These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 3754242)

  • 1. Interaction of hemoglobin Siriraj with hemoglobin S: a mild sickle cell syndrome.
    Rhoda MD; Arous N; Garel MC; Mazarin M; Monplaisir N; Braconnier F; Rosa J; Cohen-Solal M; Galacteros F
    Hemoglobin; 1986; 10(1):21-31. PubMed ID: 3754242
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 33(3):177-87. PubMed ID: 19657831
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 262(27):12920-5. PubMed ID: 2888754
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effect of chloride ion on the oxygen affinity of hemoglobin York (alpha 2 beta 2(146)Pro) and S-York hybrid hemoglobin (alpha 2 beta S beta York). Role of the beta 82 lysyl and beta 146 histydyl residues in chloride binding to hemoglobin.
    Adachi H; Asakura T; Adachi K
    J Biol Chem; 1983 Nov; 258(22):13422-4. PubMed ID: 6417128
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hb S/Hb Lepore with mild sickling symptoms: a hemoglobin variant with mostly delta-chain sequences ameliorates sickle-cell disease.
    Fairbanks VF; McCormick DJ; Kubik KS; Rezuke WN; Black D; Ochaney MS; Schwartz D
    Am J Hematol; 1997 Feb; 54(2):164-5. PubMed ID: 9034293
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Compound heterozygosity for two beta chain variants: Hb S [beta 6(A3)Glu-->Val] and the high affinity variant Hb San Diego [beta 109(G11)Val-->Met].
    Williamson D; Perry DJ; Brown K; Langdown JV; de Silva C
    Hemoglobin; 1995; 19(1-2):27-32. PubMed ID: 7615400
    [No Abstract]   [Full Text] [Related]  

  • 7. [Clinical and biological studies of an hybrid S/Stanleyville II hemoglobin (alpha 2 78 Asn replaced by Lys beta 2 6 Glu replaced by Val) (author's transl)].
    North ML; Hassan W; Thillet J; Schwartz M; Taubert C; Ritter J; Gandar R; Rosa J
    Nouv Rev Fr Hematol (1978); 1980; 22(3):235-41. PubMed ID: 6782549
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hemoglobinopathy S with an interaction of HbS and Hb G-Ferrara].
    Cañizares ME; Martínez G; Hernández S; Raymond P; Colombo B
    Sangre (Barc); 1983; 28(6):770-4. PubMed ID: 6673168
    [No Abstract]   [Full Text] [Related]  

  • 9. Hemoglobin Hofu or alpha 2 beta 2 [126 (H4) Va1 leads to Glu] found in combination with hemoglobin S.
    Brittenham G; Lozoff B; Harris JW; Nayudu NV; Gravely M; Wilson JB; Lam H; Huisman TH
    Hemoglobin; 1978; 2(6):541-9. PubMed ID: 750554
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional studies and polymerization of recombinant hemoglobin Glu-alpha2beta26(A3) --> Val/Glu-7(A4) --> Ala.
    Lesecq S; Baudin V; Kister J; Marden MC; Poyart C; Pagnier J
    J Biol Chem; 1996 Jul; 271(29):17211-4. PubMed ID: 8663330
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cyanate and sickle-cell disease.
    Cerami A; Peterson CM
    Sci Am; 1975 Apr; 232(4):44-50. PubMed ID: 1114310
    [No Abstract]   [Full Text] [Related]  

  • 12. Hemoglobin Kariya [alpha 40 (C5) Lys leads to Glu]: a new hemoglobin variant with an increased oxygen affinity.
    Harano T; Harano K; Shibata S; Ueda S; Imai K; Tsuneshige A; Yamada H; Seki M; Fukui H
    FEBS Lett; 1983 Mar; 153(2):332-4. PubMed ID: 6137414
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Roles of alpha 114 and beta 87 amino acid residues in the polymerization of hemoglobin S: implications for gene therapy.
    Ho C; Willis BF; Shen TJ; Dazhen NT; Sun DP; Tam MF; Suzuka SM; Fabry ME; Nagel RL
    J Mol Biol; 1996 Nov; 263(3):475-85. PubMed ID: 8918602
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hb Hope [beta136(H14)Gly-->Asp (GGT-->GAT)]: interactions with Hb S [beta6(A3)Glu-->Val (GAG-->GTG)], other variant hemoglobins and thalassemia.
    Ingle J; Adewoye A; Dewan R; Okoli M; Rollins L; Eung SH; Luo HY; Chui DH; Steinberg MH
    Hemoglobin; 2004; 28(4):277-85. PubMed ID: 15658184
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular stability and function of hemoglobins Hasharon (alpha(2)47 (CD5)Asp----His beta 2) and Hasharon (alpha(2)47 (CD5)Asp----His delta 2).
    Bender JW; Reilly MP; Asakura T
    Hemoglobin; 1984; 8(1):61-73. PubMed ID: 6724992
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapid turnover of newly-synthesized beta S chains in reticulocytes from individuals with sickle cell trait.
    DeSimone J; Kleve L; Longley MA; Shaeffer J
    Biochem Biophys Res Commun; 1974 Mar; 57(1):248-54. PubMed ID: 4828186
    [No Abstract]   [Full Text] [Related]  

  • 17. Hb S-Hb Lufkin disease in a black male infant.
    Gu LH; Leonova J Ye; Huisman TH
    Hemoglobin; 1995 Sep; 19(5):291-4. PubMed ID: 8537234
    [No Abstract]   [Full Text] [Related]  

  • 18. A biochemical and biophysical characterization of recombinant mutants of fetal hemoglobin and their interaction with sickle cell hemoglobin.
    Larson SC; Fisher GW; Ho NT; Shen TJ; Ho C
    Biochemistry; 1999 Jul; 38(29):9549-55. PubMed ID: 10413533
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comparisons of the kinetic stability of normal and sickle cell human hemoglobins at extremes of pH.
    Jones DD; McGrath WP; Carroll D; Steinhardt J
    Biochemistry; 1973 Sep; 12(20):3818-24. PubMed ID: 4745648
    [No Abstract]   [Full Text] [Related]  

  • 20. Hemoglobin S Travis: a sickling hemoglobin with two amino acid substitutions [beta6(A3)glutamic acid leads to valine and beta142 (h20) alanine leads to valine).
    Moo-Penn WF; Schmidt RM; Jue DL; Bechtel KC; Wright JM; Horne MK; Haycraft GL; Roth EF; Nagel RL
    Eur J Biochem; 1977 Aug; 77(3):561-6. PubMed ID: 19257
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.