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An interspecies heart-to-heart: Using to uncover the genetic basis of congenital heart disease.种间心连心:利用(此处原文“Using”后缺少内容)揭示先天性心脏病的遗传基础。
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Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy.非洲爪蟾作为出生缺陷——先天性心脏病和内脏反位的模式生物
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A Matter of the Heart: The African Clawed Frog Xenopus as a Model for Studying Vertebrate Cardiogenesis and Congenital Heart Defects.心脏问题:非洲爪蟾作为研究脊椎动物心脏发生和先天性心脏缺陷的模型
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Philos Trans R Soc Lond B Biol Sci. 2016 Dec 19;371(1710). doi: 10.1098/rstb.2015.0406.

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本文引用的文献

1
Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia.先天性心脏病遗传学揭示了纤毛处核孔蛋白的上下文依赖性组织和功能。
Dev Cell. 2016 Sep 12;38(5):478-92. doi: 10.1016/j.devcel.2016.08.002. Epub 2016 Sep 1.
2
Trends in Congenital Heart Disease: The Next Decade.先天性心脏病的发展趋势:未来十年
Circulation. 2016 Jun 21;133(25):2716-33. doi: 10.1161/CIRCULATIONAHA.116.023544.
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De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.伴有神经发育及其他先天性异常的先天性心脏病中的新发突变。
Science. 2015 Dec 4;350(6265):1262-6. doi: 10.1126/science.aac9396.
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CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus.CRISPR/Cas9:一种用于在非洲爪蟾中筛选人类疾病基因的廉价且高效的功能丧失工具。
Dev Biol. 2015 Dec 15;408(2):196-204. doi: 10.1016/j.ydbio.2015.11.003. Epub 2015 Nov 4.
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The NIMA-like kinase Nek2 is a key switch balancing cilia biogenesis and resorption in the development of left-right asymmetry.类NIMA激酶Nek2是左右不对称发育过程中平衡纤毛生成与纤毛吸收的关键开关。
Development. 2015 Dec 1;142(23):4068-79. doi: 10.1242/dev.126953. Epub 2015 Oct 22.
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Infant Mortality Statistics From the 2013 Period Linked Birth/Infant Death Data Set.来自2013年时期关联出生/婴儿死亡数据集的婴儿死亡率统计数据。
Natl Vital Stat Rep. 2015 Aug 6;64(9):1-30.
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Reciprocal regulation of cilia and autophagy via the MTOR and proteasome pathways.通过MTOR和蛋白酶体途径对纤毛和自噬进行相互调节。
Autophagy. 2015 Apr 3;11(4):607-16. doi: 10.1080/15548627.2015.1023983.
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Global genetic analysis in mice unveils central role for cilia in congenital heart disease.对小鼠的全基因组分析揭示了纤毛在先天性心脏病中的核心作用。
Nature. 2015 May 28;521(7553):520-4. doi: 10.1038/nature14269. Epub 2015 Mar 25.
9
Dual developmental role of transcriptional regulator Ets1 in Xenopus cardiac neural crest vs. heart mesoderm.转录调节因子Ets1在非洲爪蟾心脏神经嵴与心脏中胚层中的双重发育作用。
Cardiovasc Res. 2015 Apr 1;106(1):67-75. doi: 10.1093/cvr/cvv043. Epub 2015 Feb 17.
10
Complex genetics and the etiology of human congenital heart disease.复杂遗传学与人类先天性心脏病的病因学
Cold Spring Harb Perspect Med. 2014 Jul 1;4(7):a013953. doi: 10.1101/cshperspect.a013953.

种间心连心:利用(此处原文“Using”后缺少内容)揭示先天性心脏病的遗传基础。

An interspecies heart-to-heart: Using to uncover the genetic basis of congenital heart disease.

作者信息

Garfinkel Alexandra MacColl, Khokha Mustafa K

机构信息

Pediatric Genomics Discovery Program, Departments of Pediatrics and Genetics; Yale University School of Medicine.

出版信息

Curr Pathobiol Rep. 2017 Jun;5(2):187-196. doi: 10.1007/s40139-017-0142-x. Epub 2017 May 6.

DOI:10.1007/s40139-017-0142-x
PMID:29082114
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5658036/
Abstract

PURPOSE OF REVIEW

Given the enormous impact congenital heart disease has on child health, it is imperative that we improve our understanding of the disease mechanisms that underlie patient phenotypes and clinical outcomes. This review will outline the merits of using the frog model, as a tool to study human cardiac development and left-right patterning mechanisms associated with congenital heart disease.

RECENT FINDINGS

Patient-driven gene discovery continues to provide new insight into the mechanisms of congenital heart disease, and by extension, patient phenotypes and outcomes. By identifying gene variants in CHD patients, studies in have elucidated the molecular mechanisms of how these candidate genes affect cardiac development, both cardiogenesis as well as left-right patterning, which can have a major impact on cardiac morphogenesis. has also proved to be a useful screening tool for the biological relevance of identified patient-mutations, and ongoing investigations continue to illuminate disease mechanisms.

SUMMARY

Analyses in model organisms can help to elucidate the disease mechanisms underlying CHD patient phenotypes. Using to disentangle the genotype-phenotype relationships of well-known and novel disease genes could enhance the ability of physicians to efficaciously treat patients and predict clinical outcomes, ultimately improving quality of life and survival rates of patients born with congenital heart disease.

摘要

综述目的

鉴于先天性心脏病对儿童健康的巨大影响,我们必须加深对构成患者表型和临床结果基础的疾病机制的理解。本综述将概述使用青蛙模型作为研究与先天性心脏病相关的人类心脏发育和左右模式形成机制的工具的优点。

最新发现

由患者推动的基因发现继续为先天性心脏病的机制以及由此延伸的患者表型和结果提供新的见解。通过识别先天性心脏病患者的基因变异,相关研究阐明了这些候选基因如何影响心脏发育的分子机制,包括心脏发生以及左右模式形成,这可能对心脏形态发生产生重大影响。青蛙模型也已被证明是一种用于筛选已识别的患者突变的生物学相关性的有用工具,并且正在进行的研究继续阐明疾病机制。

总结

在模式生物中进行的分析有助于阐明先天性心脏病患者表型背后的疾病机制。使用青蛙模型来理清已知和新发现的疾病基因的基因型-表型关系,可以提高医生有效治疗患者和预测临床结果的能力,最终改善先天性心脏病患者的生活质量和生存率。