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The role of primary myogenic regulatory factors in the developing diaphragmatic muscle in the nitrofen-induced diaphragmatic hernia

机译:肌原性调节因子在硝基芬诱发的diaphragm肌疝中发展的diaphragm肌中的作用

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摘要

The nitrofen model of congenital diaphragmatic hernia (CDH) is widely used to investigate the pathogenesis of CDH. However, the exact pathomechanism of the diaphragmatic defect is still unclear. Diaphragmatic muscularization represents the last stage of diaphragmatic development. Myogenic differentiation 1 (MyoD) and myogenic factor 5 (Myf5) play a crucial role in muscularization. MyoD−/− : Myf5+/− mutant mice show reduced diaphragmatic size, whereas MyoD+/− : Myf5−/− mutants have normal diaphragms. We designed this study to investigate diaphragmatic gene expression of MyoD and Myf5 in the nitrofen CDH model.
机译:先天性diaphragm肌疝(CDH)的nitrofen模型被广泛用于研究CDH的发病机理。但是,the肌缺损的确切发病机制仍不清楚。 Dia肌肌肉化代表diaphragm肌发育的最后阶段。成肌分化1(MyoD)和成肌因子5(Myf5)在肌肉形成过程中起着至关重要的作用。 MyoD-/-:Myf5 +/- 突变小鼠显示出较小的reduced肌大小,而MyoD + /-:Myf5-//-突变小鼠具有正常的s肌。我们设计了这项研究,以调查在硝基芬CDH模型中MyoD和Myf5的隔膜基因表达。

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