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- W2021805029 endingPage "3274" @default.
- W2021805029 startingPage "3260" @default.
- W2021805029 abstract "Abstract Retinoic acid (RA), a vitamin A derivative, is synthesized by specific cell populations and acts as a diffusible embryonic signal activating ligand‐inducible transcription factors, the RA receptors (RARs). RA‐activatable transgenic systems have revealed many discrete, transient sites of RA action during development. However, there has been no attempt to permanently label the RA‐activated cell lineages during mouse ontogenesis. We describe the characterization of a RA‐activatable Cre transgene, which through crosses with a conditional reporter strain (the ROSA26R lacZ reporter), leads to a stable labeling of the cell populations experiencing RA signaling during embryogenesis. RA response‐element (RARE) ‐driven Cre activity mimics at early stages the known activity of the corresponding RARE‐ lacZ transgene (Rossant et al., 1991 ). Stable labeling of the Cre‐excised cell populations allows to trace the distribution of the RA‐activated cell lineages at later stages. These are described in relationship with current models of RA activity in various developmental systems, including the embryonic caudal region, limb buds, hindbrain, sensory organs, and heart. Developmental Dynamics 239:3260–3274, 2010. © 2010 Wiley‐Liss, Inc." @default.
- W2021805029 created "2016-06-24" @default.
- W2021805029 creator A5001884543 @default.
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- W2021805029 creator A5056381305 @default.
- W2021805029 creator A5075630822 @default.
- W2021805029 creator A5079263362 @default.
- W2021805029 date "2010-11-02" @default.
- W2021805029 modified "2023-10-18" @default.
- W2021805029 title "Fate of retinoic acid-activated embryonic cell lineages" @default.
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