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Journal Abstract Search

166 related items for PubMed ID: 6871109

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  • 3. Rational design of pyridyl derivatives of vanillin for the treatment of sickle cell disease.
    Pagare PP, Ghatge MS, Musayev FN, Deshpande TM, Chen Q, Braxton C, Kim S, Venitz J, Zhang Y, Abdulmalik O, Safo MK.
    Bioorg Med Chem; 2018 May 15; 26(9):2530-2538. PubMed ID: 29655608
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  • 4. GBT440 increases haemoglobin oxygen affinity, reduces sickling and prolongs RBC half-life in a murine model of sickle cell disease.
    Oksenberg D, Dufu K, Patel MP, Chuang C, Li Z, Xu Q, Silva-Garcia A, Zhou C, Hutchaleelaha A, Patskovska L, Patskovsky Y, Almo SC, Sinha U, Metcalf BW, Archer DR.
    Br J Haematol; 2016 Oct 15; 175(1):141-53. PubMed ID: 27378309
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  • 6. New developments in anti-sickling agents: can drugs directly prevent the polymerization of sickle haemoglobin in vivo?
    Oder E, Safo MK, Abdulmalik O, Kato GJ.
    Br J Haematol; 2016 Oct 15; 175(1):24-30. PubMed ID: 27605087
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  • 7. Effect of 2, 3-diphosphoglycerate on the solubility of deoxy-sickle hemoglobin.
    Swerdlow PH, Bryan RA, Bertles JF, Poillon WN, Magdoff-Fairchild B, Milner PF.
    Hemoglobin; 1977 Oct 15; 1(6):527-37. PubMed ID: 914634
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  • 8. Effect of liganded hemoglobin S and hemoglobin A on the aggregation of deoxy-hemoglobin S.
    Adachi K, Asakura T.
    J Biol Chem; 1982 May 25; 257(10):5738-44. PubMed ID: 7068616
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  • 9. A Triazole Disulfide Compound Increases the Affinity of Hemoglobin for Oxygen and Reduces the Sickling of Human Sickle Cells.
    Nakagawa A, Ferrari M, Schleifer G, Cooper MK, Liu C, Yu B, Berra L, Klings ES, Safo RS, Chen Q, Musayev FN, Safo MK, Abdulmalik O, Bloch DB, Zapol WM.
    Mol Pharm; 2018 May 07; 15(5):1954-1963. PubMed ID: 29634905
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  • 15. Treatment of sickle cell disease by increasing oxygen affinity of hemoglobin.
    Henry ER, Metaferia B, Li Q, Harper J, Best RB, Glass KE, Cellmer T, Dunkelberger EB, Conrey A, Thein SL, Bunn HF, Eaton WA.
    Blood; 2021 Sep 30; 138(13):1172-1181. PubMed ID: 34197597
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  • 16. Hb Shelby [beta 131(H9)Gln-->Lys] in association with Hb S [beta 6(A3)Glu-->Val]: characterization, stability, and effects on Hb S polymerization.
    Adachi K, Surrey S, Tamary H, Kim J, Eck HS, Rappaport E, Ohene-Frempong K.
    Hemoglobin; 1993 Aug 30; 17(4):329-43. PubMed ID: 8226094
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  • 18. Crystallographic analysis of human hemoglobin elucidates the structural basis of the potent and dual antisickling activity of pyridyl derivatives of vanillin.
    Abdulmalik O, Ghatge MS, Musayev FN, Parikh A, Chen Q, Yang J, Nnamani I, Danso-Danquah R, Eseonu DN, Asakura T, Abraham DJ, Venitz J, Safo MK.
    Acta Crystallogr D Biol Crystallogr; 2011 Nov 30; 67(Pt 11):920-8. PubMed ID: 22101818
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  • 19. Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes.
    Monplaisir N, Merault G, Poyart C, Rhoda MD, Craescu C, Vidaud M, Galacteros F, Blouquit Y, Rosa J.
    Proc Natl Acad Sci U S A; 1986 Dec 30; 83(24):9363-7. PubMed ID: 3467311
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