Sentence examples for mutants share the from inspiring English sources
Negative, non permeable, mutants share the opposite feature since they are monomorphic.
Note that all mutants share the same set of users (U), roles (R), permissions (Pr) and inputs (I) of the original policy P. The set ( mathcal {R}^{P}_{fault}) of faulty policies is generated by making changes using two kinds of operators: mutation operators and element modification operators.
Consistent with this idea, let-418 and mep-1 mutants share the same phenotype that includes an L1 larval arrest and derepression of germline specific genes in somatic cells of the arrested larvae.
All the mutants were expressed in bacteria and purified as wild type CrSPI-1-D1 (Figure S1).The CD spectrum was recorded on all 15 mutants of CrSPI-1-D1, whindicatedathatthesethese mutants share the same α/β structure as the wild type CrSPI-1-D1 (Figure S2).
Another link between a potential plant heterotrimeric G protein and LRR-RLKs was demonstrated by the observation that gpa1 mutants share the same level of insensitivity to GAs during seed germination as mutants for the LRR-RLK protein BRI1 [ 33].
All knockout mutants shared the same genetic background of the overcompensating Col-4 genotype; mutants with the L er genetic background were not available.
The H251A mutant shared the same GlcNAc-binding site as the WT during most of the simulation time.
In contrast to previous findings (Rasmussen et al. 1994), we found that the Aspergillus nidulans calcineurin catalytic subunit (calcineurin A, or CnaA) was not essential and that the cnaA deletion mutant shared the morphological phenotypes observed in the corresponding A. fumigatus mutant, calAΔ (Soriani et al. 2008).
These mutants share in common with the bubR1 mutant, the property of high rates of chromosome nondisjunction.
Because dachs and ft dachs mutants share a similar phenotype, the defect in Fz-EYFP localization is likely due to the lack of Dachs.
This is absolutely in line with our observation that the three mutants share a common signalling pattern which is independent of the location of the mutation within the receptor chain.
