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Fig. S11

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ZDB-FIG-190114-20
Publication
Olcese et al., 2017 - X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3
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Fig. S11

Rescue of hi1392Tg mutant phenotypes by injection of zebrafish pih1d3

(a, b) Representative clutches of 72 hpf hi1392Tg mutant embryos injected at one-cell stage with 250 pg of zebrafish pih1d3 mRNA, showing rescue of mutant phenotypes (b) compared to non-injected siblings (a). (c) Quantification of common phenotypes in 48 hpf hi1392Tg mutant embryos (red columns) versus embryos injected with 250pg of zebrafish pih1d3 mRNA (green columns). There was complete or significant rescue of ventral body axis curvature, pronephric cysts and abnormal cardiac looping (images not shown). Columns represent data from 3 separate experiments with n=29-111 per experiment. Error bars show standard deviation, significance calculated using two way ANOVA, p value *<0.05, **<0.005, ***<0.001.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
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