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Applying other normalization methods also revealed significant differences between tissues (data not shown).
Computational methods also revealed a set of "transcription factor" proteins that regulate the expression of clusters of these genes.
However, our methods also revealed a T. cruzi-dependent block in the host cell cycle, at the level of cytokinesis, previously unrecognized for this pathogen-host cell interaction.
The new LC-MS/MS method, which is both more efficient and more sensitive than previous methods, also revealed novel features of the oxidant-specific distribution of these G oxidation products.
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Three different indirect methods also reveal the similar difference in size distribution in nanosystems synthesized in nonionic and anionic branched polymer matrices.
fMRI methods also reveal insight into the brain activity by demonstrating different activation patterns in subjects with RBT.
Our method also revealed that CNT dispersibility in solvent correlated with the pore sizes of CNT agglomerates.
The proposed method also revealed additional minor depositional processes on the sand flat, namely, the deposition of fluvial-channel lags and muddy particles.
The method also revealed the structure and function of many biological molecules, including vitamins, drugs, proteins and nucleic acids such as DNA.
The method also revealed notable differences of octapeptide sensitivity to PK in different types of human prion disease (figures 3 and 4).
Clustering analysis of the three networks by the depth-first-search method also revealed several 'orphan' reactions that were completely unconnected in their respective networks.
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