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哥伦比亚人群中MSX1与非综合征性唇腭裂的关联。

Association of MSX1 with nonsyndromic cleft lip and palate in a Colombian population.

作者信息

Otero Liliana, Gutiérrez Sandra, Cháves Margarita, Vargas C, Bérmudez Luis

机构信息

Pontificia Universidad Javeriana, Bogotá, Colombia.

出版信息

Cleft Palate Craniofac J. 2007 Nov;44(6):653-6. doi: 10.1597/06-097.1.


DOI:10.1597/06-097.1
PMID:18177186
Abstract

OBJECTIVE: To evaluate the association between MSX1 CA polymorphism and nonsyndromic cleft lip with or without cleft palate (CL+/-P) in a group of patients from Operation Smile Colombia. DESIGN: Four alleles from MSX1 CA microsatellite sequence were analyzed. Polymerase chain reaction was carried out. The amplifications were performed by Short Tandem Repeats (STRs) in ABI PRISM 310 genetic analyzer. Chi-square and odds ratio tests were used to determine the association between genotype frequencies and the risk to the cleft lip/palate in a Colombian group population. SETTING: Operation Smile Colombia. PARTICIPANTS: Ninety-four affected patients (49 men and 45 women with CL+/-P) and 93 control individuals (43 men and 50 women). RESULTS: A significant statistical difference (p<.0106) was found between the patients who carried allele 3 and CL+/-P. In addition, allele 4 (heterozygous and homozygous form) was the most frequent in CL+/-P (74%) patients and in the control group (82%). CONCLUSIONS: These findings show a positive association between the MSX1 CA polymorphism and CL+/-P in a Colombian group population.

摘要

目的:在一组来自哥伦比亚“微笑行动”的患者中,评估MSX1 CA多态性与非综合征性唇裂伴或不伴腭裂(CL+/-P)之间的关联。 设计:分析MSX1 CA微卫星序列的四个等位基因。进行聚合酶链反应。扩增通过ABI PRISM 310基因分析仪中的短串联重复序列(STRs)进行。卡方检验和比值比检验用于确定哥伦比亚人群中基因型频率与唇腭裂风险之间的关联。 地点:哥伦比亚“微笑行动”。 参与者:94例受影响患者(49名男性和45名女性患有CL+/-P)和93名对照个体(43名男性和50名女性)。 结果:携带等位基因3的患者与CL+/-P之间存在显著统计学差异(p<.0106)。此外,等位基因4(杂合子和纯合子形式)在CL+/-P患者(74%)和对照组(82%)中最为常见。 结论:这些发现表明,在哥伦比亚人群中,MSX1 CA多态性与CL+/-P之间存在正相关。

相似文献

[1]
Association of MSX1 with nonsyndromic cleft lip and palate in a Colombian population.

Cleft Palate Craniofac J. 2007-11

[2]
[Association study on microsatellite polymorphisms of MSX1 gene and nonsyndromic cleft lip and palate].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007-6

[3]
Association between MSX1 variants and oral clefts in Han Chinese in western China.

DNA Cell Biol. 2011-6-20

[4]
SNPs and interaction analyses of IRF6, MSX1 and PAX9 genes in patients with non‑syndromic cleft lip with or without palate.

Mol Med Rep. 2013-8-6

[5]
Association between MSX1 SNPs and nonsyndromic cleft lip with or without cleft palate in the Korean population.

J Korean Med Sci. 2013-3-27

[6]
MSX1 gene polymorphisms in Mexican patients with non-syndromic cleft lip/palate.

Int J Pediatr Otorhinolaryngol. 2016-11

[7]
[Association between polymorphism of IRF6 rs2235371 locus and nonsyndromic cleft lip with or without cleft palate].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012-4

[8]
Mutation analysis of the MSX1 gene exons and intron in patients with nonsyndromic cleft lip and palate.

Stomatologija. 2006

[9]
Family-based association study of the MTHFR polymorphism C677T in patients with nonsyndromic cleft lip and palate from central Europe.

Cleft Palate Craniofac J. 2008-5

[10]
MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.

Eur J Oral Sci. 2010-6

引用本文的文献

[1]
Expressional Analysis of MSX1 (Human) Revealed its Role in Sagittal Jaw Relationship.

J Clin Diagn Res. 2017-8

[2]
Deleterious coding variants in multi-case families with non-syndromic cleft lip and/or palate phenotypes.

Sci Rep. 2016-7-26

[3]
Genomic expression in non syndromic cleft lip and palate patients: A review.

J Oral Biol Craniofac Res. 2015

[4]
MSX1 gene and nonsyndromic oral clefts in a Southern Brazilian population.

Braz J Med Biol Res. 2013-7-16

[5]
Molecular signaling along the anterior-posterior axis of early palate development.

Front Physiol. 2013-1-7

[6]
Roles of BMP signaling pathway in lip and palate development.

Front Oral Biol. 2012

[7]
No evidence of HAND2 involvement in nonsyndromic cleft lip with or without cleft palate.

Clin Oral Investig. 2011-3-24

[8]
Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations.

Eur J Hum Genet. 2010-1-20

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