spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


Right arrow Help viewing high resolution images
Right arrow Return to article
(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.


Figure 10


Fig. 10. AVE defects in Nap1khlo mutants. (A-D) Cells of the AVE, marked by expression of Cerl at E6.5 (A,B) and Hex at E7.5 (C,D), were present at the embryonic-extraembryonic boundary of wild-type embryos (A,C), but failed to migrate completely in half of the Nap1khlo mutants examined (B,D, brackets). Anterior is to the left. (E-H) All Hex-GFP-expressing cells migrated towards the anterior of wild-type embryos at E6.0 (E,G), but some Hex-GFP cells remained distal (F, arrow) or migrated to the posterior (H, arrows) in half of the Nap1khlo embryos examined (green, Hex-GFP; red, phalloidin). Anterior is out in E and F, and to the left in G and H. (I,J) High magnification anterior views of the Hex-GFP-expressing cells in E6.0 wild-type (I) and Nap1khlo (J) embryos. Vertical arrows in I and J represent the orientation of the proximodistal axis. Note that that although the wild-type AVE cells are elongated along the proximodistal axis, the Nap1khlo cells are not. Scale bars in E-J: 50 µm.





Right arrow Return to article