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[杂合β和δ-β地中海贫血病例中的信使核糖核酸。生物合成及杂交研究]

[Messenger RNA in cases of heterozygous beta and delta-beta Thalassemia. Biosynthetic and hybridization studies].

作者信息

Bernardi F, Marchetti G, Del Senno L, Perrotta C, Conconi F, Borsetto C, Paolini A R

出版信息

Boll Soc Ital Biol Sper. 1980 Jun 15;56(11):1127-32.

PMID:7448019
Abstract

mRNA-cDNA hybridization, intact reticulocytes biosynthesis and heterologous cell-free translation studies have been performed in cases of heterozygous beta and delta beta thalassaemia. Results obtained have shown that the relative amount of beta mRNA is higher in Ferrara microcytes than in other heterozygous including delta beta. This indicates that transcription of beta globin gene takes place in Ferrara beta 0 thalassaemia. On the contrary globin biosynthesis studies have failed to show clear-cut differences among the various heterozygous considered and cannot evaluate the translatability of beta thal. FemRNA.

摘要

在杂合子β和δβ地中海贫血病例中进行了mRNA - cDNA杂交、完整网织红细胞生物合成及异源无细胞翻译研究。所获结果表明,费拉拉小红细胞中β mRNA的相对量高于包括δβ在内的其他杂合子。这表明β珠蛋白基因的转录发生在费拉拉β0地中海贫血中。相反,珠蛋白生物合成研究未能在各种所考虑的杂合子之间显示出明显差异,且无法评估β地中海贫血FemRNA的可翻译性。

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