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Fig. 5. FGF signaling is not sufficient to position the RA-responsive domain in
the PSM. (A,B) Cyp26 expression in the posterior
region of the Fgfr1f/f;T-Cre (B) mutant is downregulated
compared with that in Fgfr1f/+;T-Cre control (A) embryos.
(C,D) There is a lack of significant change in RA activity, as
detected by crossing to RARE-lacZ reporter mice, in
Fgfr1f/f;T-Cre mutant (D) compared with the
Fgfr1f/+;T-Cre control (C) embryos. (E,F)
Expression of Raldh2 is not significantly changed in the PSM of
Fgfr1f/f;T-Cre mutant embryos (F) compared with control
Fgfr1f/+;T-Cre (E) embryos.