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The median symptom score of control patients did not differ between unrestricted diet (1.8; 0 – 4.1) and potato-rice diet (2.1; 0 – 5.9).
Cumulative symptom scores were calculated for each plant line replicate, and the mean cumulative score for each transgenic line compared to the mean cumulative score of control line K (100%).
We measured how the decision score of the SVM corresponded to the observed error rate as measured by the number of mismatches for each predicted quality score of control reads to their respective genome.
Cells exposed to medium from chelated DDs had a larger increase (3.89%, 3.88%, 3.98%, 4.97% and 5.3% increase for HGF and 9.88%, 9.69%, 11.22%, 12.91% and 12.83% for HaCaT at ZA 0.5, 1, 3, 5 and 10 μM, respectively) compared with the NM control (raw data score of control cultures were averaged over three separate runs: 194 and 272 cells per 10,000 events in HGF and HaCaT cells respectively).
The chelated models of fresh HaCaT cells exposed for 24 hours to medium from chelated DDs demonstrated a combined decrease in cell proliferation (12%, 14%, 19.4%, 19.9% decrease at ZA 1, 3, 5 and 10 μM, respectively) compared with the NM control (raw data score of control cultures were averaged over three separate runs: 156 and 352 cells per 10,000 events in HGF and HaCaT cells respectively).
Results at 24 hours showed that fresh HaCaT cells exposed to medium from non-chelated DDs treated with ZA (0.5, 1, 3, 5 and 10 μM) failed to demonstrate a significant difference in cell proliferation from the NM control (raw data score of control cultures were averaged over three separate runs: 156 and 352 cells per 10,000 events in HGF and HaCaT cells respectively).
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PCNA staining scores of control groups were higher than for treated groups, independently of the scheme and the radiation dose considered.
Statistical analysis between the pre-test and post-test scores of the experimental group showed significant difference (p = 0.000) and scores of control and experimental group showed significant difference (p = 0.000) in all dependent variables in the post-test.
c Synovial histopathology scores of control joints and joints undergoing ACLT and receiving weekly intra-articular injections of PBS (n = 9), IL-1 ra (n = 13), PLGA IL-1 ra (n = 14) or PLGA (n = 6) for 4 weeks starting one week following ACLT.
a Cartilage histopathology scores of control joints and joints undergoing ACLT and receiving weekly intra-articular injections of PBS (n = 9), IL-1 ra (n = 13), PLGA-encapsulated IL-1 ra (PLGA IL-1 ra; n = 14) or PLGA microspheres (PLGA; n = 6) for 4 weeks starting one week following ACLT.
US military donor scores were compared with those scores of control donors who denied any travel to P. papatasi-endemic regions.
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