Wang et al., 2015 - Point mutations in KAL1 and the mitochondrial gene MT-tRNA(cys) synergize to produce Kallmann syndrome phenotype. Scientific Reports   5:13050 Full text @ Sci. Rep.

Fig. 5

cars2 gene knockdown with Morpholinos in Danio rerio affected the migration of GnRH3 neurons.

Whole mount in situ hybridization of the control (b (b'),d,f,h) and cars2 morphants (a (a'),c,e,g) embryos with gnrh3 (a (a'),b (b')), gnrh2 (c,d), kal1a (e,f), and kal1b (g,h) probes at 56 hpf. (a,b) front views, dorsal up; (a',b',c–h) dorsal view, anterior up. Results shown were representative figures from three independent experiments and the frequency of embryos with the indicated expression patterns were shown in the bottom left corner of each panel. Red arrows indicated the affected GnRH3 neurons by knockdown cars2. Scale bar: 0.1 mm.

Fig. S8 ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions.

Acknowledgments:
ZFIN wishes to thank the journal Scientific Reports for permission to reproduce figures from this article. Please note that this material may be protected by copyright. Full text @ Sci. Rep.