Molecular basis of α-thalassemia associated with the structural mutant hemoglobin Suan-Dok (α2109LEU→ARG)

No abstract is available for this paper.

• Publication year

  1990

• Venue

  Blood

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers

  No identifiers available.

• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• Molecular Cloning: A Laboratory Manual

  2001cited by this paper
• A review of the molecular genetics of the human alpha-globin gene cluster.

  1989cited by this paper
• Detection of minimal disease in hematopoietic malignancies of the B-cell lineage by using third-complementarity-determining region (CDR-III)-specific probes.

  1989cited by this paper
• An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype.

  1987cited by this paper
• Molecular basis for nondeletion alpha-thalassemia in American blacks. Alpha 2(116GAG----UAG).

  1987cited by this paper
• Effects of the position of the simian virus 40 enhancer on expression of multiple transcription units in a single plasmid

  1986cited by this paper
• Human alpha-globin gene expression. The dominant role of the alpha 2-locus in mRNA and protein synthesis.

  1986cited by this paper
• A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.

  1986cited by this paper
• Destabilization of messenger RNA/complementary DNA duplexes by the elongating 80 S ribosome.

  1986cited by this paper
• Alpha thalassaemia in an Italian population

  1986cited by this paper
• Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries.

  1985cited by this paper
• Gene synthesis machines: DNA chemistry and its uses.

  1985cited by this paper
• alpha‐Thalassaemia associated with the deletion of two nucleotides at position ‐2 and ‐3 preceding the AUG codon.

  1985cited by this paper
• The molecular basis of alpha‐thalassaemia in Thailand.

  1984cited by this paper
• Functional messenger RNAs are produced by SP6 in vitro transcription of cloned cDNAs.

  1984cited by this paper
• Initiation codon mutation as a cause of alpha thalassemia.

  1984cited by this paper
• Acquired alpha-thalassemia in preleukemia is due to decreased expression of all four alpha-globin genes.

  1983cited by this paper
• α-Thalassaemia caused by a polyadenylation signal mutation

  1983cited by this paper
• Oligonucleotide-directed mutagenesis of DNA fragments cloned into M13 vectors.

  1983cited by this paper
• a-Thalassemia Caused by an Unstable a-Globin Mutant

  1983cited by this paper
• Abnormal RNA splicing causes one form of alpha thalassemia.

  1982cited by this paper
• Globin structural mutant α125Leu→Pro is a novel cause of α-thalassaemia

  1982cited by this paper
• Genetic and molecular diversity in nondeletion Hb H disease.

  1981cited by this paper
• Molecular Characteristics of a Non‐deletion α‐Thalassaemia of the Po River Delta

  1981cited by this paper
• Mutation in an intervening sequence splice junction in man.

  1981cited by this paper
• Differentiation of the mRNA transcripts originating from the alpha 1- and alpha 2-globin loci in normals and alpha-thalassemics.

  1981cited by this paper
• Homology and concerted evolution at the alpha 1 and alpha 2 loci of human alpha-globin.

  1981cited by this paper
• Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.

  1980cited by this paper
• Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.

  1980cited by this paper
• The varied arrangement of the alpha globin genes in alpha thalassemia and Hb H disease in American blacks.

  1980cited by this paper
• Partial deletion of the α-globin structural gene in human α-thalassaemia

  1980cited by this paper
• Sequencing end-labeled DNA with base-specific chemical cleavages.

  1980cited by this paper
• A new genetic basis for hemoglobin-H disease.

  1980cited by this paper
• AN UNSTABLE VARIANT ASSOCIATED WITH a-THALASSEMIA

  1979cited by this paper
• α-Globin gene organisation in blacks precludes the severe form of α-thalassaemia

  1979cited by this paper
• Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.

  1979cited by this paper
• alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia.

  1979cited by this paper
• Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease.

  1979cited by this paper
• The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease.

  1979cited by this paper
• Resolution of hemoglobin subunits by electrophoresis in acid urea polyacrylamide gels containing Triton X-100.

  1978cited by this paper
• DNA sequencing with chain-terminating inhibitors.

  1977cited by this paper
• A general method for isolation of high molecular weight DNA from eukaryotes.

  1976cited by this paper
• Detection of specific sequences among DNA fragments separated by gel electrophoresis.

  1975cited by this paper
• Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain.

  1971cited by this paper
• Β-thalassemia -a Review

  year unknowncited by this paper

• In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia

  2020cites this paper
• An α0-Thalassemia-Like Mutation: Hb Suan-Dok [α109(G16)Leu→Arg] Carried by a Recombinant −α3.7 Gene

  2008cites this paper
• Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia

  2008cites this paper
• Hb Suan‐Dok [α109(G16)Leu→Arg; CTG→CGG (α2)] Described in a Patient of African Ancestry

  2004cites this paper
• Erythroid cell-specific mRNA stability elements in the alpha 2-globin 3' nontranslated region

  1995cites this paper
• Erythroid cell-specific determinants of alpha-globin mRNA stability

  1994cites this paper
• A Novel 13 BP Deletion in the 3′UTR of the β-Globin Gene Causes β-Thalassemia in a Turkish Patient

  1993cites this paper
• Human α-globin gene expression is silenced by terminal truncation of chromosome 16p beginning immediately 3′ of the ζ-globin gene

  1992cites this paper