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. 2008 Sep 29;9:445. doi: 10.1186/1471-2164-9-445

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Copyright © 2008 Fortes et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Quantitative RT-PCR analysis. Complementary cDNAs were used encoding a metallothionein (Hl3889, Hlct1310), sucrose synthase (Hlsuc), glycolate oxidase (Hl1696), 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase (Hl1812), cinnamic acid hydroxylase (Hl1751) and peroxidases (Hl1 and Hl4578). Hl1812 and Hl1751 are both involved in secondary metabolism and were grouped together. Values are the mean of three-four experiments; bars represent SE. Graphs are plotted against relative cDNA concentration (Y axis) assessed by plasmid.