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Methods: HER2 was silenced in ovarian SKOV-3 cells, a genome-wide expression analysis of PTPs and DSPs was performed, the effects on cell motility were analysed and compared with those of PTPN12-silencing, focusing on FAK.
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Sperm motility was analysed using a Hamilton CASA IVOS Integrated Visual Optical System.
Motility was analysed using a wound-healing assay as described (Hein et al, 2009).
To further establish the pro-migratory effect of PKC the cell motility was analysed with a scratch assay (Fig 3).
Motility patterns were analysed with Motilis-dedicated software for the upper gastro-intestinal tract (MTS_Tool, Motilis, Lausanne, Switzerland).
The effects of MU on motility and invasiveness were analysed under the condition of Has1 and/or Has3 knockdown.
To evaluate the effect of carprofen and mavacoxib on the metastatic potential of the cell lines, motility and invasiveness were analysed using a transwell migration and invasion assay.
The samples were analysed for motility and concentration according to a manual for the project based on the WHO manual for basic semen analysis [ 24].
Cineradiographies were analysed in reference to motility.
The accelerometry data were analysed as total wheeled physical activity, sedentary time and motility.
TbPFR2 expression and cell motility were analyzed.
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