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

Benzer Materyaller

• The deletion of the distal CCAAT box region of the A gamma-globin gene in black HPFH abolishes the binding of the erythroid specific protein NFE3 and of the CCAAT displacement protein.
  Yazar:: Mantovani, R, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• Role of the duplicated CCAAT box region in gamma-globin gene regulation and hereditary persistence of fetal haemoglobin.
  Yazar:: Ronchi, A, ve diğerleri
  Baskı/Yayın Bilgisi: (1996)
• A novel C-T transition within the distal CCAAT motif of the G gamma-globin gene in the Japanese HPFH: implication of factor binding in elevated fetal globin expression.
  Yazar:: Fucharoen, S, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• Gamma thalassemia resulting from the deletion of a gamma-globin gene.
  Yazar:: Sukumaran, P K, ve diğerleri
  Baskı/Yayın Bilgisi: (1983)
• G gamma and A gamma globin genes are identical from -471 of the promoter midway through gamma IVSII in a Benin beta s haplotype associated with elevated fetal hemoglobin.
  Yazar:: Mishima, N, ve diğerleri
  Baskı/Yayın Bilgisi: (1991)