BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 12173405)

  • 21. Receptor-mediated binding of milk lactoferrin to nursing piglet enterocytes: a model for studies on absorption of lactoferrin-bound iron.
    Gíslason J; Douglas GC; Hutchens TW; Lönnerdal B
    J Pediatr Gastroenterol Nutr; 1995 Jul; 21(1):37-43. PubMed ID: 8576812
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Utilization of lactoferrin-bound and transferrin-bound iron by Campylobacter jejuni.
    Miller CE; Rock JD; Ridley KA; Williams PH; Ketley JM
    J Bacteriol; 2008 Mar; 190(6):1900-11. PubMed ID: 18203832
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Reduction of exogenous ferric iron by a surface-associated ferric reductase of Listeria spp.
    Deneer HG; Healey V; Boychuk I
    Microbiology (Reading); 1995 Aug; 141 ( Pt 8)():1985-1992. PubMed ID: 7551061
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Iron uptake and increased intracellular enzyme activity follow host lactoferrin binding by Trichomonas vaginalis receptors.
    Peterson KM; Alderete JF
    J Exp Med; 1984 Aug; 160(2):398-410. PubMed ID: 6088662
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The mammalian neuroendocrine hormone norepinephrine supplies iron for bacterial growth in the presence of transferrin or lactoferrin.
    Freestone PP; Lyte M; Neal CP; Maggs AF; Haigh RD; Williams PH
    J Bacteriol; 2000 Nov; 182(21):6091-8. PubMed ID: 11029429
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Iron uptake from transferrin and lactoferrin by rat intestinal brush-border membrane vesicles.
    Kawakami H; Dosako S; Lönnerdal B
    Am J Physiol; 1990 Apr; 258(4 Pt 1):G535-41. PubMed ID: 2333967
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Iron accumulation by bovine aortic endothelial cells.
    Vijayaraghavan P; Rafelson ME; Bezkorovainy A
    Clin Physiol Biochem; 1992; 9(4):138-44. PubMed ID: 1302169
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Amonabactin-mediated iron acquisition from transferrin and lactoferrin by Aeromonas hydrophila: direct measurement of individual microscopic rate constants.
    Stintzi A; Raymond KN
    J Biol Inorg Chem; 2000 Feb; 5(1):57-66. PubMed ID: 10766437
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Protein disulfide isomerase (PDI) associates with NADPH oxidase and is required for phagocytosis of Leishmania chagasi promastigotes by macrophages.
    Santos CX; Stolf BS; Takemoto PV; Amanso AM; Lopes LR; Souza EB; Goto H; Laurindo FR
    J Leukoc Biol; 2009 Oct; 86(4):989-98. PubMed ID: 19564574
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Elucidation of the mechanism by which catecholamine stress hormones liberate iron from the innate immune defense proteins transferrin and lactoferrin.
    Sandrini SM; Shergill R; Woodward J; Muralikuttan R; Haigh RD; Lyte M; Freestone PP
    J Bacteriol; 2010 Jan; 192(2):587-94. PubMed ID: 19820086
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multivalent metal-induced iron acquisition from transferrin and lactoferrin by myeloid cells.
    Olakanmi O; Rasmussen GT; Lewis TS; Stokes JB; Kemp JD; Britigan BE
    J Immunol; 2002 Aug; 169(4):2076-84. PubMed ID: 12165535
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Leishmania infantum chagasi: a genome-based approach to identification of excreted/secreted proteins.
    DebRoy S; Keenan AB; Ueno N; Jeronimo SM; Donelson JE; Wilson ME
    Exp Parasitol; 2010 Dec; 126(4):582-91. PubMed ID: 20542033
    [TBL] [Abstract][Full Text] [Related]  

  • 33. LFR1 ferric iron reductase of Leishmania amazonensis is essential for the generation of infective parasite forms.
    Flannery AR; Huynh C; Mittra B; Mortara RA; Andrews NW
    J Biol Chem; 2011 Jul; 286(26):23266-79. PubMed ID: 21558274
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Efficient iron uptake via a reductive mechanism in procyclic Trypanosoma brucei.
    Mach J; Tachezy J; Sutak R
    J Parasitol; 2013 Apr; 99(2):363-4. PubMed ID: 22924933
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Lactoferrin effects of phagocytic cell function. II. The presence of iron is required for the lactoferrin molecule to stimulate intracellular killing by macrophages but not to enhance the uptake of particles and microorganisms.
    Lima MF; Kierszenbaum F
    J Immunol; 1987 Sep; 139(5):1647-51. PubMed ID: 3114372
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Trypanothione efficiently intercepts nitric oxide as a harmless iron complex in trypanosomatid parasites.
    Bocedi A; Dawood KF; Fabrini R; Federici G; Gradoni L; Pedersen JZ; Ricci G
    FASEB J; 2010 Apr; 24(4):1035-42. PubMed ID: 19952282
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Plasma membrane Fe2-transferrin reductase and iron uptake in K562 cells are not directly related.
    Goldenberg H; Dodel B; Seidl D
    Eur J Biochem; 1990 Sep; 192(2):475-80. PubMed ID: 2209603
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Influence of copper depletion on iron uptake mediated by SFT, a stimulator of Fe transport.
    Yu J; Wessling-Resnick M
    J Biol Chem; 1998 Mar; 273(12):6909-15. PubMed ID: 9506995
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Acquisition of iron by Legionella pneumophila: role of iron reductase.
    Johnson W; Varner L; Poch M
    Infect Immun; 1991 Jul; 59(7):2376-81. PubMed ID: 1904841
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Iron-dependent binding of 8-anilinonaphthalene-1-sulphonate by both lactoferrin and transferrin.
    Bilić N; Casey M; Blanc B
    Biochem J; 1976 Jul; 157(1):233-5. PubMed ID: 9066
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.