Optimizing and extending light-sculpting microscopy for fast functional imaging in neuroscience

Biomedical Optics Express

Volumn 6, Issue 2, 2015, Pages 353-368

  Rupprecht, Peter ^a,b,c   Prevedel, Robert ^a,b   Groessl, Florian ^a   Haubensak, Wulf E ^a   Vaziri, Alipasha ^a,b  

^a RESEARCH INSTITUTE OF MOLECULAR PATHOLOGY   (Austria)

^b UNIVERSITY OF VIENNA   (Austria)

^c FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN; COMMERCE; DYNAMICS; ECONOMIC AND SOCIAL EFFECTS; HIGH SPEED CAMERAS; IMAGE ENHANCEMENT; IMAGING TECHNIQUES; NEURONS; TISSUE;

CELLULAR POPULATIONS; DEPTH PENETRATION; FUNCTIONAL IMAGING; HIGH SPEED IMAGING; NEURONAL DYNAMICS; NEURONAL NETWORKS; SCATTERING EFFECTS; SINGLE-CELL LEVEL;

NEURAL NETWORKS;

ANIMAL TISSUE; ARTICLE; CAENORHABDITIS ELEGANS; CALCIUM IMAGING; CELL SYNCHRONIZATION; COMPARATIVE STUDY; FLUORESCENCE MICROSCOPY; FUNCTIONAL NEUROIMAGING; IMAGE QUALITY; IMAGE SIZE; IMAGING; IMAGING SPEED; LIGHT SCATTERING; LIGHT SCULPTING MICROSCOPY; MOUSE; NEUROSCIENCE; NONHUMAN; PROCEDURES; SCANNING ELECTRON MICROSCOPY; SIMULATION; ZEBRA FISH;

EID: 84922206369     PISSN: None     EISSN: 21567085     Source Type: Journal    
DOI: 10.1364/BOE.6.000353     Document Type: Article

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