[角膜形态发生的分子遗传机制]。

I G Panova, Yu V Markitantova, Yu A Smirnova, R D Zinovieva
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引用次数: 0

摘要

在本文中,我们分析了自己的研究结果和已发表的有关脊椎动物角膜形态发生过程中编码转录因子Pax6/PAX6、Pitx2/PITX2、Fox1/FOXC1、Prox1/PROX1、Oct4/OCT4、Nanog/NANOG和TGFβ2信号蛋白的调控基因表达的数据。我们考虑了模型动物(主要是小鼠)角膜和人类胎儿角膜的研究结果。对人类和动物模型的眼球形态发生进行比较研究是建立脊椎动物在健康和疾病情况下眼球发育共同机制的主要可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Molecular-genetic mechanisms of cornea morphogenesis].

In this paper, we analyzed our own results and published data on the expression of regulatory genes encoding transcription factors Pax6/PAX6, Pitx2/PITX2, Fox1/FOXC1, Prox1/PROX1, Oct4/OCT4, Nanog/NANOG, and TGFβ2 signaling protein during morphogenesis of the cornea in vertebrates. We considered the results obtained for the cornea of model animals, primarily mice, and human fetal cornea. The main possibility of establishing common mechanisms of eye development in vertebrates in health and disease is comparative studies of eye morphogenesis of humans and animal models.

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