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Similar methods could be used once future studies identified the molecules that are exchanged through GJIC.
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Future studies identifying ATL9's targets and its possible interacting partners will be integral in order to better assess its role in innate immunity and defense against fungal pathogens.
Future studies identifying such a reductase would be taken as support for a NOD function for SynHb but, more importantly, this observation demonstrates the potential use of E. coli AG1000 as a background for reductase screening in co-expression experiments.
Future studies identifying how these phosphatases and kinases regulate ER and its cooperating factors might improve the anti-estrogen therapies.
It is very important that future studies identify potential markers of response to everolimus and validate their role.
Future studies identifying the molecules involved in cell cell contact formation and separation will be needed to interpret the outcome separation measurements in relation to the adhesion energy.
Future studies identifying and assessing the effect of genetic variation on AMH levels may look to integrate such genetic data into these diagnostic tests to improve predictive power.
Thus, it will not be possible to determine which alleles are ancestral vs. derived until future studies identify causal genes/mutations.
It is hoped that future studies identify specific clinical signs or biomarkers that more specifically point toward specific underlying neuropathologies, with respect to both their quantity and quality.
Future studies identifying further dysregulated miRNAs may discover novel pathways involved in islet dysfunction that could provide novel therapeutic targets for diabetes treatment.
It will be interesting to see whether future studies identify the new activity of Cdk9 of our study as being the same or different from any of the previously reported mechanisms.
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