Publications by authors named "Christopher J Crowley"

Conduction velocity (CV) slowing is associated with atrial fibrillation (AF) and reentrant ventricular tachycardia (VT). Clinical electroanatomical mapping systems used to localize AF or VT sources as ablation targets remain limited by the number of measuring electrodes and signal processing methods to generate high-density local activation time (LAT) and CV maps of heterogeneous atrial or trabeculated ventricular endocardium. The morphology and amplitude of bipolar electrograms depend on the direction of propagating electrical wavefront, making identification of low-amplitude signal sources commonly associated with fibrotic area difficulty.

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Despite a long and rich history of scientific investigation, fluid turbulence remains one of the most challenging problems in science and engineering. One of the key outstanding questions concerns the role of coherent structures that describe frequently observed patterns embedded in turbulence. It has been suggested, but not proved, that coherent structures correspond to unstable, recurrent solutions of the governing equation of fluid dynamics.

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Article Synopsis
  • Cardiac arrhythmias are primarily caused by changes in cell membrane ionic channels and calcium handling, which affect heart tissue behavior and can lead to conditions like QT prolongation in patients.
  • An innovative optical-mapping technique allows for simultaneous measurement of voltage and calcium signals without interference, helping to analyze heart cell and tissue reactions to treatments or structural changes.
  • Researchers have identified a specific range of excitation wavelengths, called semasbestic, that enable effective recording of heart signals from different dyes without any cross-talk, optimizing the study of heart conditions across multiple species.
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Optical mapping methods utilize fluorescence dyes to measure dynamic response of cardiac tissue such as changes in transmembrane potential (V). For the commonly used V sensitive dyes, a dye absorption and emission spectra shift as V changes. Signals relevant to V are calculated as a relative fluorescence change with respect to the fluorescence baseline.

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