Sentence examples for contributions to progression from inspiring English sources
These observations indicate that deregulated expression of EEF1A2 might be a common contributor to the pathogenesis of mouse PCT and a subset of human MM in ways affecting disease initiation although contributions to progression are also possible.
They are treated as time-varying covariates, which means that their contributions to progression and regression of GORD may depend on the status they had at the time preceding the next transition during a given epoch.
On the basis of in silico analyses, we then compared the genes expressed in BM in stage IV GC patients to determine their contribution to progression.
There was no significant difference between the observed (14%) and expected (16%) contribution to progression of the thoracic segment (P = 0.70).
Thus the same genes that regulate EMT in epithelial cancer cells also regulate functional contributions to malignant progression from the tumor stroma.
Closer inspection of the two EMT gene sets reveals that many of the genes driving the enrichment in skin fibroblasts (i.e. the core enriched genes) are cell surface and secreted molecules that have been implicated in stromal contributions to tumor progression (Figure 6).
These strategies are likely to clarify the functional attributes of Treg and their contributions to disease progression.
Such an approach would permit multi-platform analyses that link together genetic, epigenetic and genomic contributions to cancer progression.
The discovery of this compound will enable further investigations into the biological activities of MRCK proteins and their contributions to cancer progression.
Thus, as smoking status changed with time, its effect in each epoch makes different contributions to disease progression and regression in the same individual.
Presently, whole exome sequencing with NGS may be a cost-effective way of screening for genetic mutations in coding regions, both in patients with familial ALS without an identified mutation, and to identify clustering of genetic variations in sporadic ALS that may help clarify genetic contributions to disease progression.
