<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hillman EM</submitter><funding>Simons Foundation Collaboration on the Global Brain</funding><funding>NEI NIH HHS</funding><funding>Kavli Institute for Brain Science</funding><funding>NHLBI NIH HHS</funding><funding>Coulter Foundation</funding><funding>Columbia-Coulter Translational Research Partnership</funding><funding>NINDS NIH HHS</funding><funding>Department of Defense MURI</funding><funding>National Institutes of Health</funding><funding>National Science Foundation</funding><pagination>190-200</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6002850</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>50</volume><pubmed_abstract>As optical reporters and modulators of cellular activity have become increasingly sophisticated, the amount that can be learned about the brain via high-speed cellular imaging has increased dramatically. However, despite fervent innovation, point-scanning microscopy is facing a fundamental limit in achievable 3D imaging speeds and fields of view. A range of alternative approaches are emerging, some of which are moving away from point-scanning to use axially-extended beams or sheets of light, for example swept confocally aligned planar excitation (SCAPE) microscopy. These methods are proving effective for high-speed volumetric imaging of the nervous system of small organisms such as Drosophila (fruit fly) and D. Rerio (Zebrafish), and are showing promise for imaging activity in the living m</pubmed_abstract><journal>Current opinion in neurobiology</journal><pubmed_title>High-speed 3D imaging of cellular activity in the brain using axially-extended beams and light sheets.</pubmed_title><pmcid>PMC6002850</pmcid><funding_grant_id>5U01NS094296</funding_grant_id><funding_grant_id>P30 EY019007</funding_grant_id><funding_grant_id>W911NF-12-1-0594</funding_grant_id><funding_grant_id>CBET-0954796</funding_grant_id><funding_grant_id>U19 NS104649</funding_grant_id><funding_grant_id>R01HL13143801A1</funding_grant_id><funding_grant_id>U01 NS094296</funding_grant_id><funding_grant_id>R01 HL131438</funding_grant_id><funding_grant_id>UF1 NS108213</funding_grant_id><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Galwaduge PT</pubmed_authors><pubmed_authors>Voleti V</pubmed_authors><pubmed_authors>Benezra SE</pubmed_authors><pubmed_authors>Bruno RM</pubmed_authors><pubmed_authors>Perez-Campos C</pubmed_authors><pubmed_authors>Hillman EM</pubmed_authors><pubmed_authors>Yu H</pubmed_authors><pubmed_authors>Patel K</pubmed_authors></additional><is_claimable>false</is_claimable><name>High-speed 3D imaging of cellular activity in the brain using axially-extended beams and light sheets.</name><description>As optical reporters and modulators of cellular activity have become increasingly sophisticated, the amount that can be learned about the brain via high-speed cellular imaging has increased dramatically. However, despite fervent innovation, point-scanning microscopy is facing a fundamental limit in achievable 3D imaging speeds and fields of view. A range of alternative approaches are emerging, some of which are moving away from point-scanning to use axially-extended beams or sheets of light, for example swept confocally aligned planar excitation (SCAPE) microscopy. These methods are proving effective for high-speed volumetric imaging of the nervous system of small organisms such as Drosophila (fruit fly) and D. Rerio (Zebrafish), and are showing promise for imaging activity in the living m</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jun</publication><modification>2025-04-25T19:54:33.489Z</modification><creation>2019-07-01T13:40:34Z</creation></dates><accession>S-EPMC6002850</accession><cross_references><pubmed>29642044</pubmed><doi>10.1016/j.conb.2018.03.007</doi></cross_references></HashMap>