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Bone measurements at implants on the CBCT scans was done using 3D image diagnostic and treatment planning software (NobelClinician, version 2.1 (Nobel Biocare - Guided Surgery Center, Mechelen, Belgium).
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Tomographic scans were done using the General Electric Phoenix V| Tome |X s high-resolution CT scanner.
Combinatorial scans were done using multiscan [10] to identify and quantify Cbf1/Met31 cooperatively acting binding sites in the genome.
Mosaic scans were done using a motorized x y stage (Maerzhaeuser).
The simulation CT scans were done using 5 mm slices from the head to the level of diaphragm.
In Calgary, scans were done using a Marconi PQ5000 VisionMaster/Picker, and in Edmonton, using a Phillips/Marconi MX8000 multislice scanner.
In situ temperature-dependent specular X-ray diffraction scans were done using the DHS900 (Anton Paar GmbH, Austria) under an ambient atmosphere.
The mice were scanned 60 to 90 min after injection for 20 min, and only one mouse per scan was done using view A with small binning.
The mice were scanned 45 to 90 min after injection for a duration of 5 min, and only one mouse per scan was done using view A with small binning (4.0 cm × 4.0 cm field of view, 480 × 480 pixels, 0.083 mm × 0.083 mm pixel size, f/stop = f/1).
Scanning was done using 2 line averaging and a resolution of 5 µm.
briggsae ortholog pairs that exhibited detectable expression in our microarray data (background dataset) The motif scan was done using a previously described tool, PWM_SCAN [50].
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