Point mutation associated with hereditary persistence of fetal hemoglobin decreases RNA polymerase III transcription upstream of the affected gamma-globin gene.

Samankaltaisia teoksia

• Balanced Globin Chain Synthesis in Hereditary Persistence of Fetal Hemoglobin
  Tekijä: Natta, C. L., et al.
  Julkaistu: (1974)
• Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobin.
  Tekijä: Stoeckert, C J, et al.
  Julkaistu: (1987)
• Nuclear proteins that bind the human gamma-globin gene promoter: alterations in binding produced by point mutations associated with hereditary persistence of fetal hemoglobin.
  Tekijä: Gumucio, D L, et al.
  Julkaistu: (1988)
• Hereditary persistence of fetal hemoglobin
  Tekijä: Sharma, Dharmesh Chandra, et al.
  Julkaistu: (2020)
• Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.
  Tekijä: Tuan, D, et al.
  Julkaistu: (1983)