Fig. 3
- ID
- ZDB-FIG-220908-25
- Publication
- Ma et al., 2022 - Ercc2/Xpd deficiency results in failure of digestive organ growth in zebrafish with elevated nucleolar stress
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Digestive organ bud initiation is unaffected in ercc2/xpd mutants (A) Whole-mount in situ hybridization (WISH) of marker genes for digestive organ budding in ercc2/xpd mutants and siblings at 2 dpf. Dorsal view, anterior to the top. l, liver; p, pancreas; i, intestine. After individual imaging, embryos were subjected to individual genotyping. Scale bars, 100 μm. (B) WISH of marker genes for early development of digestive organs in ercc2/xpd mutants and siblings at 3 and 4 dpf. Upper: dorsal view, anterior to the top; lower: lateral view, anterior to the left. After individual imaging, embryos were subjected to individual genotyping. Scale bars, 100 μm. (C) Tg(fabp10a:dsRed; ela3l:GFP) revealed early development of digestive organs in ercc2/xpd mutants and siblings at 4 dpf. After individual imaging, embryos were subjected to individual genotyping. Scale bars, 100 μm. |
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Anatomical Terms: | |
Stage Range: | Long-pec to Day 4 |
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Observed In: | |
Stage Range: | Protruding-mouth to Day 4 |