4D in in vivo 2-photon laser scanning fluorescence microscopy with sample motion in 6 degrees of freedom

Journal of Neuroscience Methods

Volumn 200, Issue 1, 2011, Pages 47-53

  Scheibe, Sabine ^a   Dorostkar, Mario M ^a   Seebacher, Christian ^a   Uhl, Rainer ^a   Lison, Frank ^b   Herms, Jochen ^a  

^a UNIVERSITY OF MUNICH   (Germany)

^b TILL Photonics GmbH   (Germany)

Author keywords

Angle adjustment; Chronic imaging; Hexapod; In vivo imaging; Orientation; Volume alignment

Indexed keywords

YELLOW FLUORESCENT PROTEIN;

ALZHEIMER DISEASE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN; COMPUTER PROGRAM; CONTROLLED STUDY; FLUORESCENCE MICROSCOPE; FOUR DIMENSIONAL IMAGING; IMAGING AND DISPLAY; IN VIVO STUDY; LASER; MOTION; MOUSE; MULTIPHOTON MICROSCOPY; NERVE CELL; NEUROIMAGING; NONHUMAN; PRIORITY JOURNAL; SAMPLING; STRUCTURE ANALYSIS; TWO PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY;

ALZHEIMER DISEASE; ANIMALS; BACTERIAL PROTEINS; DISEASE MODELS, ANIMAL; EQUIPMENT DESIGN; FLUORESCENT DYES; IMAGE PROCESSING, COMPUTER-ASSISTED; IMAGING, THREE-DIMENSIONAL; LUMINESCENT PROTEINS; MICE; MICE, TRANSGENIC; MICROSCOPY, CONFOCAL; MICROSCOPY, FLUORESCENCE; NEURONS; SOFTWARE; SOFTWARE VALIDATION;

EID: 79960892379     PISSN: 01650270     EISSN: 1872678X     Source Type: Journal    
DOI: 10.1016/j.jneumeth.2011.06.013     Document Type: Article

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