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Furthermore, collapsing the density distribution to 1D profiles along the vertical axis (Fig. 4 B ) allowed for direct comparison with previously reported profiles obtained from dendrite morphologies traced from in vitro preparations (Meyer, Wimmer, Hemberger, et al. 2010).
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To quantify the change in mitochondrial morphology, mitochondria were traced from TEM micrographs, and their morphology was analyzed as previously described (Picard et al, 2013).
Since the morphology of neuronal trees corresponds to the continuous bounds of their cytosolic membrane, the 3D location and thickness of each branch are typically traced from the image stack of the membrane label.
Earlier changes were traced from literature review.
The theoretical curves are traced from (17).
Digital representation of neuronal morphology using light microscopy has traditionally relied on manual tracing from a computer screen [30], [31], and is prone to subjective errors.
Red traces in AI and white traces in Q maps fault traces from corresponding coherency map.
Black lines fault traces from coherency map.
White lines fault traces from coherency.
(D ) Example traces from touching RBC pair.
(B ) Sample eyelid position signal traces from a mouse undergoing trace eyeblink conditioning.
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