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CELL-TO-CELL MODELING OF THE INTERFACE BETWEEN ATRIAL AND SINOATRIAL ANISOTROPIC HETEROGENEOUS NETS
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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/ar.a.20109openalex-snapshot
Cytoarchitecture and intercalated disks of the working myocardium and the conduction system in the mammalian heart
inferredcites →https://doi.org/10.1007/s00232-012-9466-yopenalex-snapshot
The Noncanonical Functions of Cx43 in the Heart
inferredcites →https://doi.org/10.1016/0025-5564(93)90001-qopenalex-snapshot
Spreading of excitation in 3-d models of the anisotropic cardiac tissue. I. validation of the eikonal model
inferredcites →https://doi.org/10.1016/0167-2789(95)00059-dopenalex-snapshot
Re-entry in three-dimensional Fitzhugh-Nagumo medium with rotational anisotropy
inferredcites →https://doi.org/10.1016/j.pbiomolbio.2008.05.002openalex-snapshot
Dynamics of human atrial cell models: Restitution, memory, and intracellular calcium dynamics in single cells
inferredcites →https://doi.org/10.1016/j.pbiomolbio.2015.12.011openalex-snapshot
Human sinoatrial node structure: 3D microanatomy of sinoatrial conduction pathways
inferredcites →https://doi.org/10.1016/s0006-3495(86)83559-7openalex-snapshot
Propagation through electrically coupled cells. How a small SA node drives a large atrium
inferredcites →https://doi.org/10.1016/s0008-6363(00)00135-8openalex-snapshot
The sinoatrial node, a heterogeneous pacemaker structure
inferredcites →https://doi.org/10.1016/s0022-2828(84)80714-2openalex-snapshot
Pacemaker cell types in the rabbit sinus node: A correlative ultrastructural and electrophysiological study
inferredcites →https://doi.org/10.1016/s0025-5564(97)00093-xopenalex-snapshot
Spread of excitation in 3-D models of the anisotropic cardiac tissue. II. Effects of fiber architecture and ventricular geometry
inferredcites →https://doi.org/10.1111/an.1999.40.2.6openalex-snapshot
The Massachusetts Institute of Technology
inferredcites →https://doi.org/10.1113/jphysiol.2012.229435openalex-snapshot
An updated computational model of rabbit sinoatrial action potential to investigate the mechanisms of heart rate modulation
inferredcites →https://doi.org/10.1142/s0218202504003489openalex-snapshot
A PARALLEL SOLVER FOR REACTION–DIFFUSION SYSTEMS IN COMPUTATIONAL ELECTROCARDIOLOGY
inferredcites →https://doi.org/10.1152/ajpheart.00515.2013openalex-snapshot
Are SR Ca content fluctuations or SR refractoriness the key to atrial cardiac alternans?: insights from a human atrial model
inferredcites →https://doi.org/10.1152/ajpheart.1996.271.4.h1666openalex-snapshot
A model of the action potential and underlying membrane currents in a rabbit atrial cell
inferredcites →https://doi.org/10.1152/ajpheart.1998.275.1.h301openalex-snapshot
Ionic mechanisms underlying human atrial action potential properties: insights from a mathematical model
inferredcites →https://doi.org/10.1152/ajpheart.2000.279.1.h397openalex-snapshot
Mathematical models of action potentials in the periphery and center of the rabbit sinoatrial node
inferredcites →https://doi.org/10.1152/ajpheart.2000.279.4.h1767openalex-snapshot
Mathematical analysis of canine atrial action potentials: rate, regional factors, and electrical remodeling
inferredcites →https://doi.org/10.1152/ajpheart.2001.280.5.h2103openalex-snapshot
Gap junctions in the rabbit sinoatrial node
inferredcites →https://doi.org/10.1161/01.cir.0000152100.04087.dbopenalex-snapshot
Computer Three-Dimensional Reconstruction of the Sinoatrial Node
inferredcites →https://doi.org/10.1161/01.cir.103.4.584openalex-snapshot
Gradient Model Versus Mosaic Model of the Sinoatrial Node
inferredcites →https://doi.org/10.1161/01.cir.97.16.1623openalex-snapshot
Distribution of Atrial and Nodal Cells Within the Rabbit Sinoatrial Node
inferredcites →https://doi.org/10.1161/01.res.64.3.563openalex-snapshot
Distribution and three-dimensional structure of intercellular junctions in canine myocardium.
inferredcites →https://doi.org/10.1161/01.res.73.3.473openalex-snapshot
Immunohistochemical delineation of the conduction system. I: The sinoatrial node.
inferredcites →https://doi.org/10.1161/01.res.76.3.366openalex-snapshot
The Stochastic Nature of Cardiac Propagation at a Microscopic Level
inferredcites →https://doi.org/10.1161/01.res.80.5.673openalex-snapshot
Characterization of Gap Junction Channels in Adult Rabbit Atrial and Ventricular Myocardium
inferredcites →https://doi.org/10.1161/01.res.82.1.63openalex-snapshot
Mathematical Model of an Adult Human Atrial Cell
inferredcites →https://doi.org/10.1177/002215549904700708openalex-snapshot
Connexin45, a Major Connexin of the Rabbit Sinoatrial Node, Is Co-expressed with Connexin43 in a Restricted Zone at the Nodal-Crista Terminalis Border
inferredcites →https://doi.org/10.1371/journal.pcbi.1001041openalex-snapshot
Determinants of Heterogeneity, Excitation and Conduction in the Sinoatrial Node: A Model Study
inferredcites →https://doi.org/10.1371/journal.pone.0094565openalex-snapshot
Importance of Gradients in Membrane Properties and Electrical Coupling in Sinoatrial Node Pacing
inferredcites →https://doi.org/10.7551/mitpress/2526.001.0001openalex-snapshot
Dynamical Systems in Neuroscience
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/103259openalex-snapshot
Cell-to-cell Modeling of the interface between Atrial and Sinoatrial Anisotropic Heterogeneous Nets II: Mechanisms Underlying Nets Dynamics
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