An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.
about
Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron.The molecular basis of β-thalassemia.The thalassemias: molecular mechanisms of human genetic disease.alpha-Thalassemia caused by an unstable alpha-globin mutant.Direct detection of the common Mediterranean beta-thalassemia gene with synthetic DNA probes. An alternative approach for prenatal diagnosis.Determination of the spectrum of beta-thalassemia genes in Spain by use of dot-blot analysis of amplified beta-globin DNAFive nucleotide changes in the large intervening sequence of a beta globin gene in a beta+ thalassemia patient.Restriction fragment length polymorphism of the rat albumin gene in Sprague-Dawley rats and its application in genetic study of analbuminemiaA beta-thalassemia lesion abolishes the same Mst II site as the sickle mutationStructure and expression of a cloned beta o thalassaemic globin gene.Two cloned beta thalassemia genes are associated with amber mutations at codon 39.Presence of albumin mRNA precursors in nuclei of analbuminemic rat liver lacking cytoplasmic albumin mRNA.RNA processing errors in patients with beta-thalassemia.Posttranscriptional defects in beta-globin messenger RNA metabolism in beta-thalassemia: abnormal accumulation of beta-messenger RNA precursor sequencesA seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.Abnormal splice in a mutant human beta-globin gene not at the site of a mutation."Silent" nucleotide substitution in a beta+-thalassemia globin gene activates splice site in coding sequence RNA.A journey in science: early lessons from the hemoglobin fieldThe ovalbumin gene family: complete sequence and structure of the Y gene.mRNA-deficient beta o-thalassemia results from a single nucleotide deletion.Deletion analysis of a unique 3' splice site indicates that alternating guanine and thymine residues represent an efficient splicing signal.The beta-globin gene in Sardinian delta beta 0-thalassemia carries a C----T nonsense mutation at codon 39The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia.beta (+)-Thalassaemia in the Po river delta region (northern Italy): genotype and beta globin synthesisThe beta- and delta-thalassemia repository.Ectopic synthesis of high-Mr calcitonin by the BEN lung carcinoma cell line reflects aberrant proteolytic processing.Real-time multiplex analysis of four beta-thalassemia mutations employing surface plasmon resonance and biosensor technology.Isolation and characterization of the translation product of a β-globin gene nonsense mutation (β121 GAA→TAA)Hereditary anaemias: genetic basis, clinical features, diagnosis, and treatment. WHO working group[Hereditary anemia: genetic basis, clinical characteristics, diagnosis and treatment. WHO Workgroup]
P2860
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P2860
An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.
description
1981 nî lūn-bûn
@nan
1981年の論文
@ja
1981年論文
@yue
1981年論文
@zh-hant
1981年論文
@zh-hk
1981年論文
@zh-mo
1981年論文
@zh-tw
1981年论文
@wuu
1981年论文
@zh
1981年论文
@zh-cn
name
An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.
@ast
An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.
@en
type
label
An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.
@ast
An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.
@en
prefLabel
An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.
@ast
An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.
@en
P2860
P356
P1476
An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.
@en
P2093
D Westaway
R Williamson
P2860
P304
P356
10.1093/NAR/9.8.1777
P407
P577
1981-04-01T00:00:00Z