(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.

Fig. 7. Roof plate ablation causes loss of Wnt1 and c1 populations, and
reduces cerebellar anlage proliferation at E10.5. (A) Schematic of
the genetic strategy to ablate roof plate cells. (B-I) Whole-mount in
situ staining of E10.5 embryos with markers and genotypes indicated. (B,C and
H,I) Dorsal views with broken line in C demarking the dorsal edge of the open
neural tube. (D-G) Side views. Arrows in B-E indicate position of r1 roof
plate. Arrowheads `o' and `v' mark normal otic and ventral midbrain
Lmx1a expression in panels B and C. Upper and lower insets in panel E
show Wnt1 and Fgf8 isthmic expression. Arrows in panels F
and G point to the cerebellar rhombic lip. Arrows in panel H show broad
expression of cyclin D2 which is eliminated in roof plate-ablated
embryos (I). Weak staining in I is ventral, visible because of the open neural
tube. Dark lines on dorsal edges are artifact. (J,K) Schematic
illustration of E10.5 wild-type and roof plate-ablated embryos demonstrating
the consequences of ablation. (L) Hematoxylin and eosin-stained
sections at the level of the horizontal line in panels J and K in time series.
Arrows point to the most dorsal neuroepithelium of roof plate-ablated embryo
(M-P) Immunostained transverse sections at E10.5 demonstrating that
cell proliferation and cyclin D2 expression is reduced across the entire
cerebellar anlage in ablated embryos. Arrowheads point to the developing
cerebellar anlage.