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Ca2+-dependent calcineurin/NFAT signaling in β-adrenergic-induced cardiac hypertrophy

https://doi.org/10.4149/gpb_2017022

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/wsbm.1322openalex-snapshot

Modeling calcium regulation of contraction, energetics, signaling, and transcription in the cardiac myocyte

inferredcites →https://doi.org/10.1006/jmcc.1996.0086openalex-snapshot

A Cardiac Muscle Model Relating Sarcomere Dynamics to Calcium Kinetics

inferredcites →https://doi.org/10.1006/jmcc.2002.2038openalex-snapshot

Calcium, Calmodulin, and Calcium-Calmodulin Kinase II: Heartbeat to Heartbeat and Beyond

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Simulating Complex Calcium-Calcineurin Signaling Network

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Excitation-Contraction Coupling and Cardiac Contractile Force

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NFAT and NFκB Activation in T Lymphocytes: A Model of Differential Activation of Gene Expression

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Investigating β-adrenergic-induced cardiac hypertrophy through computational approach: classical and non-classical pathways

inferredcites →https://doi.org/10.1016/0022-2828(92)90114-fopenalex-snapshot

Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum

inferredcites →https://doi.org/10.1016/j.bbrc.2004.07.121openalex-snapshot

Calcium–calcineurin signaling in the regulation of cardiac hypertrophy

inferredcites →https://doi.org/10.1016/j.bbrc.2005.06.152openalex-snapshot

Kinetics of calmodulin binding to calcineurin

inferredcites →https://doi.org/10.1016/j.bpj.2008.11.064openalex-snapshot

Sensitivity of NFAT Cycling to Cytosolic Calcium Concentration: Implications for Hypertrophic Signals in Cardiac Myocytes

inferredcites →https://doi.org/10.1016/j.bpj.2011.03.060openalex-snapshot

In Situ Calibration of Nucleoplasmic versus Cytoplasmic Ca2+ Concentration in Adult Cardiomyocytes

inferredcites →https://doi.org/10.1016/j.cardiores.2004.01.021openalex-snapshot

Calcineurin?NFAT signaling regulates the cardiac hypertrophic response in coordination with the MAPKs

inferredcites →https://doi.org/10.1016/j.cardiores.2004.04.026openalex-snapshot

Role of Ca2+/calmodulin-dependent protein kinase II in cardiac hypertrophy and heart failure

inferredcites →https://doi.org/10.1016/j.cellsig.2008.01.023openalex-snapshot

System-level investigation into the regulatory mechanism of the calcineurin/NFAT signaling pathway

inferredcites →https://doi.org/10.1016/j.etap.2014.05.008openalex-snapshot

Astragalus polysaccharide inhibits isoprenaline-induced cardiac hypertrophy via suppressing Ca2+-mediated calcineurin/NFATc3 and CaMKII signaling cascades

inferredcites →https://doi.org/10.1016/j.febslet.2006.09.064openalex-snapshot

Switching feedback mechanisms realize the dual role of MCIP in the regulation of calcineurin activity

inferredcites →https://doi.org/10.1016/j.ijcard.2014.02.035openalex-snapshot

MicroRNA-328 as a regulator of cardiac hypertrophy

inferredcites →https://doi.org/10.1016/j.yjmcc.2009.10.016openalex-snapshot

β-Adrenergic receptor signaling in the heart: Role of CaMKII

inferredcites →https://doi.org/10.1016/j.yjmcc.2011.05.001openalex-snapshot

Unraveling the secrets of a double life: Contractile versus signaling Ca2+ in a cardiac myocyte

inferredcites →https://doi.org/10.1016/j.yjmcc.2011.10.016openalex-snapshot

Epac enhances excitation–transcription coupling in cardiac myocytes

inferredcites →https://doi.org/10.1016/j.yjmcc.2013.11.001openalex-snapshot

PKA catalytic subunit compartmentation regulates contractile and hypertrophic responses to β-adrenergic signaling

inferredcites →https://doi.org/10.1016/s0021-9258(18)92938-8openalex-snapshot

Calcium binding to calmodulin and its globular domains

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Src Tyrosine Kinase Is a Novel Direct Effector of G Proteins

inferredcites →https://doi.org/10.1021/bi00188a015openalex-snapshot

Dual Calcium Ion Regulation of Calcineurin by Calmodulin and Calcineurin B

inferredcites →https://doi.org/10.1023/a:1008969032563openalex-snapshot

Models of Calmodulin Trapping and CaM Kinase II Activation in a Dendritic Spine

inferredcites →https://doi.org/10.1038/31960openalex-snapshot

Calcium oscillations increase the efficiency and specificity of gene expression

inferredcites →https://doi.org/10.1038/357692a0openalex-snapshot

FK-506- and CsA-sensitive activation of the interleukin-2 promoter by calcineurin

inferredcites →https://doi.org/10.1038/382370a0openalex-snapshot

Role of kinases and the phosphatase calcineurin in the nuclear shuttling of transcription factor NF-AT4

inferredcites →https://doi.org/10.1038/386855a0openalex-snapshot

Differential activation of transcription factors induced by Ca2+ response amplitude and duration

inferredcites →https://doi.org/10.1038/40912openalex-snapshot

Differential activation of transcription factors induced by Ca2+ response amplitude and duration

inferredcites →https://doi.org/10.1038/nature04678openalex-snapshot

NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21

inferredcites →https://doi.org/10.1042/bj20021824openalex-snapshot

A computational model on the modulation of mitogen-activated protein kinase (MAPK) and Akt pathways in heregulin-induced ErbB signalling

inferredcites →https://doi.org/10.1042/bst0350957openalex-snapshot

Calcium in the heart: when it's good, it's very very good, but when it's bad, it's horrid

inferredcites →https://doi.org/10.1073/pnas.0712316105openalex-snapshot

Ca 2+ oscillation frequency decoding in cardiac cell hypertrophy: Role of calcineurin/NFAT as Ca 2+ signal integrators

inferredcites →https://doi.org/10.1073/pnas.96.12.7059openalex-snapshot

Progressive hypertrophy and heart failure in β 1 -adrenergic receptor transgenic mice

inferredcites →https://doi.org/10.1074/jbc.271.32.19443openalex-snapshot

Role of c-Src Tyrosine Kinase in G Protein-coupled Receptorand Gβγ Subunit-mediated Activation of Mitogen-activated Protein Kinases

inferredcites →https://doi.org/10.1074/jbc.274.14.9760openalex-snapshot

Both Gs and Gi Proteins Are Critically Involved in Isoproterenol-induced Cardiomyocyte Hypertrophy

inferredcites →https://doi.org/10.1074/jbc.275.3.1855openalex-snapshot

Electrical Stimulation of Neonatal Cardiac Myocytes Activates the NFAT3 and GATA4 Pathways and Up-regulates the Adenylosuccinate Synthetase 1 Gene

inferredcites →https://doi.org/10.1074/jbc.m103166200openalex-snapshot

Glycogen Synthase Kinase 3β Regulates GATA4 in Cardiac Myocytes

inferredcites →https://doi.org/10.1074/jbc.m804902200openalex-snapshot

Differential Integration of Ca2+-Calmodulin Signal in Intact Ventricular Myocytes at Low and High Affinity Ca2+-Calmodulin Targets

inferredcites →https://doi.org/10.1093/bib/bbv039openalex-snapshot

Systems biological approaches to the cardiac signaling network

inferredcites →https://doi.org/10.1093/emboj/cdg381openalex-snapshot

NFAT functions as a working memory of Ca2+ signals in decoding Ca2+ oscillation

inferredcites →https://doi.org/10.1097/00007890-199911150-00023openalex-snapshot

THE TEMPORAL PROFILE OF CALCINEURIN INHIBITION BY CYCLOSPORINE IN VIVO1

inferredcites →https://doi.org/10.1101/cshperspect.a004242openalex-snapshot

Calcium Signaling in Cardiac Myocytes

inferredcites →https://doi.org/10.1113/jphysiol.2002.025619openalex-snapshot

Mechanisms Underlying the Frequency Dependence of Contraction and [Ca2+]i Transients in Mouse Ventricular Myocytes

inferredcites →https://doi.org/10.1113/jphysiol.2003.053579openalex-snapshot

Pacing‐induced calcineurin activation controls cardiac Ca2+ signalling and gene expression

inferredcites →https://doi.org/10.1113/jphysiol.2006.120048openalex-snapshot

Regulation of the nuclear export of the transcription factor NFATc1 by protein kinases after slow fibre type electrical stimulation of adult mouse skeletal muscle fibres

inferredcites →https://doi.org/10.1113/jphysiol.2007.133066openalex-snapshot

The cAMP binding protein Epac modulates Ca 2+ sparks by a Ca 2+ /calmodulin kinase signalling pathway in rat cardiac myocytes

inferredcites →https://doi.org/10.1124/mol.113.090951openalex-snapshot

Modeling the Effects of β1-Adrenergic Receptor Blockers and Polymorphisms on Cardiac Myocyte Ca2+ Handling

inferredcites →https://doi.org/10.1126/science.1079206openalex-snapshot

Myocyte Adrenoceptor Signaling Pathways

inferredcites →https://doi.org/10.1126/science.283.5400.381openalex-snapshot

Emergent Properties of Networks of Biological Signaling Pathways

inferredcites →https://doi.org/10.1126/stke.2003.166.pe4openalex-snapshot

Excitation-Transcription Coupling: Signaling by Ion Channels to the Nucleus

inferredcites →https://doi.org/10.1128/mcb.25.3.865-878.2005openalex-snapshot

Direct and Indirect Interactions between Calcineurin-NFAT and MEK1-Extracellular Signal-Regulated Kinase 1/2 Signaling Pathways Regulate Cardiac Gene Expression and Cellular Growth

inferredcites →https://doi.org/10.1146/annurev.physiol.70.113006.100455openalex-snapshot

Calcium Cycling and Signaling in Cardiac Myocytes

inferredcites →https://doi.org/10.1152/ajpcell.1983.245.1.c1openalex-snapshot

Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum

inferredcites →https://doi.org/10.1152/ajpheart.00007.2015openalex-snapshot

Chasing cardiac physiology and pathology down the CaMKII cascade

inferredcites →https://doi.org/10.1152/ajpheart.00733.2011openalex-snapshot

Constitutive overexpression of phosphomimetic phospholemman S68E mutant results in arrhythmias, early mortality, and heart failure: potential involvement of Na+/Ca2+ exchanger

inferredcites →https://doi.org/10.1152/ajpheart.01072.2009openalex-snapshot

Isoform- and tissue-specific regulation of the Ca2+-sensitive transcription factor NFAT in cardiac myocytes and heart failure

inferredcites →https://doi.org/10.1152/ajprenal.00036.2008openalex-snapshot

Role of AQP1 in endotoxemia-induced acute kidney injury

inferredcites →https://doi.org/10.1152/physiolgenomics.00107.2002openalex-snapshot

Abnormal contractile activity and calcium cycling in cardiac myocytes isolated from dmpk knockout mice

inferredcites →https://doi.org/10.1161/01.res.0000059562.91384.1aopenalex-snapshot

Familial Hypertrophic Cardiomyopathy-Linked Mutant Troponin T Causes Stress-Induced Ventricular Tachycardia and Ca 2+ -Dependent Action Potential Remodeling

inferredcites →https://doi.org/10.1161/circresaha.107.153007openalex-snapshot

Intact β-Adrenergic Response and Unmodified Progression Toward Heart Failure in Mice With Genetic Ablation of a Major Protein Kinase A Phosphorylation Site in the Cardiac Ryanodine Receptor

inferredcites →https://doi.org/10.1161/circresaha.110.223602openalex-snapshot

Computational Models Reduce Complexity and Accelerate Insight Into Cardiac Signaling Networks

inferredcites →https://doi.org/10.1161/circresaha.111.247148openalex-snapshot

Fluorescence Resonance Energy Transfer–Based Sensor Camui Provides New Insight Into Mechanisms of Calcium/Calmodulin-Dependent Protein Kinase II Activation in Intact Cardiomyocytes

inferredcites →https://doi.org/10.1161/circresaha.111.247338openalex-snapshot

Short Communication: Flecainide Exerts an Antiarrhythmic Effect in a Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia by Increasing the Threshold for Triggered Activity

inferredcites →https://doi.org/10.1161/circulationaha.107.754051openalex-snapshot

Phospholemman-Mediated Activation of Na/K-ATPase Limits [Na] i and Inotropic State During β-Adrenergic Stimulation in Mouse Ventricular Myocytes

inferredcites →https://doi.org/10.1161/hc2601.090987openalex-snapshot

Isoproterenol Activates Extracellular Signal–Regulated Protein Kinases in Cardiomyocytes Through Calcineurin

inferredcites →https://doi.org/10.1161/hh0102.102271openalex-snapshot

β-Adrenergic Stimulation Modulates Ryanodine Receptor Ca 2+ Release During Diastolic Depolarization to Accelerate Pacemaker Activity in Rabbit Sinoatrial Nodal Cells

inferredcites →https://doi.org/10.1172/jci27824openalex-snapshot

Dichotomy of Ca2+ in the heart: contraction versus intracellular signaling

inferredcites →https://doi.org/10.1196/annals.1341.008openalex-snapshot

Calcium Signaling in Cardiac Ventricular Myocytes

inferredcites →https://doi.org/10.1196/annals.1380.026openalex-snapshot

Cardiac β‐Adrenergic Signaling

inferredcites →https://doi.org/10.1196/annals.1420.008openalex-snapshot

Cardiac Cell Hypertrophy In Vitro

inferredcites →https://doi.org/10.1210/en.133.1.376openalex-snapshot

Targeted developmental overexpression of calmodulin induces proliferative and hypertrophic growth of cardiomyocytes in transgenic mice

inferredcites →https://doi.org/10.1210/me.2002-0350openalex-snapshot

Pressure Overload Selectively Up-Regulates Ca2+/Calmodulin-Dependent Protein Kinase IIin Vivo

inferredcites →https://doi.org/10.1242/jcs.076034openalex-snapshot

A hidden incoherent switch regulates RCAN1 in the calcineurin–NFAT signaling network

inferredcites →https://doi.org/10.1371/journal.pone.0089113openalex-snapshot

A Compartmentalized Mathematical Model of the β1-Adrenergic Signaling System in Mouse Ventricular Myocytes

inferredcites →https://doi.org/10.1529/biophysj.107.118505openalex-snapshot

A Simulation Study on the Activation of Cardiac CaMKII δ-Isoform and Its Regulation by Phosphatases

inferredcites →https://doi.org/10.1529/biophysj.108.128728openalex-snapshot

Calmodulin Mediates Differential Sensitivity of CaMKII and Calcineurin to Local Ca2+ in Cardiac Myocytes

inferredcites →https://doi.org/10.2147/jrlcr.s36375openalex-snapshot

Myocardial calcium signaling in physiology and disease

inferredcites →https://doi.org/10.3389/fphar.2014.00009openalex-snapshot

Modeling CaMKII in cardiac physiology: from molecule to tissue

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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In vitro ischemic preconditioning mediates the Ca2+/CaN/NFAT pathway to protect against oxygen-glucose deprivation-induced cellular damage and inflammatory responses

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Continuous exposure to isoprenaline reduced myotube size by delaying myoblast differentiation and fusion through the NFAT-MEF2C signaling pathway

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The Calcineurin–Nuclear Factor of Activated T Cells Signaling Axis in Hypertrophic Cardiomyopathy: Molecular Insights and Therapeutic Implications

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Cell shape regulates subcellular organelle location to control early Ca 2+ signal dynamics in Vascular Smooth Muscle Cells

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Mechanisms underlying divergent relationships between Ca 2+ and YAP/TAZ signaling

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Mechanisms underlying divergent relationships between Ca2+ and YAP/TAZ signalling

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