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. 2015 Jun 12;66(17):5217–5227. doi: 10.1093/jxb/erv293

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© The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 8. — Endosperm-specific expression of CLE19 _G6T led to defective cotyledon establishment in embryos. (A) Seed abortions (indicated by arrowheads) observed in the pALE1:CLE19 _G6T transgenic plant, as compared with the wild type (WT). (B and C) Defected cotyledon establishment (indicated by arrowheads) in embryos from pALE1:CLE19 _G6T transgenic plants (C), as compared with the wild type (B) at the same stage (7 DAP). (D and E) Cytohistological examination of ovules from the wild type (D) and pALE1:CLE19 _G6T transgenic plants (E), showing establishment of the defective cotyledon (E, indicated by arrowheads). Note the cellularized endosperms (indicated by asterisks). c, cotyledon primordia. Scale bars: in A=1mm; in B–E=100 μm.