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Journal Abstract Search

385 related items for PubMed ID: 186485

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  • 3. Electron paramagnetic resonance of Hb St Louis beta28 (B10) Leu replaced by Gln.
    Hyafil F, Guéron M, Thillet J.
    Biochim Biophys Acta; 1976 Oct 28; 446(2):472-8. PubMed ID: 186113
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  • 6. Hemoglobin Louisville (beta-42 (CD1) phe-leu): an unstable variant causing mild hemolytic anemia.
    Keeling MM, Ogden LL, Wrightstone RN, Wilson JB, Reynolds CA, Kitchens JL, Huisman TH.
    J Clin Invest; 1971 Nov 28; 50(11):2395-402. PubMed ID: 5096522
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  • 7. Effects of substitutions of lysine and aspartic acid for asparagine at beta 108 and of tryptophan for valine at alpha 96 on the structural and functional properties of human normal adult hemoglobin: roles of alpha 1 beta 1 and alpha 1 beta 2 subunit interfaces in the cooperative oxygenation process.
    Tsai CH, Shen TJ, Ho NT, Ho C.
    Biochemistry; 1999 Jul 06; 38(27):8751-61. PubMed ID: 10393550
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  • 8. Studies of hemoglobin denaturation and Heinz body formation in the unstable hemoglobins.
    Winterbourn CC, Carrell RW.
    J Clin Invest; 1974 Sep 06; 54(3):678-89. PubMed ID: 4854449
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  • 11. The role of hemoglobin heme loss in Heinz body formation: studies with a partially heme-deficient hemoglobin and with genetically unstable hemoglobins.
    Jacob HS, Winterhalter KH.
    J Clin Invest; 1970 Nov 06; 49(11):2008-16. PubMed ID: 5475984
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  • 12. [Erythrocytosis due to a high-affinity hemoglobulin: mutant hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr with a change in the 2,3-diphosphoglycerate binding site].
    Rochette J, Boissel JP, Labie D, Wajcman H, Poyart C, Bohn B, Varet B.
    Nouv Rev Fr Hematol (1978); 1984 Nov 06; 26(2):75-7. PubMed ID: 6546989
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  • 14. A new hemoglobin variant, hemoglobin Nunobiki [alpha 141 (HC3) Arg----Cys]. Notable influence of the carboxy-terminal cysteine upon various physico-chemical characteristics of hemoglobin.
    Shimasaki S.
    J Clin Invest; 1985 Feb 06; 75(2):695-701. PubMed ID: 3973024
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  • 17. Hemoglobin Okayama [beta 2 (NA 2) His replaced by Gln]: a new 'silent' hemoglobin variant with substituted amino acid residue at the 2,3-diphosphoglycerate binding site.
    Harano T, Harano K, Shibata S, Ueda S, Mori H, Arimasa N.
    FEBS Lett; 1983 May 30; 156(1):20-2. PubMed ID: 6852251
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  • 19. Hb Chile [beta28(B10)Leu-->Met]: an unstable hemoglobin associated with chronic methemoglobinemia and sulfonamide or methylene blue-induced hemolytic anemia.
    Hojas-Bernal R, McNab-Martin P, Fairbanks VF, Holmes MW, Hoyer JD, McCormick DJ, Kubik KS.
    Hemoglobin; 1999 May 30; 23(2):125-34. PubMed ID: 10335980
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  • 20. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct 30; 64(4):1024-32. PubMed ID: 479366
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