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In contrast, gene mutation-dependent EGFR activation, being constitutive, might not vary in different cell compartments determining a similar basal potential of response in CSCs and differentiated cells.
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One of the challenges in comparing results across studies is that studies typically assess a somewhat different list of possible characteristics as potential moderators of response to treatment.
To investigate potential predictors of response to conventional DMARDs in RA.
In Experiment 2 we eliminated the potential effect of response bias.
As with all surveys constructed with a middle response option, potential sources of response error exist.
A dataset of immunohistochemistry stains in 411 patients was mined to identify potential markers of response.
The potential limitation of response bias has been widely described [ 37- 42].
In this context, PD-L1 expression has been proposed as a potential biomarker of response.
A further objective was to identify potential biomarkers of response to the combined cilengitide/PFE treatment.
Clearly, other potential markers of response, such as B-RAF status, require assessment in this context.
In further analyses other potential predictors of response to treatment are examined.
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