Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytes.
about
Nucleotide sequences of human globin messenger RNA2003 William Allan Award address. The Thalassemias: the role of molecular genetics in an evolving global health problemThe genetic control of protein synthesis: The haemoglobin modelImbalance in alpha and beta globin synthesis associated with a hemoglobinopathy.Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.Hemoglobin messenger RNA from human bone marrow. Isolation and translation in homozygous and heterozygous beta-thalassemia.Messenger RNA in animal cells.Increased efficiency of exogenous messenger RNA translation in a Krebs ascites cell lysate.Hemoglobin switching in sheep and goats: change in functional globin messenger RNA in reticulocytes and bone marrow cells.Authentic beta-globin mRNA sequences in homozygous betaO-thalassemia.Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia.Further evidence of a quantitative deficiency of chain-specific globin mRNA in the thalassemia syndromes.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.Quantitative deficiency of chain-specific globin messenger ribonucleic acids in the thalassemia syndromes.Decreased globin messenger RNA in thalassemia detected by molecular hybridization.A limited number of globin genes in human DNA.An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.Translation and stability of human globin mRNA in Xenopus oocytesProcessing of human beta-globin mRNA precursor to mRNA is defective in three patients with beta+-thalassemia.Cell-free transcription of mammalian chromatin: transcription of globin messenger RNA sequences from bone-marrow chromatin with mammalian RNA polymerase.Thalassemia 2016: Modern medicine battles an ancient disease.The molecular biology of the thalassemia syndromes.The molecular basis of thalassemia.Translational control of hemoglobin synthesis in thalassemic bone marrow.Clinical Features of β-Thalassemia and Sickle Cell Disease.Molecular basis for some disorders of haemoglobin synthesis. II.
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P2860
Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytes.
description
1971 nî lūn-bûn
@nan
1971 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1971 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1971年の論文
@ja
1971年学术文章
@wuu
1971年学术文章
@zh-cn
1971年学术文章
@zh-hans
1971年学术文章
@zh-my
1971年学术文章
@zh-sg
1971年學術文章
@yue
name
Isolation and translation of h ...... nd normal human reticulocytes.
@ast
Isolation and translation of h ...... nd normal human reticulocytes.
@en
Isolation and translation of h ...... nd normal human reticulocytes.
@nl
type
label
Isolation and translation of h ...... nd normal human reticulocytes.
@ast
Isolation and translation of h ...... nd normal human reticulocytes.
@en
Isolation and translation of h ...... nd normal human reticulocytes.
@nl
prefLabel
Isolation and translation of h ...... nd normal human reticulocytes.
@ast
Isolation and translation of h ...... nd normal human reticulocytes.
@en
Isolation and translation of h ...... nd normal human reticulocytes.
@nl
P2860
P356
P1476
Isolation and translation of h ...... nd normal human reticulocytes.
@en
P2093
Anderson WF
Nienhuis AW
P2860
P304
P356
10.1172/JCI106745
P407
P577
1971-11-01T00:00:00Z