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Fig. 5 Displacement vectors at cutting direction of {100} < 001>, and slice plane of (a) B-B, (b) C-C; cutting direction of {100} < 011>, and slice plane of (c) B-B, (d) C-C; cutting direction of {110} < 001>, and slice plane of (e) B-B, (f) C-C.

This slice plane was chosen to cover the cortex and brainstem with the smallest number of slices possible.

Incorrect slice plane positioning excluded the experiments of one subject, and a significant motion artifact excluded the D4 experiments of subject 1.

The same holds for V3, though some phases are not seen in Figure 2A because they are out of the slice plane.

We selected neurons with dendrites positioned at an angle of ∼30° 45° from the slice plane and imaged the entire dendrite over multiple planes to localize and quantify Δ[Ca2+]i signals using two-photon microscopy.

From each image, a random microvessel oriented parallel to the slice plane was selected.

Unlike conventional tomography, DTS is not limited to reconstruction of a single plane, but can generate an arbitrary number of slice planes orthogonal to the projection direction.

The pulse sequence begins with m temporally sequential excitation pulses to produce signal in multiple adjacent slice planes.

Nine contiguous pseudocoronal 5-mm thick functional slice planes (1.5×1.5 mm resolution in-plane) were sampled, and 72 such volumes were collected over each 216-s experiment.

Such symmetry was occasionally evident in individual pseudocoronal slice planes that happened to include both pre- and postcentral gyri (Fig. 3).

After coregistering a subject's functional and anatomical slice planes, phase-coded functional data were assigned to one of the regions of interest (ROIs).