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The P-domain boundaries were deduced from the X-ray structure of CNX and the NMR structure of the rat CRT P-domain [10], [11].
Gene specific primers that encompass one intron were defined for each transcript (except for HOXA9 gene) using the program Primer Express version 2. To design intron-spanning primers, putative intron-exon boundaries were deduced from the Genome Browser Database (http://genome.ucsc.edu/cgibin/hgGateway?hgsid=105081852&clade=vertebrate&org=Cow&db=0).
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Finally, the following expressions for the velocity field components on the boundary are deduced from (27) using the connection between the two systems of numbering, and returning to the global one: u ( x ¯ i ) = ∑ k = 1 3 N u i k f k, v ( x ¯ i ) = ∑ k = 1 3 N v i k f k, (31).
The intron-exon boundaries were deduced by comparing the sequences obtained from the genomic clones and the respective cDNAs.
Exon-intron boundaries, position and orientation of ADH genes were deduced from the amphibian and reptilian genome assemblies, thus revealing syntenic regions and gene rearrangements with respect to the human genome.
Shear velocities were deduced from velocity profiles above the sand.
The specific wear rates were deduced from mass loss.
Results were deduced from 1000 simulations.
Amino acid sequences were deduced from nucleic acid sequences.
The peptide sequences were deduced from DNA sequencing.
Allele frequencies were deduced from the genotype distribution.
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