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Cells expressing FRNK, FAK siRNA or their respective control cells were plated on three different substrates; fibronectin, collagen and matrigel, at low densities in the presence of serum, and their random motility were monitored by time-lapse microscopy.
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SO motility was monitored with conventional low-compliance, continuous perfusion technique at ERCP (n = 9) or via percutaneous transhepatic cholangioscopy (n = 2).
Nanoparticle motility was monitored using multi-color, time-lapse fluorescence microscopy for the formation of actin comet tails attached to the fluorescently labeled vehicle.
Macrophage motility was monitored by time-lapse videomicroscopy.
Motility was monitored in GN-11 neurons for control pSil-empty and α1-b, α1-c and α2-a clones by wound healing assays.
mTECs random motility was monitored by tracking cell nuclei every 10 min for 7 h with an FV10i microscopic time-lapse imaging system (Olympus).
Return of motility and beating cilia were monitored for up to 2 h.
However, sperm motility and viability (using propidium iodide as a vital stain) were monitored.
However, sperm motility and viability (using propitium iodide as a vital stain) were monitored.
On the day of the motility studies, appetite, satiety, nausea, epigastric fullness and epigastric pain (or discomfort) were monitored by the visual analogue scale (VAS) [ 27].
Mice were monitored daily and killed at signs of illness (anemia, weight loss and reduced motility).
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