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Functionally, muscle contraction became severely affected within weeks of birth, with specific force generation dropping as low as ∼65% and ∼27% of control values in the extensor digitorum longus and soleus muscles respectively.
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Here, the stamp with line patterns descends into the polymer and then both of the materials are squeezed with a specific force.
Soleus muscles from 4 week old lmna−/− mice showed a significant reduction in force generation, with muscle specific force only ∼70% of controls (Figure 6a).
Consistent with maximal specific force measurements, twitch force was modestly decreased in Mbnl1+ /ΔE3 / Mbnl2 GT2/GT2 animals, with intermediate and maximal reduction in this series being observed in Mbnl1 ΔE3/ΔE3 and Mbnl1 ΔE3/ΔE3/mice3 ΔE2 mice, respectively (Pt decreased 26.2% and 29.3% compared to wild type mice for Mbnl1 ΔE3/ΔE3 and Mbnl1 ΔE3/ΔE3/mice3 ΔE2 mice, respectively).
Membrane-stabilizing effects of VBP15, but not prednisolone, are consistent with increases in specific force observed for VBP15 but not for prednisolone.
Expanded cells from all ten sources formed functional myobundles that contracted in response to electrical stimulation with an average specific force of 2.1 ± 0.9 mN/mm and 7.0 ± 2.2 mN/mm for twitch and tetanus, respectively.
In particular, the 1st principal component closely correlated with tetanic force and specific force, while the 2nd principal component closely correlated with the fatigue index and fatigue time (the variables correlated with the two principal components can be identified by the highest score coefficients in the absolute values shown in Table 3).
We hypothesized that fiber size and fiber force-generating capacity would decrease in parallel, thus resulting in no change in specific force with either age or inactivity.
The mechanization equations (1) together with measurements of the specific force f ~ k and the angular rates ω ~ k, provided by the inertial sensors, are used to propagate position p ̂ k, velocity v ̂ k, and orientation q ̂ k state estimates.
The decline in muscle specific force with age is a highly consistent finding among studies on rodents [10] [11], [13] [16].
EPA administration attenuated endotoxin-induced reductions in diaphragm specific force, with maximum specific force levels of 27 ± 1, 14 ± 1, 23 ± 1, and 24 ± 1 N/cm, respectively, for control, endotoxin, endotoxin + EPA, and EPA treated groups (P < 0.001).
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