A cluster of overlapping inserts was observed for p88, p153, and p360; these produced outlier values for both of the Mexican isolates.
For the clinical application, dynamic states of contact on the tibial insert were observed including axial rotation and unilateral loading during knee flexion, and post-cam contact of posterior stabilized TKA.
In clone P5.b.3 a dominant insert is observed in chromosome 13/14 but by TAIL-PCR we were able to identify 10 different inserts in different chromosomes.
Also in the three clones P5.i.1-3 one dominant insert was observed in the group of chromosomes 9-11 but faint hybridization signals are also observed in other chromosomes, indicating the presence of additional inserts.
(iv) A duplication of a genomic region including the atp9 open reading frame interrupted by a 488 bp insert was observed in P. subalpina, leading to the annotation of ORF_01.
Species in group 1 possess an additional tRNA-Cys between cox1 and ORF_02 except for A. applanata and no insert was observed in the duplicated region including the atp9 ORF.
Within the peripherally inserted umbilical cord, paracentral insertion was observed in 136/185 (73.5%) UC, battledore insertion in 44/185 (23.8%) UC, and velamentous insertion in 5/185 (2.7%) UC (Table 1).
Although both human isolates contained the insertion, amino acid changes within the inserted sequence were observed compared with the avian AVFV2 sequence, indicating that sequence drift occurred after the initial insertion event.
