Hostname: page-component-848d4c4894-ttngx Total loading time: 0 Render date: 2024-05-30T15:15:38.175Z Has data issue: false hasContentIssue false
  • English
  • Français

Binucleate Cell Atlasing: An Intracellular Object Localization Tool for Single-Cell Fluorescence Microscopy

Published online by Cambridge University Press:  30 July 2020

Andrew Soltisz ,
Rengasayee Veeraraghavan  and
Seth Weinberg
Andrew Soltisz
Affiliation:
The Ohio State University, Columbus, Ohio, United States
Rengasayee Veeraraghavan
Affiliation:
The Ohio State University, Columbus, Ohio, United States
Seth Weinberg
Affiliation:
The Ohio State University, Columbus, Ohio, United States

Abstract

An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Illuminating Health and Disease at New Frontiers of Spatiotemporal Resolution and Adaptive Microscopy
Information
Microscopy and Microanalysis , Volume 26 , Supplement S2 , August 2020 , pp. 602 - 604
Check for updates
Copyright
Copyright © Microscopy Society of America 2020

References

Veeraraghavan, R and Gourdie, R. Stochastic Optical Reconstruction Microscopy-based Relative Localization Analysis (STORM-RLA) for Quantitative Nanoscale Assessment of Spatial Protein Organization. Molecular biology of the cell. 2016;27:3583-3590.10.1091/mbc.e16-02-0125CrossRefGoogle ScholarPubMed
Veeraraghavan, R, Hoeker, GS, et al. The adhesion function of the sodium channel beta subunit (beta1) contributes to cardiac action potential propagation. Elife. 2018;7.10.7554/eLife.37610CrossRefGoogle ScholarPubMed
Veeraraghavan, R, Lin, J, et al. Sodium channels in the Cx43 gap junction perinexus may constitute a cardiac ephapse: an experimental and modeling study. Pflugers Arch. 2015;467:2093-2105.10.1007/s00424-014-1675-zCrossRefGoogle ScholarPubMed
Veeraraghavan, R, Lin, J, et al. Potassium channels in the Cx43 gap junction perinexus modulate ephaptic coupling: an experimental and modeling study. Pflugers Arch. 2016;468:1651-61.10.1007/s00424-016-1861-2CrossRefGoogle ScholarPubMed
Radwanski, PB, Brunello, L, et al. Neuronal Na+ channel blockade suppresses arrhythmogenic diastolic Ca2+ release. Cardiovascular research. 2015;106:143-52.10.1093/cvr/cvu262CrossRefGoogle ScholarPubMed
Radwański, PB, Ho, H-T, et al. Neuronal Na+ Channels Are Integral Components of Pro-Arrhythmic Na+/Ca2+ Signaling Nanodomain That Promotes Cardiac Arrhythmias During β-Adrenergic Stimulation. JACC: Basic to Translational Science. 2016;1:251-266.Google ScholarPubMed
Struckman, HL, Baine, S, et al. Super-Resolution Imaging Using a Novel High-Fidelity Antibody Reveals Close Association of the Neuronal Sodium Channel NaV1.6 with Ryanodine Receptors in Cardiac Muscle. Microsc Microanal. 2020:1-9.Google Scholar
Koleske, M, Bonilla, I, et al. Tetrodotoxin-sensitive Navs contribute to early and delayed afterdepolarizations in long QT arrhythmia models. The Journal of general physiology. 2018.10.1085/jgp.201711909CrossRefGoogle ScholarPubMed