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Left-right asymmetry and congenital cardiac defects: getting to the heart of the matter in vertebrate left-right axis determination.

机译:左右不对称和先天性心脏缺陷:在脊椎动物左右轴确定中到达问题的心脏。

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摘要

Cellular and molecular left-right differences that are present in the mesodermal heart fields suggest that the heart is lateralized from its inception. Left-right asymmetry persists as the heart fields coalesce to form the primary heart tube, and overt, morphological asymmetry first becomes evident when the heart tube undergoes looping morphogenesis. Thereafter, chamber formation, differentiation of the inflow and outflow tracts, and position of the heart relative to the midline are additional features of heart development that exhibit left-right differences. Observations made in human clinical studies and in animal models of laterality disease suggest that all of these features of cardiac development are influenced by the embryonic left-right body axis. When errors in left-right axis determination happen, they almost always are associated with complex congenital heart malformations. The purpose of this review is to highlight what is presently known about cardiac development and upstream processes of left-right axis determination, and to consider how perturbation of the left-right body plan might ultimately result in particular types of congenital heart defects.
机译:中胚层心脏区域中存在的细胞和分子左右差异表明,心脏从开始就被侧向化。随着心脏场的合并形成初级心管,左右不对称性持续存在,并且明显地,当心管经历环状形态发生时,形态不对称首先变得明显。此后,腔的形成,流入和流出通道的区分以及心脏相对于中线的位置是心脏发育的其他特征,表现出左右差异。在人类临床研究和偏侧性疾病动物模型中所做的观察表明,心脏发育的所有这些特征均受胚胎左右身体轴的影响。当左右轴确定错误发生时,它们几乎总是与复杂的先天性心脏畸形有关。这篇综述的目的是强调当前关于心脏发育和左右轴确定的上游过程的已知知识,并考虑左右身体计划的扰动最终可能导致特定类型的先天性心脏缺陷的原因。

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