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Chromatin Compaction in Noncompaction Cardiomyopathy.

作者信息

Cashman Timothy J, Trivedi Chinmay M

机构信息

Division of Cardiovascular Medicine (T.J.C., C.M.T.), UMass Chan Medical School, Worcester, MA.

Department of Medicine (T.J.C., C.M.T.), UMass Chan Medical School, Worcester, MA.

出版信息

Circ Res. 2023 Jun 23;133(1):68-70. doi: 10.1161/CIRCRESAHA.123.323015. Epub 2023 Jun 22.

Abstract
摘要

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本文引用的文献

1
Missense Mutation in Human CHD4 Causes Ventricular Noncompaction by Repressing ADAMTS1.
Circ Res. 2023 Jun 23;133(1):48-67. doi: 10.1161/CIRCRESAHA.122.322223. Epub 2023 May 31.
2
Noncompaction Cardiomyopathy-History and Current Knowledge for Clinical Practice.
J Clin Med. 2021 Jun 1;10(11):2457. doi: 10.3390/jcm10112457.
3
N-Acetyl Transferases: New Insights Into Human Congenital Cardiovascular Defects.
Circ Res. 2021 Apr 16;128(8):1170-1172. doi: 10.1161/CIRCRESAHA.121.319049. Epub 2021 Apr 15.
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Histone deacetylases 1 and 2 silence cryptic transcription to promote mitochondrial function during cardiogenesis.
Sci Adv. 2020 Apr 10;6(15):eaax5150. doi: 10.1126/sciadv.aax5150. eCollection 2020 Apr.
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A systematic review and meta-analysis of the prevalence of left ventricular non-compaction in adults.
Eur Heart J. 2020 Apr 7;41(14):1428-1436. doi: 10.1093/eurheartj/ehz317.
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CHD4 and the NuRD complex directly control cardiac sarcomere formation.
Proc Natl Acad Sci U S A. 2018 Jun 26;115(26):6727-6732. doi: 10.1073/pnas.1722219115. Epub 2018 Jun 11.
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Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.
J Am Coll Cardiol. 2018 Feb 20;71(7):711-722. doi: 10.1016/j.jacc.2017.12.019.
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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Nat Genet. 2017 Nov;49(11):1593-1601. doi: 10.1038/ng.3970. Epub 2017 Oct 9.
10

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