The NIH-SSM was developed based on the NINR intramural research program's success in designing and implementing methods for examining identified symptoms or symptom clusters.
As noted in a recent review (Bellinger 2009), researchers conducting observational studies have great latitude in how exposure and outcome are measured and expressed, which methods for examining associations are employed, and which analyses among the myriad typically conducted are reported.
However, existing antibody-based methods for phosphorylation detection have been found to lack specificity, and methods developed for examining PPIs in vitro cannot be easily adapted for tissues samples.
Different methods for examining and isolating FZT metacercariae in fish fry and juveniles are needed because compression of whole fish bodies is efficient for processing of small fry and detecting any metacercariae present.
To qualitatively and quantitatively compare both models and thus highlight the effect of third and fourth infection we used a variety of methods for examining serotype and incidence dynamics.
The following review will highlight the advantages and challenges of using fluorescence spectroscopic methods for examining protein dynamics with a special emphasis on fluorescence resonance energy transfer and fluorescence anisotropy.
The Tu-L11 and Tu-tRNA assays provide convenient methods for examining the selectivity of TC binding to 70SIC programmed at the decoding center with cognate (UUU) and near-cognate (CUC) codons, and the ability of the misreading-inducing aminoglycoside antibiotics streptomycin (STR) and paromomycin (PAR) to modulate such selectivity.
Other chapters describe current methods for examining antibiotic resistance, mechanisms of resistance, and subtyping infectious strains.
We develop several numerical methods for examining the frequency dependence of both the outgoing solution and the FDRK.
