ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Microscopy, Fluorescence, Multiphoton

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Diagnosis ∟ Diagnostic Techniques and Procedures ∟ Diagnostic Imaging ∟ Microscopy ∟ Microscopy, Fluorescence ∟ Microscopy, Fluorescence, Multiphoton Medical Subject Headings (MeSH) ∟ Investigative Techniques ∟ Microscopy ∟ Microscopy, Fluorescence ∟ Microscopy, Fluorescence, Multiphoton Medical Subject Headings (MeSH) ∟ Natural Sciences ∟ Physics ∟ Optics ∟ Microscopy ∟ Microscopy, Fluorescence ∟ Microscopy, Fluorescence, Multiphoton X
Broader terms:	Medical Subject Headings (MeSH) ∟ Diagnosis ∟ Diagnostic Techniques and Procedures ∟ Diagnostic Imaging ∟ Microscopy ∟ Microscopy, Fluorescence ∟ Microscopy, Fluorescence, Multiphoton Medical Subject Headings (MeSH) ∟ Investigative Techniques ∟ Microscopy ∟ Microscopy, Fluorescence ∟ Microscopy, Fluorescence, Multiphoton Medical Subject Headings (MeSH) ∟ Natural Sciences ∟ Physics ∟ Optics ∟ Microscopy ∟ Microscopy, Fluorescence ∟ Microscopy, Fluorescence, Multiphoton Microscopy, Fluorescence > Microscopy > Diagnostic Imaging > Diagnostic Techniques and Procedures > Diagnosis > Medical Subject Headings (MeSH) Microscopy, Fluorescence > Microscopy > Investigative Techniques > Medical Subject Headings (MeSH) Microscopy, Fluorescence > Microscopy > Optics > Physics > Natural Sciences > Medical Subject Headings (MeSH) X
History note:	Microscopy, Confocal (1997-2002) \| Microscopy, Fluorescence (1996-2002)X
historyNote*:	2003 X
publicMeSHNote*:	2003 X
Scope note:	Fluorescence microscopy utilizing multiple low-energy photons to produce the excitation event of the fluorophore. 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. X
activeMeSHYear*:	2005 \| 2005A \| 2006 \| 2007X
dateCreated*:	2002-07-03X
dateEstablished*:	2003-01-01X
dateRevised*:	2004-07-28X
recordAuthorizer*:	jlsX
recordMaintainer*:	jlsX
recordOriginator*:	agsX
Type:	Concept X
URI:	X
Labels and equivalent concepts:	Multifotonifluoresenssimikroskopia (fi) Multiphoton Fluorescence Microscopy (en, replaced) Fluorescence Microscopy, Multiphoton (en, replaced) X
Share:	X