FIGURE

Fig. EV5

ID
ZDB-FIG-201012-119
Publication
Pini et al., 2020 - ALX1-related frontonasal dysplasia results from defective neural crest cell development and migration
Other Figures
All Figure Page
Back to All Figure Page
Fig. EV5

Qualitative and quantitative characterization of zebrafish mutants

The number of embryos displaying craniofacial phenotypes increased with increasing concentration of Alx1DN mRNA injected into the single cell stage embryo. Overview of the relationship of the results of injections of 25, 50, and 100 pg of control mRNA and Alx1DN mRNA with the outcomes of wild‐type zebrafish (green), a craniofacial phenotype (gray), and dead zebrafish (magenta).

The number of embryos displaying craniofacial phenotypes injected with alx1uw2016 mRNA was very low. Overview of the percent of injected wild‐type zebrafish displaying a craniofacial phenotype (gray), compared with uninjected wild‐type zebrafish from the identical clutches (gray). Data of the injections are presented as a comparative percentage.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ EMBO Mol. Med.