Sentence examples for mutations are somewhat from inspiring English sources

Notably, disease-causing mutations are somewhat equally distributed in all four Nav channel domains, which account for more than 20 sodium channelopathies (Fig. 4C).

Therefore, nmdΔ mutations are somewhat unusual in that they result in short telomeres but suppress cdc13-1.

Estimates that as many as 23% of amino acid mutations are somewhat deleterious, and present mostly in heterozygous individuals [ 35], suggests that consanguinity should increase homozygosity at these sites and lead to more pronounced effects in inbred populations.

Other studies have found that the relative risks associated with CHEK2 1100delC and ATM mutations are somewhat higher at young ages (The CHEK2 Breast Cancer Case Control Consortium, 2004; Thompson et al, 2005).

The conditions for such faster-X evolution for beneficial mutations are somewhat more relaxed when the effective sex ratio is biased toward females, or there is a higher variance of fitness in males (Vicoso and Charlesworth 2009).

The cell type specific effect of the PTB binding site mutations is somewhat intriguing and may be due to the apparent heterogeneity of PTB expression in AK-D cells (Fig 11b).

During the intermediate follow-up period that varied from 9 to 22 months after transmission between recipients, we found only one reverting mutation and very few forward mutations in Gag while in Env and Nef the numbers of AA reversions and forward mutations were somewhat higher albeit still low.

Furthermore, the general pattern of base substitution in the NBS patients (829 mutations) was somewhat different from that in controls (750 mutations), with significantly more transversions (49.3% vs. 44.3%, χ2 test, p<0.05) and substitutions occurring at G residues (41.4% vs. 35.6%, χ2 test, p<0.05; Fig. 1C).

The clinical impact and outcome of having BRCA mutations is somewhat unclear in humans [ 12- 15].

This incidence of UVB signature mutations is somewhat higher than the frequencies reported in other studies.

For the 'B' families, the predicted number of BRCA2 mutations is very similar to the observed number, but the number of BRCA1 mutations is somewhat higher than predicted (21 vs 15.30 respectively for the polygenic model).