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Figure 1


Fig. 1. Morphogenetic movement defects in developing mouse eyes deficient for RA synthesis. (A-D) Hematoxylin and eosin staining of frontal sections through the eye of E14.5 wild-type (WT), Raldh1-/- (R1-/-), Raldh3-/- (R3-/-) and Raldh1-/-;Raldh3-/- double null (R1;R3-/-) embryos. The double-arrow indicates thickening of the neural retina in R3-/- and R1;R3-/- embryos; notice the lack of a vitreous body and the presence of a retrolenticular membrane in these mutants. (E-H) Expression of RARE-lacZ (an RA-reporter transgene) in whole-mount E10.5 wild-type and mutant embryos. Note the near complete loss of RARE-lacZ expression in eyes of R1;R3-/- embryos. Olfactory pit staining is completely dependent upon Raldh3, but forebrain staining is not dependent upon Raldh1 or Raldh3. c, cornea; D, dorsal; e, eye; el, eyelid; f, forebrain; olf, olfactory pit; pm, perioptic mesenchyme; rlm, retrolenticular membrane; V, ventral; vb, vitreous body.





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