Highly versatile confocal microscopy system based on a tunable femtosecond Er: Fiber source

Journal of Biophotonics

Volumn 1, Issue 1, 2008, Pages 53-61

  Trautlein D ^a   Adler, F ^a   Moutzouris, K ^a   Jeromin, A ^b   Leitenstorfer, A ^a   Ferrando May, E ^a  

^a UNIVERSITY OF KONSTANZ   (Germany)

^b ALLEN INSTITUTE FOR BRAIN SCIENCE   (United States)

Author keywords

DNA damage; Femtosecond technology; Fluorescent protein; Multiphoton microscopy; Photomanipulation; Three photon absorption

Indexed keywords

DNA DAMAGES; FEMTOSECOND TECHNOLOGY; FLUORESCENT PROTEIN; MULTI-PHOTON MICROSCOPY; PHOTOMANIPULATION; THREE PHOTON ABSORPTION;

FLUORESCENCE; IMAGING TECHNIQUES; LASER EXCITATION; LIGHT ABSORPTION;

CONFOCAL MICROSCOPY;

FLUORESCENT DYE;

ANIMAL; ARTICLE; CATTLE; CHEMISTRY; CONFOCAL MICROSCOPY; CYTOLOGY; DNA DAMAGE; ENDOTHELIUM CELL; HELA CELL; HUMAN; METHODOLOGY; MULTIPHOTON MICROSCOPY; PYRAMIDAL NERVE CELL; RADIATION EXPOSURE;

ANIMALS; CATTLE; DNA DAMAGE; ENDOTHELIAL CELLS; FLUORESCENT DYES; HELA CELLS; HUMANS; MICROSCOPY, CONFOCAL; MICROSCOPY, FLUORESCENCE, MULTIPHOTON; PYRAMIDAL CELLS;

EID: 58449111083     PISSN: 1864063X     EISSN: 18640648     Source Type: Journal    
DOI: 10.1002/jbio.200710019     Document Type: Article

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