Sentence examples for mutants for other from inspiring English sources
It should be noted that in the cells grown on YPD plates, Rho3-mediated suppression in the Apm1 deletion cells was less prominent than that in the mutants for other subunits of the AP-1 complex.
We reasoned that if deletion mutants for other members of a particular protein complex share anc1Δ's damage sensitivity profile, this would pinpoint the complex via which Anc1 helps cells survive after chemical damage.
In addition, we found that a different neuron, PDA, is misguided in lin-44/Wnt and lin-17/Fz mutants but not in mutants for other components of the canonical pathway, including gsk-3, pry-1/Axin and bar-1/β-catenin (G.S.M., data not shown).
Next, we tested biofilm-deficient mutants for other FLO11 -dependent phenotypes.
Nevertheless, we are not aware of mutants for other genes with a similar or even close impact on the global response to Cu deficiency as spl7 mutants have.
A similar and specific increase in the number of R7 cells has been observed in eye tissue mutant for other negative regulators of EGFR signaling including argos, gap1, and sprouty [12], [16] [18].
By contrast, dRASSF levels were unaffected in clones mutant for other Hpo-pathway members, such as ex, sav, and wts.
(B) Since btd-GAL4 is inserted in the promoter of btd, we could not do the rescue by using btd-GAL4 to drive the expression of UAS-mSp8 or UAS-btd in type II NB clones homozygous mutant for other btd mutant alleles, such as btd XG81.
The key findings of this present study are that the sclera of M2 mutant mice has higher expression of collagen type I and lower expression of collagen type V than do wild-type mice and mice that are mutant for other muscarinic subtypes, and, therefore, M2 mutant mice were resistant to the development of experimental myopia.
Mutants deleted for other genes in the GABA shunt, including uga1 and gad1, have similar intracellular GABA levels as wild-type (WT) cells (Kamei et al, 2011).
Mutants for two other error-free pathway components, MMS2 and UBC13, showed a synergistic pattern of sensitivity to MMS when combined with the ANC1 mutation (Figure 3C, D).
