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Journal Abstract Search
189 related items for PubMed ID: 4767302
1. The solubility of hemoglobin beta 4 S, the mutant subunits of sickle cell hemoglobin. Benesch R, Benesch RE, Yung S. Biochem Biophys Res Commun; 1973 Nov 16; 55(2):261-5. PubMed ID: 4767302 [No Abstract] [Full Text] [Related]
2. Studies on the mechanism of action of cyanate in sickle cell disease. Oxygen affinity and gelling properties of hemoglobin S carbamylated on specific chains. Nigen AM, Njikam N, Lee CK, Manning JM. J Biol Chem; 1974 Oct 25; 249(20):6611-6. PubMed ID: 4421180 [No Abstract] [Full Text] [Related]
3. Mechanical stability of hemoglobin subunits: an abnormality in betaS-subunits of sickle hemoglobin. Asakura T, Adachi K, Sono M, Friedman S, Schwartz E. Biochem Biophys Res Commun; 1974 Apr 08; 57(3):780-6. PubMed ID: 4827832 [No Abstract] [Full Text] [Related]
11. Studies on abnormal hemoglobins. VI. Electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon. SINGER K, FISHER B. Blood; 1953 Mar 15; 8(3):270-5. PubMed ID: 13032196 [No Abstract] [Full Text] [Related]
12. Haemoglobin D Punjab in a Cuban family and its interaction with haemoglobin S. Uriarte A, Perez Atencio R, Colombo B. Acta Haematol; 1973 Mar 15; 50(5):315-20. PubMed ID: 4202636 [No Abstract] [Full Text] [Related]
13. [Stanleyville II, a variant of the abnormal alpha-chain hemoglobin frequent in the north of Zaire. Apropos of a case of sickle cell anemia with S and Stanleyville II/S hemoglobins]. Van Ros G. Ann Soc Belg Med Trop; 1974 Mar 15; 54(6):483-501. PubMed ID: 4469969 [No Abstract] [Full Text] [Related]