Abstract

<p><b>A</b>) Strategy for expressing <i>RockDN</i> construct in NCC. <b>B</b>) Quantitative real time PCR for the <i>CAT</i> gene cassette, using RNA extracted from pharyngeal arches 1 and 2, from E11.5 mutant <i>RockDN<sup>+</sup>;Wnt1-cre<sup>+</sup></i> and control embryos. There is a statistically significant (P<0.05 *), 13 fold decrease, in the expression of the <i>CAT</i> box in the mutant sample, as calculated using the one-way Anova test.</p

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