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lhx1xenopus otic region 

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Experiment details for lhx1

Comparative Functional Analysis of ZFP36 Genes during Xenopus Development.

Comparative Functional Analysis of ZFP36 Genes during Xenopus Development.

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Gene Clone Species Stages Anatomy
lhx1.L laevis NF stage 26 otic region

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  Figure 8. Zfp36 mRNA overexpression alters the formation of pronephros and affects pronephric marker genes expression. (A) 250 pg of Xenopus zfp36 mRNA were injected into one ventral blastomere of 8-cell stage embryos and developing embryos were fixed at stage 39 before immunhistochemistry analysis with the pronephros specific markers 3G8 and 4A6. Arrows in b and d mark the pronephros (pn) alteration on the injected side. (B) 250 pg of Xenopus zfp36 (a) or zfp36l1 (e) mRNA was injected into one ventral blastomere of 8-cell stage embryos and developing embryos were fixed at stage 22 (a, b and e) or stage 26 (c, d) before in situ hybridization analysis for pax8 or lim1 expression. Arrows in b, d, f and h mark the pronephros (pn) alteration on the injected side. (C) Two-cell stage embryos were injected or not (NI) with 250 pg of the different Xenopus zfp36 mRNAs. Animal caps were explanted at stage 8.5 and treated with activin plus retinoic acid (RA) before analysis by RT-PCR for smp30 expression when control embryos reached stage 35. Stage 35 embryo (Emb) or untreated animal caps (-) were assayed by RT-PCR in parallel. Odc was used as control of loading and a reaction was performed in the absence of reverse transcriptase to check for genomic DNA contamination (-RT).
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