首页> 外文期刊>Hemoglobin: International Journal for Hemoglobin Research >Regulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for beta-Globin Chain Deficiency?
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Regulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for beta-Globin Chain Deficiency?

机译:调节单核苷酸多态性RS368698783(g> a):仅在β-珠蛋白链缺乏的促红细胞生成应力特征下产生HB F的遗传改性剂?

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摘要

A regulatory single nucleotide polymorphism (rSNP), the Ay (+25G>A) (rs368698783) (NG_000007.3: g47783G>A) located in the HBG1 proximal promoter, is a significant predictor of clinical severity by elevating Hb F levels in p-thalassemia (P-thal). In this study, the presence of the Ay (+25 G>A) and Ay (+25 A>A) genotypes was investigated in four subgroups from a total of 611 subjects, including 88 a-thalassemia (a-thal) carriers (group A), 162 p-thal carriers of point mutations (group B), 57 carriers of p-thal deletions (group C) and 152 non thalassemic individuals (group D). The result is that the genotypes G>A and A>A exhibit significantly high levels of Hb F compared with the genotype G>G in both groups B and C, while no significant difference was observed in both groups A and D. We assume that the effect of Ay (+25G>A) polymorphism on Hb F production is only under erythropoietic stress characteristic for p-globin chain deficiency.
机译:调节单核苷酸多态性(RSNP),位于HBG1近端启动子中的AY(+ 25g> A)(RS368698783)(NG_000007.3:G47783G> A)是通过在P中升高HB F水平来实现临床严重程度的显着预测因子 -ThalAssemia(第p-Thal)。 在该研究中,在共有611个受试者中,在四个亚组中研究了AY(+ 25g> a)和Ay(+ 25A> a)基因型的存在,其中包括88个A-Thalassemia(A-THAL)载体( A组),点突变(B组)的162个P-Thal载体,第57个缺失(C组)和152个非丘脑血症个体(D组)。 结果是基因型G> A和A> A>与B和C组中的基因型G> G相比,显着高水平的HB F,同时在A和D两组中观察到没有显着差异。我们假设 AY(+ 25g> a)多态性对Hb F产生的影响仅在P-珠蛋白链缺乏的促红细胞生成应力特征下。

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