Post-translational control of human hemoglobin synthesis The role of the differential affinity between globin chains in the control of mutated globin gene expression

This publication has 47 references indexed in Scilit:

• Decrease of Alpha‐Hasharon Globin in Beta‐Thalassaemia
  British Journal of Haematology, 1978
• Is the trimodality of Hb leslie (α2β2131Gln → 0) in heterozygotes the result of a variable number of active α-chain genes? Evidence for posttranslational control of hemoglobin synthesis
  American Journal of Hematology, 1978
• Haemoglobin Hasharon in a north Italian community.
  Journal of Medical Genetics, 1975
• Haemoglobin C/α Thalassaemia: Haematological and Biosynthetic Studies
  British Journal of Haematology, 1975
• Rapid turnover of newly-synthesized βS chains in reticulocytes from individuals with sickle cell trait
  Biochemical and Biophysical Research Communications, 1974
• Haemoglobin Inkster (α₂⁸⁵ aspartic acid → valineβ₂) Coexisting with β‐Thalassaemia in a Caucasian Family
  British Journal of Haematology, 1974
• Haemoglobin G St. José in an Italian Family
  Acta Haematologica, 1974
• alpha-Chain and Globin: Intermediates in the Synthesis of Rabbit Hemoglobin
  European Journal of Biochemistry, 1967
• Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)
  Journal of Molecular Biology, 1966
• Studies on the structure of hemoglobin
  Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects, 1964