Sentence examples for muscles at different from inspiring English sources

(J) Pax7 mRNA levels in uninjured (0 d) and injured muscles at different times after injury (1, 3, 5, and 7 d) from RNF13-/ and RNF13+/+ mice were determined by qRT-PCR.

To further confirm this result, we examined Pax7 expression in muscles at different time points after damage using qRT-PCR and Western blotting analysis (Figs. 2J, S1A, and S1B).

Considering that cytokines and chemokines are important in muscle regeneration, we determined the presence of 18 different cytokines/chemokines secreted in TA muscles at different time points after CTX-induced damage (0, 4, and 12 h, and 1 d and 3 d) by using a Luminex multiplex platform (Table S2).

The few other studies [21], [22], like our own, investigating intersegmental mechanisms modulating activity between heteronymous muscles at different joints in hemiparetic subjects did not find correlations between modulation changes and spasticity levels after stroke.

The secondary aim is the evaluation of the activity of synergistic muscles at different orientations of the pelvis.

To investigate whether the differential expression of MST1 kinase in fast- and slow-dominant muscles is established during postnatal development, we examined expression of MST1 kinase in fast- and slow-dominant muscles at different postnatal stages.

The experimental protocol consisted of an isometric task selective for the upper trapezius muscle at different force levels (10 80% of maximal voluntary contraction MVC, in steps of 10%MVC) and one fatiguing contraction (constant force level at 50%MVC until exhaustion).

We looked at the site of the fracture as a potential risk factor because the tibial shaft has various muscle attachments and varying bulk of muscle at different levels.

To study the influence of this overexpression during aging, we have analyzed changes in mitochondrial activity and biogenesis in skeletal muscle at different ages: 2, 6, 11 and 23 months.

This will enable visual examination of the muscle at different stages of the worm's lifespan.

Collection of patient samples, e.g. from peripheral tissues such as muscle at different disease stages might shed more light on the regulation of gene expression during disease progression.