Sentence examples for mutations when compared from inspiring English sources

We show that pyrosequencing pooled surveillance specimens can cost-competitively detect protease TDR mutations when compared with conventional methods.

Sequences contained from one to 28 (on the average 11) mutations, when compared to the HIV-1 subtype B consensus sequence reported at the Stanford database [35].

Further, in the HA gene, the Ck/India/WB-NIV2812/08 isolate of Birbhum showed a maximum of six unique mutations when compared to other Indian isolates.

Our data combined with the data of Kastritis et al. show a significantly lower frequency of truncating mutations when compared with data obtained for colorectal cancer from the COSMIC database (p<0.0001, Chi-2).

Thus, no decrease in BRG1 expression levels was observed in patients with Pro327Pro and Pro1297Pro mutations when compared to controls.

In parallel to the effect on serum ceruloplasmin oxidase activities we observed an earlier onset of WD in patients with truncating ATP7B mutations when compared to missense mutations.

We had previously shown that there is a correlation between degree of detachment and degree of deafness associated with ck/MyoVIIA mutations when comparing antennae with no, partial, or complete JO organization [8].

There were no significant differences in frequencies of SPINK1, CFTR and CTRC mutations when comparing the male and female patients.

Also, we have previously shown that the positively selected gene CT105 (a pseudogene for ocular strains) has a significant overrepresentation of nonsynonymous mutations when comparing sequences between urogenital and LGV strains (Borges et al. 2012), indicating that it has been evolutionarily diverging toward niche-specific adaptation.

Microarray analysis confirmed this dysregulation: elevated expression (1.5 fold) of the LDL receptor gene was readily detected in NPC fibroblasts homozygous for the I1061T mutation when compared with normal fibroblasts (Table 1).

DNMT3L methylation percentage across all CpG sites analysed for cases with BRAF and KRAS mutation revealed increased methylation of the DNMT3L promoter in cases with a KRAS mutation when compared with polyps with the normal variant (p = 0.0053), however due to small number of cases this observation need to be investigated in a larger number of polyps harbouring KRAS mutation.