Secondly, we used a posterior restraint in order to recreate external rotation, which might alter glenohumeral joint kinematics.
Secondly, we used the capability of HA in acting as a solid support in the nanoparticles' production procedure [25].
Secondly, we used a method similar to Wang and Qian [16].
Secondly, we used evolutionary conserved sequence features to predict mitochondrial proteins.
Secondly, we used virus-like particles to assign Vpx functions to HIV-1-derived vectors, thus allowing monocyte transduction.
Secondly, we used a deterministic, discrete time formula that has been shown to be suitable for use in large populations.
Secondly, we used a relaxed (uncorrelated lognormal) molecular clock method [68] as implemented in BEAST version 1.4.6 [69].
Secondly, we used permutations to establish stringent genome-wide thresholds for declaring significant association for each phenotype.
Secondly, we used a previously described Cry1Ab mutant R99E, located in helix α-3 that showed impaired toxin oligomerization [21].
Secondly, we used the same approach as that taken by Manzano et al. [34] for in vitro reconstitution of pneumococcal pili using SrtC1.
Secondly, we used the MNI template for registration (spatial normalization) and segmentation instead of a customized template from our samples of controls and KS patients.
