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本文引用的文献

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Translation of Human-Induced Pluripotent Stem Cells: From Clinical Trial in a Dish to Precision Medicine.人类诱导多能干细胞的翻译:从培养皿中的临床试验到精准医学
J Am Coll Cardiol. 2016 May 10;67(18):2161-2176. doi: 10.1016/j.jacc.2016.01.083.
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Human induced pluripotent stem cell-derived cardiomyocytes recapitulate the predilection of breast cancer patients to doxorubicin-induced cardiotoxicity.人诱导多能干细胞衍生的心肌细胞重现了乳腺癌患者对阿霉素诱导的心脏毒性的易感性。
Nat Med. 2016 May;22(5):547-56. doi: 10.1038/nm.4087. Epub 2016 Apr 18.
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Induced pluripotent stem cells: at the heart of cardiovascular precision medicine.诱导多能干细胞:心血管精准医学的核心。
Nat Rev Cardiol. 2016 Jun;13(6):333-49. doi: 10.1038/nrcardio.2016.36. Epub 2016 Mar 24.
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Complex Interdependence Regulates Heterotypic Transcription Factor Distribution and Coordinates Cardiogenesis.复杂的相互依赖调节异型转录因子分布并协调心脏发生。
Cell. 2016 Feb 25;164(5):999-1014. doi: 10.1016/j.cell.2016.01.004. Epub 2016 Feb 11.
5
Genetic Variation, Not Cell Type of Origin, Underlies the Majority of Identifiable Regulatory Differences in iPSCs.遗传变异而非起源细胞类型,是诱导多能干细胞中大多数可识别调控差异的基础。
PLoS Genet. 2016 Jan 26;12(1):e1005793. doi: 10.1371/journal.pgen.1005793. eCollection 2016 Jan.
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Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correction.3型长QT综合征的人诱导多能干细胞模型概括了基于药物的表型校正。
Basic Res Cardiol. 2016 Mar;111(2):14. doi: 10.1007/s00395-016-0530-0. Epub 2016 Jan 23.
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Genetic and Epigenetic Regulation of Human Cardiac Reprogramming and Differentiation in Regenerative Medicine.再生医学中人类心脏重编程与分化的遗传和表观遗传调控
Annu Rev Genet. 2015;49:461-84. doi: 10.1146/annurev-genet-112414-054911.
8
Efficient attenuation of Friedreich's ataxia (FRDA) cardiomyopathy by modulation of iron homeostasis-human induced pluripotent stem cell (hiPSC) as a drug screening platform for FRDA.通过调节铁稳态有效减轻弗里德赖希共济失调(FRDA)心肌病——以人诱导多能干细胞(hiPSC)作为FRDA的药物筛选平台
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Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells.利用人诱导多能干细胞模拟RBM20家族性扩张型心肌病的结构和功能缺陷。
Hum Mol Genet. 2016 Jan 15;25(2):254-65. doi: 10.1093/hmg/ddv468. Epub 2015 Nov 24.
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Reprogramming barriers and enhancers: strategies to enhance the efficiency and kinetics of induced pluripotency.重编程的障碍与增强因素:提高诱导多能性效率和动力学的策略
Cell Regen. 2015 Nov 11;4:10. doi: 10.1186/s13619-015-0024-9. eCollection 2015.

人类诱导多能干细胞作为个性化精准心血管医学的一个平台

Human Induced Pluripotent Stem Cells as a Platform for Personalized and Precision Cardiovascular Medicine.

作者信息

Matsa Elena, Ahrens John H, Wu Joseph C

机构信息

Stanford Cardiovascular Institute, Department of Medicine, Division of Cardiology, and Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California.

出版信息

Physiol Rev. 2016 Jul;96(3):1093-126. doi: 10.1152/physrev.00036.2015.

DOI:10.1152/physrev.00036.2015
PMID:27335446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6345246/
Abstract

Human induced pluripotent stem cells (hiPSCs) have revolutionized the field of human disease modeling, with an enormous potential to serve as paradigm shifting platforms for preclinical trials, personalized clinical diagnosis, and drug treatment. In this review, we describe how hiPSCs could transition cardiac healthcare away from simple disease diagnosis to prediction and prevention, bridging the gap between basic and clinical research to bring the best science to every patient.

摘要

人类诱导多能干细胞(hiPSC)彻底改变了人类疾病建模领域,具有巨大潜力,可作为临床前试验、个性化临床诊断和药物治疗的范式转变平台。在本综述中,我们描述了hiPSC如何能够将心脏医疗从简单的疾病诊断转变为预测和预防,弥合基础研究与临床研究之间的差距,为每位患者带来最佳科学成果。