DNA sequences regulating human globin gene transcription in nondeletional hereditary persistence of fetal hemoglobin (Q28239881)

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R Mantovani

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S Nicolis

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A Ronchi

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B Giglioni

The human beta-globin gene 3' enhancer contains multiple binding sites for an erythroid-specific protein.

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language of work or name

English

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publication date

1989

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523-41

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cites work

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G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene

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A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin

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G to A substitution in the distal CCAAT box of the A gamma-globin gene in Greek hereditary persistence of fetal haemoglobin

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A frequent A gamma-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with beta-thalassemia.

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Distal CCAAT box deletion in the A gamma globin gene of two black adolescents with elevated fetal A gamma globin

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Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients

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Human fetal G gamma- and A gamma-globin genes: complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes

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A history of the human fetal globin gene duplication

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An erythroid specific nuclear factor binding to the proximal CACCC box of the beta-globin gene promoter

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A protein factor binding to an octamer motif in the gamma-globin promoter disappears upon induction of differentiation and hemoglobin synthesis in K562 cells

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The effects of HPFH mutations in the human gamma-globin promoter on binding of ubiquitous and erythroid specific nuclear factors

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Increased gamma-globin expression in a nondeletion HPFH mediated by an erythroid-specific DNA-binding factor

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Nuclear proteins that bind the human gamma-globin gene promoter: alterations in binding produced by point mutations associated with hereditary persistence of fetal hemoglobin

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The immunoglobulin octanucleotide: independent activity and selective interaction with enhancers

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Human CCAAT-binding proteins have heterologous subunits

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Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobin

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A fetal globin gene mutation in A gamma nondeletion hereditary persistence of fetal hemoglobin increases promoter strength in a nonerythroid cell

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The British type of non-deletion HPFH: characterization of developmental changes in vivo and erythroid growth in vitro

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Hereditary persistence of foetal haemoglobin with β-chain synthesis in cis position (Gγ-β+-HPFH) in a negro family

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Multiple mutations produce delta beta 0 thalassemia in Sardinia.

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Position-independent, high-level expression of the human beta-globin gene in transgenic mice

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Deforestation alters denitrification in a lowland tropical rain forest

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Mutually exclusive interaction of the CCAAT-binding factor and of a displacement protein with overlapping sequences of a histone gene promoter

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The protein CDP, but not CP1, footprints on the CCAAT region of the γ-globin gene in unfractionated B-cell extracts

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