地中海贫血中与多核糖体相关的珠蛋白信使核糖核酸活性降低。 - Suppr

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超能文献

Decreased globin messenger RNA activity associated with polyribosomes in thalassaemia.

作者信息

Grossbard E, Terada M, Dow L W, Bank A

出版信息

Nat New Biol. 1973 Feb 14;241(111):209-11. doi: 10.1038/newbio241209a0.

DOI:10.1038/newbio241209a0

PMID:4512586

Abstract

摘要

相似文献

Decreased globin messenger RNA activity associated with polyribosomes in thalassaemia.地中海贫血中与多核糖体相关的珠蛋白信使核糖核酸活性降低。

Nat New Biol. 1973 Feb 14;241(111):209-11. doi: 10.1038/newbio241209a0.

Globin messenger RNA in hemoglobin H disease.

Blood. 1973 Dec;42(6):825-33.

Globin-chain synthesis in Hb H disease: the activity of red cell precursors and their mRNA.血红蛋白H病中的珠蛋白链合成：红细胞前体的活性及其信使核糖核酸

Isr J Med Sci. 1978 Nov;14(11):1102-6.

Globin synthesis of intact cells and activity of isolated mRNA in -thalassaemia.β地中海贫血中完整细胞的珠蛋白合成及分离mRNA的活性

Nat New Biol. 1973 May 23;243(125):114-6.

Globin messenger RNA in the thalassemia syndromes.

Ann N Y Acad Sci. 1974;232(0):76-87. doi: 10.1111/j.1749-6632.1974.tb20574.x.

Decreased beta globin mRNA activity in bone marrow cells in homozygous and heterozygous beta thalassaemia.纯合子和杂合子β地中海贫血患者骨髓细胞中β珠蛋白mRNA活性降低。

Nat New Biol. 1973 Aug 29;244(139):280-1. doi: 10.1038/newbio244280a0.

Globin chain synthesis in the marrow and reticulocytes of beta thalassemia, hemoglobin H disease, and beta delta thalassemia.β地中海贫血、血红蛋白H病和βδ地中海贫血患者骨髓及网织红细胞中的珠蛋白链合成

Blood. 1972 Jul;40(1):105-11.

Induction of -globin synthesis in the -thalassaemia of Ferrara.费拉拉β地中海贫血中β珠蛋白合成的诱导

Nat New Biol. 1972 Jul 19;238(81):83-7. doi: 10.1038/newbio238083a0.

Hemoglobin Lepore trait: globin synthesis in bone marrow and peripheral blood.血红蛋白Lepore特性：骨髓和外周血中的珠蛋白合成。

Science. 1972 Nov 10;178(4061):623-5. doi: 10.1126/science.178.4061.623.

Cell-free synthesis of globin chains: an overview.无细胞体系合成珠蛋白链：概述

Ann N Y Acad Sci. 1974 Nov 29;241(0):142-55. doi: 10.1111/j.1749-6632.1974.tb21874.x.

引用本文的文献

Translational control of hemoglobin synthesis in thalassemic bone marrow.地中海贫血骨髓中血红蛋白合成的翻译控制

J Clin Invest. 1974 Apr;53(4):955-63. doi: 10.1172/JCI107661.

Decreased globin messenger RNA in thalassemia detected by molecular hybridization.通过分子杂交检测到地中海贫血中珠蛋白信使核糖核酸减少。

Proc Natl Acad Sci U S A. 1973 Jun;70(6):1886-90. doi: 10.1073/pnas.70.6.1886.

Quantitative deficiency of chain-specific globin messenger ribonucleic acids in the thalassemia syndromes.地中海贫血综合征中链特异性珠蛋白信使核糖核酸的定量缺乏。

Proc Natl Acad Sci U S A. 1973 Jun;70(6):1809-13. doi: 10.1073/pnas.70.6.1809.

Relative numbers of human globin genes assayed with purified alpha and beta complementary human DNA.用纯化的α和β互补人类DNA检测人类珠蛋白基因的相对数量。

Proc Natl Acad Sci U S A. 1975 Apr;72(4):1550-4. doi: 10.1073/pnas.72.4.1550.

Further evidence of a quantitative deficiency of chain-specific globin mRNA in the thalassemia syndromes.地中海贫血综合征中特定链珠蛋白mRNA定量缺乏的进一步证据。

Proc Natl Acad Sci U S A. 1975 Feb;72(2):567-71. doi: 10.1073/pnas.72.2.567.

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