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When directly monitoring the segregation of chromosome 2 in bub3Δ cells by using live-cell imaging, we observed only a slight increase in mis-segregation compared to wild-type cells (Fig 2B; Vanoosthuyse et al, 2004).
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The aim was to monitor the segregation of phosphorus and carbon through temperature ranges which offered the extremes of both solutes having long-range lattice mobility to that where only carbon was mobile.
To quantitatively assess the FLO11 phenotype we used a FLO11pr:: GFP construct to monitor the segregation of FLO11 transcription in S288c tec1 Δ × Sigma tec1 Δ crosses.
In summary, although the characteristics of cell cycle in meiosis are different from those in mitosis, as a core member of SAC, Bub3 is required for monitoring the chromosome segregation in mammalian oocytes.
We can monitor the chromosome segregation process by measuring the mitotic stability of the non-essential minichromosome Ch16.
The first utilizes biparental mapping populations to monitor the co-segregation of QTL and marker loci.
Some gene inserts were over balancers that segregate ebony (Table 1), scores were corrected for segregation bias by monitoring the Tubby phenotype (e.g., +/e and e/e vs. e/e, Tb).
The spindle checkpoint ensures the accurate segregation of chromosomes by monitoring the status of kinetochore attachment to microtubules.
The transparency of the zebrafish embryo has allowed us to monitor the in vivo chromosome segregation dynamics in real time and revealed the dynamic chromosome segregation defects in the esco2 mutants.
The spindle checkpoint acts to monitor the fidelity of chromosome segregation during mitosis [ 57].
Authors have monitored the dependence of the local segregation order parameter on system size and found algebraic scaling and different characteristic exponent values for enveloping and engulfed cells.
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