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Is the common 844ins68 polymorphism in the cystathionine beta-synthase gene associated with atherosclerosis?

作者信息

Orendác M, Musková B, Richterová E, Zvárová J, Stefek M, Zaykova E, Kraus J P, Stríbrný J, Hyánek J, Kozich V

机构信息

Institute of Inherited Metabolic Diseases, 1st Faculty of Medicine, Charles University, Prague, Czech Republic.

出版信息

J Inherit Metab Dis. 1999 Jun;22(5):674-5. doi: 10.1023/a:1005554702861.

DOI:10.1023/a:1005554702861
PMID:10399104
Abstract
摘要

相似文献

1
Is the common 844ins68 polymorphism in the cystathionine beta-synthase gene associated with atherosclerosis?胱硫醚β-合酶基因常见的844ins68多态性与动脉粥样硬化有关吗？
J Inherit Metab Dis. 1999 Jun;22(5):674-5. doi: 10.1023/a:1005554702861.
2
The 844ins68 polymorphism of the cystathionine beta-synthase gene is associated with schizophrenia.胱硫醚β-合酶基因 844ins68 多态性与精神分裂症有关。
Psychiatry Res. 2009 Dec 30;170(2-3):168-71. doi: 10.1016/j.psychres.2008.07.007. Epub 2009 Nov 10.
3
The frequency of 844ins68 mutation in the cystathionine beta-synthase gene is not increased in patients with venous thrombosis.胱硫醚β-合酶基因突变844ins68在静脉血栓形成患者中的频率并未增加。
Haematologica. 1998 Nov;83(11):1006-8.
4
Cystathionine beta-synthase 844ins68 polymorphism is unrelated to susceptibility to neural tube defects.胱硫醚β合酶 844ins68 多态性与神经管缺陷易感性无关。
Gene. 2014 Feb 10;535(2):119-23. doi: 10.1016/j.gene.2013.11.052. Epub 2013 Dec 4.
5
Presence of 844ins68 in the cystathionine beta-synthase gene in Asians (Koreans).
Thromb Haemost. 2001 Oct;86(4):1130.
6
Cystathionine beta-synthase T833C/844ins68 polymorphism and stroke.
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7
Heterogeneous ethnic distribution of the 844ins68 in the cystathionine beta-synthase gene.胱硫醚β-合酶基因中844ins68的异质种族分布。
Hum Hered. 1998 Nov-Dec;48(6):338-42. doi: 10.1159/000022826.
8
CBS c.844ins68 Polymorphism Frequencies in Control Populations: Implications on Nonsyndromic Cleft Lip With or Without Cleft Palate.对照组人群中CBS基因c.844ins68多态性频率：对非综合征性唇裂伴或不伴腭裂的影响
Cleft Palate Craniofac J. 2015 Jan;52(1):49-53. doi: 10.1597/13-051.
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Contribution of the cystathionine beta-synthase gene (844ins68) polymorphism to the risk of early-onset venous and arterial occlusive disease and of fasting hyperhomocysteinemia.胱硫醚β-合酶基因（844ins68）多态性对早发性静脉和动脉闭塞性疾病以及空腹高同型半胱氨酸血症风险的影响。
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Thromb Res. 2003 Apr 15;110(1):7-12. doi: 10.1016/s0049-3848(03)00293-7.

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本文引用的文献

1
A common 844INS68 insertion variant in the cystathionine beta-synthase gene.
Biochem Mol Med. 1997 Oct;62(1):23-5. doi: 10.1006/bmme.1997.2623.
2
A 68-bp insertion found in a homocystinuric patient is a common variant and is skipped by alternative splicing of the cystathionine beta-synthase mRNA.在一名同型胱氨酸尿症患者中发现的一个68个碱基对的插入是一个常见变异，并且在胱硫醚β-合酶信使核糖核酸的可变剪接过程中被跳过。
Am J Hum Genet. 1996 Dec;59(6):1391-3.
3
High prevalence of a mutation in the cystathionine beta-synthase gene.胱硫醚β-合酶基因突变的高患病率。
携带最常见同型胱氨酸尿症突变c.833T>C的胱硫醚β-合酶单倍型的多样性：基因转换的可能作用。
Hum Mutat. 2007 Mar;28(3):255-64. doi: 10.1002/humu.20430.
4
Candidate genes and confirmed genetic polymorphisms associated with cardiovascular diseases: a tabular assessment.与心血管疾病相关的候选基因和已证实的基因多态性：表格评估
J Thromb Thrombolysis. 2001 Feb;11(1):49-81. doi: 10.1023/a:1008956327032.
Am J Hum Genet. 1996 Dec;59(6):1262-7.
4
Hyperhomocysteinemia in premature arterial disease: examination of cystathionine beta-synthase alleles at the molecular level.早产动脉疾病中的高同型半胱氨酸血症：分子水平上胱硫醚β-合酶等位基因的检测
Hum Mol Genet. 1995 Apr;4(4):623-9. doi: 10.1093/hmg/4.4.623.
5
Hyperhomocysteinemia: an independent risk factor for vascular disease.高同型半胱氨酸血症：血管疾病的独立危险因素。
N Engl J Med. 1991 Apr 25;324(17):1149-55. doi: 10.1056/NEJM199104253241701.