| P50 | author | Rodney D. Newberry | Q38523760 |
| | Robin G. Lorenz | Q50229441 |
| P2860 | cites work | LIGHT, a new member of the TNF superfamily, and lymphotoxin alpha are ligands for herpesvirus entry mediator | Q24308657 |
| | 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 |
| | RORgamma t, a novel isoform of an orphan receptor, negatively regulates Fas ligand expression and IL-2 production in T cells | Q24657337 |
| | Hepatic expression of secondary lymphoid chemokine (CCL21) promotes the development of portal-associated lymphoid tissue in chronic inflammatory liver disease | Q24669792 |
| | 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 |
| | RORgammaT, a thymus-specific isoform of the orphan nuclear receptor RORgamma / TOR, is up-regulated by signaling through the pre-T cell receptor and binds to the TEA promoter | Q28140633 |
| | Epithelial M cells: differentiation and function | Q28141133 |
| | A chemokine-driven positive feedback loop organizes lymphoid follicles | Q28142202 |
| | An essential function for the nuclear receptor RORgamma(t) in the generation of fetal lymphoid tissue inducer cells | Q28235728 |
| | Genomic structure and chromosomal mapping of the nuclear orphan receptor ROR gamma (RORC) gene | Q28256851 |
| | Thymic origin of intestinal alphabeta T cells revealed by fate mapping of RORgammat+ cells | Q28271481 |
| | A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen | Q28300225 |
| | Aberrant expansion of segmented filamentous bacteria in IgA-deficient gut | Q28505481 |
| | Basis for the age-related decline in intestinal mucosal immunity | Q28569785 |
| | In situ demonstration of dendritic cell migration from rat intestine to mesenteric lymph nodes: relationships to maturation and role of chemokines | Q28570463 |
| | Abnormal development of secondary lymphoid tissues in lymphotoxin beta-deficient mice | Q28587099 |
| | OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis | Q28589430 |
| | Class switch recombination and hypermutation require activation-induced cytidine deaminase (AID), a potential RNA editing enzyme | Q29547201 |
| | Mesenteric B cells centrally inhibit CD4+ T cell colitis through interaction with regulatory T cell subsets | Q33836834 |
| | Antigen processing and presentation by intestinal epithelial cells - polarity and complexity | Q33846429 |
| | CCR6 mediates dendritic cell localization, lymphocyte homeostasis, and immune responses in mucosal tissue. | Q33904793 |
| | Collaboration of epithelial cells with organized mucosal lymphoid tissues. | Q33955758 |
| | The gastrointestinal ecosystem: a precarious alliance among epithelium, immunity and microbiota | Q34156291 |
| | RelB is required for Peyer's patch development: differential regulation of p52-RelB by lymphotoxin and TNF | Q34167602 |
| | Lymphotoxin beta receptor induces sequential activation of distinct NF-kappa B factors via separate signaling pathways | Q34173731 |
| | IL-12 and Th1 immune responses in human Peyer's patches | Q34232529 |
| | Modulating the intestinal immune system: the role of lymphotoxin and GALT organs | Q34298341 |
| | Defective lymphoid development in mice lacking expression of the common cytokine receptor gamma chain. | Q34307135 |
| | Isolated lymphoid follicles can function as sites for induction of mucosal immune responses | Q34554635 |
| | Peyer's patches are required for oral tolerance to proteins | Q34725322 |
| | The role of CD45+CD4+CD3- cells in lymphoid organ development | Q35005856 |
| | Peyer's patches: organized lymphoid structures for the induction of mucosal immune responses in the intestine | Q35022309 |
| | Concerted action of the chemokine and lymphotoxin system in secondary lymphoid-organ development | Q35084291 |
| | Organogenesis of lymphoid tissues | Q35096187 |
| | Biology of the TRANCE axis | Q35145622 |
| | The impact of CCR7 and CXCR5 on lymphoid organ development and systemic immunity | Q35216957 |
| | Characterisation of mucosal lymphoid aggregates in ulcerative colitis: immune cell phenotype and TcR-gammadelta expression | Q35361010 |
| | The IL-12 family of heterodimeric cytokines: new players in the regulation of T cell responses | Q35582560 |
| | Role of chemokines in the development of secondary and tertiary lymphoid tissues | Q35682757 |
| | 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 |
| | Regulation of IgA synthesis at mucosal surfaces | Q35768869 |
| | Regulatory T cells and mechanisms of immune system control | Q35852343 |
| | Improving M cell mediated transport across mucosal barriers: do certain bacteria hold the keys? | Q35863373 |
| | Use of fluorescence imaging to investigate the structure and function of intestinal M cells. | Q35935149 |
| | Mucosal immunity and tolerance in the elderly | Q35962900 |
| | Surveillance B lymphocytes and mucosal immunoregulation | Q35988828 |
| | Cellular interactions in lymph node development | Q35990072 |
| | Insights into the mechanism of oral tolerance derived from the study of models of mucosal inflammation | Q36024783 |
| | Two gut intraepithelial CD8+ lymphocyte populations with different T cell receptors: a role for the gut epithelium in T cell differentiation | Q36229868 |
| | Regulation of murine lymphokine production in vivo. III. The lymphoid tissue microenvironment exerts regulatory influences over T helper cell function | Q36350855 |
| | Thymic and extrathymic origins of gut intraepithelial lymphocyte populations in mice | Q36363572 |
| | Identification of novel lymphoid tissues in murine intestinal mucosa where clusters of c-kit+ IL-7R+ Thy1+ lympho-hemopoietic progenitors develop | Q36367413 |
| | 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 |
| | Freshly isolated Peyer's patch, but not spleen, dendritic cells produce interleukin 10 and induce the differentiation of T helper type 2 cells | Q36375116 |
| | Chemokine receptor CCR9 contributes to the localization of plasma cells to the small intestine | Q36399163 |
| | Enterocyte expression of interleukin 7 induces development of gammadelta T cells and Peyer's patches | Q36404323 |
| | Differential expression of lectin-binding sites defines mouse intestinal M-cells | Q36697340 |
| | Intestinal villous M cells: an antigen entry site in the mucosal epithelium | Q37647153 |
| | Targeted disruption of LIGHT causes defects in costimulatory T cell activation and reveals cooperation with lymphotoxin beta in mesenteric lymph node genesis | Q38288045 |
| | Antigen transport into Peyer's patches: increased uptake by constant numbers of M cells | Q38584534 |
| | The lymphotoxin-beta receptor induces different patterns of gene expression via two NF-kappaB pathways | Q40696432 |
| | Ligation of MHC class II molecules differentially upregulates TNF beta gene expression in B cell lines of different MHC class II haplotypes | Q40949280 |
| | Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kappa b-inducing kinase | Q40954925 |
| | Alpha 4 beta 7 integrin mediates lymphocyte binding to the mucosal vascular addressin MAdCAM-1. | Q41541656 |
| | 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 |
| | Surface lymphotoxin alpha/beta complex is required for the development of peripheral lymphoid organs | Q42196937 |
| | Morphology of colorectal lymphoid aggregates in cancer, diverticular and inflammatory bowel diseases | Q42471311 |
| | Hapten-induced colitis is associated with colonic patch hypertrophy and T helper cell 2-type responses | Q42944018 |
| | Elimination of colonic patches with lymphotoxin beta receptor-Ig prevents Th2 cell-type colitis | Q43710164 |
| | Critical roles of activation-induced cytidine deaminase in the homeostasis of gut flora | Q44218058 |
| | Lack of oral tolerance in aging is due to sequential loss of Peyer's patch cell interactions | Q44310063 |
| | Analysis of adhesion molecules involved in leukocyte homing into the basolateral pockets of mouse Peyer's patch M cells | Q47326860 |
| | IgA class switch occurs in the organized nasopharynx- and gut-associated lymphoid tissue, but not in the diffuse lamina propria of airways and gut. | Q47644148 |
| | The lymphotoxin beta receptor controls organogenesis and affinity maturation in peripheral lymphoid tissues | Q47713235 |
| | Induction of protective IgA by intestinal dendritic cells carrying commensal bacteria | Q47962035 |
| | Targeting of secretory IgA to Peyer's patch dendritic and T cells after transport by intestinal M cells. | Q51024807 |
| | Murine Peyer's patches favor development of an IL-10-secreting, regulatory T cell population. | Q52012319 |
| | The role of dendritic cells, B cells, and M cells in gut-oriented immune responses. | Q52020473 |
| | Presumptive lymph node organizers are differentially represented in developing mesenteric and peripheral nodes. | Q52087999 |
| | Defective lymphotoxin-beta receptor-induced NF-kappaB transcriptional activity in NIK-deficient mice. | Q52542561 |
| | Visualization of peptide presentation following oral application of antigen in normal and Peyer's patches-deficient mice. | Q52951733 |
| | Postgestational lymphotoxin/lymphotoxin beta receptor interactions are essential for the presence of intestinal B lymphocytes. | Q53971848 |
| | Oral tolerance in humans: failure to suppress an existing immune response by oral antigen administration. | Q53987614 |
| | Role of gut cryptopatches in early extrathymic maturation of intestinal intraepithelial T cells. | Q54758426 |
| P304 | page(s) | 6-21 | |
| P577 | publication date | 2005-08-01 | |
| P1433 | published in | Immunological Reviews | Q15724582 |
| P1476 | title | Organizing a mucosal defense | |
| P478 | volume | 206 | |