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Exact(20)
All models were also estimated with lagged predictors measured at time t – 1 but results (not reported, available upon request) were substantively similar.
Alternative analyses, available upon request, were also run with dimensions set at two and three, respectively, but these analyses did not produce sufficiently consistent additional dimensions (Cronbach alpha scores <.6).
Specifically, oligonucleotide primers (sequences available upon request) were designed to amplify each region.
The primers (exact sequences available upon request) were designed to include flight muscle specific exons when applicable (exon 3 for Tn I and exon 11e for mhc).
Expression vectors for AP-1 and CREB factors (maps available upon request) were constructed by cloning the respective cDNAs in the pcDNA3 vector (Invitrogen).
PCR primers (available upon request) were designed for the specific amplification of region B insertion junctions and conventional chromosomes, similar to those of S288C.
Similar(40)
The results, available upon request, are consistent with the four-outcome multinomial probit estimation.
A computer program (available upon request) was implemented to allow analysis of conserved and variable sites.
A Perl script utilizing BioPerl modules (available upon request) was used for completeness analysis.
A standard rating scale (available upon request) was developed and utilized to rate the tapes.
A series of primer pairs (available upon request) was designed to span the intron-exon junctions.
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