Validity and test-retest reliability of a resistance training device for Smith machine back squat exercise.

This study evaluated the validity and test-retest reliability of a resistance training device Jueying (Beijing, China) for Smith machine back squat exercise. Twelve male participants completed two test sessions with an interval of one week. In each test session, participants completed 30%, 45%, 60%, and 75% of 1RM back squats on a Smith machine equipped with Jueying and a linear position transducer GymAware (Canberra, Australia), which measured the velocity and power during the movement simultaneously. Results showed that Jueying was both valid (Pearson correlation coefficient [r] = 0.896-0.999, effect size [ES] = 0.004-0.192) when compared with GymAware and consistent between two tests in terms of reliability (intraclass correlation coefficient [ICC] = 0.79-0.95) to assess speed and power within all exercises. The device could be applied to provide athletes and coaches with effective and reliable data in actual application.

Sequence-related amplified polymorphism, an effective molecular approach for studying genetic variation in Fasciola spp. of human and animal health significance.

In the present study, a recently described molecular approach, namely sequence-related amplified polymorphism (SRAP), which preferentially amplifies ORFs, was evaluated for the studies of genetic variation among Fasciola hepatica, Fasciola gigantica and the "intermediate" Fasciola from different host species and geographical locations in mainland China. Five SRAP primer combinations were used to amplify 120 Fasciola samples after ten SRAP primer combinations were evaluated. The number of fragments amplified from Fasciola samples using each primer combination ranged from 12 to 20, with an average of 15 polymorphic bands per primer pair. Fifty-nine main polymorphic bands were observed, ranging in size from 100 to 2000 bp, and SRAP bands specific to F. hepatica or F. gigantica were observed. SRAP fragments common to F. hepatica and the "intermediate" Fasciola, or common to F. gigantica and the "intermediate" Fasciola were identified, excised and confirmed by PCR amplification of genomic DNA using primers designed based on sequences of these SRAP fragments. Based on SRAP profiles, unweighted pair-group method with arithmetic averages clustering algorithm categorized all of the examined representative Fasciola samples into three groups, representing the F. hepatica, the "intermediate" Fasciola, or the F. gigantica. These results demonstrated the usefulness of the SRAP technique for revealing genetic variability between F. hepatica, F. gigantica and the "intermediate" Fasciola, and also provided genomic evidence for the existence of the "intermediate" Fasciola between F. hepatica and F. gigantica. This technique provides an alternative and a useful tool for the genetic characterization and studies of genetic variability in parasites.