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Developmentally regulated expression of MSX1, MSX2 and Fgfs in the developing mouse cranial base.

机译:MSX1,MSX2和Fgfs在发育中的小鼠颅底中的发育调控表达。

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OBJECTIVE: To examine the expression pattern of the Fgf and Msx genes in cranial base development. MATERIALS AND METHODS: To detect the expression of these genes, antisense riboprobes were synthesized by in vitro transcription. Radioactive in situ hybridization was performed on parasagittal sections of embryonic mouse heads. RESULTS: Msx2 was observed in the underlying perichondrium at restricted stages. Msx1 was not observed in cranial base development. Fgf1 was localized in osteogenic cells from the time of ossification; Fgf10 was highly expressed in the occipital-vertebral joint during E13 to E14; Fgf2, Fgf7, and Fgf18 were localized in the perichondria; Fgf12 was transitorily expressed at early chondrocranium; Fgf9 was seen in the hypertrophic chondrocytes. CONCLUSIONS: The Fgf and Msx gene expression in the cranial base was different from that of other skeletons.
机译:目的:探讨Fgf和Msx基因在颅底发育中的表达模式。材料与方法:为了检测这些基因的表达,通过体外转录合成了反义核糖。在胚胎小鼠头部的矢状旁切面进行放射性原位杂交。结果:Msx2在受限的阶段在底层软骨膜中观察到。在颅底发育中未观察到Msx1。从骨化开始,Fgf1就定位在成骨细胞中。在E13至E14期间,Fgf10在枕-椎关节中高表达。 Fgf2,Fgf7和Fgf18定位在软骨膜中; Fgf12在早期软骨中短暂表达。在肥大的软骨细胞中发现了Fgf9。结论:Fgf和Msx基因在颅底的表达不同于其他骨骼。

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