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DOI: http://dx.doi.org/10.7554/eLife.09617.014 Comparison of the anchor residues in TAPBPR-permitted versus TAPBPR-restricted peptides suggests TAPBPR enhances the selection of peptides with canonical anchor residues and consequently may help reduce the cell surface presentation of peptides with lower affinity.

The presence of an RNA secondary structure (nt 1 355-1 384) within the long 5′-UTR enhances the selection of the downstream AUG1397-1399 as the initiation codon to produce the 50-kDa isoform, whereas the two upstream RNA secondary structures (nt 1 255-1 268 and nt 1 286-1 342), involving sequences transcribed from two different chromosomes, are required to produce the 56-kDa isoform.

In gp250 SC mice with the well-established MCC-specific T cell features, we argued one positively selecting self-peptide enhanced the selection of certain TCRs with conserved CDR3 features to dominate in a given antigen response (such as gp250 favors the selection of MCC-specific T cells).

In many patients, the amount of drug delivered beyond the tip of the endotracheal tube may be negligible, and low drug pulmonary concentrations may enhance the selection of drug-resistant bacteria.

To enhance the selection of Pol II transcripts we have developed an efficient method of purifying RNA polymerase II (Pol II) transcripts regardless of their 3' polyadenylation status.

Our results will enhance the selection of appropriate targets for immunotherapeutic treatment of this disease.

The self-peptide gp250 enhanced the selection of Vα11+Vβ3+ T cells, which were the dominant TCR pair against MCC.

Therefore, identification of the vernalization and photoperiod response alleles will enhance the selection of cultivars with wide adaptability to a set of environments.

These results suggest that, like tapasin (Chen and Bouvier, 2007), TAPBPR can enhance the selection of high affinity peptides for binding to MHC I in vitro.

This assumption was supported by the finding of both qnrB and aac(6′ )-Ib-cr in two two ciprofloxacin resistant isolates as both genes have the ability to enhance the selection of chromosomal mutations [ 2].

To identify a surrogate pharmacodynamic marker that would be applicable to the broader AML/MDS population, and to enhance the selection of patients most likely to benefit from the addition of panobinostat, a quantitative flow cytometric assay was employed.