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. 2019 Oct 16;9(12):4149–4157. doi: 10.1534/g3.119.400585

Figure 2.

Figure 2

Phenotype of rps9 deficient embryos is partially rescued by rps9 mRNA injections. (A-B) Whole mount in situ hybridization for rps9 in mutants and siblings at 24 hpf or 48 hpf. (C) qPCR analysis of rps9 transcript levels. *, P < 0.05. (C) In vitro transcribed rps9 mRNA (400 pg) partially rescues phenotype in rps9 mutants. Arrowhead indicates morphological improvement in the hindbrain and trunk.