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Many approaches on automated animal analysis require human interaction for the detection of animals.
Existing approaches on animal analysis frequently operate in highly controlled environments, for example, with a fixed camera, in a well-defined location, with static background, and without interfering environmental factors, such as occlusions, different lighting conditions, and interfering objects [3, 4].
Furthermore, the gravid mouse had only three placentas confirming the reduced fluorescence observed in whole animal analysis.
Profiling isolated cells identified ten times more sex-biased transcripts than whole animal analysis during the same period.
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k, Dmrt3−/− mice displayed increased burst and interburst durations compared to control animals, analysis made on L2s (n = 6 per genotype, P = 0.02, burst; P = 0.001, interburst).
We used voxels of about 0.26 × 0.26 × 1 mm to construct images sufficient for small-animal analysis.
Single-animal analysis confirmed our previous data detecting an induction of 4.0 ± 0.4 that is significantly (p = 0.001) different from sham controls [see Supplemental Material, Figure 2 (http://www.ehponline.org/members/2008/11370/suppl.pdf)].
In animals, analysis of mutants with deleted tetraspanins showed no effect on development, but often had slightly altered phenotypes.
In contrast to the all-or-nothing phenotype obtained from knockout animals, analysis of gene dosage effects may be possible by using siRNAs with variable silencing efficiency.
The different estimation procedures showed different results for the young animals' analysis, with lower estimates for most variables in the LL procedure (Table 4).
The swelling (in mm; n = number of animals; analysis of variance ANOVA P < 0.0001; Student-Newman-Keuls multiple comparisons test; P < 0.001), erythema, and cyanosis were the main macroscopic characteristics of the hind paws of arthritic animals.
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