Sentence examples for markers we propose from inspiring English sources

Based on their location, sequence features, and nucleosomal markers we propose that these might be part of subtelomeric regions of T. gondii.

Awaiting analysis of nuclear markers, we propose full species status for T. g. graeca (T. graeca) and T. g. ibera (T. ibera), based upon their divergent mtDNA lineages, with subspecies to be defined.

In the absence of more specific markers, we propose that the effective translation of the CSC hypothesis into patient benefit will necessitate the use of a panel of markers to robustly identify tumours enriched for CSCs.

Since these relationships are consistent between the two gene markers, we propose the new tribe Aleiodini nov. for the members of the Aleiodes clade, within which we recognise two genera, Aleiodes and Heterogamus stat.

Based on our findings and in the absence of more specific CSC markers, we propose that it may be necessary to utilise a panel of CSC markers in order to effectively translate knowledge of CSCs into patient benefit.

In view of its differential sensitivity to BFA in different root cells and its co-localization with different endosomal markers, we propose that ATM1 participates in various stages of endosomes biogenesis and function.

Instead of searching for a deficiency in any single marker, we propose that CFS is associated with a profound imbalance in the regulation of immune function forcing a departure from standard pre-programmed responses.

For a given marker, we propose a comparison of the associated LOD score with the distribution of the maximum LOD score at that marker.

Because immobilization does not change any of the autophagy markers studied, we propose that autophagy is not a regulator of long-term disuse atrophy.

Second, rather than performing the TDT at each marker separately, we propose a single test statistic that follows a X2 distribution with 1 df, under the null hypothesis of no linkage or linkage disequilibrium to the region.

Summarizing our data on the different marker molecules, we propose the following model of different fibroblast subpopulations in the human kidney (Fig. 10): Cadherin-9 is expressed by all fibroblast subpopulations of the human kidney defined in this study.