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Unveiling novel genetic insights into arterial calcification.

作者信息

Goettsch Claudia

机构信息

Department of Internal Medicine I, Cardiology, University Hospital, Medical Faculty, RWTH Aachen, Aachen, Germany.

出版信息

Nat Cardiovasc Res. 2023 Dec;2(12):1102-1103. doi: 10.1038/s44161-023-00379-8.

DOI:10.1038/s44161-023-00379-8
PMID:39196144
Abstract
摘要

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Unveiling novel genetic insights into arterial calcification.揭示动脉钙化的新基因见解。
Nat Cardiovasc Res. 2023 Dec;2(12):1102-1103. doi: 10.1038/s44161-023-00379-8.
2
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本文引用的文献

1
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.多民族全基因组研究鉴定出冠状动脉钙化的效应基因和可用药途径。
Nat Genet. 2023 Oct;55(10):1651-1664. doi: 10.1038/s41588-023-01518-4. Epub 2023 Sep 28.
2
eXclusionarY: 10 years later, where are the sex chromosomes in GWASs?排除性研究:10 年后,GWAS 研究中的性染色体在哪里?
Am J Hum Genet. 2023 Jun 1;110(6):903-912. doi: 10.1016/j.ajhg.2023.04.009.
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Cardiovascular Calcification Heterogeneity in Chronic Kidney Disease.
慢性肾脏病中心血管钙化的异质性。
Circ Res. 2023 Apr 14;132(8):993-1012. doi: 10.1161/CIRCRESAHA.123.321760. Epub 2023 Apr 13.
4
Heritability of Coronary Artery Disease: Insights From a Classical Twin Study.冠状动脉疾病的遗传性:来自经典双胞胎研究的见解。
Circ Cardiovasc Imaging. 2022 Mar;15(3):e013348. doi: 10.1161/CIRCIMAGING.121.013348. Epub 2022 Mar 15.
5
Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis.亚临床动脉粥样硬化的多民族外显子组全关联研究
Circ Cardiovasc Genet. 2016 Dec;9(6):511-520. doi: 10.1161/CIRCGENETICS.116.001572. Epub 2016 Nov 21.
6
Racial differences in the burden of coronary artery calcium and carotid intima media thickness between Blacks and Whites.黑人和白人在冠状动脉钙化负担和颈动脉内膜中层厚度方面的种族差异。
Neth Heart J. 2015 Jan;23(1):44-51. doi: 10.1007/s12471-014-0610-4.
7
Genetics of coronary artery calcification among African Americans, a meta-analysis.非裔美国人冠状动脉钙化的遗传学:一项荟萃分析。
BMC Med Genet. 2013 Jul 19;14:75. doi: 10.1186/1471-2350-14-75.
8
A prospective study of brachytelephalangic chondrodysplasia punctata: identification of arylsulfatase E mutations, functional analysis of novel missense alleles, and determination of potential phenocopies.前瞻性研究短指-点状软骨发育不良:鉴定芳基硫酸酯酶 E 突变,新型错义等位基因的功能分析,以及确定潜在的表型模拟。
Genet Med. 2013 Aug;15(8):650-7. doi: 10.1038/gim.2013.13. Epub 2013 Mar 7.
9
X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variability.X连锁隐性点状软骨发育不良:芳基硫酸酯酶E基因突变谱及临床变异性扩大
Am J Med Genet A. 2003 Mar 1;117A(2):164-8. doi: 10.1002/ajmg.a.10950.
10
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy.Xp22.3上的一组硫酸酯酶基因:点状软骨发育不良(CDPX)中的突变及其对华法林胚胎病的影响。
Cell. 1995 Apr 7;81(1):15-25. doi: 10.1016/0092-8674(95)90367-4.