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PUBMED FOR HANDHELDS

Journal Abstract Search


209 related items for PubMed ID: 12792024

  • 1. Validation of the hexose transporter of Plasmodium falciparum as a novel drug target.
    Joet T, Eckstein-Ludwig U, Morin C, Krishna S.
    Proc Natl Acad Sci U S A; 2003 Jun 24; 100(13):7476-9. PubMed ID: 12792024
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  • 2. The hexose transporter of Plasmodium falciparum is a worthy drug target.
    Joët T, Krishna S.
    Acta Trop; 2004 Feb 24; 89(3):371-4. PubMed ID: 14744563
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  • 3. Why is the Plasmodium falciparum hexose transporter a promising new drug target?
    Joët T, Morin C, Fischbarg J, Louw AI, Eckstein-Ludwig U, Woodrow C, Krishna S.
    Expert Opin Ther Targets; 2003 Oct 24; 7(5):593-602. PubMed ID: 14498822
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  • 4. Interaction of O-(undec-10-en)-yl-D-glucose derivatives with the Plasmodium falciparum hexose transporter (PfHT).
    Ionita M, Krishna S, Léo PM, Morin C, Patel AP.
    Bioorg Med Chem Lett; 2007 Sep 01; 17(17):4934-7. PubMed ID: 17587575
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  • 5. Analysis of Plasmodium vivax hexose transporters and effects of a parasitocidal inhibitor.
    Joët T, Chotivanich K, Silamut K, Patel AP, Morin C, Krishna S.
    Biochem J; 2004 Aug 01; 381(Pt 3):905-9. PubMed ID: 15107012
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  • 6. Comparative characterization of hexose transporters of Plasmodium knowlesi, Plasmodium yoelii and Toxoplasma gondii highlights functional differences within the apicomplexan family.
    Joët T, Holterman L, Stedman TT, Kocken CH, Van Der Wel A, Thomas AW, Krishna S.
    Biochem J; 2002 Dec 15; 368(Pt 3):923-9. PubMed ID: 12238947
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  • 7. Probing structure/affinity relationships for the Plasmodium falciparum hexose transporter with glucose derivatives.
    Fayolle M, Ionita M, Krishna S, Morin C, Patel AP.
    Bioorg Med Chem Lett; 2006 Mar 01; 16(5):1267-71. PubMed ID: 16361099
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  • 8. Life cycle studies of the hexose transporter of Plasmodium species and genetic validation of their essentiality.
    Slavic K, Straschil U, Reininger L, Doerig C, Morin C, Tewari R, Krishna S.
    Mol Microbiol; 2010 Mar 01; 75(6):1402-13. PubMed ID: 20132450
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  • 9. Inhibition of hexose transport and abrogation of pH homeostasis in the intraerythrocytic malaria parasite by an O-3-hexose derivative.
    Saliba KJ, Krishna S, Kirk K.
    FEBS Lett; 2004 Jul 16; 570(1-3):93-6. PubMed ID: 15251446
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  • 11. Docking, QM/MM, and molecular dynamics simulations of the hexose transporter from Plasmodium falciparum (PfHT).
    Fonseca AL, Nunes RR, Braga VM, Comar M, Alves RJ, Varotti Fde P, Taranto AG.
    J Mol Graph Model; 2016 May 16; 66():174-86. PubMed ID: 27131282
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  • 17. Hexose permeation pathways in Plasmodium falciparum-infected erythrocytes.
    Woodrow CJ, Burchmore RJ, Krishna S.
    Proc Natl Acad Sci U S A; 2000 Aug 29; 97(18):9931-6. PubMed ID: 10954735
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  • 18. A constitutive pan-hexose permease for the Plasmodium life cycle and transgenic models for screening of antimalarial sugar analogs.
    Blume M, Hliscs M, Rodriguez-Contreras D, Sanchez M, Landfear S, Lucius R, Matuschewski K, Gupta N.
    FASEB J; 2011 Apr 29; 25(4):1218-29. PubMed ID: 21169382
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  • 19. Use of a selective inhibitor to define the chemotherapeutic potential of the plasmodial hexose transporter in different stages of the parasite's life cycle.
    Slavic K, Delves MJ, Prudêncio M, Talman AM, Straschil U, Derbyshire ET, Xu Z, Sinden RE, Mota MM, Morin C, Tewari R, Krishna S, Staines HM.
    Antimicrob Agents Chemother; 2011 Jun 29; 55(6):2824-30. PubMed ID: 21402842
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  • 20. Intraerythrocytic Plasmodium falciparum expresses a high affinity facilitative hexose transporter.
    Woodrow CJ, Penny JI, Krishna S.
    J Biol Chem; 1999 Mar 12; 274(11):7272-7. PubMed ID: 10066789
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