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Compared with the SPR measurement, selective binding to the imprinted cavity can be more precisely detected by the proposed method, enabling us to prepare a new class of protein recognizable materials with the ability of the specific signal transduction of protein binding events.
We provide an alternative method enabling us to quantify the role of cell motility and cell proliferation separately.
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Notably, the SmartAmp2 method enables us to analyze mutations using a drop of whole blood and the dried blood spot.
Third, the use of a propensity-based method enabled us to address the challenge of potential confounding that has hampered previous analyses.
The direct visualization in 3-D using a synchrotron X-ray imaging method enabled us to study the growth patterns of acervuli in human PG and suggest their growth process.
This method enabled us to see the difference according to rosiglitazone use when the patients had the same level of baseline covariates between the cases and the controls.
The use of an automated brain segmentation method enabled us to estimate accurate, reproducible, and sensitive volumetric assessments of the brain.
This method enabled us to analyze the transcriptome of king penguin by using microarrays dedicated to the chicken.
However, use of this ultra thin needle extraction method enabled us to isolate cultivable strains, including Bacillus and Paenibacillus.
Application of the DD tomography method enables us to jointly determine hypocenter locations and the 3D velocity structure using absolute and relative event locations.
This encoding method enables us to quickly check the number of mismatches between two bit-strings, using two 'XOR' and one 'OR' bitwise operations.
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