Results 211 to 220 of about 204,284 (265)

Antibody-Dependent and Antibody-Independent Hemolysis in Sickle Cell Disease. [PDF]

Antibodies (Basel)
Glover RT, Maitta RW.
europepmc   +1 more source

Suzetrigine for Vaso-Occlusive Pain in Sickle Cell Disease: A Three-Patient Case Series. [PDF]

Orthop Rev (Pavia)
Joudeh S, Moore D, Hasoon J, Robinson CL, Idowu M, Oso T.   +5 more
europepmc   +1 more source

Sickle cell hemoglobin, primaquine sensitivity and their correlation. 1. Sickle cell hemoglobin.

Journal of postgraduate medicine, 1966
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Effect of piracetam on sickle erythrocytes and sickle hemoglobin

Biochimica Et Biophysica Acta (BBA) - Protein Structure, 1981
Piracetam, 2-oxo-1-pyrrolidine acetamide, inhibits sickling of red cells containing sickle hemoglobin (Hb S). The concentration required for 50% inhibition is about 300 mM. Addition of piracetam into the supersaturated Hb S solution in concentrated phosphate buffer prolongs the delay time prior to gelation.
Meral Özgüç, Elias Schwartz, Kazuhiko Adachi   +2 more
exaly   +3 more sources

Sickle Cell Anemia and Fetal Hemoglobin

American Journal of the Medical Sciences, 1994
Fetal hemoglobin, the predominant hemoglobin of the fetus, is good for sickle cell anemia. This hemoglobin inhibits the polymerization of sickle hemoglobin. Clinical studies have shown that at any level of fetal hemoglobin, the more that is present, the better off is the patient.

exaly   +3 more sources

Sickle Cell Hemoglobin

2020
Sickle cell hemoglobin (HbS) is an example of a genetic variant of human hemoglobin where a point mutation in the β globin gene results in substitution of glutamic acid to valine at sixth position of the β globin chain. Association between tetrameric hemoglobin molecules through noncovalent interactions between side chain residue of βVal6 and ...
Amit Kumar, Mandal, Amrita, Mitra, Rajdeep, Das   +2 more
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Alternative diaspirins for modification of hemoglobin and sickle hemoglobin

Archives of Biochemistry and Biophysics, 1984
Studies of modification of hemoglobin and of sickle hemoglobin by alternative aspirins have been extended to a series of new bis esters with a variety of substituted bridging diacids and to a group of mono esters with polar acyl groups. Rates of hydrolysis of these alternative aspirins have also been examined, and they reveal that a careful balance ...
E J, Delaney, S E, Massil, G Y, Shi, I M, Klotz   +3 more
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Crowding and the polymerization of sickle hemoglobin

Journal of Molecular Recognition, 2004
AbstractUnder physiological conditions, sickle hemoglobin, a natural mutant of human hemoglobin A with a surface hydrophobic valine in place of a negatively charged glutamic acid, polymerizes at high volume occupancy. Equilibrium solubility of sickle hemoglobin entails activity coefficients that can approach 103 at high concentrations.
Frank A, Ferrone, Maria A, Rotter
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