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In summary, MyoR is not an exclusive marker of branchiomeric muscles as previously described [16], [40], but also labels extra ocular muscles in both chick and mouse embryos.
Our data thus question the relevance of FOXP3 as an exclusive marker for T-Regs, as has been emphasized recently by others [63], as well as the role of FOXP3 in T-Reg-mediated active suppression.
We demonstrated that Pou4f3, an exclusive marker for hair cells in the ear with limited expression outside the ear [33], [35], was expressed in hair cell-like cells in the remaining ganglia of the Neurod1 CKO ear (Fig. 3H) and colocalized with Myo VIIa (data not shown) identical to Atoh1 (Fig. 2H, H').
There is ample evidence that GFAP is not an exclusive marker of astrocytes.
However, there is strong agreement that α-SMA is not an exclusive marker for activated PSC.
FOXP3 represents a typical, although not exclusive, marker of regulatory CD4+ T-cells.
Similar(42)
These genes are potentially the exclusive markers of μG.
Extreme case 1: mutually exclusive markers for each subtype.
Surface antigens previously regarded as exclusive markers of naive T cells, such as L-selectin (CD62L), can also be detected on some memory T cells.
Exclusive markers extracted from serum, other biological fluids, or any sample obtained through minimally invasive techniques, can be realistically employed to discriminate cancers or other pathologies.
Hence, exclusive markers (i.e. having private alleles occurring only in native or exogenous populations) obtained good results even with few markers (5 10), and more markers were required when alleles were segregating in both native and exogenous populations at intermediate frequencies (i.e. more similar populations).
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