Sentence examples for mutants at an from inspiring English sources

The classification of mutants based on secondary structure (helix, strand, turn and coil) and solvent accessibility (buried, partially buried, partially exposed and exposed) distinguished the stabilizing/destabilizing mutants at an average accuracy of 81% and 80%, respectively for ΔΔG and ΔΔGH2O.

In addition, the number of Brn3-positive retinal ganglion cells is remarkably reduced in the mutants, although in this region the retinal layers are similar to wild-type eyes (Fig.  9B, a c and f h), indicating that the retinal ganglion cells are affected in mutants at an early postnatal period (3 weeks).

It is likely that such changes would have widespread consequences for ionic homeostasis in the inner ear and that altered osmolalities between compartments might lead to expansion of the endolymphatic space seen in the Atp6v0a4 mutants at an early developmental stage.

Mutagenesis and screening of 11,000 mutants at sites A-G generated ~500 mutants with higher activity toward carboxymethyl cellulose (CMC) after pre-incubation at 50°C for 45 min than the wild-type TrEGI expressed using cell-free synthesis.

Fig. 7 Oxidation of benzopyrene by CueO and its mutants at a pH 3.5 and 30 °C, and b pH 3.5 and 60 °C.

To analyze the unfolding process of active AQN mutants at a fixed temperature, changes in the CD spectra of the wild-type enzyme, D17N, E237Q, D212N or D183N as a function of time were recorded at 70°C and 80°C.

Initial populations are clonal, but at division, each clone generates mutants at a rate μ that differ in fitness from the parent clone.

The low copy number wild type was able to back invade the higher copy mutants at a much smaller copy number when non-conjugal plasmids were present.

Probability generating function is used to study the probability of colony extinction, probability of treatment success, and the probability of having resistant mutants at a given colony size.

To analyze when reinforcement takes place, we introduce mutants at a locus for female mating preference and study under which circumstances such mutants can invade, and whether this results in divergence at the preference locus.

This link, discovered during an extensive analysis of dna(Ts) suppressors, is very strong as some metabolic alterations fully restore growth of dna(Ts) mutants at a temperature at which a lethal arrest of DNA synthesis otherwise occurs.