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114 related items for PubMed ID: 723949
1. Competition of normal beta chains and sickle haemoglobin beta chains for alpha chains as a post-translational control mechanism. Shaeffer JR, Kingston RE, McDonald MJ, Bunn HF. Nature; 1978 Dec 07; 276(5688):631-3. PubMed ID: 723949 [No Abstract] [Full Text] [Related]
2. Patterns of hemoglobin assembly in reticulocytes of sickle cell trait individuals. Shaeffer JR, Longley MA, DeSimone J, Kleve LJ. J Biol Chem; 1975 Nov 25; 250(22):8630-4. PubMed ID: 1184582 [Abstract] [Full Text] [Related]
3. Proportions of haemoglobin S in sickle-cell trait. Alayash AI. Med Lab Sci; 1989 Apr 25; 46(2):162-3. PubMed ID: 2593776 [No Abstract] [Full Text] [Related]
4. Evidence for rapid loss of newly synthesized haemoglobin S molecules in sickle cell anaemia and sickle cell trait. DeSimone J, Adams JG, Shaeffer J. Br J Haematol; 1977 Mar 25; 35(3):373-85. PubMed ID: 870003 [Abstract] [Full Text] [Related]
5. Clinical, hematologic and biosynthetic studies in sickle cell-betao-thalassemia: a comparison with sickle cell anemia. Steinberg MH, Dreiling BJ. Am J Hematol; 1976 Mar 25; 1(1):35-44. PubMed ID: 984035 [Abstract] [Full Text] [Related]
6. Increasing haemoglobin oxygen affinity to prevent sickling: abnormal haemoglobin variants as models. Franklin IM, Huehns ER, Rosemeyer MA. Br J Haematol; 1986 Oct 25; 64(2):319-29. PubMed ID: 3778826 [Abstract] [Full Text] [Related]
7. Detection of alpha thalassaemia in sickle cell trait patients by Hb-Bart's screening & quantitation of Hb-A & Hb-S. Misra RC. Indian J Med Res; 1989 Dec 25; 90():459-62. PubMed ID: 2628314 [Abstract] [Full Text] [Related]
8. Premature neonate with apnea and trace amounts of hemoglobin S and A detected by high-performance liquid chromatography. Sickle cell trait/disease in a prematurely born baby with hampered switch from gamma-globin to beta-globin chain synthesis. Uzquiano M, Risin SA. Arch Pathol Lab Med; 2006 May 25; 130(5):733-4. PubMed ID: 16683895 [No Abstract] [Full Text] [Related]
9. The development of haemoglobin A2 in normal negro infants and in sickle cell disease. Serjeant BE, Mason KP, Serjeant GR. Br J Haematol; 1978 Jun 25; 39(2):259-65. PubMed ID: 678477 [Abstract] [Full Text] [Related]
10. Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytes. Nienhuis AW, Anderson WF. J Clin Invest; 1971 Nov 25; 50(11):2458-60. PubMed ID: 5096528 [Abstract] [Full Text] [Related]
11. Modification of hemoglobin H disease by sickle trait. Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF. J Clin Invest; 1979 Oct 25; 64(4):1024-32. PubMed ID: 479366 [Abstract] [Full Text] [Related]
12. Synthesis of globin chains in sickle -thalassemia. Gill FM, Schwartz E. J Clin Invest; 1973 Mar 25; 52(3):709-14. PubMed ID: 4685090 [Abstract] [Full Text] [Related]
13. Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia. Honig GR, Shamsuddin M, Mason RG, Vida LN, Tremaine LM, Tarr GE, Shahidi NT. Blood; 1980 Jan 25; 55(1):131-7. PubMed ID: 7350933 [Abstract] [Full Text] [Related]
14. [Drepanocytosis with alpha and beta(o) thalassemia: a case report]. Désidéri-Vaillant C, Olivro J, Valéro E, Kerdoncuff C, Lafontaine Y, Laborde JP. Ann Biol Clin (Paris); 2009 Jan 25; 67(3):349-52. PubMed ID: 19411239 [Abstract] [Full Text] [Related]
16. Genetic model for observed distributions of proportions of haemoglobin in sickle-cell trait. Brittenham G. Nature; 1977 Aug 18; 268(5621):635-6. PubMed ID: 895858 [No Abstract] [Full Text] [Related]
17. Defect in messenger RNA for human hemoglobin synthesis in beta thalassemia. Benz EJ, Forget BG. J Clin Invest; 1971 Dec 18; 50(12):2755-60. PubMed ID: 5129324 [Abstract] [Full Text] [Related]
18. Hemoglobin messenger RNA from human bone marrow. Isolation and translation in homozygous and heterozygous beta-thalassemia. Nienhuis AW, Canfield PH, Anderson WF. J Clin Invest; 1973 Jul 18; 52(7):1735-45. PubMed ID: 4718962 [Abstract] [Full Text] [Related]
19. Hemoglobin A2 levels in healthy persons, sickle cell disease, sickle cell trait, and beta-thalassemia by capillary isoelectric focusing. Craver RD, Abermanis JG, Warrier RP, Ode DL, Hempe JM. Am J Clin Pathol; 1997 Jan 18; 107(1):88-91. PubMed ID: 8980373 [Abstract] [Full Text] [Related]
20. Plasma, erythrocyte and urinary selenium levels in sickle cell homozygotes and traits. Kilinç Y. Turk J Pediatr; 1993 Jan 18; 35(2):105-9. PubMed ID: 8249189 [Abstract] [Full Text] [Related] Page: [Next] [New Search]