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This proposed label-free impedimetric biosensor is simple, cost-effective and feasible to detect changes in the lindane concentration as low as 120 μg L−1 in less than 2 days without sample pretreatment.
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Biomarker validation studies should use standardized collection conditions, use multiple control groups, and/or collect samples from cases prior to influence of diagnosis whenever feasible to detect and correct for potential biases associated with sample collection.
However, it was feasible to detect lung and brain metastases from breast and lung cancer.
The pilot demonstrated that it was feasible to detect, monitor and treat depression in routine general practice alongside the usual biophysical measures, and identified moderate-to-severe depression in 34% of participants.
We found that it is technically feasible to detect normal and atypical breast ductal epithelial cells using routine cytologic preparation methods and a modified classification system, adapted from King et al [ 4].
In past years, with the development of new methods, such as cardiac and respiratory gating [ 75– 78], it has been shown that DTI and magnetization transfer (MT) imaging were feasible to detect changes in the spinal cord in ALS [ 79– 81].
Early work indicates that it is feasible to detect the higher elasticity and stiffness of malignant breast tissue and benign masses or normal parenchyma, though clearly some overlap between stiff glandular parenchyma and soft malignancies would be expected [ 68, 69].
Consequently, it may not be feasible to detect all pairwise (and higher order) interactions given a large set of pollutants.
In other diseases it is frequently not feasible to detect correlations between objective measurements and quality of life evaluations.
Results obtained with simulated and experimental data at 10 Å suggest that it is also feasible to detect the correct superfamily of the domains when dealing with electron microscopy maps containing multi-domain proteins.
In the current study, we tested whether it was feasible to detect circulating FRα in ovarian cancer patients and whether the circulating FRα was full-length and functional.
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