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Using isolated mitochondria as well as model lipid Langmuir monolayers coupled with Brewster Angle Microscopy, we explored systematically and comparatively the membrane activity and membrane-peptide interactions of fragments derived from the central helical hairpin of BAX, BCL-xL and BID.
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Next, we explored by electron microscopy how the loss of PGC-1α affects mitochondria in nigral dopaminergic neurons.
Because the Ca2+ channel genes detected encode targets of THI, we explored the distribution of the proteins in IDCs using confocal microscopy.
Based on the favorable photon yields exhibited by compounds 8, 15, and 21 we explored the utility of these dyes in a cellular super-resolution microscopy experiment.
We explored the usefulness of a new technology, live-imaging laser scanning confocal microscopy, as a tool for characterizing coral health state based on the signature of endogenous fluorescence.
Next, we explored the effects of regulatory elements on protein expression by using quantitative confocal microscopy.
We explored the hotel.
"We explored those over time".
In those times, we explored.
We explored the limits".
Here, we explored neurogenesis in fetal-derived human neural progenitors using the single cell analysis and direct lineage tracing capabilities afforded by time-lapse microscopy.
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CEO of Professional Science Editing for Scientists @ prosciediting.com