首页> 外文期刊>Orthodontics & craniofacial research >Further evidence for the role of WNT 10A, WNT 10B WNT WNT 10A, WNT WNT 10B and GREM 2 GREM GREM 2 as candidate genes for isolated tooth agenesis
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Further evidence for the role of WNT 10A, WNT 10B WNT WNT 10A, WNT WNT 10B and GREM 2 GREM GREM 2 as candidate genes for isolated tooth agenesis

机译:WNT 10A,WNT 10B WNT 10A,WNT WNT 10B和GREM 2 GREM GREM 2作为候选基因的进一步证据作为分离的牙齿刺激的候选基因

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Structured Abstract Objective To investigate the association of single nucleotide variants in the candidate genes WNT 10A, WNT 10B and GREM 2 with isolated tooth agenesis. Setting and sample population A total of 435 Caucasian individuals (88 cases with isolated tooth agenesis and 347 unrelated controls) were ascertained at the University of Texas Health Science Center at Houston School of Dentistry. Clinical and radiographic examination by orthodontists confirmed the diagnosis of tooth agenesis. Genetic evaluation excluded syndromic forms of tooth agenesis. Materials and methods Saliva samples were collected as source of genomic DNA . Fourteen variants in/nearby WNT 10A , WNT 10B and GREM 2 were genotyped to test for association with tooth agenesis. Genotyping was performed using TaqMan chemistry in a real‐time polymerase chain reaction assay. Allelic and haplotype frequencies were compared among cases and controls using chi‐square tests as implemented in PLINK v.1.06. Bonferroni correction was used and P ?≤?0.004 indicates statistical differences between groups. Results Significant associations were found between individual SNP s and SNP combinations in WNT 10A, WNT 10B and GREM 2 SNP s with isolated tooth agenesis ( P ??0.004). Conclusion Our findings further support a role for variants in WNT 10A, WNT 10B and GREM 2 genes in the aetiology of isolated tooth agenesis. Functional studies are necessary to investigate the biological effects of these gene variants in tooth agenesis phenotypes.
机译:结构化摘要目的探讨候选基因Wnt 10a,wnt 10b和grem 2中的单核苷酸变体与分离的牙齿刺激的关联。在德克萨斯州休斯顿牙科学院的德克萨斯州卫生科学中心,共设定和样本人口共有435名白种人个人(88例患有孤立的牙齿发作和347例无关控制)。正畸医生的临床和放射线检查证实牙齿刺激的诊断。遗传评估排除综合症形式的牙齿刺激。材料和方法唾液样品被收集为基因组DNA的来源。在/附近的14个变体10a,wnt 10b和grem 2中进行基因分型以测试与牙齿刺激相关的关联。在实时聚合酶链反应测定中使用Taqman化学进行基因分型。使用Chi-Square测试在PLINK V.1.06中实现的情况下比较了等位基因和单倍型频率。使用Bonferroni校正,P?≤≤004表示组之间的统计差异。结果WNT 10A,WNT 10B和GREM 2 SNP S中的单个SNP S和SNP组合在分离出牙齿刺激(P 1 0.004)之间存在显着的关联。结论我们的研究结果进一步支持WNT 10A,WNT 10B和GREM 2基因的变体的作用,在分离的牙齿止血中的病毒中。有必要的功能研究来研究这些基因变体在牙齿血液缺血表型中的生物学效应。

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