Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling.
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Mitochondrial Ca(2+) uptake by the voltage-dependent anion channel 2 regulates cardiac rhythmicity.
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MICU1 Serves as a Molecular Gatekeeper to Prevent In Vivo Mitochondrial Calcium Overload.
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The antiarrhythmic compound efsevin directly modulates voltage-dependent anion channel 2 by binding to its inner wall and enhancing mitochondrial Ca2+ uptake.
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Implantable cardioverter-defibrillator explantation for overdiagnosed or overtreated congenital long QT syndrome.
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Sudden death after inappropriate shocks of implantable cardioverter defibrillator in a catecholaminergic polymorphic ventricular tachycardia case with a novel RyR2 mutation.
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Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases.
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Efficacy of implantable cardioverter defibrillators in young patients with catecholaminergic polymorphic ventricular tachycardia: success depends on substrate.
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EL20, a potent antiarrhythmic compound, selectively inhibits calmodulin-deficient ryanodine receptor type 2.
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The zebrafish reference genome sequence and its relationship to the human genome.
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Istaroxime treatment ameliorates calcium dysregulation in a zebrafish model of phospholamban R14del cardiomyopathy.
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The Genetic Puzzle of Familial Atrial Fibrillation.
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Constructing Adult Zebrafish Einthoven's Triangle to Define Electrical Heart Axes.
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Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis.
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Spen deficiency interferes with Connexin 43 expression and leads to heart failure in zebrafish.
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Cardiac specification during gastrulation - The Yellow Brick Road leading to Tinman.
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A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.
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Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.