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Journal Abstract Search
384 related items for PubMed ID: 7937904
1. Recombinant human hemoglobins designed for gene therapy of sickle cell disease. McCune SL, Reilly MP, Chomo MJ, Asakura T, Townes TM. Proc Natl Acad Sci U S A; 1994 Oct 11; 91(21):9852-6. PubMed ID: 7937904 [Abstract] [Full Text] [Related]
6. High expression of human beta S- and alpha-globins in transgenic mice: hemoglobin composition and hematological consequences. Fabry ME, Nagel RL, Pachnis A, Suzuka SM, Costantini F. Proc Natl Acad Sci U S A; 1992 Dec 15; 89(24):12150-4. PubMed ID: 1465454 [Abstract] [Full Text] [Related]
15. Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr]. Zanella-Cleon I, Préhu C, Joly P, Riou J, Becchi M, Wajcman H, Francina A. Hemoglobin; 2009 Feb 02; 33(3):177-87. PubMed ID: 19657831 [Abstract] [Full Text] [Related]
16. Polymerization and solubility of recombinant hemoglobins alpha 2 beta 2 (6Val) (Hb S) and alpha 2 beta 2(6Leu) (Hb Leu). Adachi K, Rappaport E, Eck HS, Konitzer P, Kim J, Surrey S. Hemoglobin; 1991 Feb 02; 15(5):417-30. PubMed ID: 1802884 [Abstract] [Full Text] [Related]
17. Towards a transgenic mouse model of sickle cell disease: hemoglobin SAD. Trudel M, Saadane N, Garel MC, Bardakdjian-Michau J, Blouquit Y, Guerquin-Kern JL, Rouyer-Fessard P, Vidaud D, Pachnis A, Roméo PH. EMBO J; 1991 Nov 02; 10(11):3157-65. PubMed ID: 1915288 [Abstract] [Full Text] [Related]
20. Effect of amino acid at the beta 6 position on surface hydrophobicity, stability, solubility, and the kinetics of polymerization of hemoglobin. Comparisons among Hb A (Glu beta 6), Hb C (Lys beta 6), Hb Machida (Gln beta 6), and Hb S (Val beta 6). Adachi K, Kim J, Travitz R, Harano T, Asakura T. J Biol Chem; 1987 Sep 25; 262(27):12920-5. PubMed ID: 2888754 [Abstract] [Full Text] [Related] Page: [Next] [New Search]