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The intensity and position of stains in epithelial tissue positive for this marker were also analyzed.
This indicates a redundancy for this marker at this stage in neural differentiation.
The population attributable risk for this marker was estimated to be 10.7%.
Hence, the allelic frequencies for this marker will increase and decrease purely by random genetic drift.
Taken together, these results may indicate a role for this marker in cancer progression, raising new possibilities for research, targeting FOXP3.
In the United Kingdom, Clarke said, 21 labs test for this marker, but only two use the test approved by U.K. regulators.
The researchers then inserted the DNA that codes for this marker into the zebrafish genome, tying it to a specific protein found only in neurons.
The positive area for this marker was measured in the dentate gyrus.
MATP's single allelic dropout rate was incalculable since all samples were homozygous for this marker.
Sensitivity and specificity values of 86.7% and 100%, respectively, were obtained for this marker.
Statistical power to evaluate interactions for this marker of exposure is not sufficient.
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