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Root emergence was delayed by ∼1 2 days in all genotypes compared with shoot emergence and was enhanced in both primed and pre-soaked seeds, with greater effects in the two flooding-intolerant lines (Fig. 2B).
Although radicle emergence in B. coccinea and C. cauliflora occurred within 21 ± 8 and 3 ± 2 days, respectively (from the beginning of incubation), shoot emergence was delayed until ∼77 ± 14 and 38 ± 4 days, respectively, after radicle protrusion.
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About a week to a week and a half after emerging from their eggs (or the following spring if emergence is delayed), hatchlings begin feeding to support growth.
In addition, the onset of both pupariation and adult emergence are delayed in dGPHR null flies compared to wild-type controls (Fig. 2D).
His emergence from anesthesia was delayed, his respiration was suppressed, and premature ventricular contractions occurred; all of which are symptoms of LAST.
As a result of this low growth rate, shoot emergence in C. cauliflora was delayed ∼38 days from radicle emergence.
The levels of PPAR γ-2 and C/EBP α were decreased, and the emergence of lipid droplets was delayed in MSCs groups in adipogenic differentiation medium subject to strain stimulation, as compared with in unstrained groups.
Follicle wave emergence in EB-treated llamas was delayed (P < 0.05) by 2.3 days compared with non-treated llamas.
Hence, a more likely alternative explanation for the higher larval densities of the Mt. Hood population detected in fall at low elevation is that larval emergence of the lowland populations was delayed due to their later oviposition relative to the Mt. Hood population.
In all these MEFs, the emergence of visible AP+ colonies was delayed compared to the standard three-factor cocktail (3F-OKS) (4 weeks versus 2 weeks) and the average efficiency was about 100-fold lower (9 × 10−5 in p27 null/2F-OK versus 8 × 10−3 in WT/3F-OKS).
We next analyzed NeuroD EGFP cells in the islet of morphant embryos at 3 dpf to determine if emergence of second wave endocrine cells was delayed.
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