| Literature DB >> 23831260 |
Yicong Wu1, Ryan Christensen, Daniel Colón-Ramos, Hari Shroff.
Abstract
Over the past decade, developmental neuroscience has been transformed by the widespread application of confocal and two-photon fluorescence microscopy. Even greater progress is imminent, as recent innovations in microscopy now enable imaging with increased depth, speed, and spatial resolution; reduced phototoxicity; and in some cases without external fluorescent probes. We discuss these new techniques and emphasize their dramatic impact on neurobiology, including the ability to image neurons at depths exceeding 1mm, to observe neurodevelopment noninvasively throughout embryogenesis, and to visualize neuronal processes or structures that were previously too small or too difficult to target with conventional microscopy. Published by Elsevier Ltd.Entities:
Mesh:
Year: 2013 PMID: 23831260 PMCID: PMC3830703 DOI: 10.1016/j.conb.2013.06.008
Source DB: PubMed Journal: Curr Opin Neurobiol ISSN: 0959-4388 Impact factor: 6.627