Quantitative deficiency of chain-specific globin messenger ribonucleic acids in the thalassemia syndromes. - Wikidata - wikimedia - TriplyDB

Quantitative deficiency of chain-specific globin messenger ribonucleic acids in the thalassemia syndromes.

Quantitative deficiency of chain-specific globin messenger ribonucleic acids in the thalassemia syndromes.

http://www.wikidata.org/entity/Q35106363

about

Nucleotide sequences of human globin messenger RNA The genetic control of protein synthesis: The haemoglobin model Imbalance in alpha and beta globin synthesis associated with a hemoglobinopathy.Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.Effects of 5-bromo-2' -deoxyuridine on production of globin messenger RNA in dimethyl sulfoxide-stimulated Friend leukemia cells.Authentic beta-globin mRNA sequences in homozygous betaO-thalassemia.Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia.Molecular evolution of human and rabbit beta-globin mRNAs.Further evidence of a quantitative deficiency of chain-specific globin mRNA in the thalassemia syndromes.Synthesis of DNA complementary to separated human alpha and beta globin messenger RNAs.Relative numbers of human globin genes assayed with purified alpha and beta complementary human DNA.Human globin gene analysis for a patient with beta-o/delta beta-thalassemia.Nucleotide sequences of the 3'-terminal untranslated region of messenger RNA for human beta globin chain.Nucleotide sequence analysis of RNA synthesized from rabbit globin complementary DNA A limited number of globin genes in human DNA.An unusual "morphologic" variant of BF S The thalassemias: molecular mechanisms of human genetic disease.beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0].Base substitution in an intervening sequence of a beta+-thalassemic human globin gene Mutation in an intervening sequence splice junction in man Translation and stability of human globin mRNA in Xenopus oocytes Insertion of synthetic copies of human globin genes into bacterial plasmids.Activation of human beta-globin genes from nonerythroid cells by fusion with murine erythroleukemia cells Embryonic-fetal erythroid characteristics of a human leukemic cell line Processing of human beta-globin mRNA precursor to mRNA is defective in three patients with beta+-thalassemia.Transcription of adenovirus RNA in permissive and nonpermissive infections.Molecular analysis of the beta-thalassemia phenotype associated with inheritance of hemoglobin E (alpha 2 beta2(26)Glu leads to Lys).Defects in DNA and globin messenger RNA in homozygotes for hemoglobin Lepore.Cell-free transcription of mammalian chromatin: transcription of globin messenger RNA sequences from bone-marrow chromatin with mammalian RNA polymerase.Demonstration of non-functional beta-globin mRNA in homozygous beta (0) thalassemia The molecular biology of the thalassemia syndromes.The potential molecular mechanism of thalassemias and related disorders.The molecular basis of thalassemia.The structure of the human beta-globin gene in beta-thalassaemia.Translational control of hemoglobin synthesis in thalassemic bone marrow.Immunological purification and characterization of hemoglobin chain-synthesizing polysomes: a derivative hypothesis for regulatory and evolutionary interrelationships in hemoglobin biosynthesis.Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.beta (+)-Thalassaemia in the Po river delta region (northern Italy): genotype and beta globin synthesis The thalassemias and related disorders.Assay of thalassaemic messenger RNA in the wheat germ system.

P2860

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P2860

Quantitative deficiency of chain-specific globin messenger ribonucleic acids in the thalassemia syndromes.

http://www.wikidata.org/entity/Q35106363

description

1973 nî lūn-bûn

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1973 թուականի Յունիսին հրատարակուած գիտական յօդուած

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1973 թվականի հունիսին հրատարակված գիտական հոդված

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1973年の論文

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1973年論文

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1973年論文

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1973年論文

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1973年論文

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1973年論文

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1973年论文

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name

Quantitative deficiency of cha ...... in the thalassemia syndromes.

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Quantitative deficiency of cha ...... in the thalassemia syndromes.

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Quantitative deficiency of cha ...... in the thalassemia syndromes.

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Quantitative deficiency of cha ...... in the thalassemia syndromes.

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Proceedings of the National Academy of Sciences of the United States of America

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Quantitative deficiency of cha ...... in the thalassemia syndromes.

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P2093

Benz EJ Jr

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Forget BG

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Housman D

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Skoultchi A

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P2860

In vitro synthesis of DNA complementary to purified rabbit globin mRNA (RNA-dependent DNA polymerase-reticulocyte-hemoglobin-density gradient centrifugation-oligo(dT) primer)

Cell-free hemoglobin synthesis in beta-thalassemia

Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytes.

Protein synthesis in a cell free human reticulocyte system: ribosome function in thalassemia.

Messenger RNA for globin in the postribosomal supernatant of rabbit reticulocytes

Separation and translation of the mRNAs coding for and chains of rabbit globin.

Beta thalassemia and translation of globin messenger RNA.

Translation of -globin m-RNA in -thalassemia and the S and C hemoglobinopathies

Defect in messenger RNA for human hemoglobin synthesis in beta thalassemia.

Association of an endoribonuclease with the avian myeloblastosis virus deoxyribonucleic acid polymerase.

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1809-1813

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scholarly article

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10.1073/PNAS.70.6.1809

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6

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70

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19041956

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4124305

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433602

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