BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

266 related articles for article (PubMed ID: 1447137)

  • 1. Characterization of a high-affinity iron transport system in Acinetobacter baumannii.
    Echenique JR; Arienti H; Tolmasky ME; Read RR; Staneloni RJ; Crosa JH; Actis LA
    J Bacteriol; 1992 Dec; 174(23):7670-9. PubMed ID: 1447137
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Isolation and Characterization of the Acinetobactin and Baumannoferrin Siderophores Produced by Acinetobacter baumannii.
    Penwell WF; Actis LA
    Methods Mol Biol; 2019; 1946():259-270. PubMed ID: 30798562
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic organization of an Acinetobacter baumannii chromosomal region harbouring genes related to siderophore biosynthesis and transport.
    Dorsey CW; Tolmasky ME; Crosa JH; Actis LA
    Microbiology (Reading); 2003 May; 149(Pt 5):1227-1238. PubMed ID: 12724384
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Catechol Siderophore Transport by Vibrio cholerae.
    Wyckoff EE; Allred BE; Raymond KN; Payne SM
    J Bacteriol; 2015 Sep; 197(17):2840-9. PubMed ID: 26100039
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Effect of iron-limiting conditions on growth of clinical isolates of Acinetobacter baumannii.
    Actis LA; Tolmasky ME; Crosa LM; Crosa JH
    J Clin Microbiol; 1993 Oct; 31(10):2812-5. PubMed ID: 8253994
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of 2,3-dihydroxybenzoic acid as a Brucella abortus siderophore.
    López-Goñi I; Moriyón I; Neilands JB
    Infect Immun; 1992 Nov; 60(11):4496-503. PubMed ID: 1398964
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Pseudomonas aeruginosa pirA gene encodes a second receptor for ferrienterobactin and synthetic catecholate analogues.
    Ghysels B; Ochsner U; Möllman U; Heinisch L; Vasil M; Cornelis P; Matthijs S
    FEMS Microbiol Lett; 2005 May; 246(2):167-74. PubMed ID: 15899402
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Influence of iron on growth, production of siderophore compounds, membrane proteins, and lipase activity in Acinetobacter calcoaceticus BD 413.
    Nudel C; Gonzalez R; Castañeda N; Mahler G; Actis LA
    Microbiol Res; 2001 Mar; 155(4):263-9. PubMed ID: 11297356
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Production of catechol-siderophore and utilization of transferrin-bound iron in Bacillus cereus.
    Park RY; Choi MH; Sun HY; Shin SH
    Biol Pharm Bull; 2005 Jun; 28(6):1132-5. PubMed ID: 15930764
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Influence of iron on growth and extracellular products of Acinetobacter baumannii.
    Goel VK; Kapil A; Das B; Rao DN
    Jpn J Med Sci Biol; 1998 Nov; 51(1):25-33. PubMed ID: 10211429
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Catechol siderophores repress the pyochelin pathway and activate the enterobactin pathway in Pseudomonas aeruginosa: an opportunity for siderophore-antibiotic conjugates development.
    Gasser V; Baco E; Cunrath O; August PS; Perraud Q; Zill N; Schleberger C; Schmidt A; Paulen A; Bumann D; Mislin GL; Schalk IJ
    Environ Microbiol; 2016 Mar; 18(3):819-32. PubMed ID: 26718479
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Iron acquisition functions expressed by the human pathogen Acinetobacter baumannii.
    Zimbler DL; Penwell WF; Gaddy JA; Menke SM; Tomaras AP; Connerly PL; Actis LA
    Biometals; 2009 Feb; 22(1):23-32. PubMed ID: 19130255
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Iron limitation enhances acyl homoserine lactone (AHL) production and biofilm formation in clinical isolates of Acinetobacter baumannii.
    Modarresi F; Azizi O; Shakibaie MR; Motamedifar M; Mosadegh E; Mansouri S
    Virulence; 2015; 6(2):152-61. PubMed ID: 25622119
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Siderophore production by Aeromonas salmonicida.
    Hirst ID; Hastings TS; Ellis AE
    J Gen Microbiol; 1991 May; 137(5):1185-92. PubMed ID: 1830896
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Iron-binding compounds and related outer membrane proteins in Vibrio cholerae non-O1 strains from aquatic environments.
    Amaro C; Aznar R; Alcaide E; Lemos ML
    Appl Environ Microbiol; 1990 Aug; 56(8):2410-6. PubMed ID: 2144956
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Proteomic analysis of iron-regulated membrane proteins identify FhuE receptor as a target to inhibit siderophore-mediated iron acquisition in Acinetobacter baumannii.
    Tiwari V; Rajeswari MR; Tiwari M
    Int J Biol Macromol; 2019 Mar; 125():1156-1167. PubMed ID: 30579900
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Siderophore-mediated iron transport correlates with the presence of specific iron-regulated proteins in the outer membrane of Rhizobium meliloti.
    Reigh G; O'Connell M
    J Bacteriol; 1993 Jan; 175(1):94-102. PubMed ID: 8416915
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Species selectivity of new siderophore-drug conjugates that use specific iron uptake for entry into bacteria.
    Diarra MS; Lavoie MC; Jacques M; Darwish I; Dolence EK; Dolence JA; Ghosh A; Ghosh M; Miller MJ; Malouin F
    Antimicrob Agents Chemother; 1996 Nov; 40(11):2610-7. PubMed ID: 8913474
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Iron transport-mediated drug delivery using mixed-ligand siderophore-beta-lactam conjugates.
    Ghosh A; Ghosh M; Niu C; Malouin F; Moellmann U; Miller MJ
    Chem Biol; 1996 Dec; 3(12):1011-9. PubMed ID: 9000006
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Acinetobacter baumannii can use multiple siderophores for iron acquisition, but only acinetobactin is required for virulence.
    Sheldon JR; Skaar EP
    PLoS Pathog; 2020 Oct; 16(10):e1008995. PubMed ID: 33075115
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.