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本文引用的文献

1
Aberrant pulmonary lymphatic development in the nitrofen mouse model of congenital diaphragmatic hernia.先天性膈疝硝基酚模型鼠肺淋巴管发育异常。
J Pediatr Surg. 2013 Jun;48(6):1198-204. doi: 10.1016/j.jpedsurg.2013.03.013.
2
Current concepts on the pathogenesis and etiology of congenital diaphragmatic hernia.先天性膈疝发病机制和病因的现代概念。
Respir Physiol Neurobiol. 2013 Nov 1;189(2):232-40. doi: 10.1016/j.resp.2013.04.015. Epub 2013 May 9.
3
Antenatal imatinib treatment reduces pulmonary vascular remodeling in a rat model of congenital diaphragmatic hernia.产前伊马替尼治疗可减少先天性膈疝大鼠模型的肺血管重构。
Am J Physiol Lung Cell Mol Physiol. 2012 Jun 1;302(11):L1159-66. doi: 10.1152/ajplung.00325.2010. Epub 2012 Mar 23.
4
Defective pulmonary innervation and autonomic imbalance in congenital diaphragmatic hernia.先天性膈疝中肺神经支配缺陷和自主神经失衡。
Am J Physiol Lung Cell Mol Physiol. 2012 Feb 15;302(4):L390-8. doi: 10.1152/ajplung.00275.2011. Epub 2011 Nov 23.
5
Local fetal lung renin-angiotensin system as a target to treat congenital diaphragmatic hernia.局部胎儿肺肾素-血管紧张素系统作为治疗先天性膈疝的靶点。
Mol Med. 2012 Mar 27;18(1):231-43. doi: 10.2119/molmed.2011.00210.
6
The pulmonary mesenchymal tissue layer is defective in an in vitro recombinant model of nitrofen-induced lung hypoplasia.体外重组硝呋酚诱导肺发育不良模型中肺间质组织层存在缺陷。
Am J Pathol. 2012 Jan;180(1):48-60. doi: 10.1016/j.ajpath.2011.09.032. Epub 2011 Nov 4.
7
Results of fetal endoscopic tracheal occlusion for congenital diaphragmatic hernia and the set up of the randomized controlled TOTAL trial.先天性膈疝胎儿内镜气管封堵术的结果及随机对照 TOTAL 试验的建立。
Early Hum Dev. 2011 Sep;87(9):619-24. doi: 10.1016/j.earlhumdev.2011.08.001.
8
Dynamic tracheal occlusion improves lung morphometrics and function in the fetal lamb model of congenital diaphragmatic hernia.动态气管阻塞改善先天性膈疝胎儿羊模型的肺形态计量学和功能。
J Pediatr Surg. 2011 Jun;46(6):1150-7. doi: 10.1016/j.jpedsurg.2011.03.049.
9
Antenatal sildenafil treatment attenuates pulmonary hypertension in experimental congenital diaphragmatic hernia.产前西地那非治疗可减轻实验性先天性膈疝的肺动脉高压。
Circulation. 2011 May 17;123(19):2120-31. doi: 10.1161/CIRCULATIONAHA.108.845909. Epub 2011 May 2.
10
Abnormal development of the enteric nervous system in rat embryos and fetuses with congenital diaphragmatic hernia.先天性膈疝大鼠胚胎和胎儿肠道神经系统的异常发育。
Pediatr Surg Int. 2011 Feb;27(2):165-73. doi: 10.1007/s00383-010-2788-x.

先天性膈疝的新见解-外科医生对 CDH 动物模型的介绍。

New Insights into Congenital Diaphragmatic Hernia - A Surgeon's Introduction to CDH Animal Models.

机构信息

Division of Pediatric General and Thoracic Surgery, Department of Surgery, The Hospital for Sick Children, University of Toronto , Toronto, ON , Canada.

出版信息

Front Pediatr. 2014 Apr 29;2:36. doi: 10.3389/fped.2014.00036. eCollection 2014.

DOI:10.3389/fped.2014.00036
PMID:24809040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4010792/
Abstract

In recent decades, new research into the developmental defects and pathophysiological basis of congenital diaphragmatic hernia (CDH) has revealed opportunities for the development of innovative therapies. Importantly, the use of animal models to represent this anomaly in the laboratory has resulted in the discovery of many important genetic, epigenetic, and other molecular contributors to this condition. In this review, the most commonly used and newly devised animal models of CDH are presented to familiarize the reader with the latest innovations in the basic sciences.

摘要

近几十年来,对先天性膈疝 (CDH) 的发育缺陷和病理生理学基础的新研究揭示了开发创新疗法的机会。重要的是,使用动物模型在实验室中代表这种异常,导致发现了许多对这种情况有重要贡献的遗传、表观遗传和其他分子因素。在这篇综述中,介绍了最常用和新设计的 CDH 动物模型,以使读者熟悉基础科学的最新创新。