• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Polymorphisms at regions 1p22.1 (rs560426) and 8q24 (rs1530300) are risk markers for nonsyndromic cleft lip and/or palate in the Brazilian population.

作者信息

Bagordakis Elizabete, Paranaiba Lívia Máris Ribeiro, Brito Luciano Abreu, de Aquino Sibele Nascimento, Messetti Ana Camila, Martelli-Junior Hercílio, Swerts Mario Sergio Oliveira, Graner Edgard, Passos-Bueno Maria Rita, Coletta Ricardo D

机构信息

Department of Oral Diagnosis, School of Dentistry, State University of Campinas, Piracicaba, São Paulo, Brazil.

出版信息

Am J Med Genet A. 2013 May;161A(5):1177-80. doi: 10.1002/ajmg.a.35830. Epub 2013 Mar 26.

DOI:10.1002/ajmg.a.35830
PMID:23532876
Abstract
摘要

相似文献

1
Polymorphisms at regions 1p22.1 (rs560426) and 8q24 (rs1530300) are risk markers for nonsyndromic cleft lip and/or palate in the Brazilian population.1p22.1区域（rs560426）和8q24区域（rs1530300）的多态性是巴西人群非综合征性唇裂和/或腭裂的风险标志物。
Am J Med Genet A. 2013 May;161A(5):1177-80. doi: 10.1002/ajmg.a.35830. Epub 2013 Mar 26.
2
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry.巴西一个非洲血统比例高的人群中，非综合征性唇裂伴或不伴腭裂的遗传风险因素。
Am J Med Genet A. 2015 Oct;167A(10):2344-9. doi: 10.1002/ajmg.a.37181. Epub 2015 Jul 22.
3
Case-control and family-based association studies of novel susceptibility locus 8q24 in nonsyndromic cleft lip with or without cleft palate in a Southern Han Chinese population located in Guangdong Province.广东汉族人群非综合征型唇裂伴或不伴腭裂中新的易感位点 8q24 的病例对照和家系关联研究。
DNA Cell Biol. 2012 May;31(5):700-5. doi: 10.1089/dna.2011.1383. Epub 2011 Nov 1.
4
Association between single-nucleotide polymorphisms on chromosome 1p22 and 20q12 and nonsyndromic cleft lip with or without cleft palate: new data in Han Chinese and meta-analysis.1p22和20q12染色体上的单核苷酸多态性与非综合征性唇裂伴或不伴腭裂之间的关联：汉族人群新数据及荟萃分析
Birth Defects Res A Clin Mol Teratol. 2012 Jun;94(6):469-76. doi: 10.1002/bdra.23013. Epub 2012 Apr 21.
5
No evidence of association between 8q24 and susceptibility to nonsyndromic cleft lip with or without palate in Japanese population.在日本人群中，没有证据表明8q24与非综合征性唇裂伴或不伴腭裂易感性之间存在关联。
Cleft Palate Craniofac J. 2012 Nov;49(6):714-7. doi: 10.1597/10-242. Epub 2011 Oct 7.
6
rs1801133C>T polymorphism in MTHFR is a risk factor for nonsyndromic cleft lip with or without cleft palate in the Brazilian population.亚甲基四氢叶酸还原酶（MTHFR）基因中的rs1801133C>T多态性是巴西人群非综合征性唇裂伴或不伴腭裂的一个风险因素。
Birth Defects Res A Clin Mol Teratol. 2015 Apr;103(4):292-8. doi: 10.1002/bdra.23365. Epub 2015 Mar 24.
7
Potential genetic markers for nonsyndromic oral clefts in the Brazilian population: A systematic review and meta-analysis.巴西人群中非综合征性口腔裂的潜在遗传标志物：系统评价和荟萃分析。
Birth Defects Res. 2018 Jun 1;110(10):827-839. doi: 10.1002/bdr2.1208. Epub 2018 Feb 15.
8
Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients.爱沙尼亚和立陶宛患者中8号染色体q24区域非综合征性唇裂伴或不伴腭裂新易感基因座的复制研究
Am J Med Genet A. 2009 Nov;149A(11):2551-3. doi: 10.1002/ajmg.a.33024.
9
Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen.阿拉伯人群中伴有或不伴有腭裂的非综合征性唇裂：对也门新招募的病例对照样本中15个风险位点的基因分析。
Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):307-13. doi: 10.1002/bdra.23221. Epub 2014 Mar 13.
10
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25.中美洲人群非综合征性唇裂伴或不伴腭裂的遗传风险因素：IRF6以及8q24和10q25处变异的证据
Birth Defects Res A Clin Mol Teratol. 2010 Jul;88(7):535-7. doi: 10.1002/bdra.20689.

引用本文的文献

1
A Large Multicenter Brazilian Case-Control Study Exploring Genetic Variations in Interferon Regulatory Factor 6 and the Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate.一项大型多中心巴西病例对照研究，探索干扰素调节因子6的基因变异与非综合征性唇裂伴或不伴腭裂的风险。
Int J Mol Sci. 2025 Apr 7;26(7):3441. doi: 10.3390/ijms26073441.
2
Brazilian Multiethnic Association Study of Genetic Variant Interactions among , and in the Risk of Nonsyndromic Cleft Lip with or without Cleft Palate.巴西多民族协会关于、和基因变异相互作用与非综合征性唇裂伴或不伴腭裂风险的研究。 （注：原文中存在部分缺失内容，导致翻译可能不太完整准确，正常应该是具体的基因等相关内容。）
Dent J (Basel). 2022 Dec 26;11(1):7. doi: 10.3390/dj11010007.
3
Polymorphisms of (rs560426 and rs481931) and Non-Syndromic Cleft Lip/Palate: A Meta-Analysis.
（rs560426和rs481931）多态性与非综合征性唇腭裂：一项荟萃分析。
Life (Basel). 2021 Jan 15;11(1):58. doi: 10.3390/life11010058.
4
DOT: Gene-set analysis by combining decorrelated association statistics.基因集分析通过结合去相关关联统计。
PLoS Comput Biol. 2020 Apr 14;16(4):e1007819. doi: 10.1371/journal.pcbi.1007819. eCollection 2020 Apr.
5
Polymorphic variants in VAX1 and the risk of nonsyndromic cleft lip with or without cleft palate in a population from northern China.VAX1基因多态性变异与中国北方人群非综合征性唇裂伴或不伴腭裂的风险
Medicine (Baltimore). 2017 Apr;96(14):e6550. doi: 10.1097/MD.0000000000006550.
6
Association between IRF6 and 8q24 polymorphisms and nonsyndromic cleft lip with or without cleft palate: Systematic review and meta-analysis.IRF6与8q24基因多态性和非综合征性唇裂伴或不伴腭裂之间的关联：系统评价与荟萃分析
Birth Defects Res A Clin Mol Teratol. 2016 Sep;106(9):773-88. doi: 10.1002/bdra.23540. Epub 2016 Aug 11.
7
Family-based association analysis between nonsyndromic cleft lip with or without cleft palate and IRF6 polymorphism in an Iranian population.伊朗人群中唇腭裂（伴或不伴腭裂）与IRF6基因多态性的家系关联分析
Clin Oral Investig. 2015 May;19(4):891-4. doi: 10.1007/s00784-014-1305-3. Epub 2014 Sep 16.
8
Further evidence suggesting a role for variation in ARHGAP29 variants in nonsyndromic cleft lip/palate.进一步的证据表明ARHGAP29基因变异在非综合征性唇腭裂中发挥作用。
Birth Defects Res A Clin Mol Teratol. 2014 Sep;100(9):679-85. doi: 10.1002/bdra.23286. Epub 2014 Aug 27.
9
Genetics and genomics in Brazil: a promising future.巴西的遗传学与基因组学：前景光明。
Mol Genet Genomic Med. 2014 Jul;2(4):280-91. doi: 10.1002/mgg3.95.
10
Polymorphisms in FGF12, VCL, CX43 and VAX1 in Brazilian patients with nonsyndromic cleft lip with or without cleft palate.巴西非综合征性唇裂伴或不伴腭裂患者中 FGF12、VCL、CX43 和 VAX1 的多态性。
BMC Med Genet. 2013 May 16;14:53. doi: 10.1186/1471-2350-14-53.