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Su et al. validated a higher risk of ESRD in HCV males than females, but Tsui et al. did not examine this.
The RT-qPCR analysis validated a higher expression of YABBY members at an early stage of seed hair development and a relative low level of expression at later developmental stages, equivalent to the period of seed hair trichome elongation.
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To perform our analyses, we first devised and validated a high-throughput whole-genome single-cell sequencing method using two lymphoblastoid cell line single cells.
In this study, we developed and validated a high-density microarray for simultaneous screening of 14 bacterial pathogens using an approach that employs gold labeling with silver enhancement (GLS) protocol.
Khambay et al. [17] validated a high-resolution 3D imaging system (Di3D™, Dimensional Imaging Ltd., Glasgow, Scotland, UK) using only ten landmarks on facial plaster casts, comparing the results with those obtained by a coordinate-measuring machine (CMM), reporting a system error of 0.2 mm and a reproducibility error of less than 0.5 mm.
We validated a high number of variables that are regarded to be important for the study of AML prognosis.
Using this system, we developed and validated a high-throughput assay to screen small chemicals for an effect on Aβ42 oligomer formation.
For that reason we have recently developed and validated a high throughput yolk infection model using M. marinum with an automated microinjection system [ 12].
To address this limitation, we developed and validated a high-throughput and scalable SPR-based strategy for characterizing aptamer binding to small molecules.
Toward this objective we designed and validated a high throughput assay for general chromatin sensitivity to DNase I (GCSDI) as a powerful approach to determine chromatin compactness across genome.
The primary aim of this study was to validate a higher dosing regimen for amikacin in patients with severe sepsis and septic shock.
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