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166 related items for PubMed ID: 2513289

  • 1. Hb Hinsdale [beta 139 (H17)Asn----Lys]: a variant in the central cavity showing reduced affinity for oxygen and 2,3-diphosphoglycerate.
    Moo-Penn WF, Johnson MH, Jue DL, Lonser R.
    Hemoglobin; 1989; 13(5):455-64. PubMed ID: 2513289
    [Abstract] [Full Text] [Related]

  • 2. Chloride masks effects of opposing positive charges in Hb A and Hb Hinsdale (beta 139 Asn-->Lys) that can modulate cooperativity as well as oxygen affinity.
    Bonaventura C, Arumugam M, Cashon R, Bonaventura J, Moo-Penn WF.
    J Mol Biol; 1994 Jun 17; 239(4):561-8. PubMed ID: 8006968
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  • 3. Hemoglobin Detroit: beta95 (FG2) lysine leads to asparagine.
    Moo-Penn WF, Schneider RG, Andrian S, Das DK.
    Biochim Biophys Acta; 1978 Sep 26; 536(1):283-8. PubMed ID: 708768
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  • 4. Hb Geelong [beta 139(H17)Asn----Asp].
    Como PF, Hocking DR, Swinton GW, Trent RJ, Holland RA, Tibben EA, Wilkinson T, Kronenberg H.
    Hemoglobin; 1991 Sep 26; 15(1-2):85-95. PubMed ID: 1917539
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  • 5. Hemoglobin Tarrant: alpha126(H9) Asp leads to Asn. A new hemoglobin variant in the alpha1beta1 contact region showing high oxygen affinity and reduced cooperativity.
    Moo-Penn WF, Jue DL, Johnson MH, Wilson SM, Therrell B, Schmidt RM.
    Biochim Biophys Acta; 1977 Feb 22; 490(2):443-51. PubMed ID: 13856
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  • 6. Hb Rancho Mirage [beta 143(H21)His----Asp]; a variant in the 2,3-DPG binding site showing normal oxygen affinity at physiological pH.
    Moo-Penn WF, Hine TK, Johnson MH, Jue DL, Holland S, George S, Pierce AM, Michalski LA, McDonald MJ.
    Hemoglobin; 1992 Feb 22; 16(1-2):35-44. PubMed ID: 1634360
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  • 7. Hemoglobin Shelby [beta 131(H9) Gln----Lys] a correction to the structure of hemoglobin Deaconess and hemoglobin Leslie.
    Moo-Penn WF, Johnson MH, McGuffey JE, Jue DL.
    Hemoglobin; 1984 Feb 22; 8(6):583-93. PubMed ID: 6526653
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Molecular characterization of a rare hemoglobin variant: Hb-Hinsdale: beta139(H17)ASN-->Lys.
    Degani V, Leone D, Murtas R, De Angelis S, Rabino-Massa E.
    Minerva Med; 2001 Feb 06; 92(1):57-9. PubMed ID: 11317140
    [Abstract] [Full Text] [Related]

  • 10. 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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  • 11. Hemoglobin providence. Functional consequences of two alterations of the 2,3-diphosphoglycerate binding site at position beta 82.
    Bonaventura J, Bonaventura C, Sullivan B, Ferruzzi G, McCurdy PR, Fox J, Moo-Penn WF.
    J Biol Chem; 1976 Dec 10; 251(23):7563-71. PubMed ID: 12172
    [Abstract] [Full Text] [Related]

  • 12. Hemoglobin Deer Lodge (beta 2 His replaced by Arg). Consequences of altering the 2,3-diphosphoglycerate binding site.
    Bonaventura J, Bonaventura C, Sullivan B, Godette G.
    J Biol Chem; 1975 Dec 25; 250(24):9250-5. PubMed ID: 393
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  • 13. Identification of a new high oxygen affinity hemoglobin variant: Hb Aurora [beta 139(H17) Asn-->Tyr].
    Lafferty J, Ali M, Matthew K, Eng B, Patterson M, Waye JS.
    Hemoglobin; 1995 Dec 25; 19(6):335-41. PubMed ID: 8718692
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  • 15. Hemoglobin Warsaw (Phe beta 42(CD1)----Val), an unstable variant with decreased oxygen affinity. Characterization of its synthesis, functional properties, and structure.
    Honig GR, Vida LN, Rosenblum BB, Perutz MF, Fermi G.
    J Biol Chem; 1990 Jan 05; 265(1):126-32. PubMed ID: 2294098
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  • 19. Hemoglobin Windsor or beta 11 (A8)Val----Asp: a new unstable beta-chain hemoglobin variant producing a hemolytic anemia.
    Gilbert AT, Fleming PJ, Sumner DR, Hughes WG, Holland RA, Tibben EA.
    Hemoglobin; 1989 Jan 05; 13(5):437-53. PubMed ID: 2599880
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  • 20. The presurgical management with erythrocytapheresis of a patient with a high-oxygen-affinity, unstable Hb variant (Hb Bryn Mawr).
    Larson PJ, Friedman DF, Reilly MP, Kattamis AC, Asakura T, Fortina P, Cohen AR, Kim HC, Manno CS.
    Transfusion; 1997 Jul 05; 37(7):703-7. PubMed ID: 9225933
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