| P2093 | author name string | Spahn TW | |
| | Kucharzik T | |
| P2860 | cites work | Intestinal tuberculosis: return of an old disease | Q74642709 |
| | Regulation of mucosal dendritic cell function by receptor activator of NF-kappa B (RANK)/RANK ligand interactions: impact on tolerance induction | Q74817249 |
| | Induction and mechanism of action of transforming growth factor-beta-secreting Th3 regulatory cells | Q77291206 |
| | Role of appendix and spleen in experimental colitis | Q77326686 |
| | Identification of multiple isolated lymphoid follicles on the antimesenteric wall of the mouse small intestine | Q77373865 |
| | CCR6 expression distinguishes mouse myeloid and lymphoid dendritic cell subsets: demonstration using a CCR6 EGFP knock-in mouse | Q77380495 |
| | IL-7 receptor alpha+ CD3(-) cells in the embryonic intestine induces the organizing center of Peyer's patches | Q77756301 |
| | Expansion of CD8+ T cells with regulatory function after interaction with intestinal epithelial cells | Q78439525 |
| | Different cytokines induce surface lymphotoxin-alphabeta on IL-7 receptor-alpha cells that differentially engender lymph nodes and Peyer's patches | Q78651212 |
| | RANK is essential for osteoclast and lymph node development | Q24598872 |
| | Retinoid-related orphan receptor gamma (RORgamma) is essential for lymphoid organogenesis and controls apoptosis during thymopoiesis | Q24642725 |
| | A chemokine expressed in lymphoid high endothelial venules promotes the adhesion and chemotaxis of naive T lymphocytes | Q24681916 |
| | Requirement for RORgamma in thymocyte survival and lymphoid organ development | Q28139666 |
| | Severe osteopetrosis, defective interleukin-1 signalling and lymph node organogenesis in TRAF6-deficient mice | Q28140546 |
| | A chemokine-driven positive feedback loop organizes lymphoid follicles | Q28142202 |
| | A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen | Q28300225 |
| | Characterization of M cell development during indomethacin-induced ileitis in rats | Q28369380 |
| | Abnormal development of peripheral lymphoid organs in mice deficient in lymphotoxin | Q28507630 |
| | Lymphotoxin-alpha-deficient mice. Effects on secondary lymphoid organ development and humoral immune responsiveness | Q28510392 |
| | Overlapping roles of CXCL13, interleukin 7 receptor alpha, and CCR7 ligands in lymph node development | Q28585776 |
| | Distinct roles for lymphotoxin-alpha and tumor necrosis factor in organogenesis and spatial organization of lymphoid tissue | Q28586439 |
| | Abnormal development of secondary lymphoid tissues in lymphotoxin beta-deficient mice | Q28587099 |
| | Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta-deficient mice | Q28587819 |
| | Interleukin-2 receptor α chain regulates the size and content of the peripheral lymphoid compartment | Q28587823 |
| | OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis | Q28589430 |
| | Ulcerative colitis-like disease in mice with a disrupted interleukin-2 gene | Q28593669 |
| | The Ikaros gene is required for the development of all lymphoid lineages | Q28594316 |
| | A CD4+ T-cell subset inhibits antigen-specific T-cell responses and prevents colitis | Q29619339 |
| | Dendritic cells express tight junction proteins and penetrate gut epithelial monolayers to sample bacteria | Q29619620 |
| | Critical role for tumor necrosis factor alpha in controlling the number of lumenal pathogenic bacteria and immunopathology in infectious colitis | Q33552079 |
| | Yersinia enterocolitica: overview and epidemiologic correlates | Q33797319 |
| | Development of peripheral lymphoid organs and natural killer cells depends on the helix-loop-helix inhibitor Id2. | Q33854381 |
| | Role of M cells in intestinal barrier function. | Q34148556 |
| | RelB is required for Peyer's patch development: differential regulation of p52-RelB by lymphotoxin and TNF | Q34167602 |
| | Defective lymphoid development in mice lacking expression of the common cytokine receptor gamma chain. | Q34307135 |
| | Selective defects in the development of the fetal and adult lymphoid system in mice with an Ikaros null mutation | Q34412659 |
| | Tropomyosin isoforms in intestinal mucosa: production of autoantibodies to tropomyosin isoforms in ulcerative colitis | Q34465376 |
| | Regulatory T cell clones induced by oral tolerance: suppression of autoimmune encephalomyelitis | Q34719541 |
| | Peyer's patches are required for oral tolerance to proteins | Q34725322 |
| | Organogenesis of lymphoid tissues | Q35096187 |
| | Characterisation of mucosal lymphoid aggregates in ulcerative colitis: immune cell phenotype and TcR-gammadelta expression | Q35361010 |
| | Regression of Peyer's patches in G alpha i2 deficient mice prior to colitis is associated with reduced expression of Bcl-2 and increased apoptosis. | Q35594988 |
| | Protective role of appendicectomy on onset and severity of ulcerative colitis and Crohn's disease | Q35595179 |
| | Effects of appendicectomy on the course of ulcerative colitis | Q35595250 |
| | Induction of colitis in mice deficient of Peyer's patches and mesenteric lymph nodes is associated with increased disease severity and formation of colonic lymphoid patches | Q35748193 |
| | Peyer's patch organogenesis is intact yet formation of B lymphocyte follicles is defective in peripheral lymphoid organs of mice deficient for tumor necrosis factor and its 55-kDa receptor | Q36184139 |
| | Evidence for function of Ia molecules on gut epithelial cells in man. | Q36357485 |
| | Role of appendix in the development of inflammatory bowel disease in TCR-alpha mutant mice | Q36367158 |
| | Localization of distinct Peyer's patch dendritic cell subsets and their recruitment by chemokines macrophage inflammatory protein (MIP)-3alpha, MIP-3beta, and secondary lymphoid organ chemokine | Q36368440 |
| | Regulation of peripheral lymph node genesis by the tumor necrosis factor family member TRANCE | Q36368551 |
| | The CCR7 ligand elc (CCL19) is transcytosed in high endothelial venules and mediates T cell recruitment | Q36369301 |
| | Freshly isolated Peyer's patch, but not spleen, dendritic cells produce interleukin 10 and induce the differentiation of T helper type 2 cells | Q36375116 |
| | The requirement of membrane lymphotoxin for the presence of dendritic cells in lymphoid tissues | Q36375299 |
| | Oxazolone colitis: A murine model of T helper cell type 2 colitis treatable with antibodies to interleukin 4. | Q36401302 |
| | Enterocyte expression of interleukin 7 induces development of gammadelta T cells and Peyer's patches | Q36404323 |
| | Disrupted splenic architecture, but normal lymph node development in mice expressing a soluble lymphotoxin-beta receptor-IgG1 fusion protein. | Q36688075 |
| | Targeted disruption of LIGHT causes defects in costimulatory T cell activation and reveals cooperation with lymphotoxin beta in mesenteric lymph node genesis | Q38288045 |
| | Cooperating mechanisms of CXCR5 and CCR7 in development and organization of secondary lymphoid organs | Q40590092 |
| | Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kappa b-inducing kinase | Q40954925 |
| | Lymph node germinal centers form in the absence of follicular dendritic cell networks | Q41853947 |
| | Essential role of nuclear factor (NF)-kappaB-inducing kinase and inhibitor of kappaB (IkappaB) kinase alpha in NF-kappaB activation through lymphotoxin beta receptor, but not through tumor necrosis factor receptor I | Q42015911 |
| | Lymphopenia in interleukin (IL)-7 gene-deleted mice identifies IL-7 as a nonredundant cytokine. | Q42064178 |
| | Molecular basis for hematopoietic/mesenchymal interaction during initiation of Peyer's patch organogenesis. | Q42076869 |
| | Surface lymphotoxin alpha/beta complex is required for the development of peripheral lymphoid organs | Q42196937 |
| | Defective Peyer's patch organogenesis in mice lacking the 55-kD receptor for tumor necrosis factor | Q42943618 |
| | Elimination of colonic patches with lymphotoxin beta receptor-Ig prevents Th2 cell-type colitis | Q43710164 |
| | Oxazolone colitis, a Th2 colitis model resembling ulcerative colitis, is mediated by IL-13-producing NK-T cells | Q44217456 |
| | A novel method in the induction of reliable experimental acute and chronic ulcerative colitis in mice | Q44753508 |
| | A high endothelial cell-derived chemokine induces rapid, efficient, and subset-selective arrest of rolling T lymphocytes on a reconstituted endothelial substrate. | Q46115193 |
| | Lymph node genesis is induced by signaling through the lymphotoxin beta receptor | Q47713223 |
| | The lymphotoxin beta receptor controls organogenesis and affinity maturation in peripheral lymphoid tissues | Q47713235 |
| | Both the lymphotoxin and tumor necrosis factor pathways are involved in experimental murine models of colitis | Q48709458 |
| | Expression of alpha(4)beta(7) integrin defines a distinct pathway of lymphoid progenitors committed to T cells, fetal intestinal lymphotoxin producer, NK, and dendritic cells. | Q51063633 |
| | The role of dendritic cells, B cells, and M cells in gut-oriented immune responses. | Q52020473 |
| | Lymphocyte-filled villi: comparison with other lymphoid aggregations in the mucosa of the human small intestine. | Q52036578 |
| | Chemokines and the arrest of lymphocytes rolling under flow conditions. | Q52040689 |
| | Developmental defects of lymphoid cells in Jak3 kinase-deficient mice. | Q52204302 |
| | Defective lymphotoxin-beta receptor-induced NF-kappaB transcriptional activity in NIK-deficient mice. | Q52542561 |
| | Abnormal organogenesis of Peyer's patches in mice deficient for NF-kappaB1, NF-kappaB2, and Bcl-3. | Q52546319 |
| | Ulcerative colitis and adenocarcinoma of the colon in G alpha i2-deficient mice. | Q53463453 |
| | Postgestational lymphotoxin/lymphotoxin beta receptor interactions are essential for the presence of intestinal B lymphocytes. | Q53971848 |
| | Mesenteric lymph nodes are critical for the induction of high-dose oral tolerance in the absence of Peyer's patches. | Q53975385 |
| | Impaired On/Off Regulation of TNF Biosynthesis in Mice Lacking TNF AU-Rich Elements | Q62819809 |
| | TNF and lymphotoxin beta cooperate in the maintenance of secondary lymphoid tissue microarchitecture but not in the development of lymph nodes | Q63968518 |
| | Antigen presentation by epithelial cells of the rat small intestine. II. Selective induction of suppressor T cells | Q68963289 |
| | Induction of oral tolerance in rats without Peyer's patches | Q69994772 |
| | Anti-gamma delta T cell antibody blocks the induction and maintenance of oral tolerance to ovalbumin in mice | Q71288342 |
| | Expression of ICAM-I on M cells covering isolated lymphoid follicles of the human colon | Q72064118 |
| | A new mutation, aly, that induces a generalized lack of lymph nodes accompanied by immunodeficiency in mice | Q72753495 |
| | Spontaneous, heritable colitis in a new substrain of C3H/HeJ mice | Q72800593 |
| | The accessory cell populations in ulcerative colitis: a comparison between the colon and appendix in colitis and acute appendicitis | Q73094359 |
| | Gamma delta T lymphocytes regulate the induction and maintenance of oral tolerance | Q73224605 |
| | Organogenic role of B lymphocytes in mucosal immunity | Q73232930 |
| | gammadelta T cells regulate mucosally induced tolerance in a dose-dependent fashion | Q73254532 |
| | Gut cryptopatches: direct evidence of extrathymic anatomical sites for intestinal T lymphopoiesis | Q73291761 |
| | Isolated lymphoid follicle formation is inducible and dependent upon lymphotoxin-sufficient B lymphocytes, lymphotoxin beta receptor, and TNF receptor I function | Q73419615 |
| | New gut associated lymphoid tissue "cryptopatches" breed murine intestinal intraepithelial T cell precursors | Q73605525 |
| | Unique functions of CD11b+, CD8 alpha+, and double-negative Peyer's patch dendritic cells | Q73720806 |
| | Induction of oral tolerance to cellular immune responses in the absence of Peyer's patches | Q73740471 |
| | Alternate mucosal immune system: organized Peyer's patches are not required for IgA responses in the gastrointestinal tract | Q73755884 |
| | Newly-formed lymph nodes in the submucosa in chronic inflammatory bowel disease | Q73768616 |
| | Lymphoid precursors in intestinal cryptopatches express CCR6 and undergo dysregulated development in the absence of CCR6 | Q73827790 |
| | Signaling via LTbetaR on the lamina propria stromal cells of the gut is required for IgA production | Q74082070 |
| | Essential role of IL-7 receptor alpha in the formation of Peyer's patch anlage | Q74261728 |
| | Pulmonary dendritic cells producing IL-10 mediate tolerance induced by respiratory exposure to antigen | Q74286698 |
| | Generation of intestinal T cells from progenitors residing in gut cryptopatches | Q74424059 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 456-465 | |
| P577 | publication date | 2004-03-01 | |
| P1433 | published in | Gut | Q5621669 |
| P1476 | title | Modulating the intestinal immune system: the role of lymphotoxin and GALT organs | |
| P478 | volume | 53 | |