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1.
Appl Opt ; 54(2): 184-8, 2015 Jan 10.
Artigo em Inglês | MEDLINE | ID: mdl-25967615

RESUMO

We extend the principles of time-resolved super-resolution source localization from diffractive microscopy to the imaging of objects through scattering media. We show that isolation and localization of the scattering (versus diffractive) point-spread function can be done by individually illuminating or individually darkening image segments. We experimentally demonstrate reconstruction of both bright and dark sources. Further, we show that self-focusing nonlinearity improves the localization accuracy for bright sources.

2.
J Biophotonics ; 5(5-6): 425-36, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22461190

RESUMO

In this work we present how to entirely remove the scattering ambiguity present in existing multiphoton multifocal systems. This is achieved through the development and implementation of single-element detection systems that incorporate high-speed photon-counting electronics. These systems can be used to image entire volumes in the time it takes to perform a single transverse scan (four depths simultaneously at a rate of 30 Hz). In addition, this capability is further exploited to accomplish single-element detection of multiple modalities (two photon excited fluorescence and second harmonic generation) and to perform efficient image deconvolution. Finally, we demonstrate a new system that promises to significantly simplify this promising technology.


Assuntos
Microscopia de Fluorescência por Excitação Multifotônica/métodos , Imagem Molecular/métodos , Espalhamento de Radiação , Animais , Celulose/metabolismo , Drosophila melanogaster/citologia , Processamento de Imagem Assistida por Computador , Proteínas Luminescentes/metabolismo , Amido/química , Zea mays/química , Proteína Vermelha Fluorescente
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