Author

Clemenceau Acquaye

Observed names: C Acquaye, C T Acquaye, C. T. A. ACQUAYE, C. T. A. Acquaye, C. T. ACQUAYE, C.T.A. Acquaye

Observed institutions: National Institutes of Health, Wayne State University, Kwame Nkrumah University of Science and Technology, National Institute of Diabetes and Digestive and Kidney Diseases, Weizmann Institute of Science

OpenAlex ID: A5055627675

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

1979 · S. OTTOLENGHI, B. GIGLIONI, et al. · Nature · 73

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

1977 · B. Ringelhann, C. T. A. Acquaye, et al. · Biochemical Genetics · 27

Antisickling activity of amino acid benzyl esters.

1980 · M Gorecki, C T Acquaye, et al. · Proceedings of the National Academy of Sciences · 24

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

1982 · C.T.A. Acquaye, J.D. Young, et al. · Biochimica et Biophysica Acta (BBA) - Biomembranes · 19

Blood-donor Homozygous for Hereditary Persistence of Fetal Hæmoglobin

1977 · C.T.A. Acquaye, J.H. Oldham, et al. · The Lancet · 12

Electron microscopic studies of the intracellular polymerization of sickle hemoglobin.

1988 · C Acquaye, E J Blanchette-Mackie, et al. · PubMed · 9

Variants of haemoglobin and glucose-6-phosphate dehydrogenase-I. distribution in Southern Ghana.

1973 · C T Acquaye, J H Oldham · PubMed · 7

The development of a filtration system for evaluating flow characteristics of erythrocytes

1987 · Clemenceau Acquaye, Elijah C. Walker, et al. · Microvascular Research · 4

Bepridil as an antisickling agent: Membrane internalization and cell rigidity

1994 · Robert M. Johnson, Clemenceau Acquaye, et al. · American Journal of Hematology · 2

Modified celluloses for erythrocyte deformability fractionation.

1993 · C Acquaye, R M Johnson · PubMed · 2

Strategies for tackling sickle cell disease

1981 · Clemenceau Acquaye, Meir Wilchek, et al. · Trends in Biochemical Sciences · 2

Isolation and quantitation of human erythrocyte deformability classes.

1990 · C Acquaye, R M Johnson · PubMed · 1

2,6‐Di(isobutyrylamino)hexanoic Acid as a Potential Therapeutic Agent for the Treament of Sickle Cell Disease

1989 · C. T. ACQUAYE, T. L. CARTER, et al. · Annals of the New York Academy of Sciences · 1

Antisickling activity of amino acid benzyl esters (sickle cell disease/hydrophobic bonding/cell penetration/erythrocyte flexibility)

2016 · Marian Gorecki, Clemenceau Acquaye, et al.

Analysis of the γ Chains in a Homozygote for HPFH Negro Type and in Three Related Heterozygotes

2009 · A. Guerrasio, C.T.A. Acquaye, et al. · Acta Haematologica

Observation of Intracellular Sickle Cell Hemoglobin Polymers with a Differential Polarization Microscopea

1989 · H. MIZUKAMI, D. A. BEACH, et al. · Annals of the New York Academy of Sciences

A preliminary report on survey and characterization of haemoglobins and glucose-6-phosphate dehydrogenase variants in Ghana.

1974 · C T Acquaye, J H Oldham · PubMed

Works count: 17

Citation count: 183

H-index: 7

I10-index: 5