Sentence examples for mutants with severe from inspiring English sources
The fraction of mutants with severe deletions in the Hprt locus after exposure to oxygen ions increases from 65% at 60 keV/μm up to a maximum (100%) at 300 keV/μm and declines with higher LET values to 75% at 750 keV/μm.
In aux mutants with severe Notch-like mutant phenotypes, clathrin vesicle uncoating is inefficient.
Mutants with severe growth defects were eliminated from further analysis and the remaining potential biofilm mutants were reexamined for reproducibility in the biofilm assay.
However, the observation of a few cells with three TOs in the GDmg200 mutant indicates that this regulatory mechanism can be occasionally overcome in mutants with severe gliding deficiencies.
Mutants with severe defects in some sensory modalities displayed normal or nearly normal magnetic orientation.
Mature cortical cell lengths, primarily the result of cell elongation in the EZ, were indeed reduced in the mutants with severe growth defects.
In a large-scale ENU mutagenesis screen for definitive hematopoietic mutations, we obtained cas002, a novel mutant with severe hematopoietic defects and recessive lethality.
In contrast, rate of cell elongation is reduced in parallel with growth rate only for the exocyst mutants with less severe root growth defects; whereas the three exocyst mutant lines with the most severe defects in root growth (sec8-3, sec8-4 exo70and and exo84b) share the same dramatically reduced cell elongation rate.
Mutants with early, severe defects in sarcomere assembly fail to begin normal embryonic movements at mid-embryogenesis, and soon after this point the elongation process stops prematurely at the two fold length.
For these measurements, we examined the subset of sma-1 mutants with relatively severe g1P defects, as assessed using a fluorescence dissecting microscope.
The polar localization within the cells and the pattern of distribution within the root tips (e.g., the MZ) of these auxin transport proteins in two exocyst mutant lines with severe root growth defects (sec8-3, and sec8-4 exo70A1) appeared similar to wild-type, as had previously been reported for the less severe exo70A1 mutant [ 36].
