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1 thyl ester, and fluorescence was measured by laser scanning confocal microscope.
2 al imaging of the primary tumor in situ on a laser scanning confocal microscope.
3 ber of ingested beads was determined using a laser scanning confocal microscope.
4 e Fluo-3 AM and measured fluorescence with a laser scanning confocal microscope.
5 e dimensions in corneal whole-mounts using a laser scanning confocal microscope.
6 the single-particle level is obtained with a laser scanning confocal microscope.
7 oltage-clamped cut frog muscle fibers with a laser scanning confocal microscope.
8 d with the fluorescence from Fluo-5F using a laser-scanning confocal microscope.
9 Ca2+ sparks were recorded at 240 Hz using a laser scanning confocal microscope, allowing observation
10 rmed using consecutive images collected on a laser scanning confocal microscope and ANALYZE software.
12 T was detected using a spectrofluorometer, a laser scanning confocal microscope, and an inverted fluo
13 c resonance imaging (MRI), three-dimensional laser-scanning confocal microscope, and functional neuro
14 c strain measurements of the cornea, using a laser-scanning confocal microscope, are a valuable tool
17 t until now the great resolving power of the laser scanning confocal microscope has not been utilized
18 uo-3), was developed to numerically simulate laser scanning confocal microscope images of Ca(2+) "spa
19 g spatial intensity distribution analysis to laser scanning confocal microscope images of cells stabl
21 cellular ionised calcium with fluo-4 using a laser scanning confocal microscope showed local or globa
22 ssed by the TUNEL assay and evaluated with a laser scanning confocal microscope to determine the perc
23 es to image through the lens of the eye or a laser scanning confocal microscope to image through the
24 orescence recovery after photobleaching in a laser-scanning confocal microscope to visualize in real
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