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The siRNA sequences were designed as described previously [70].
For each gene of interest, specific primers were designed as described previously [78].
Zebrafish NRP-1a/NRP-1b MOs, p53 MO, and MDm2 MO were designed as described.
The primer pairs for human β-actin, human α1(I) procollagen, rat 18S were designed as described [2], [42].
Bidirectional transcription cassettes for influenza genes were designed as described by Hoffmann and Neumann et al [11], [29].
Primers used for amplification of the bacterial 16S rRNA gene V3 region were designed as described previously [37].
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The Term-lov-Term fragment was designed as described below and produced by GeneArt AG (Regensburg, Germany).
A microarray was designed as described previously and manufactured by Agilent Technology (Santa Clara, CA, USA) (Kim et al. 2009).
The lower utility arch was designed as described in the bioprogressive technique.
Oligonucleotide probes are designed as described previously [43].
The sequence of the shRNA oligo targeting human p120ctn was designed as described [52].
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were implemented as described
were structured as described
were engineered as described
were modelled as described
were developed as described
were manufactured as described
were modeled as described
were assigned as described
were transfected as described
were processed as described
were recovered as described
were designed as followed
were extracted as described
were measured as described
were designed as matched
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