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Hence we set out to validate this specific aspect of T-IhNSCs behaviour.
Hence, we set out to validate whether Usf1 might be truly causal for these eQTL.
We set out to validate ARACNe target predictions, TRNASFAC-based binding site predictions, co-factor binding predictions, and de novo motif discovery predictions.
Since antibodies for the different CDK substrates (cyclins) are not available, we set out to validate these findings by using a pan CDK p-substrate western blot.
Next we set out to validate the transformants with PCR and restriction digestions.
We set out to validate and extend our previous data using C3H/HeJ mice that demonstrated an important role for TLR4 in K. pneumoniae pneumonia.
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As an important regulatory factor of SPRY4-IT1 expression, we next set out to validate whether EZH2 could also affect NSCLC cell proliferation.
Other studies set out to validate the items and their interrelationships within a model, discussed below (see table 1 for descriptions of models).
This study set out to validate a map book system for use in urban slums with no municipal address systems, where classification has been shown to be inaccurate when address descriptions were used.
This study set out to validate the Hs27 ReadyCell assay (RCCNA) as an alternative CCNA method compared against a commonly used commercial enzyme immunoassay (EIA) method and toxigenic culture (TC) reference standard.
The present study set out to validate a single depression rating item submitted by SMS text message (R-SMS-DS) against data of the widely validated PHQ-9 concurrently collected by post, which were available for a depressed adult sub-population of the UK ACUDep trial.
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CEO of Professional Science Editing for Scientists @ prosciediting.com