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This methodology enables us to study subtle changes in MOP/plasma membrane lipid dynamics in live cells, using ethanol concentrations that are relevant for its behavioral effects, at low, clearly not intoxicating (10 mM), intermediate (20 mM) and high concentrations (40 mM).
The methodology enables us to deal with luminance changes.
The new methodology enables us to encode an arbitrary signal accurately and efficiently.
For speech movements, this methodology enables us to extract at least six components once the head movements have been removed.
This vision-based methodology enables us to track the fingertips even when some fingers are not fully stretched out or when the luminance changes.
Compared to the traditional ways, this methodology enables us to construct both decoding-performance-aware and hardware-efficiency-aware LDPC codes in a short time.
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The use of this methodology enabled us to capture the landscape of interactions between genes known to be associated with BMI and to better understand which interactions are predictive of BMI.
This methodology enabled us to resolve (i) size variations of martensite sub-units, (ii) associated dislocation sub-structures, (iii) chemical heterogeneities, and (iv) the resulting local mechanical properties.
This methodology enabled us to distinguish between potential effects on energy stores due to manipulation of the circadian clock and to different amounts of light.
This methodology enabled us to study the activity of the BMP-2/6 heterodimer in a variety of experiments that require sub-milligram amount of ligands.
This methodology enabled us to get a wide range of responses that otherwise would not have been gathered.
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