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(2010) for the Gmed posterior part. The electrodes for the biceps femoral were placed over the distal third of the long head muscle belly. The ground electrode was placed over the tibia bone. The selected muscle model was derived from previous studies (Hertel et al., 2004; Fel��cio et al., 2011; Baffa et al., 2012) with additional measurement of BF for observation of at least one hamstring muscle. 3D kinematics The kinematic data were recorded at a frequency of 200 Hz using a six-camera Vicon MX10 infra-red motion analysis system (Oxford Metrics, Oxford, UK). Cameras were spaced around the walking track with two force plates (Kistler Instrumente, Winterthur, Switzerland) in the middle. The force plates and EMG output were connected to the Montelukast Sodium Vicon software via an MX box. Reflective markers measuring 19 mm in diameter were attached bilaterally on the subject��s skin overlying the following landmarks: Epigenetics inhibitor the anterior superior iliac crest; the posterior superior iliac crest; the lateral thigh; the lateral femoral epicondyles; the tibias; the lateral malleolus; the heels; and the metatarsal head of the second toe. 3D kinematics was used to detect step cycles defined as heel-to-heel contact on the force plates with a sensitivity detection of 20N. When a non-periodical course of kinematic walking was observed during a subject��s Farmer��s walk, the attempt was excluded from the trials as ��invalid��. Statistical Analyses For statistical analysis, the participants�� results were divided into groups based on their H/Q, HAB/Hamstring (HAB/H) and HAB/quadriceps (HAB/Q) strength ratios to determine if the strength ratios predicted the electromyography amplitude of the VM, VL, BF and Gmed expressed as a %MVIC. The groups formed were participants with the results Akt molecular weight of H/Q �� 0.5 (H/Q 1), H/Q