Maximum imaging depth of two-photon autofluorescence microscopy in epithelial tissues (Q33832955)

29 July 2017

title

Maximum imaging depth of two-photon autofluorescence microscopy in epithelial tissues (English)

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29 July 2017

4

Adela Ben-Yakar

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29 July 2017

Nicholas J Durr

1

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29 July 2017

Christian T Weisspfennig

series ordinal

2

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29 July 2017

Benjamin A Holfeld

series ordinal

3

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29 July 2017

publication date

1 February 2011

1 reference

Journal of Biomedical Optics

29 July 2017

published in

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29 July 2017

volume

16

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29 July 2017

issue

2

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29 July 2017

page(s)

026008

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Imaging of epithelial tissue in vivo based on excitation of multiple endogenous nonlinear optical signals

29 July 2017

cites work

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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Multiphoton microscopy of endogenous fluorescence differentiates normal, precancerous, and cancerous squamous epithelial tissues

28 July 2018

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In vivo multiphoton fluorescence imaging: a novel approach to oral malignancy

28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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Multiphoton excitation microscopy of in vivo human skin. Functional and morphological optical biopsy based on three-dimensional imaging, lifetime measurements and fluorescence spectroscopy

28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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29 October 2018

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29 October 2018

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29 October 2018

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In vivo multimodal nonlinear optical imaging of mucosal tissue.

29 October 2018

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Measurement of group delay dispersion of high numerical aperture objective lenses using two-photon excited fluorescence

29 October 2018

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On the fundamental imaging-depth limit in two-photon microscopy.

29 October 2018

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Two-photon imaging to a depth of 1000 microm in living brains by use of a Ti:Al2O3 regenerative amplifier

29 October 2018

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Autofluorescence Microscopy of Fresh Cervical-Tissue Sections Reveals Alterations in Tissue Biochemistry with Dysplasia¶

29 October 2018

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Measurement of femtosecond pulses in the focal point of a high-numerical-aperture lens by two-photon absorption

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Epifluorescence collection in two-photon microscopy

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12 December 2020

Characterizing point spread functions of two-photon fluorescence microscopy in turbid medium

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Clinical two-photon microendoscopy

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Derivation of a Monte Carlo method for modeling heterodyne detection in optical coherence tomography systems

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In vivo nonlinear spectral imaging in mouse skin

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Simultaneous spatial and temporal focusing of femtosecond pulses

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Understanding the contributions of NADH and collagen to cervical tissue fluorescence spectra: Modeling, measurements, and implications

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Identifiers

DOI

10.1117/1.3548646

1 reference

29 July 2017

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29 July 2017

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