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For example, muscle weights of F66/Mstn+/+ males obtained from crosses with Mstn+/− females were higher than those of F66/Mstn+/+ males obtained from crosses with Mstn+/+ females.
Similarly, muscle weights of F66/Mstn+/− males obtained from crosses with Mstn−/− females were higher than those of F66/Mstn+/− males obtained from crosses with Mstn+/− females.
Muscle weights of collected tissues were measured at different ages and normalized to body weight, to account for runted phenotype of H-FRG1TG mice.
Phenotypic data for muscle weights of animals sampled for this experiment (Figure 2) show the characteristic muscle hypertrophy responses that have been previously reported for callipyge lambs [1] [3].
One objective was to identify the early transcriptional changes that lead to muscle hypertrophy, so three of the four ages used for microarray analysis (10, 20 and 30 days of age) are prior to sufficient protein accretion (4 18 kg live weight) for muscle weights of callipyge lambs to be statistically heavier than normal lambs.
Whole muscle weights of M. gast.
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(A D) Ageing mice (A) Grip power, (B) Running distance, (C) Mitochondrial amount and (D) Muscle weight of the gastrocnemius muscle), (E H) 5/6Nx mice (E) Grip power, (F) Running distance, (G) Mitochondrial amount, (H) Muscle weight of the gastrocnemius muscle).
Restoration of the contractile force and muscle weight of the extensor digitorum longus muscle began earlier in the SNAC group--after day 11--whereas the other 2 groups showed progressive atrophy until day 21, with a significant difference between the SNAC group and the other 2 groups.
By contrast, muscle weight of β2KO mice remained unchanged at 10 and 21 days post-cryolesion (Table 1).
The Tibialis anterior muscle weight of IL10KO mice was lower than that of control mice, while GSE supplementation attenuated muscle loss in IL10KO mice.
In addition, feeding AA and the combination of AA and FOS increased the breast muscle weight of broiler chicks, while feeding FOS not significantly.
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