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Fig. S2 Modulation of fbxl10 expression results in normal development of gross anatomical and craniofacial structures. (A–B) Lateral and dorsal bright-field images of 4 dpf fbxl10 morphants.(C–D) Whole-mount lateral and ventral representative images of fbxl10 morphant craniofacial structure. (E) Sagittal sectioning of Alcian blue stained craniofacial cartilage in a representative fbxl10 morphant. AC=auditory capsule, CB=ceratobranchial, CH=ceratohyal, ME=Meckel′s cartilage, PC=parachordal, PQ=palatoquadrate, and T=trabeculacranii.
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Reprinted from Developmental Biology, 382(1), Balow, S.A., Pierce, L.X., Zentner, G.E., Conrad, P.A., Davis, S., Sabaawy, H.E., McDermott, B.M., and Scacheri, P.C., Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome, 57-69, Copyright (2013) with permission from Elsevier. Full text @ Dev. Biol.