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本文引用的文献

1
Pax9 regulates a molecular network involving Bmp4, Fgf10, Shh signaling and the Osr2 transcription factor to control palate morphogenesis.Pax9 通过调节一个分子网络来控制腭部形态发生,该网络涉及 Bmp4、Fgf10、Shh 信号通路和 Osr2 转录因子。
Development. 2013 Dec;140(23):4709-18. doi: 10.1242/dev.099028. Epub 2013 Oct 30.
2
Modulation of lipid metabolic defects rescues cleft palate in Tgfbr2 mutant mice.调节脂质代谢缺陷可挽救Tgfbr2突变小鼠的腭裂。
Hum Mol Genet. 2014 Jan 1;23(1):182-93. doi: 10.1093/hmg/ddt410. Epub 2013 Aug 23.
3
Developmental epigenetics of the murine secondary palate.小鼠次生腭的发育表观遗传学
ILAR J. 2012;53(3-4):240-52. doi: 10.1093/ilar.53.3-4.240.
4
Systematic analysis of palatal transcriptome to identify cleft palate genes within TGFβ3-knockout mice alleles: RNA-Seq analysis of TGFβ3 Mice.系统分析腭转录组以鉴定 TGFβ3 敲除小鼠等位基因中的腭裂基因:TGFβ3 小鼠的 RNA-Seq 分析。
BMC Genomics. 2013 Feb 20;14:113. doi: 10.1186/1471-2164-14-113.
5
Smad4-Irf6 genetic interaction and TGFβ-mediated IRF6 signaling cascade are crucial for palatal fusion in mice.Smad4-Irf6 基因相互作用和 TGFβ 介导的 IRF6 信号级联对于小鼠腭裂融合至关重要。
Development. 2013 Mar;140(6):1220-30. doi: 10.1242/dev.089615. Epub 2013 Feb 13.
6
Mouse TU tagging: a chemical/genetic intersectional method for purifying cell type-specific nascent RNA.小鼠 TU 标签:一种用于纯化细胞类型特异性新生 RNA 的化学/遗传交叉方法。
Genes Dev. 2013 Jan 1;27(1):98-115. doi: 10.1101/gad.205278.112.
7
Identification of candidate downstream targets of TGFβ signaling during palate development by genome-wide transcript profiling.通过全基因组转录谱分析鉴定腭发育过程中 TGFβ 信号的候选下游靶标。
J Cell Biochem. 2013 Apr;114(4):796-807. doi: 10.1002/jcb.24417.
8
Periderm cells covering palatal shelves have tight junctions and their desquamation reduces the polarity of palatal shelf epithelial cells in palatogenesis.覆盖腭突的表皮细胞有紧密连接,其脱落减少了腭突上皮细胞在腭发育过程中的极性。
Genes Cells. 2012 Jun;17(6):455-72. doi: 10.1111/j.1365-2443.2012.01601.x. Epub 2012 May 9.
9
Mass spectrometry-based proteomics and network biology.基于质谱的蛋白质组学和网络生物学。
Annu Rev Biochem. 2012;81:379-405. doi: 10.1146/annurev-biochem-072909-100424.
10
Tbx1 regulates oral epithelial adhesion and palatal development.Tbx1 调节口腔上皮黏附与腭裂发育。
Hum Mol Genet. 2012 Jun 1;21(11):2524-37. doi: 10.1093/hmg/dds071. Epub 2012 Feb 27.

腭发育中的信号转导网络。

Signaling networks in palate development.

机构信息

Department of Biologic and Materials Sciences, University of Michigan School of Dentistry, Ann Arbor, MI, USA.

出版信息

Wiley Interdiscip Rev Syst Biol Med. 2014 May-Jun;6(3):271-8. doi: 10.1002/wsbm.1265. Epub 2014 Mar 18.

DOI:10.1002/wsbm.1265
PMID:24644145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3991764/
Abstract

UNLABELLED

Palatogenesis, the formation of the palate, is a dynamic process regulated by a complex series of context-dependent morphogenetic signaling events. Many genes involved in palatogenesis have been discovered through the use of genetically manipulated mouse models as well as from human genetic studies, but the roles of these genes and their products in signaling networks regulating palatogenesis are still poorly known. In this review, we give a brief overview on palatogenesis and introduce key signaling cascades leading to formation of the intact palate. Moreover, we review conceptual differences between pathway biology and network biology and discuss how some of the recent technological advances in conjunction with mouse genetic models have contributed to our understanding of signaling networks regulating palate growth and fusion. For further resources related to this article, please visit the WIREs website.

CONFLICT OF INTEREST

The authors have declared no conflicts of interest for this article.

摘要

未加标签

palateogenesis,即腭的形成,是一个由一系列复杂的、依赖上下文的形态发生信号事件调节的动态过程。许多参与 palateogenesis 的基因已经通过使用遗传操作的小鼠模型以及人类遗传研究被发现,但这些基因及其产物在调节 palateogenesis 的信号转导网络中的作用仍知之甚少。在这篇综述中,我们简要概述了 palateogenesis,并介绍了导致完整腭形成的关键信号级联反应。此外,我们还回顾了通路生物学和网络生物学之间的概念差异,并讨论了最近的一些技术进步如何结合小鼠遗传模型,促进了我们对调节腭生长和融合的信号转导网络的理解。有关本文的更多资源,请访问 WIREs 网站。

利益冲突

作者声明本文没有利益冲突。