Sentence examples for mutations which appear from inspiring English sources

Computational results in accord with experimental data show that all mutations, which appear during in vitro evolution were either neutral or favorable for the reorganization energy.

We looked for associations between polymorphisms in the enriched patterns by identifying mutations which appear together in patterns and are simultaneously strongly associated with the longevity phenotypes.

Latent drivers are non-hotspot, lower frequency mutations, which appear like passenger mutations in that they do not cause malignancy.

Interestingly, the Human Gene Mutation Database (www.hgmd.cf.ac.uk) lists more than 130 mutations, which appear to be uniformly distributed over the entire length of the gene and concern invariant amino acids as well as regions of variability.

For example, a single sample from an individual tumour might reveal mutations which appear to be clonally dominant, but are then shown to be absent from other regions of the tumour (79– 81).

With its help, it is possible to detect the heteroplasmy level of both hereditary and somatic mitochondrial genome mutations which appear during the life of an individual or in pathological processes.

The study also aims to analyse the mutations which appeared through evolution process of residential buildings and identify the invariant elements and the main trajectories of modification established in the past, confirming their compatibility with the future development of Aleppo.

At the same time, low-level contamination would generate excessive back mutations, which appeared to reverse germline common polymorphisms into wild-type alleles.

The studies presented in this section clearly suggest that, in the body, CSPGs expressions impose their functions and any mutation which appear at nucleotide sequence of CSPGs may induce changes in their functions.

Our results indicate that, like many of the previously-reported SCN5A mutations in young children, the F1473C mutation, which appeared de novo in the proband of this study, causes marked changes in Nav1.5 channel inactivation that are predicted to have severe physiological consequences.

The novel c.5763dupT mutation, which appeared in two unrelated families, was the only recurrent alteration of the BRCA2 gene identified in this study.