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2. Since the difference in susceptibility of CD4+ and CD8+ T cells to BIM-mediated AICD is a novel observation, the authors should discuss this data more extensively.
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We have now provided and discussed this data as requested.
We have now provided data showing the viral burden in a subset of infected patients and discussed this data further.
When discussing this question, data on the efficacy of routinely applicable reprocessing procedures for medical instruments against Aβ-, tau- and α-synuclein aggregates can provide helpful guidance.
The reason that we discuss these data in this study is that at first glance, this polysynaptic excitation might account for the individual variability.
In this review, we discuss the data existing in the literature regarding biocompatibility of nanoparticles for drug delivery applications.
In the next section, we discuss this process, which uses the data structures mentioned above.
The following sections summarize the toxicity data and discuss this in relation to the classification criteria for POPs and PBTs.
We have discussed all this data in the context of our hypothetical model.
As discussed, this redundancy of data can alter statistical analysis and lead to greater numbers of false discoveries.
We review the literature on this issue and discuss our data in relation to the results of this review.
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