Zobrazeno 1 - 10
of 32
pro vyhledávání: '"ocis:(180.0180) Microscopy"'
Autor:
Peter, Quicke, Stephanie, Reynolds, Mark, Neil, Thomas, Knöpfel, Simon R, Schultz, Amanda J, Foust
Publikováno v:
Biomedical Optics Express
Multifocal two-photon microscopy (MTPM) increases imaging speed over single-focus scanning by parallelizing fluorescence excitation. The imaged fluorescence’s susceptibility to crosstalk, however, severely degrades contrast in scattering tissue. He
Publikováno v:
Biomedical Optics Express
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
15 pags., 12 figs. -- OCIS codes: (170.3660) Light propagation in tissues; (050.1755) Computational electromagnetic methods; (180.0180) Microscopy; (110.4500) Optical coherence tomography. -- Corrections: 20 June 2018: Typographical corrections were
Publikováno v:
Biomedical Optics Express
We have investigated the effect of Airy illumination on the image quality and depth penetration of digitally scanned light-sheet microscopy in turbid neural tissue. We used Fourier analysis of images acquired using Gaussian and Airy light-sheets to a
Publikováno v:
Biomedical Optics Express
We report replacement of one side of a static illumination, dual sided, thin-sheet laser imaging microscope (TSLIM) with an intensity modulated laser scanner in order to implement structured illumination (SI) and HiLo image demodulation techniques fo
Publikováno v:
Biomedical Optics Express
Light sheet microscopy became a powerful tool in life sciences. Often, however, the sheet geometry is fixed, whereas it would be advantageous to adjust the sheet geometry to specimens of different dimensions. Therefore we developed an afocal cylindri
Publikováno v:
Biomedical Optics Express
Rapid and direct imaging of microscopic tissue morphology and pathology can be achieved by multiphoton imaging of intrinsic tissue fluorophores and second harmonic signals. Engineering parameters for developing this technology for clinical applicatio
Publikováno v:
Optics Express
In atomic force microscopy (AFM), finding sparsely distributed regions of interest can be difficult and time-consuming. Typically, the tip is scanned until the desired object is located. This process can mechanically or chemically degrade the tip, as
Autor:
Tatsuki Tahara, Yuki Shimozato, Motofumi Fujii, Shogo Ura, Kenichi Ito, Toshihiro Kubota, Kenzo Nishio, Takashi Kakue, Yasuhiro Awatsuji, Osamu Matoba
Publikováno v:
Biomedical Optics Express
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We propose parallel phase-shifting digital holographic microscopy (PPSDHM) which has the ability of three-dimensional (3-D) motion measurement using space-division multiplexing technique. By the PPSDHM, instantaneous information of both the 3-D struc
Publikováno v:
Biomedical Optics Express
Dipping objectives were tested for multi-photon laser scanning microscopy, since their large working distances are advantageous for thick specimens and the absence of a coverslip facilitates examination of living material. Images of fluorescent bead
Autor:
Oscar Ces, Duncan Casey, David R. Klug, Mark A. A. Neil, Ian Munro, Peter M. P. Lanigan, E. J. Grace, John Phillips
Publikováno v:
Biomedical Optics Express
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ResearcherID
This paper demonstrates spatially selective sampling of the plasma membrane by the implementation of time-multiplexed holographic optical tweezers for Smart Droplet Microtools (SDMs). High speed (>1000fps) dynamical hologram generation was computed o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c233011ff98180b4cc4d06bfc947812d
http://hdl.handle.net/10044/1/13172
http://hdl.handle.net/10044/1/13172