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This leads to the question of which cell type should be the cell source for tissue-engineering of ligament, the highly proliferating cells or the differentiated matrix producing cells.
Thus, genetic activity establishes an expression pattern, a "map", by means of which cell fate is determined depending on the relative positions of cells inside the tissue.
Similar lesions were found in control experiments in which dead cells were injected and also in the later experiments irrespective of which cell types were injected, indicating that the damage was due to the infusion regime [15].
Our data indicate that all three cytokines, regardless of which cell type they originate, contributed to MHEC induction of VCAM-1, ICAM-1, P-selectin, or E-selectin expression.
While the functional role of electrophysiology in stem cell biology is poorly understood, it has become clear that endogenous ion flows represent a powerful set of signals by means of which cell proliferation, differentiation, and migration can be controlled in regeneration and embryonic morphogenesis.
The granular layer was clearly stained, thus raising the question of which cell types and/or processes are targeted by ET: granule cells, GABAergic interneurons, the nerve fibers afferent to the granule cells (i.e. the mossy fiber nerve terminals), astrocytes or oligodendrocytes.
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The variation of which cells exhibited the highest dark current as a function of the percentage of inhibition p is shown in Table 1.
Morphological alterations were used as a gauge of which cells were efficiently silenced for SEPT2.
The observations of variable suppressive capacity of Treg expansions [14] raise the question of which cells to use in expansion protocols.
Little is known of which cells initiate and control ejaculation.
This conclusion raises the question of which cells are involved.
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