Sentence examples for supplementary mutation from inspiring English sources

The Cbioportal MutationMapper online tool (http://www.cbioportal.org/public-portal/mutation_mapper.jsp) was used for generating supplementary mutation distribution plots.

We further corrected the mutation carrier probabilities based on supplementary mutation carrier testing of relevant members in some of the families.

M35-derived chromosomes were hierarchically genotyped for 59 additional mutations whereas M215* ×M35) chromosomes were analyzed for the V16 mutation (supplementary table S2, Supplementary Material online).

Seven of 26 strains assigned as VISA by Etest had the H481Y allele, one each carried H481L and H481N mutations, while none of the VSSA strains harbored H481 mutation (supplementary table S3, Supplementary Material online).

Within this haplogroup, a shift in location assignment from western Africa to eastern Africa was observed along the lineage leading to a cluster of three (former) E-U209* samples, defined by V2580 mutation (supplementary fig. S4, Supplementary Material online).

Although EGF-stimulated Tyr-phosphorylation was not affected by Y392F mutation (Supplementary Figure S1G), Y392F mutation also abolished the interaction with Grb2 (Supplementary Figure 1F).

Our data suggest that imatinib-resistant cell lines with T315I mutation (Supplementary Figures S4b and c) can be inhibited with everolimus with downregulation of the mTOR pathway (Supplementary Figure S4d).

In both cases, HOIPRBR-LDD forms ubiquitin chains with lysine-less ubiquitin (K0) and mutated ubiquitins that contain either a single lysine or a lysine point mutation (Supplementary Figure S1E).

A total of 141 different pathogenic mutations were detected in 173 mutation-positive individuals (excluding monoallelic MUTYH mutations) (Supplementary Table S3 online).

A total of 51 Japanese local rice varieties (JRC) obtained from the DNA bank of NIAS were further used to trace the history of the single mutation (Supplementary Table 1).

We also investigated the haplotype structure in the NAT2 region by calculating the EHH [22] on both sides of each slow-causing mutation (Supplementary Fig. S2a, top line).