Microscopy, Fluorescence, Multiphoton
"Microscopy, Fluorescence, Multiphoton" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Fluorescence microscopy utilizing multiple low-energy photons to produce the excitation event of the fluorophore (endogenous fluorescent molecules in living tissues or FLUORESCENT DYES). Multiphoton microscopes have a simplified optical path in the emission side due to the lack of an emission pinhole, which is necessary with normal confocal microscopes. Ultimately this allows spatial isolation of the excitation event, enabling deeper imaging into optically thick tissue, while restricting photobleaching and phototoxicity to the area being imaged.
| Descriptor ID |
D036641
|
| MeSH Number(s) |
E01.370.350.515.458.500 E01.370.350.515.717.250 E05.595.458.500 E05.595.717.250
|
| Concept/Terms |
Microscopy, Fluorescence, Multiphoton- Microscopy, Fluorescence, Multiphoton
- Multiphoton Fluorescence Microscopy
- Microscopy, Multiphoton Fluorescence
- Fluorescence Microscopy, Multiphoton
- Multiphoton Excitation Microscopy
- Excitation Microscopies, Multiphoton
- Excitation Microscopy, Multiphoton
- Microscopies, Multiphoton Excitation
- Microscopy, Multiphoton Excitation
- Multiphoton Excitation Microscopies
|
Below are MeSH descriptors whose meaning is more general than "Microscopy, Fluorescence, Multiphoton".
- Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
- Diagnosis [E01]
- Diagnostic Techniques and Procedures [E01.370]
- Diagnostic Imaging [E01.370.350]
- Microscopy [E01.370.350.515]
- Microscopy, Fluorescence [E01.370.350.515.458]
- Microscopy, Fluorescence, Multiphoton [E01.370.350.515.458.500]
- Nonlinear Optical Microscopy [E01.370.350.515.717]
- Microscopy, Fluorescence, Multiphoton [E01.370.350.515.717.250]
- Investigative Techniques [E05]
- Microscopy [E05.595]
- Microscopy, Fluorescence [E05.595.458]
- Microscopy, Fluorescence, Multiphoton [E05.595.458.500]
- Nonlinear Optical Microscopy [E05.595.717]
- Microscopy, Fluorescence, Multiphoton [E05.595.717.250]
Below are MeSH descriptors whose meaning is more specific than "Microscopy, Fluorescence, Multiphoton".
This graph shows the total number of publications written about "Microscopy, Fluorescence, Multiphoton" by people in this website by year, and whether "Microscopy, Fluorescence, Multiphoton" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 2 | 1 | 3 |
| 2005 | 2 | 0 | 2 |
| 2006 | 0 | 1 | 1 |
| 2007 | 2 | 0 | 2 |
| 2008 | 2 | 0 | 2 |
| 2009 | 2 | 1 | 3 |
| 2010 | 1 | 0 | 1 |
| 2012 | 0 | 1 | 1 |
| 2013 | 2 | 1 | 3 |
| 2014 | 0 | 3 | 3 |
| 2015 | 2 | 1 | 3 |
| 2017 | 2 | 2 | 4 |
| 2018 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
| 2025 | 2 | 0 | 2 |
| 2026 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Microscopy, Fluorescence, Multiphoton" by people in Profiles.
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Designer indicators for two-photon recording of subthreshold voltage dynamics. Nat Methods. 2026 May; 23(5):986-997.
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Three-photon microscopy: an emerging technique for deep intravital brain imaging. Nat Rev Neurosci. 2025 Sep; 26(9):521-537.
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Multimodal optical coherence tomography and two-photon light sheet fluorescence microscopy for embryo imaging. J Biomed Opt. 2025 06; 30(6):060501.
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Two-photon frequency division multiplexing for functional in vivo imaging: a feasibility study. Opt Express. 2019 Feb 18; 27(4):4488-4503.
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Novel hemodynamic structures in the human glomerulus. Am J Physiol Renal Physiol. 2018 11 01; 315(5):F1370-F1384.
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SmartScope2: Simultaneous Imaging and Reconstruction of Neuronal Morphology. Sci Rep. 2017 08 24; 7(1):9325.
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Real-time in?vivo mitochondrial redox assessment confirms enhanced mitochondrial reactive oxygen species in diabetic nephropathy. Kidney Int. 2017 11; 92(5):1282-1287.
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In vivo three-photon imaging of activity of GCaMP6-labeled neurons deep in intact mouse brain. Nat Methods. 2017 Apr; 14(4):388-390.
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Ultraflexible nanoelectronic probes form reliable, glial scar-free neural integration. Sci Adv. 2017 Feb; 3(2):e1601966.
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Automatic Morphological Reconstruction of Neurons from Multiphoton and Confocal Microscopy Images Using 3D Tubular Models. Neuroinformatics. 2015 Jul; 13(3):297-320.