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Host-derived glucose and its transporter in the obligate intracellular pathogen Toxoplasma gondii are dispensable by glutaminolysis.

Blume M, Rodriguez-Contreras D, Landfear S, Fleige T, Soldati-Favre D, Lucius R, Gupta N.

Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):12998-3003. doi: 10.1073/pnas.0903831106. Epub 2009 Jul 17.


Metabolic Cooperation of Glucose and Glutamine Is Essential for the Lytic Cycle of Obligate Intracellular Parasite Toxoplasma gondii.

Nitzsche R, Zagoriy V, Lucius R, Gupta N.

J Biol Chem. 2016 Jan 1;291(1):126-41. doi: 10.1074/jbc.M114.624619. Epub 2015 Oct 30.


Mitochondrial metabolism of glucose and glutamine is required for intracellular growth of Toxoplasma gondii.

MacRae JI, Sheiner L, Nahid A, Tonkin C, Striepen B, McConville MJ.

Cell Host Microbe. 2012 Nov 15;12(5):682-92. doi: 10.1016/j.chom.2012.09.013.


Molecular cloning, organellar targeting and developmental expression of mitochondrial chaperone HSP60 in Toxoplasma gondii.

Toursel C, Dzierszinski F, Bernigaud A, Mortuaire M, Tomavo S.

Mol Biochem Parasitol. 2000 Dec;111(2):319-32.


A plant/fungal-type phosphoenolpyruvate carboxykinase located in the parasite mitochondrion ensures glucose-independent survival of Toxoplasma gondii.

Nitzsche R, Günay-Esiyok Ö, Tischer M, Zagoriy V, Gupta N.

J Biol Chem. 2017 Sep 15;292(37):15225-15239. doi: 10.1074/jbc.M117.802702. Epub 2017 Jul 18.


Toxoplasma gondii is dependent on glutamine and alters migratory profile of infected host bone marrow derived immune cells through SNAT2 and CXCR4 pathways.

Lee IP, Evans AK, Yang C, Works MG, Kumar V, De Miguel Z, Manley NC, Sapolsky RM.

PLoS One. 2014 Oct 9;9(10):e109803. doi: 10.1371/journal.pone.0109803. eCollection 2014.


Stimulative effects of insulin on Toxoplasma gondii replication in 3T3-L1 cells.

Zhu S, Lai DH, Li SQ, Lun ZR.

Cell Biol Int. 2006 Feb;30(2):149-53. Epub 2005 Nov 2.


Toxoplasma gondii: use of mutants to study the host-parasite relationship.

Pfefferkorn ER, Schwartzman JD, Kasper LH.

Ciba Found Symp. 1983;99:74-91.


Phosphatidylethanolamine synthesis in the parasite mitochondrion is required for efficient growth but dispensable for survival of Toxoplasma gondii.

Hartmann A, Hellmund M, Lucius R, Voelker DR, Gupta N.

J Biol Chem. 2014 Mar 7;289(10):6809-24. doi: 10.1074/jbc.M113.509406. Epub 2014 Jan 15.


Proteomics and glycomics analyses of N-glycosylated structures involved in Toxoplasma gondii--host cell interactions.

Fauquenoy S, Morelle W, Hovasse A, Bednarczyk A, Slomianny C, Schaeffer C, Van Dorsselaer A, Tomavo S.

Mol Cell Proteomics. 2008 May;7(5):891-910. doi: 10.1074/mcp.M700391-MCP200. Epub 2008 Jan 9.


Host cell egress and invasion induce marked relocations of glycolytic enzymes in Toxoplasma gondii tachyzoites.

Pomel S, Luk FC, Beckers CJ.

PLoS Pathog. 2008 Oct;4(10):e1000188. doi: 10.1371/journal.ppat.1000188. Epub 2008 Oct 24.


Behaviour of Toxoplasma gondii RH Ankara strain tachyzoites during continuous production in various cell lines.

Döskaya M, Degirmenci A, Ciçek C, Ak M, Korkmaz M, Gürüz Y, Uner A.

Parasitology. 2006 Mar;132(Pt 3):315-9. Epub 2005 Dec 1. Erratum in: Parasitology. 2006 Feb;132(Pt 2):254.


The adenosine transporter of Toxoplasma gondii. Identification by insertional mutagenesis, cloning, and recombinant expression.

Chiang CW, Carter N, Sullivan WJ Jr, Donald RG, Roos DS, Naguib FN, el Kouni MH, Ullman B, Wilson CM.

J Biol Chem. 1999 Dec 3;274(49):35255-61.


Effect of clindamycin on intracellular replication, protein synthesis, and infectivity of Toxoplasma gondii.

Blais J, Tardif C, Chamberland S.

Antimicrob Agents Chemother. 1993 Dec;37(12):2571-7.


Vero cell surface proteoglycan interaction with the microneme protein NcMIC(3) mediates adhesion of Neospora caninum tachyzoites to host cells unlike that in Toxoplasma gondii.

Naguleswaran A, Cannas A, Keller N, Vonlaufen N, Björkman C, Hemphill A.

Int J Parasitol. 2002 Jun;32(6):695-704.


Toxoplasma gondii grown in human cells uses GalNAc-containing glycosylphosphatidylinositol precursors to anchor surface antigens while the immunogenic Glc-GalNAc-containing precursors remain free at the parasite cell surface.

Azzouz N, Shams-Eldin H, Niehus S, Debierre-Grockiego F, Bieker U, Schmidt J, Mercier C, Delauw MF, Dubremetz JF, Smith TK, Schwarz RT.

Int J Biochem Cell Biol. 2006;38(11):1914-25. Epub 2006 May 27.


Comparative activity of macrolides against Toxoplasma gondii demonstrating utility of an in vitro microassay.

Chamberland S, Kirst HA, Current WL.

Antimicrob Agents Chemother. 1991 May;35(5):903-9.

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