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Impossible problems.

BioTechniques

Webb WW.
PMID: 15884665
Biotechniques. 2005 Apr;38(4):515. doi: 10.2144/05384sp01.

No abstract available.

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Webb WW. Impossible problems. Biotechniques. 2005;38(4):515doi: 10.2144/05384sp01.
Webb, W. W. (2005). Impossible problems. BioTechniques, 38(4), 515. https://doi.org/10.2144/05384sp01
Webb, Watt W. "Impossible problems." BioTechniques vol. 38,4 (2005): 515. doi: https://doi.org/10.2144/05384sp01
Webb WW. Impossible problems. Biotechniques. 2005 Apr;38(4):515. doi: 10.2144/05384sp01. PMID: 15884665.
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Quartic-phase-limited grism-based ultrashort pulse shaper.

Optics letters

Field JJ, Durfee CG, Squier JA, Kane S.
PMID: 17975610
Opt Lett. 2007 Nov 01;32(21):3101-3. doi: 10.1364/ol.32.003101.

By replacing the dispersive element in a zero-dispersion pulse shaper with a grism, we have constructed a quartic-phase-limited pulse shaper. We demonstrate compensation of 4500 fs2 without the use of a dynamic element in the pulse shaping line, which...

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Field JJ, Durfee CG, Squier JA, et al. Quartic-phase-limited grism-based ultrashort pulse shaper. Opt Lett. 2007;32(21):3101-3doi: 10.1364/ol.32.003101.
Field, J. J., Durfee, C. G., Squier, J. A., & Kane, S. (2007). Quartic-phase-limited grism-based ultrashort pulse shaper. Optics letters, 32(21), 3101-3. https://doi.org/10.1364/ol.32.003101
Field, Jeffrey J, et al. "Quartic-phase-limited grism-based ultrashort pulse shaper." Optics letters vol. 32,21 (2007): 3101-3. doi: https://doi.org/10.1364/ol.32.003101
Field JJ, Durfee CG, Squier JA, Kane S. Quartic-phase-limited grism-based ultrashort pulse shaper. Opt Lett. 2007 Nov 01;32(21):3101-3. doi: 10.1364/ol.32.003101. PMID: 17975610.
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Spatial filtering nearly eliminates the side-lobes in single- and multi-photon 4pi-type-C super-resolution fluorescence microscopy.

The Review of scientific instruments

M K, Regmi R, Mondal PP.
PMID: 24089833
Rev Sci Instrum. 2013 Sep;84(9):093704. doi: 10.1063/1.4820922.

Super-resolution microscopy has tremendously progressed our understanding of cellular biophysics and biochemistry. Specifically, 4pi fluorescence microscopy technique stands out because of its axial super-resolution capability. All types of 4pi-microscopy techniques work well in conjugation with deconvolution techniques to get...

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M K, Regmi R, Mondal PP. Spatial filtering nearly eliminates the side-lobes in single- and multi-photon 4pi-type-C super-resolution fluorescence microscopy. Rev Sci Instrum. 2013;84(9):093704doi: 10.1063/1.4820922.
M, K., Regmi, R., & Mondal, P. P. (2013). Spatial filtering nearly eliminates the side-lobes in single- and multi-photon 4pi-type-C super-resolution fluorescence microscopy. The Review of scientific instruments, 84(9), 093704. https://doi.org/10.1063/1.4820922
M, Kavya, et al. "Spatial filtering nearly eliminates the side-lobes in single- and multi-photon 4pi-type-C super-resolution fluorescence microscopy." The Review of scientific instruments vol. 84,9 (2013): 093704. doi: https://doi.org/10.1063/1.4820922
M K, Regmi R, Mondal PP. Spatial filtering nearly eliminates the side-lobes in single- and multi-photon 4pi-type-C super-resolution fluorescence microscopy. Rev Sci Instrum. 2013 Sep;84(9):093704. doi: 10.1063/1.4820922. PMID: 24089833.
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Multimodal optical imaging with multiphoton microscopy and optical coherence tomography.

Journal of biophotonics

Tang S, Zhou Y, Ju MJ.
PMID: 22461146
J Biophotonics. 2012 May;5(5):396-403. doi: 10.1002/jbio.201100138. Epub 2012 Mar 28.

Two types of combined multiphoton microscopy and optical coherence tomography (MPM/OCT) are compared for multimodal optical imaging. Single-scale multiphoton microscopy and optical coherence microscopy (MPM/OCM) is shown to acquire multiple contrasts from MPM and OCT simultaneously. Multi-scale MPM/OCT is...

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Tang S, Zhou Y, Ju MJ. Multimodal optical imaging with multiphoton microscopy and optical coherence tomography. J Biophotonics. 2012;5(5):396-403doi: 10.1002/jbio.201100138.
Tang, S., Zhou, Y., & Ju, M. J. (2012). Multimodal optical imaging with multiphoton microscopy and optical coherence tomography. Journal of biophotonics, 5(5), 396-403. https://doi.org/10.1002/jbio.201100138
Tang, Shuo, et al. "Multimodal optical imaging with multiphoton microscopy and optical coherence tomography." Journal of biophotonics vol. 5,5 (2012): 396-403. doi: https://doi.org/10.1002/jbio.201100138
Tang S, Zhou Y, Ju MJ. Multimodal optical imaging with multiphoton microscopy and optical coherence tomography. J Biophotonics. 2012 May;5(5):396-403. doi: 10.1002/jbio.201100138. Epub 2012 Mar 28. PMID: 22461146.
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Imaging of protein crystals with two-photon microscopy.

Biochemistry

Padayatti P, Palczewska G, Sun W, Palczewski K, Salom D.
PMID: 22324807
Biochemistry. 2012 Feb 28;51(8):1625-37. doi: 10.1021/bi201682q. Epub 2012 Feb 16.

Second-order nonlinear optical imaging of chiral crystals (SONICC), which portrays second-harmonic generation (SHG) by noncentrosymmetric crystals, is emerging as a powerful imaging technique for protein crystals in media opaque to visible light because of its high signal-to-noise ratio. Here...

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Padayatti P, Palczewska G, Sun W, et al. Imaging of protein crystals with two-photon microscopy. Biochemistry. 2012;51(8):1625-37doi: 10.1021/bi201682q.
Padayatti, P., Palczewska, G., Sun, W., Palczewski, K., & Salom, D. (2012). Imaging of protein crystals with two-photon microscopy. Biochemistry, 51(8), 1625-37. https://doi.org/10.1021/bi201682q
Padayatti, Pius, et al. "Imaging of protein crystals with two-photon microscopy." Biochemistry vol. 51,8 (2012): 1625-37. doi: https://doi.org/10.1021/bi201682q
Padayatti P, Palczewska G, Sun W, Palczewski K, Salom D. Imaging of protein crystals with two-photon microscopy. Biochemistry. 2012 Feb 28;51(8):1625-37. doi: 10.1021/bi201682q. Epub 2012 Feb 16. PMID: 22324807; PMCID: PMC3293215.
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High-throughput nonlinear optical microscopy.

Biophysical journal

So PT, Yew EY, Rowlands C.
PMID: 24359736
Biophys J. 2013 Dec 17;105(12):2641-54. doi: 10.1016/j.bpj.2013.08.051.

High-resolution microscopy methods based on different nonlinear optical (NLO) contrast mechanisms are finding numerous applications in biology and medicine. While the basic implementations of these microscopy methods are relatively mature, an important direction of continuing technological innovation lies in...

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So PT, Yew EY, Rowlands C. High-throughput nonlinear optical microscopy. Biophys J. 2013;105(12):2641-54doi: 10.1016/j.bpj.2013.08.051.
So, P. T., Yew, E. Y., & Rowlands, C. (2013). High-throughput nonlinear optical microscopy. Biophysical journal, 105(12), 2641-54. https://doi.org/10.1016/j.bpj.2013.08.051
So, Peter T C, et al. "High-throughput nonlinear optical microscopy." Biophysical journal vol. 105,12 (2013): 2641-54. doi: https://doi.org/10.1016/j.bpj.2013.08.051
So PT, Yew EY, Rowlands C. High-throughput nonlinear optical microscopy. Biophys J. 2013 Dec 17;105(12):2641-54. doi: 10.1016/j.bpj.2013.08.051. PMID: 24359736; PMCID: PMC3882500.
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Breaking barriers for intravital imaging.

Nature methods

Strack R.
PMID: 34239097
Nat Methods. 2021 Jul;18(7):710. doi: 10.1038/s41592-021-01210-7.

No abstract available.

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Strack R. Breaking barriers for intravital imaging. Nat Methods. 2021;18(7):710doi: 10.1038/s41592-021-01210-7.
Strack, R. (2021). Breaking barriers for intravital imaging. Nature methods, 18(7), 710. https://doi.org/10.1038/s41592-021-01210-7
Strack, Rita. "Breaking barriers for intravital imaging." Nature methods vol. 18,7 (2021): 710. doi: https://doi.org/10.1038/s41592-021-01210-7
Strack R. Breaking barriers for intravital imaging. Nat Methods. 2021 Jul;18(7):710. doi: 10.1038/s41592-021-01210-7. PMID: 34239097.
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Breaking barriers for intravital imaging.

Nature methods

Strack R.
PMID: 34239097
Nat Methods. 2021 Jul;18(7):710. doi: 10.1038/s41592-021-01210-7.

No abstract available.

Cite
Strack R. Breaking barriers for intravital imaging. Nat Methods. 2021;18(7):710doi: 10.1038/s41592-021-01210-7.
Strack, R. (2021). Breaking barriers for intravital imaging. Nature methods, 18(7), 710. https://doi.org/10.1038/s41592-021-01210-7
Strack, Rita. "Breaking barriers for intravital imaging." Nature methods vol. 18,7 (2021): 710. doi: https://doi.org/10.1038/s41592-021-01210-7
Strack R. Breaking barriers for intravital imaging. Nat Methods. 2021 Jul;18(7):710. doi: 10.1038/s41592-021-01210-7. PMID: 34239097.
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Introduction: advanced multiphoton and fluorescence lifetime imaging techniques.

Microscopy research and technique

Diaspro A.
PMID: 17393529
Microsc Res Tech. 2007 May;70(5):397. doi: 10.1002/jemt.20464.

No abstract available.

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Diaspro A. Introduction: advanced multiphoton and fluorescence lifetime imaging techniques. Microsc Res Tech. 2007;70(5):397doi: 10.1002/jemt.20464.
Diaspro, A. (2007). Introduction: advanced multiphoton and fluorescence lifetime imaging techniques. Microscopy research and technique, 70(5), 397. https://doi.org/10.1002/jemt.20464
Diaspro, Alberto. "Introduction: advanced multiphoton and fluorescence lifetime imaging techniques." Microscopy research and technique vol. 70,5 (2007): 397. doi: https://doi.org/10.1002/jemt.20464
Diaspro A. Introduction: advanced multiphoton and fluorescence lifetime imaging techniques. Microsc Res Tech. 2007 May;70(5):397. doi: 10.1002/jemt.20464. PMID: 17393529.
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Superresolved multiphoton microscopy with spatial frequency-modulated imaging.

Proceedings of the National Academy of Sciences of the United States of America

Field JJ, Wernsing KA, Domingue SR, Allende Motz AM, DeLuca KF, Levi DH, DeLuca JG, Young MD, Squier JA, Bartels RA.
PMID: 27231219
Proc Natl Acad Sci U S A. 2016 Jun 14;113(24):6605-10. doi: 10.1073/pnas.1602811113. Epub 2016 May 26.

Superresolved far-field microscopy has emerged as a powerful tool for investigating the structure of objects with resolution well below the diffraction limit of light. Nearly all superresolution imaging techniques reported to date rely on real energy states of fluorescent...

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Field JJ, Wernsing KA, Domingue SR, et al. Superresolved multiphoton microscopy with spatial frequency-modulated imaging. Proc Natl Acad Sci U S A. 2016;113(24):6605-10doi: 10.1073/pnas.1602811113.
Field, J. J., Wernsing, K. A., Domingue, S. R., Allende Motz, A. M., DeLuca, K. F., Levi, D. H., DeLuca, J. G., Young, M. D., Squier, J. A., & Bartels, R. A. (2016). Superresolved multiphoton microscopy with spatial frequency-modulated imaging. Proceedings of the National Academy of Sciences of the United States of America, 113(24), 6605-10. https://doi.org/10.1073/pnas.1602811113
Field, Jeffrey J, et al. "Superresolved multiphoton microscopy with spatial frequency-modulated imaging." Proceedings of the National Academy of Sciences of the United States of America vol. 113,24 (2016): 6605-10. doi: https://doi.org/10.1073/pnas.1602811113
Field JJ, Wernsing KA, Domingue SR, Allende Motz AM, DeLuca KF, Levi DH, DeLuca JG, Young MD, Squier JA, Bartels RA. Superresolved multiphoton microscopy with spatial frequency-modulated imaging. Proc Natl Acad Sci U S A. 2016 Jun 14;113(24):6605-10. doi: 10.1073/pnas.1602811113. Epub 2016 May 26. PMID: 27231219; PMCID: PMC4914181.
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Scope and limitation of label-free multiphoton microscopy and probe-labeled two-photon microscopy for the endomicroscopic diagnosis.

Scanning

Chun HJ, Kim ES, Cho BR.
PMID: 24375013
Scanning. 2014 Jul-Aug;36(4):462-4. doi: 10.1002/sca.21133. Epub 2013 Dec 24.

We briefly describe the advantages and limitations of label-free multiphoton microscopy and probe-labeled two-photon microscopy for the endomicroscopic diagnosis. The two methods are complementary and more information can be collected from tissues by combining the two methods. Therefore, parallel...

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Chun HJ, Kim ES, Cho BR. Scope and limitation of label-free multiphoton microscopy and probe-labeled two-photon microscopy for the endomicroscopic diagnosis. Scanning. 2013;36(4):462-4doi: 10.1002/sca.21133.
Chun, H. J., Kim, E. S., & Cho, B. R. (2014). Scope and limitation of label-free multiphoton microscopy and probe-labeled two-photon microscopy for the endomicroscopic diagnosis. Scanning, 36(4), 462-4. https://doi.org/10.1002/sca.21133
Chun, Hoon Jai, et al. "Scope and limitation of label-free multiphoton microscopy and probe-labeled two-photon microscopy for the endomicroscopic diagnosis." Scanning vol. 36,4 (2014): 462-4. doi: https://doi.org/10.1002/sca.21133
Chun HJ, Kim ES, Cho BR. Scope and limitation of label-free multiphoton microscopy and probe-labeled two-photon microscopy for the endomicroscopic diagnosis. Scanning. 2014 Jul-Aug;36(4):462-4. doi: 10.1002/sca.21133. Epub 2013 Dec 24. PMID: 24375013.
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Multiphoton microscopy in surgical oncology- a systematic review and guide for clinical translatability.

Surgical oncology

König TT, Goedeke J, Muensterer OJ.
PMID: 31654957
Surg Oncol. 2019 Dec;31:119-131. doi: 10.1016/j.suronc.2019.10.011. Epub 2019 Oct 16.

BACKGROUND: Multiphoton microscopy (MPM) facilitates three-dimensional, high-resolution functional imaging of unlabeled tissues in vivo and ex vivo. This systematic review discusses the diagnostic value, advantages and challenges in the practical use of MPM in surgical oncology.METHOD AND FINDINGS: A...

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König TT, Goedeke J, Muensterer OJ. Multiphoton microscopy in surgical oncology- a systematic review and guide for clinical translatability. Surg Oncol. 2019;31:119-131doi: 10.1016/j.suronc.2019.10.011.
König, T. T., Goedeke, J., & Muensterer, O. J. (2019). Multiphoton microscopy in surgical oncology- a systematic review and guide for clinical translatability. Surgical oncology, 31119-131. https://doi.org/10.1016/j.suronc.2019.10.011
König, Tatjana Tamara, et al. "Multiphoton microscopy in surgical oncology- a systematic review and guide for clinical translatability." Surgical oncology vol. 31 (2019): 119-131. doi: https://doi.org/10.1016/j.suronc.2019.10.011
König TT, Goedeke J, Muensterer OJ. Multiphoton microscopy in surgical oncology- a systematic review and guide for clinical translatability. Surg Oncol. 2019 Dec;31:119-131. doi: 10.1016/j.suronc.2019.10.011. Epub 2019 Oct 16. PMID: 31654957.
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Showing 1 to 12 of 21 entries