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Journal Abstract Search

152 related items for PubMed ID: 1153003

  • 41. Interactions of other hemoglobin variants with sickle-cell hemoglobin.
    Ranney HM.
    N Engl J Med; 1970 Dec 24; 283(26):1462-3. PubMed ID: 5481781
    [No Abstract] [Full Text] [Related]

  • 42. FORMATION OF FERRIHAEMOGLOBIN OF ISOLATED HUMAN HAEMOGLOBIN TYPES BY SODIUM NITRITE.
    MARTIN H, HUISMAN TH.
    Nature; 1963 Nov 30; 200():898-9. PubMed ID: 14096079
    [No Abstract] [Full Text] [Related]

  • 43. Immunochemical identification and quantitation of variant hemoglobins.
    Garver FA, Baker MM, Grenett HE.
    Tex Rep Biol Med; 1963 Nov 30; 40():167-78. PubMed ID: 6172864
    [No Abstract] [Full Text] [Related]

  • 44. Participation of hemoglobins A and F in polymerization of sickle hemoglobin.
    Goldberg MA, Husson MA, Bunn HF.
    J Biol Chem; 1977 May 25; 252(10):3414-21. PubMed ID: 16902
    [No Abstract] [Full Text] [Related]

  • 45. Location and bond type of intermolecular contacts in the polymerisation of haemoglobin S.
    Benesch RE, Kwong S, Benesch R, Edalji R.
    Nature; 1977 Oct 27; 269(5631):772-5. PubMed ID: 927499
    [Abstract] [Full Text] [Related]

  • 46. Polymerisation of haemoglobin SA hybrid tetramers.
    Bookchin RM, Balazs T, Nagel RL, Tellez I.
    Nature; 1977 Oct 06; 269(5628):526-7. PubMed ID: 909605
    [No Abstract] [Full Text] [Related]

  • 47. Thermodynamic analysis of the chemical inhibition of sickle-cell hemoglobin gelation.
    Minton AP.
    J Mol Biol; 1975 Jun 25; 95(2):289-307. PubMed ID: 241858
    [No Abstract] [Full Text] [Related]

  • 48. Nanosecond absorption study of kinetics associated with carbon monoxide rebinding to hemoglobin S and hemoglobin C following ligand photolysis.
    Shapiro DB, Paquette SJ, Esquerra RM, Che D, Goldbeck RA, Hirsch RE, Mohandas N, Kliger DS.
    Biochem Biophys Res Commun; 1994 Nov 30; 205(1):154-60. PubMed ID: 7999016
    [Abstract] [Full Text] [Related]

  • 49. Structure of sickle-cell haemoglobin.
    Finch JT, Perutz MF.
    Trans R Soc Trop Med Hyg; 1974 Nov 30; 68(2):79. PubMed ID: 4460306
    [No Abstract] [Full Text] [Related]

  • 50. [The hemoglobins. I. Structure of the normal and abnormal hemoglobins].
    Piguet H.
    Presse Med (1893); 1968 Mar 02; 76(11):519-21. PubMed ID: 5646256
    [No Abstract] [Full Text] [Related]

  • 51. Transposing sequences between fetal and adult hemoglobins indicates which subunits and regulatory molecule interfaces are functionally related.
    Chen W, Dumoulin A, Li X, Padovan JC, Chait BT, Buonopane R, Platt OS, Manning LR, Manning JM.
    Biochemistry; 2000 Apr 04; 39(13):3774-81. PubMed ID: 10736177
    [Abstract] [Full Text] [Related]

  • 52. [A CASE OF MICRODREPANOCYTIC DISEASE DUE TO S HEMOGLOBIN AND A VARIETY OF MICROCYTHEMIA WITH NORMAL QUOTA OF A2 HEMOGLOBIN AND ELEVATED QUOTA OF F HEMOGLOBIN (THIRD VARIETY OF MICRODREPANOCYTIC DISEASE)].
    SILVESTRONI E, BIANCO I.
    Prog Med (Napoli); 1964 Aug 15; 20():509-13. PubMed ID: 14235120
    [No Abstract] [Full Text] [Related]

  • 53. [Results of 3 years of screening of abnormal hemoglobins in the blood donors of Guadeloupe (French Antilles)].
    Fabritius H, Millan J, Le Corroller Y.
    Bull Soc Pathol Exot Filiales; 1978 Aug 15; 71(2):216-20. PubMed ID: 743771
    [Abstract] [Full Text] [Related]

  • 54. Surface hydrophobicity and solubility of Hb S.
    Adachi K.
    Prog Clin Biol Res; 1987 Aug 15; 240():21-30. PubMed ID: 2441415
    [No Abstract] [Full Text] [Related]

  • 55. Some properties of Hb G San Jose (beta7 glu replaced by gly): comparisons with Hb S.
    Roth EF, Schiliro G, Elbaum D, Musumeci S, Pizzarelli G, Russo G, Nagel RL.
    J Lab Clin Med; 1977 Nov 15; 90(5):837-43. PubMed ID: 20481
    [Abstract] [Full Text] [Related]

  • 56. Gelation of sickle cell hemoglobin in mixtures with normal adult and fetal hemoglobins.
    Sunshine HR, Hofrichter J, Eaton WA.
    J Mol Biol; 1979 Oct 09; 133(4):435-67. PubMed ID: 94101
    [No Abstract] [Full Text] [Related]

  • 57. Hypotonic exchange-loading of erythrocytes. II. introduction of hemoglobins S and C into normal red cells.
    Sartiano GP, Hayes RL.
    J Lab Clin Med; 1977 Jan 09; 89(1):30-40. PubMed ID: 556623
    [Abstract] [Full Text] [Related]

  • 58. 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]

  • 59. Participation of haemoglobins A, F, A2 and C in polymerisation of haemoglobin S.
    Cheetham RC, Huehns ER, Rosemeyer MA.
    J Mol Biol; 1979 Mar 25; 129(1):45-61. PubMed ID: 448738
    [No Abstract] [Full Text] [Related]

  • 60. Hemoglobin S gelation and sickle cell disease.
    Eaton WA, Hofrichter J.
    Blood; 1987 Nov 25; 70(5):1245-66. PubMed ID: 3311198
    [No Abstract] [Full Text] [Related]

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