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Developmental responses (pericardial edema, yolk sac swelling, axial malformations) were monitored by microscopy.
To examine the effects of Emuc in vitro using our viral vector transduction system, the morphology of the cultured adherent cells transduced with the viral vectors was monitored by microscopy.
Disruption of the cells was monitored by microscopy.
The development of tetrads was monitored by microscopy.
Calcium was then reintroduced to myocytes gradually to achieve a concentration of 1 mM, while being monitored by microscopy.
Haploid cell pseudohyphal growth was induced on YPD plates supplemented with 1% (v/v) 1-butanol at 30°C for 1 day, and then monitored by microscopy [30].
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The subcellular localization of IDD8-AKIN10 complexes was monitored by DIC microscopy and fluorescence microscopy.
Cellular uptake of PTX-PLGA NPs with and without aptamer conjugation was studied using GI-1 cells and monitored by confocal microscopy and phase contrast microscopy.
Depolarization-induced Ca2+ influx was monitored by TIRF microscopy (total internal fluorescent microscopy) in myotubes loaded with fluo-4-AM.
GFP or CFP fusion proteins were monitored by fluorescence microscopy and further verified by confocal microscopy as described previously (Yang et al., 2001).
The process was monitored by fluorescence microscopy.
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