
Imaging activity in brain cells: deconvolution clears the haze
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A deceptively simple signal processing method allows researchers to quantify complex and irregular patterns of high frequency neuronal activity in whole brain at single-neuron resolution by
deconvolving the slow Ca2+ signals generated by neuronal spikes. Access through your institution Buy or subscribe This is a preview of subscription content, access via your institution
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Download references AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * the Neurosciences Department, Case Western Reserve University, Cleveland, 44106, Ohio, USA Ben W Strowbridge Authors * Ben W
Strowbridge View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE
Strowbridge, B. Imaging activity in brain cells: deconvolution clears the haze. _Nat Methods_ 3, 344–346 (2006). https://doi.org/10.1038/nmeth0506-344 Download citation * Issue Date: May
2006 * DOI: https://doi.org/10.1038/nmeth0506-344 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is
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