We introduce through this study a new conceptual framework to assessing microbicide acceptability and use by evaluating the interplay between social and biophysical acceptability.
These data are important for future research in evaluating the interplay between viral and host genetics in determining risk of HPV persistence and for progression to CIN3/cancer.
Furthermore, we evaluated the interplay and significance of the possible and presently only insufficiently understood transfer mechanisms.
Geomorphology has long been recognised as a key to evaluate the interplay between tectonics and landscape geometry in the regions of active deformation.
Therefore, it is critical to adopt a rational strategy, as demonstrated here, to evaluate the interplay of these factors, thereby greatly enhancing method development efficiency.
While the biological responses to the matrices examined in this study were not as significantly different as anticipated, the type of characterizations conducted in this study represent a systematic approach to evaluate the interplay between neuronal function, viability, biomarker expression, astrocyte proliferation, and overall culture composition.
This finding contradicts previously reported findings, and hence, further investigation is necessary to evaluate the interplay between these movements.
This makes it difficult to collate data across health, social, and criminal justice agencies and to evaluate the interplay between risk factors, the delivery of services, and outcomes.
We evaluated the interplay between cortactin S405 and S418 phosphorylation with cortactin tyrosine phosphorylation in regulating cortactin conformational forms by Western blotting.
In this study, we have generated site-specific antibodies against phosphorylated cortactin S405 and S418 to determine the spatial and temporal localization of cortactin in dynamic actin structures and human tumors, and to evaluate signaling interplay between cortactin tyrosine and serine phosphorylation events.
Therefore, we evaluated the interplay of cytogenetic changes and IFNα responses in the PEGINVERA cohort.
