306 related articles for article (PubMed ID: 12732657)
1. Ectopic LT alpha beta directs lymphoid organ neogenesis with concomitant expression of peripheral node addressin and a HEV-restricted sulfotransferase.
Drayton DL; Ying X; Lee J; Lesslauer W; Ruddle NH
J Exp Med; 2003 May; 197(9):1153-63. PubMed ID: 12732657
[TBL] [Abstract][Full Text] [Related]
2. Lymphotoxin plays a crucial role in the development and function of nasal-associated lymphoid tissue through regulation of chemokines and peripheral node addressin.
Ying X; Chan K; Shenoy P; Hill M; Ruddle NH
Am J Pathol; 2005 Jan; 166(1):135-46. PubMed ID: 15632007
[TBL] [Abstract][Full Text] [Related]
3. I kappa B kinase complex alpha kinase activity controls chemokine and high endothelial venule gene expression in lymph nodes and nasal-associated lymphoid tissue.
Drayton DL; Bonizzi G; Ying X; Liao S; Karin M; Ruddle NH
J Immunol; 2004 Nov; 173(10):6161-8. PubMed ID: 15528353
[TBL] [Abstract][Full Text] [Related]
4. Lymphotoxin alpha3 induces chemokines and adhesion molecules: insight into the role of LT alpha in inflammation and lymphoid organ development.
Cuff CA; Schwartz J; Bergman CM; Russell KS; Bender JR; Ruddle NH
J Immunol; 1998 Dec; 161(12):6853-60. PubMed ID: 9862717
[TBL] [Abstract][Full Text] [Related]
5. Transgenic LacZ under control of Hec-6st regulatory sequences recapitulates endogenous gene expression on high endothelial venules.
Liao S; Bentley K; Lebrun M; Lesslauer W; Ruddle FH; Ruddle NH
Proc Natl Acad Sci U S A; 2007 Mar; 104(11):4577-82. PubMed ID: 17360566
[TBL] [Abstract][Full Text] [Related]
6. Differing activities of homeostatic chemokines CCL19, CCL21, and CXCL12 in lymphocyte and dendritic cell recruitment and lymphoid neogenesis.
Luther SA; Bidgol A; Hargreaves DC; Schmidt A; Xu Y; Paniyadi J; Matloubian M; Cyster JG
J Immunol; 2002 Jul; 169(1):424-33. PubMed ID: 12077273
[TBL] [Abstract][Full Text] [Related]
7. Detection of a sulfotransferase (HEC-GlcNAc6ST) in high endothelial venules of lymph nodes and in high endothelial venule-like vessels within ectopic lymphoid aggregates: relationship to the MECA-79 epitope.
Bistrup A; Tsay D; Shenoy P; Singer MS; Bangia N; Luther SA; Cyster JG; Ruddle NH; Rosen SD
Am J Pathol; 2004 May; 164(5):1635-44. PubMed ID: 15111310
[TBL] [Abstract][Full Text] [Related]
8. Lymphocyte traffic in lymphoid organ neogenesis: differential roles of Ltalpha and LTalphabeta.
Drayton DL; Chan K; Lesslauer W; Lee J; Ying XY; Ruddle NH
Adv Exp Med Biol; 2002; 512():43-8. PubMed ID: 12405186
[TBL] [Abstract][Full Text] [Related]
9. Transgenic expression of lymphotoxin restores lymph nodes to lymphotoxin-alpha-deficient mice.
Sacca R; Turley S; Soong L; Mellman I; Ruddle NH
J Immunol; 1997 Nov; 159(9):4252-60. PubMed ID: 9379020
[TBL] [Abstract][Full Text] [Related]
10. Tumor necrosis factor receptor regulation of peripheral node addressin biosynthetic components in tumor endothelial cells.
Rodriguez AB; Parriott G; Engelhard VH
Front Immunol; 2022; 13():1009306. PubMed ID: 36189308
[TBL] [Abstract][Full Text] [Related]
11. Understanding high endothelial venules: Lessons for cancer immunology.
Ager A; May MJ
Oncoimmunology; 2015 Jun; 4(6):e1008791. PubMed ID: 26155419
[TBL] [Abstract][Full Text] [Related]
12. Selective disruption of lymphotoxin ligands reveals a novel set of mucosal lymph nodes and unique effects on lymph node cellular organization.
Rennert PD; Browning JL; Hochman PS
Int Immunol; 1997 Nov; 9(11):1627-39. PubMed ID: 9418124
[TBL] [Abstract][Full Text] [Related]
13. Lymphoid neo-organogenesis: lymphotoxin's role in inflammation and development.
Ruddle NH
Immunol Res; 1999; 19(2-3):119-25. PubMed ID: 10493167
[TBL] [Abstract][Full Text] [Related]
14. Defining High Endothelial Venules and Tertiary Lymphoid Structures in Cancer.
Jones E; Gallimore A; Ager A
Methods Mol Biol; 2018; 1845():99-118. PubMed ID: 30141010
[TBL] [Abstract][Full Text] [Related]
15. Nasal-associated lymphoid tissue: phenotypic and functional evidence for the primary role of peripheral node addressin in naive lymphocyte adhesion to high endothelial venules in a mucosal site.
Csencsits KL; Jutila MA; Pascual DW
J Immunol; 1999 Aug; 163(3):1382-9. PubMed ID: 10415038
[TBL] [Abstract][Full Text] [Related]
16. Mucosal addressin expression and binding-interactions with naive lymphocytes vary among the cranial, oral, and nasal-associated lymphoid tissues.
Csencsits KL; Jutila MA; Pascual DW
Eur J Immunol; 2002 Nov; 32(11):3029-39. PubMed ID: 12385022
[TBL] [Abstract][Full Text] [Related]
17. A HEV-restricted sulfotransferase is expressed in rheumatoid arthritis synovium and is induced by lymphotoxin-alpha/beta and TNF-alpha in cultured endothelial cells.
Pablos JL; Santiago B; Tsay D; Singer MS; Palao G; Galindo M; Rosen SD
BMC Immunol; 2005 Mar; 6():6. PubMed ID: 15752429
[TBL] [Abstract][Full Text] [Related]
18. Differential activities of secreted lymphotoxin-alpha3 and membrane lymphotoxin-alpha1beta2 in lymphotoxin-induced inflammation: critical role of TNF receptor 1 signaling.
Sacca R; Cuff CA; Lesslauer W; Ruddle NH
J Immunol; 1998 Jan; 160(1):485-91. PubMed ID: 9552007
[TBL] [Abstract][Full Text] [Related]
19. Vascular addressins are induced on islet vessels during insulitis in nonobese diabetic mice and are involved in lymphoid cell binding to islet endothelium.
Hänninen A; Taylor C; Streeter PR; Stark LS; Sarte JM; Shizuru JA; Simell O; Michie SA
J Clin Invest; 1993 Nov; 92(5):2509-15. PubMed ID: 7693764
[TBL] [Abstract][Full Text] [Related]
20. Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta-deficient mice.
Koni PA; Sacca R; Lawton P; Browning JL; Ruddle NH; Flavell RA
Immunity; 1997 Apr; 6(4):491-500. PubMed ID: 9133428
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
