Fast widefield imaging of neuronal structure and function with optical sectioning in vivo-Reference-Cited by-同舟云学术

Fast widefield imaging of neuronal structure and function with optical sectioning in vivo

Published:2020-05-08 Issue:19 Volume:6 Page:
ISSN:2375-2548
Container-title:Science Advances
language:en
Short-container-title:Sci. Adv.

Author:

Li Ziwei¹²^ORCID,Zhang Qinrong¹^ORCID,Chou Shih-Wei³,Newman Zachary³^ORCID,Turcotte Raphaël¹^ORCID,Natan Ryan¹^ORCID,Dai Qionghai²,Isacoff Ehud Y.³⁴⁵,Ji Na¹³⁴⁶^ORCID

Affiliation:

1. Department of Physics, University of California, Berkeley, Berkeley, CA 94720, USA.

2. Department of Automation, Tsinghua University, Beijing 100084, China.

3. Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.

4. Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720, USA.

5. Bioscience Division, Lawrence Berkeley National Laboratory, Berkeley, Berkeley, CA 94720, USA.

6. Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Abstract

Adaptive optics and structured illumination enables fast and accurate imaging of neuronal structure and function in vivo.

Funder

National Institutes of Health

National Institute of Mental Health

Defense Advanced Research Projects Agency

China Scholarship Council

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference38 articles.

1. E. R. Kandel J. H. Schwartz T. M. Jessell S. A. Siegelbaum A. J. Hudspeth Principles of Neural Science Fifth Edition (McGraw-Hill Education 2012).

2. J. B. Pawley Handbook of Biological Confocal Microscopy (ed. 3 2008).

3. Optical sectioning microscopy

4. Deep tissue two-photon microscopy

5. Multiphoton Excitation Provides Optical Sections from Deeper within Scattering Specimens than Confocal Imaging

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