Label-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm

A major challenge of in vivo imaging is imaging deeper, including in turbid tissue. The authors report an adaptive optics based microscope that uses coherent single scattering signal to reduce sample-induced aberrations and enable fast deep-tissue imaging of in vivo larval zebrafish brain.

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Autores principales:	Moonseok Kim, Yonghyeon Jo, Jin Hee Hong, Suhyun Kim, Seokchan Yoon, Kyung-Deok Song, Sungsam Kang, Byunghak Lee, Guang Hoon Kim, Hae-Chul Park, Wonshik Choi
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2019
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/c3eab64dc55e4140830dd24ebc7cf2f2
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spelling	oai:doaj.org-article:c3eab64dc55e4140830dd24ebc7cf2f22021-12-02T17:01:54ZLabel-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm10.1038/s41467-019-11040-z2041-1723https://doaj.org/article/c3eab64dc55e4140830dd24ebc7cf2f22019-07-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-11040-zhttps://doaj.org/toc/2041-1723A major challenge of in vivo imaging is imaging deeper, including in turbid tissue. The authors report an adaptive optics based microscope that uses coherent single scattering signal to reduce sample-induced aberrations and enable fast deep-tissue imaging of in vivo larval zebrafish brain.Moonseok KimYonghyeon JoJin Hee HongSuhyun KimSeokchan YoonKyung-Deok SongSungsam KangByunghak LeeGuang Hoon KimHae-Chul ParkWonshik ChoiNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Moonseok Kim Yonghyeon Jo Jin Hee Hong Suhyun Kim Seokchan Yoon Kyung-Deok Song Sungsam Kang Byunghak Lee Guang Hoon Kim Hae-Chul Park Wonshik Choi Label-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm
description	A major challenge of in vivo imaging is imaging deeper, including in turbid tissue. The authors report an adaptive optics based microscope that uses coherent single scattering signal to reduce sample-induced aberrations and enable fast deep-tissue imaging of in vivo larval zebrafish brain.
format	article
author	Moonseok Kim Yonghyeon Jo Jin Hee Hong Suhyun Kim Seokchan Yoon Kyung-Deok Song Sungsam Kang Byunghak Lee Guang Hoon Kim Hae-Chul Park Wonshik Choi
author_facet	Moonseok Kim Yonghyeon Jo Jin Hee Hong Suhyun Kim Seokchan Yoon Kyung-Deok Song Sungsam Kang Byunghak Lee Guang Hoon Kim Hae-Chul Park Wonshik Choi
author_sort	Moonseok Kim
title	Label-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm
title_short	Label-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm
title_full	Label-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm
title_fullStr	Label-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm
title_full_unstemmed	Label-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm
title_sort	label-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm
publisher	Nature Portfolio
publishDate	2019
url	https://doaj.org/article/c3eab64dc55e4140830dd24ebc7cf2f2
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Label-free neuroimaging in vivo using synchronous angular scanning microscopy with single-scattering accumulation algorithm

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