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2. Treponema pallidum and Borrelia burgdorferi lipoproteins and synthetic lipopeptides activate monocytes/macrophages. Radolf JD; Arndt LL; Akins DR; Curetty LL; Levi ME; Shen Y; Davis LS; Norgard MV J Immunol; 1995 Mar; 154(6):2866-77. PubMed ID: 7876555 [TBL] [Abstract][Full Text] [Related]
3. Activation of human monocytic cells by Borrelia burgdorferi and Treponema pallidum is facilitated by CD14 and correlates with surface exposure of spirochetal lipoproteins. Sellati TJ; Bouis DA; Caimano MJ; Feulner JA; Ayers C; Lien E; Radolf JD J Immunol; 1999 Aug; 163(4):2049-56. PubMed ID: 10438943 [TBL] [Abstract][Full Text] [Related]
4. Membrane topology of Borrelia burgdorferi and Treponema pallidum lipoproteins. Jones JD; Bourell KW; Norgard MV; Radolf JD Infect Immun; 1995 Jul; 63(7):2424-34. PubMed ID: 7790053 [TBL] [Abstract][Full Text] [Related]
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7. Lipoproteins of Borrelia burgdorferi and Treponema pallidum activate cachectin/tumor necrosis factor synthesis. Analysis using a CAT reporter construct. Radolf JD; Norgard MV; Brandt ME; Isaacs RD; Thompson PA; Beutler B J Immunol; 1991 Sep; 147(6):1968-74. PubMed ID: 1890308 [TBL] [Abstract][Full Text] [Related]
8. Treponema pallidum and Borrelia burgdorferi lipoproteins and synthetic lipopeptides activate monocytic cells via a CD14-dependent pathway distinct from that used by lipopolysaccharide. Sellati TJ; Bouis DA; Kitchens RL; Darveau RP; Pugin J; Ulevitch RJ; Gangloff SC; Goyert SM; Norgard MV; Radolf JD J Immunol; 1998 Jun; 160(11):5455-64. PubMed ID: 9605148 [TBL] [Abstract][Full Text] [Related]
9. Activation of human monocytic cells by Treponema pallidum and Borrelia burgdorferi lipoproteins and synthetic lipopeptides proceeds via a pathway distinct from that of lipopolysaccharide but involves the transcriptional activator NF-kappa B. Norgard MV; Arndt LL; Akins DR; Curetty LL; Harrich DA; Radolf JD Infect Immun; 1996 Sep; 64(9):3845-52. PubMed ID: 8751937 [TBL] [Abstract][Full Text] [Related]
10. Solid-phase synthesis of biologically active lipopeptides as analogs for spirochetal lipoproteins. DeOgny L; Pramanik BC; Arndt LL; Jones JD; Rush J; Slaughter CA; Radolf JD; Norgard MV Pept Res; 1994; 7(2):91-7. PubMed ID: 8012126 [TBL] [Abstract][Full Text] [Related]
11. Interaction of spirochetes with the host. Hindersson P; Thomas D; Stamm L; Penn C; Norris S; Joens LA Res Microbiol; 1992; 143(6):629-39. PubMed ID: 1475523 [TBL] [Abstract][Full Text] [Related]
12. Antigenic cross-reactivity between Borrelia burgdorferi, Borrelia recurrentis, Treponema pallidum, and Treponema phagedenis. Luther B; Moskophidis M Zentralbl Bakteriol; 1990 Nov; 274(2):214-26. PubMed ID: 2085371 [TBL] [Abstract][Full Text] [Related]
13. Similarity between the 38-kilodalton lipoprotein of Treponema pallidum and the glucose/galactose-binding (MglB) protein of Escherichia coli. Becker PS; Akins DR; Radolf JD; Norgard MV Infect Immun; 1994 Apr; 62(4):1381-91. PubMed ID: 8132345 [TBL] [Abstract][Full Text] [Related]
14. Immunogenic integral membrane proteins of Borrelia burgdorferi are lipoproteins. Brandt ME; Riley BS; Radolf JD; Norgard MV Infect Immun; 1990 Apr; 58(4):983-91. PubMed ID: 2318538 [TBL] [Abstract][Full Text] [Related]
15. Role of outer membrane architecture in immune evasion by Treponema pallidum and Borrelia burgdorferi. Radolf JD Trends Microbiol; 1994 Sep; 2(9):307-11. PubMed ID: 7812663 [TBL] [Abstract][Full Text] [Related]
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