Clemenceau Acquaye

Globin gene deletion in HPFH, δ°β° thalassaemia and Hb Lepore disease

Sergio Ottolenghi, Barbára Giglioni, Paola Comi et al. · Nature · 1979 · 77 citations

Mendelian Disorder, Heme Homeostasis, Genetic Disorder +12

Homozygotes for the hereditary persistence of fetal hemoglobin: The ratio of G? to A? chains and biosynthetic studies

B Ringelhann, Clemenceau Acquaye, J.H. Oldham et al. · Biochemical Genetics · 1977 · 28 citations

Biology, Heme Degradation, Genetics +9

Antisickling activity of amino acid benzyl esters.

Marian Gorecki, Clemenceau Acquaye, Meir Wilchek et al. · Proceedings of the National Academy of Sciences · 1980 · 24 citations · Full text

Inhibitory Activity, Sickle Cell Disease, Biochemistry +14

Mode of transport and possible mechanism of action of l-phenylalanine benzyl ester as an anti-sickling agent

Clemenceau Acquaye, Duncan Young, J. Clive Ellory et al. · Biochimica et Biophysica Acta (BBA) - Biomembranes · 1982 · 19 citations

L-phenylalanine Benzyl Ester, Bioorganic Chemistry, Biochemistry +6