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At the cell-type level, bulk labeling of VPM boutons in combination with in vitro-labeled dendrite morphologies was used previously to estimate the number and 1D innervation profile of VPM synapses for L2, L3, L4ss/sp, L5st/tt, and L6 neurons.
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Manganese dioxides (α−MnO2) with different morphologies are used as reactive templates as well as oxidants.
Thus, an image processing technique based on mathematical morphology was used to solve this problem.
Morphology was used to identify subspecies such as the Barbary lion and Cape lion.
Gut morphology was used to stage the embryos.
Their distinctive cellular morphology was used to confirm that the cells were epithelial.
DNA morphology was used to identify cells at the desired stage of the cell cycle.
A specific script for automated detection of neurons and analysis of their morphology was used.
Morphology was used to define the second group of populations (deep or shallow types).
For example, keratocyte morphology was used as an experimental indicator of cornea hydration state.
This effect of swelling on keratocyte morphology was used as real-time indicator of corneal hydration during NLOM-OCM measurements.
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