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. 2018 Mar 1;145(5):dev158105. doi: 10.1242/dev.158105

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© 2018. Published by The Company of Biologists Ltd

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 use, distribution and reproduction in any medium provided that the original work is properly attributed.

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Fig. 4. — ETT, IND, BP, RPL and SEU activity is conserved between Arabidopsis and B. rapa. (A,B) B. rapa R-o-18 wild-type plant (A) and colour-coded gynoecium (B): cyan, stigma; pink, style; green, valves; red, valve margin; orange, replum. (C-I) SEM images of gynoecium tops (left) and optical microscopy images of whole gynoecium (right) of wild-type R-o-18 (C) and brett.a (D), brett.b (E), brind (F), brbp (G), brrpl.a/brrpl.c (H) and brseu (I) mutants. Insets are SEM images of apical view of gynoecium tops. (J) Valve-margin defects in brind mutant (right, asterisks) compared to wild-type R-o-18 (left, asterisks). (K) Pedicel defects with horizontal orientation of fruits in brbp mutant (right) compared to wild-type R-o-18 (left). (L) Replum defect in brrpl.a/brrpl.c double mutant (right, arrowhead), compared to wild-type R-o-18 (left, arrowhead). Scale bars: 200 µm in SEM images in C-I, 100 µm in SEM images in J and K, 1 mm in optical microscope images.