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Atrial Septal Defect (ASD) associated long non-coding RNA maintains time-course of cardiomyocyte differentiation.

作者信息

Liu Yingjuan, Choy Mun-Kit, Abraham Sabu, Tenin Gennadiy, Black Graeme C, Keavney Bernard D

机构信息

Division of Cardiovascular Sciences, University of Manchester, Manchester M13 9PL, UK.

Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester M13 9NQ, UK.

出版信息

Genes Dis. 2022 Aug 8;10(4):1150-1153. doi: 10.1016/j.gendis.2022.07.010. eCollection 2023 Jul.

DOI:10.1016/j.gendis.2022.07.010
PMID:37397526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10311013/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d76/10311013/c1325f1d3ac7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d76/10311013/c1325f1d3ac7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d76/10311013/c1325f1d3ac7/gr1.jpg

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本文引用的文献

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BMC Dev Biol. 2021 Oct 6;21(1):14. doi: 10.1186/s12861-021-00245-5.
2
Quantified growth of the human embryonic heart.人类胚胎心脏的定量生长。
Biol Open. 2021 Feb 10;10(2):bio057059. doi: 10.1242/bio.057059.
3
Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies.全球先天性心脏病的出生患病率：1970-2017 年更新的 260 项研究系统评价和荟萃分析。
先天性心脏病：类型、病理生理学、诊断及治疗选择。
MedComm (2020). 2024 Jul 5;5(7):e631. doi: 10.1002/mco2.631. eCollection 2024 Jul.
4
Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population.与4p16风险基因座相关的自闭症谱系障碍的表型及芬兰人群中自闭症谱系障碍患者新的全基因组关联研究
Circ Genom Precis Med. 2023 Oct;16(5):486-489. doi: 10.1161/CIRCGEN.123.004070. Epub 2023 Aug 14.
Int J Epidemiol. 2019 Apr 1;48(2):455-463. doi: 10.1093/ije/dyz009.
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Stepwise Clearance of Repressive Roadblocks Drives Cardiac Induction in Human ESCs.逐步清除抑制性障碍驱动人类胚胎干细胞的心脏诱导。
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