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However these markers appear specific to particular tumours and no marker has identified cancer stem cells across tumour types.
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Given the fact that BDNF effects on MRS markers appear to be regionally specific (as indicated by the present and other results), this highlights the importance of investigating clearly defined and (presumably) functionally homogeneous brain regions.
Genic-SSR markers appear to be tightly linked to specific gene functions and perhaps even play a direct role in controlling important traits [ 25, 26].
Although alone no marker is absolutely specific for pericytes, collectively these markers appear to selectively identify an MSC-like pericyte.
Skewed markers appeared to be concentrated in specific areas for the different parents.
As TACAs are more or less associated with lymph node invasion and/or restricted to specific groups of patients, their use as prognosis markers appears rather limited.
Co-localization of fluorescent markers appeared yellow.
Two markers appeared to correlate with response.
Of the 205 markers genotyped, 128 markers appeared to amplify single marker regions and were polymorphic.
RICTOR (mTORC2 marker) and LAMP1 (lysosome marker) appear in fine granules distinct from GC foci.
In contrast, the Ins227bp marker appears to be more specific for Thoroughbreds, Quarter horses and related breeds and is distributed across other breeds only at minor frequency [ 11, 15].
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