FIGURE

Fig. 3.

ID
ZDB-FIG-230420-80
Publication
Snodgrass et al., 2023 - Therapeutic targeting of vascular malformation in a zebrafish model of hereditary haemorrhagic telangiectasia
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Fig. 3.

Vegf inhibition between 2 and 3 dpf rescues the abnormal trunk and cerebral vessel phenotypes of engmu130 mutants. (A) Experimental plan for rescuing the eng mutant phenotype in zebrafish using AV951. dpf, days post fertilisation. (B) Representative maximum-intensity projection of the trunk vasculature of engmu130 and WT embryos±AV951 (25 nM) treatment for 24 h. DA, dorsal aorta; PCV, posterior cardinal vein. Scale bar: 150 μm. (C) Representative maximum-intensity projection of the cerebral vasculature of engmu130 and WT embryos±AV951 (25 nM) treatment for 24 h. Scale bar: 100 μm. (D) DA diameter in engmu130 and WT embryos±AV951 treatment. (E) PCV diameter in engmu130 and WT embryos±AV951 treatment. (F) Intersegmental blood vessel (ISV) diameters in engmu130 and WT embryos±AV951 treatment. (G) Percentage of open ISVs in engmu130 and WT embryos±AV951 treatment. (H) Number of kugeln in engmu130 and WT embryos±AV951 treatment. (I) BA diameter in engmu130 and WT embryos±25 nM AV951 treatment. *P<0.05, **P<0.01, ***P<0.001, ****P<0.0001; ns, not significant (two-way ANOVA with Tukey post-hoc test, 10 animals/group).

Expression Data
Gene:
Fish:
Condition:
Anatomical Terms:
Stage: Protruding-mouth

Expression Detail
Antibody Labeling
Phenotype Data
Fish:
Condition:
Observed In:
Stage: Protruding-mouth

Phenotype Detail
Acknowledgments
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