| scholarly article | Q13442814 |
| P2093 | author name string | Troy D Randall | |
| Javier Rangel-Moreno | |||
| Damian Carragher | |||
| P2860 | cites work | Retinoid-related orphan receptor gamma (RORgamma) is essential for lymphoid organogenesis and controls apoptosis during thymopoiesis | Q24642725 |
| Follicular B helper T cells express CXC chemokine receptor 5, localize to B cell follicles, and support immunoglobulin production | Q24676570 | ||
| CCR10 expression is a common feature of circulating and mucosal epithelial tissue IgA Ab-secreting cells | Q24684754 | ||
| Multiple exposures to swine barn air induce lung inflammation and airway hyper-responsiveness | Q24814407 | ||
| TRANCE is a TNF family member that regulates dendritic cell and osteoclast function | Q28137948 | ||
| Requirement for RORgamma in thymocyte survival and lymphoid organ development | Q28139666 | ||
| A chemokine-driven positive feedback loop organizes lymphoid follicles | Q28142202 | ||
| Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis | Q28183279 | ||
| A common mucosal chemokine (mucosae-associated epithelial chemokine/CCL28) selectively attracts IgA plasmablasts | Q28184989 | ||
| IgA Fc receptors | Q28202739 | ||
| CCL9 is secreted by the follicle-associated epithelium and recruits dome region Peyer's patch CD11b+ dendritic cells | Q28205502 | ||
| An essential function for the nuclear receptor RORgamma(t) in the generation of fetal lymphoid tissue inducer cells | Q28235728 | ||
| Chemokine receptor CCR7 guides T cell exit from peripheral tissues and entry into afferent lymphatics | Q28268587 | ||
| 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 | ||
| The nature of small-airway obstruction in chronic obstructive pulmonary disease | Q29618682 | ||
| Bronchoscopy in the intensive care unit (ICU). | Q33504077 | ||
| Lymphoid neo-organogenesis: lymphotoxin's role in inflammation and development | Q33735993 | ||
| Intranasal immunization with cytotoxic T-lymphocyte epitope peptide and mucosal adjuvant cholera toxin: selective augmentation of peptide-presenting dendritic cells in nasal mucosa-associated lymphoid tissue | Q33769366 | ||
| Lymphotoxin-alpha-deficient mice can clear a productive infection with murine gammaherpesvirus 68 but fail to develop splenomegaly or lymphocytosis | Q33800151 | ||
| Development of peripheral lymphoid organs and natural killer cells depends on the helix-loop-helix inhibitor Id2. | Q33854381 | ||
| Evaluation of trivalent, live, cold-adapted (CAIV-T) and inactivated (TIV) influenza vaccines in prevention of virus infection and illness following challenge of adults with wild-type influenza A (H1N1), A (H3N2), and B viruses | Q33882108 | ||
| Bronchus-associated lymphoid tissue (BALT) is not present in the normal adult lung but in different diseases | Q33946194 | ||
| Generation of gut-homing IgA-secreting B cells by intestinal dendritic cells | Q34000967 | ||
| Intestinal IgA synthesis: regulation of front-line body defences | Q34168492 | ||
| Transcriptional profiling identifies Id2 function in dendritic cell development | Q34179059 | ||
| Lymphoid neogenesis: de novo formation of lymphoid tissue in chronic inflammation through expression of homing chemokines. | Q34191599 | ||
| Lymphocyte homing to bronchus-associated lymphoid tissue (BALT) is mediated by L-selectin/PNAd, alpha4beta1 integrin/VCAM-1, and LFA-1 adhesion pathways | Q34198405 | ||
| Chemokines determine local lymphoneogenesis and a reduction of circulating CXCR4+ T and CCR7 B and T lymphocytes in thyroid autoimmune diseases. | Q34204159 | ||
| Selective imprinting of gut-homing T cells by Peyer's patch dendritic cells | Q34211233 | ||
| NALT- versus Peyer's-patch-mediated mucosal immunity | Q34345343 | ||
| Bronchus associated lymphoid tissue (BALT) in human lung: its distribution in smokers and non-smokers | Q34348834 | ||
| Lymphotoxin alpha/beta and tumor necrosis factor are required for stromal cell expression of homing chemokines in B and T cell areas of the spleen | Q34488105 | ||
| Interaction of mature CD3+CD4+ T cells with dendritic cells triggers the development of tertiary lymphoid structures in the thyroid. | Q34568588 | ||
| Inducible bronchus-associated lymphoid tissue (iBALT) in patients with pulmonary complications of rheumatoid arthritis. | Q34586903 | ||
| Regulatory T cells interfere with the development of bronchus-associated lymphoid tissue | Q34610191 | ||
| Chemokines and the homing of dendritic cells to the T cell areas of lymphoid organs | Q34756572 | ||
| Resident lung antigen-presenting cells have the capacity to promote Th2 T cell differentiation in situ | Q34826220 | ||
| Regulation of spleen white pulp structure and function by lymphotoxin | Q34982817 | ||
| The role of CD45+CD4+CD3- cells in lymphoid organ development | Q35005856 | ||
| Role of T and NK cells and IL7/IL7r interactions during neonatal maturation of lymph nodes | Q35037300 | ||
| Lymphotoxin plays a crucial role in the development and function of nasal-associated lymphoid tissue through regulation of chemokines and peripheral node addressin | Q35083503 | ||
| Ectopic Germinal Center Formation in Rheumatoid Synovitis | Q35119934 | ||
| Organogenesis of peripheral lymphoid organs. | Q35216947 | ||
| Regulation of secondary lymphoid organ development by the nuclear factor-kappaB signal transduction pathway | Q35216951 | ||
| Lymphoid microenvironment in the gut for immunoglobulin A and inflammation. | Q35216967 | ||
| Targeted delivery of antigen to hamster nasal lymphoid tissue with M-cell-directed lectins | Q35556883 | ||
| Lymphotoxin beta receptor signaling is required for inflammatory lymphangiogenesis in the thyroid. | Q35691047 | ||
| Regulation of IgA synthesis at mucosal surfaces | Q35768869 | ||
| Current status of live attenuated influenza virus vaccine in the US. | Q35784263 | ||
| Pediatric AIDS-associated lymphocytic interstitial pneumonia and pulmonary arterio-occlusive disease: role of VCAM-1/VLA-4 adhesion pathway and human herpesviruses | Q35786936 | ||
| Specific History of Heterologous Virus Infections Determines Anti-Viral Immunity and Immunopathology in the Lung | Q35792192 | ||
| Lymphoid tissue homing chemokines are expressed in chronic inflammation | Q35810009 | ||
| Coexpression of the chemokines ELC and SLC by T zone stromal cells and deletion of the ELC gene in the plt/plt mouse | Q35822641 | ||
| Commitment to natural killer cells requires the helix-loop-helix inhibitor Id2 | Q35866730 | ||
| Citrullinated proteins in rheumatoid arthritis. | Q35969051 | ||
| Cellular interactions in lymph node development | Q35990072 | ||
| The response of rat bronchus-associated lymphoid tissue to local antigenic challenge | Q36091228 | ||
| Chemokine-mediated control of T cell traffic in lymphoid and peripheral tissues. | Q36097429 | ||
| Peptidylarginine deiminase type 4, anticitrullinated peptide antibodies, and rheumatoid arthritis. | Q36127494 | ||
| Independent signals regulate development of primary and secondary follicle structure in spleen and mesenteric lymph node | Q36157845 | ||
| Two sides of a cellular coin: CD4(+)CD3- cells regulate memory responses and lymph-node organization | Q36202186 | ||
| Bronchus- and nasal-associated lymphoid tissues | Q36209686 | ||
| Follicular B helper T cells in antibody responses and autoimmunity. | Q36302329 | ||
| The role of nasopharyngeal lymphoid tissue | Q36307154 | ||
| Chronic inflammation caused by lymphotoxin is lymphoid neogenesis | Q36366337 | ||
| CXC chemokine receptor 5 expression defines follicular homing T cells with B cell helper function | Q36368291 | ||
| 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 | ||
| Subspecialization of CXCR5+ T cells: B helper activity is focused in a germinal center-localized subset of CXCR5+ T cells | Q36368917 | ||
| Isotype-specific selection of high affinity memory B cells in nasal-associated lymphoid tissue | Q36369657 | ||
| Splenic T zone development is B cell dependent | Q36369671 | ||
| Ectopic LTαβ Directs Lymphoid Organ Neogenesis with Concomitant Expression of Peripheral Node Addressin and a HEV-restricted Sulfotransferase | Q36370988 | ||
| Chemokine requirements for B cell entry to lymph nodes and Peyer's patches. | Q36371105 | ||
| Lymphotoxin-alpha (LTalpha) supports development of splenic follicular structure that is required for IgG responses | Q36377326 | ||
| Interleukin-5 expression in the lung epithelium of transgenic mice leads to pulmonary changes pathognomonic of asthma | Q36377337 | ||
| CD4+CD3- cells regulate the organization of lymphoid tissue and T-cell memory for antibody responses | Q36380502 | ||
| Osteoclast differentiation independent of the TRANCE-RANK-TRAF6 axis | Q36402845 | ||
| Rapid interferon gamma-dependent clearance of influenza A virus and protection from consolidating pneumonitis in nitric oxide synthase 2-deficient mice | Q36404225 | ||
| Lymphoid neogenesis in chronic inflammatory diseases. | Q36405080 | ||
| Development of T lymphocytes in the nasal-associated lymphoid tissue (NALT) from growing Wistar rats | Q36509917 | ||
| CCR6 and CCL20: partners in intestinal immunity and lymphorganogenesis | Q36631416 | ||
| Dysregulated LIGHT expression on T cells mediates intestinal inflammation and contributes to IgA nephropathy | Q36752354 | ||
| Differential regulation of CCL21 in lymphoid/nonlymphoid tissues for effectively attracting T cells to peripheral tissues | Q36991047 | ||
| Structure and function of bronchus-associated lymphoid tissue (BALT). | Q38656795 | ||
| On the development and immune reactivity of the so-called bronchus-associated lymphoid tissue (BALT) in rabbits and humans: experimental and anatomoclinical observations | Q39848023 | ||
| Production of IgA monoclonal antibody against Shiga toxin binding subunits employing nasal-associated lymphoid tissue | Q40403001 | ||
| Stimulation of bronchus-associated lymphoid tissue in rats by repeated inhalation of aerosolized lipopeptide MALP-2. | Q40585880 | ||
| Lymphotoxin pathway directs thymic Aire expression | Q40630236 | ||
| The lymphotoxin-beta receptor induces different patterns of gene expression via two NF-kappaB pathways | Q40696432 | ||
| Nasal-associated lymphoid tissue is a mucosal inductive site for virus-specific humoral and cellular immune responses | Q40753138 | ||
| Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kappa b-inducing kinase | Q40954925 | ||
| Effects of microbial stimulation on the number, size and activity of bronchus-associated lymphoid tissue (BALT) structures in the pig | Q41167882 | ||
| Lymphotoxin-alpha-deficient and TNF receptor-I-deficient mice define developmental and functional characteristics of germinal centers | Q41492256 | ||
| The Peyer's patch high endothelial receptor for lymphocytes, the mucosal vascular addressin, is induced on a murine endothelial cell line by tumor necrosis factor-alpha and IL-1. | Q41514338 | ||
| Alpha 4 beta 7 integrin mediates lymphocyte binding to the mucosal vascular addressin MAdCAM-1. | Q41541656 | ||
| Chemokine Up-regulation and activated T cell attraction by maturing dendritic cells | Q41648813 | ||
| Thyroid autoimmune disease: demonstration of thyroid antigen-specific B cells and recombination-activating gene expression in chemokine-containing active intrathyroidal germinal centers | Q41873772 | ||
| Molecular basis for hematopoietic/mesenchymal interaction during initiation of Peyer's patch organogenesis. | Q42076869 | ||
| An early CD4+ T cell-dependent immunoglobulin A response to influenza infection in the absence of key cognate T-B interactions | Q42105732 | ||
| Surface lymphotoxin alpha/beta complex is required for the development of peripheral lymphoid organs | Q42196937 | ||
| Lymphotoxin-beta receptor signaling is required for the homeostatic control of HEV differentiation and function | Q42486404 | ||
| Nasal lymphoid tissue in the rat. | Q42498543 | ||
| Development of bronchus associated lymphoid tissue (BALT) in human lung disease: a normal host defence mechanism awaiting therapeutic exploitation? | Q42507235 | ||
| Mature follicular dendritic cell networks depend on expression of lymphotoxin beta receptor by radioresistant stromal cells and of lymphotoxin beta and tumor necrosis factor by B cells | Q42753323 | ||
| Safety and immunogenicity of low and high doses of trivalent live cold-adapted influenza vaccine administered intranasally as drops or spray to healthy children | Q43152415 | ||
| Is the bronchus-associated lymphoid tissue (BALT) an integral structure of the lung in normal mammals, including humans? | Q43453033 | ||
| Antibody-forming cells in the nasal-associated lymphoid tissue during primary influenza virus infection | Q43654251 | ||
| A novel antigen is common to the dome epithelium of gut- and bronchus-associated lymphoid tissues | Q43714835 | ||
| In situ class switching and differentiation to IgA-producing cells in the gut lamina propria | Q43776134 | ||
| Cutting edge: organogenesis of nasal-associated lymphoid tissue (NALT) occurs independently of lymphotoxin-alpha (LT alpha) and retinoic acid receptor-related orphan receptor-gamma, but the organization of NALT is LT alpha dependent | Q43860707 | ||
| Changes in lymphocyte subsets in the bronchus-associated lymphoid tissue of goats naturally infected with different Mycoplasma species | Q44885467 | ||
| Germinal center dark and light zone organization is mediated by CXCR4 and CXCR5. | Q44999948 | ||
| Role of inducible bronchus associated lymphoid tissue (iBALT) in respiratory immunity | Q45018410 | ||
| Cytokine mRNAs in the nasal-associated lymphoid tissue during influenza virus infection and nasal vaccination | Q45745329 | ||
| Intrinsic lymphotoxin-beta receptor requirement for homeostasis of lymphoid tissue dendritic cells. | Q46496003 | ||
| Bronchial lymphoid tissue. I. Morphologic characteristics | Q46542725 | ||
| Cellular basis of ectopic germinal center formation and autoantibody production in the target organ of patients with Sjögren's syndrome | Q47389814 | ||
| 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 | ||
| 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 | ||
| Role of CXC chemokine ligand 13, CC chemokine ligand (CCL) 19, and CCL21 in the organization and function of nasal-associated lymphoid tissue | Q47714667 | ||
| IgA antibody-forming cell responses in the nasal-associated lymphoid tissue of mice vaccinated by intranasal, intravenous and/or subcutaneous administration | Q47773345 | ||
| Blocking lymphotoxin-beta receptor activation diminishes inflammation via reduced mucosal addressin cell adhesion molecule-1 (MAdCAM-1) expression and leucocyte margination in chronic DSS-induced colitis | Q47927327 | ||
| Intranasal immunization with polymer-grafted microparticles activates the nasal-associated lymphoid tissue and draining lymph nodes | Q48003924 | ||
| IgA production without mu or delta chain expression in developing B cells | Q50114613 | ||
| The spleen and organized lymph nodes are not essential for the development of gut-induced mucosal immune responses in lymphotoxin-alpha deficient mice | Q50128939 | ||
| Nasal-associated lymphoid tissue is an inductive site for rat tear IgA antibody responses | Q50194063 | ||
| Synchrony of high endothelial venules and lymphatic vessels revealed by immunization. | Q50476530 | ||
| Bronchial-associated lymphoid tissue (BALT) response to airway challenge with cigarette smoke, bovine antigen and anti-pulmonary serum | Q50792018 | ||
| Intracerebral expression of CXCL13 and BAFF is accompanied by formation of lymphoid follicle-like structures in the meninges of mice with relapsing experimental autoimmune encephalomyelitis. | Q51027456 | ||
| 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 | ||
| Nasal-associated lymphoid tissue (NALT): frequency and localization in young children. | Q51642503 | ||
| Membranous cells in nasal-associated lymphoid tissue: a portal of entry for the respiratory mucosal pathogen group A streptococcus. | Q51658028 | ||
| Lymphotoxin-alpha-deficient mice make delayed, but effective, T and B cell responses to influenza. | Q51700316 | ||
| Development of bronchus-associated lymphoid tissue in chronic hypersensitivity pneumonitis. | Q52035275 | ||
| I kappa B kinase complex alpha kinase activity controls chemokine and high endothelial venule gene expression in lymph nodes and nasal-associated lymphoid tissue. | Q52085932 | ||
| Presumptive lymph node organizers are differentially represented in developing mesenteric and peripheral nodes. | Q52087999 | ||
| Developmental study of immunocompetent cells in the bronchus-associated lymphoid tissue (BALT) from Wistar rats. | Q52168040 | ||
| Generation of polymeric immunoglobulin receptor-deficient mouse with marked reduction of secretory IgA. | Q52536939 | ||
| Site of antigen delivery can influence T cell priming: pulmonary environment promotes preferential Th2-type differentiation. | Q52920487 | ||
| Mycobacterium tuberculosis triggers formation of lymphoid structure in murine lungs. | Q52928677 | ||
| Cutting edge: Uniqueness of lymphoid chemokine requirement for the initiation and maturation of nasopharynx-associated lymphoid tissue organogenesis. | Q53588599 | ||
| Specific antibody formation in mucosa associated lymphoid tissue after intratracheal and intra-intestinal administration of TNP-KLH; differences between BALT and GALT. | Q53699463 | ||
| Study of bronchus-associated lymphoid tissue in patients with diffuse panbronchiolitis. | Q54061360 | ||
| BALT development and augmentation of hyperoxic lung injury in mice deficient in NQO1 and NQO2. | Q54603321 | ||
| Primary induction of CD4 T cell responses in nasal associated lymphoid tissue during group A streptococcal infection. | Q54701595 | ||
| Distinct Gene Expression Profiles Characterize Cellular Phenotypes of Follicle-Associated Epithelium and M Cells | Q57273143 | ||
| Superior Relative Efficacy of Live Attenuated Influenza Vaccine Compared With Inactivated Influenza Vaccine in Young Children With Recurrent Respiratory Tract Infections | Q59397235 | ||
| Characterization of a B220+ Lymphoid Cell Subpopulation with Immune Modulatory Functions in Nasal-Associated Lymphoid Tissues | Q61689662 | ||
| Sustained interleukin‐6 signalling leads to the development of lymphoid organ‐like structures in the lung | Q64377813 | ||
| Nasopharyngeal-associated lymphoreticular tissue (NALT) immunity: fimbriae-specific Th1 and Th2 cell-regulated IgA responses for the inhibition of bacterial attachment to epithelial cells and subsequent inflammatory cytokine production | Q64449832 | ||
| Characterization of the inflammatory reaction in the peripheral airways of cigarette smokers using immunocytochemistry | Q68083065 | ||
| Lymphoid and non-lymphoid cells in nasal-associated lymphoid tissue (NALT) in the rat. An immuno- and enzyme-histochemical study | Q68780778 | ||
| Anti-TNP-forming cells in bronchus-associated lymphoid tissue (BALT) and paratracheal lymph node (PTLN) of the rat after intratracheal priming and boosting with TNP-KLH | Q68865489 | ||
| Bronchial lymphoid tissue. II. Functional characterisitics | Q69272970 | ||
| Specific antibody-forming cells in bronchus-associated lymphoid tissue (BALT) and lung of the rat after intratracheal challenge with horseradish peroxidase | Q69872682 | ||
| Histological changes in rat bronchus-associated lymphoid tissue after administration of five different antigens | Q69901994 | ||
| Gut- and bronchus-associated lymphoid tissue | Q70224535 | ||
| Development of bronchus associated lymphoid tissue (BALT) in the rat, with special reference to T- and B-cells | Q70985369 | ||
| Role of lymphotoxin and the type I TNF receptor in the formation of germinal centers | Q71095987 | ||
| The immunological architecture of B-lymphocyte aggregates in cryptogenic fibrosing alveolitis | Q71459210 | ||
| Absence of lymph nodes in lymphotoxin-alpha(LT alpha)-deficient mice is due to abnormal organ development, not defective lymphocyte migration | Q71798712 | ||
| Cellular distribution of bronchus-associated lymphoid tissue in rheumatoid arthritis | Q71907067 | ||
| Abnormal organisation of the splenic marginal zone and the correlated leukocytosis in lymphotoxin-alpha and tumor necrosis factor alpha double deficient mice | Q73017940 | ||
| "Lymphoid" chemokine messenger RNA expression by epithelial cells in the chronic inflammatory lesion of the salivary glands of Sjögren's syndrome patients: possible participation in lymphoid structure formation | Q73565836 | ||
| Compartmentalization of Peyer's patch anlagen before lymphocyte entry | Q73586921 | ||
| The presence of specialized epithelial cells on the bronchus-associated lymphoid tissue (BALT) in the mouse | Q73688373 | ||
| Unique functions of CD11b+, CD8 alpha+, and double-negative Peyer's patch dendritic cells | Q73720806 | ||
| Comparison of murine nasal-associated lymphoid tissue and Peyer's patches | Q73833235 | ||
| Developing lymph nodes collect CD4+CD3- LTbeta+ cells that can differentiate to APC, NK cells, and follicular cells but not T or B cells | Q73838320 | ||
| Ultrastructural study on the follicle-associated epithelium of nasal-associated lymphoid tissue in specific pathogen-free (SPF) and conventional environment-adapted (SPF-CV) rats | Q73896417 | ||
| A primitive T cell-independent mechanism of intestinal mucosal IgA responses to commensal bacteria | Q73919528 | ||
| Evidence of M cells as portals of entry for antigens in the nasopharyngeal lymphoid tissue of humans | Q74077692 | ||
| Signaling via LTbetaR on the lamina propria stromal cells of the gut is required for IgA production | Q74082070 | ||
| Distribution of T-cell subsets and immunoglobulin-containing cells in nasal-associated lymphoid tissue (NALT) of chickens | Q74236692 | ||
| Essential role of IL-7 receptor alpha in the formation of Peyer's patch anlage | Q74261728 | ||
| The CXC chemokine murine monokine induced by IFN-gamma (CXC chemokine ligand 9) is made by APCs, targets lymphocytes including activated B cells, and supports antibody responses to a bacterial pathogen in vivo | Q74500133 | ||
| Initiation of NALT organogenesis is independent of the IL-7R, LTbetaR, and NIK signaling pathways but requires the Id2 gene and CD3(-)CD4(+)CD45(+) cells | Q74548133 | ||
| Glycoconjugate expression in follicle-associated epithelium (FAE) covering the nasal-associated lymphoid tissue (NALT) in specific pathogen-free and conventional rats | Q74584600 | ||
| HIV mucosal vaccine: nasal immunization with rBCG-V3J1 induces a long term V3J1 peptide-specific neutralizing immunity in Th1- and Th2-deficient conditions | Q77137007 | ||
| Ectopic expression of the B cell-attracting chemokine BCA-1 (CXCL13) on endothelial cells and within lymphoid follicles contributes to the establishment of germinal center-like structures in Sjögren's syndrome | Q77179303 | ||
| Nasal immune system: distinctive Th0 and Th1/Th2 type environments in murine nasal-associated lymphoid tissues and nasal passage, respectively | Q77530752 | ||
| IL-7 receptor alpha+ CD3(-) cells in the embryonic intestine induces the organizing center of Peyer's patches | Q77756301 | ||
| Nasal immunization induces Haemophilus influenzae-specific Th1 and Th2 responses with mucosal IgA and systemic IgG antibodies for protective immunity | Q77828306 | ||
| Peyer's patch organogenesis as a programmed inflammation: a hypothetical model | Q77903801 | ||
| 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 | Q78025404 | ||
| CD4+CD3- cells induce Peyer's patch development: role of alpha4beta1 integrin activation by CXCR5 | Q78298267 | ||
| Persistence and responsiveness of immunologic memory in the absence of secondary lymphoid organs | Q79257160 | ||
| Recruitment and activation of naive T cells in the islets by lymphotoxin beta receptor-dependent tertiary lymphoid structure | Q80171529 | ||
| Involvement of dendritic cell subsets in the induction of oral tolerance and immunity | Q81341599 | ||
| The membrane-bound chemokine CXCL16 expressed on follicle-associated epithelium and M cells mediates lympho-epithelial interaction in GALT | Q81645766 | ||
| Frequency and potential cause of bronchus-associated lymphoid tissue in fetal lungs | Q81826288 | ||
| P433 | issue | 1 | |
| P921 | main subject | lymphoid tissue | Q3529455 |
| P304 | page(s) | 13-28 | |
| P577 | publication date | 2007-01-01 | |
| P1433 | published in | Inmunologia (Barcelona, Spain : 1987) | Q27722465 |
| P1476 | title | Role of lymphotoxin and homeostatic chemokines in the development and function of local lymphoid tissues in the respiratory tract | |
| P478 | volume | 26 |
| Q33694988 | A Unique Cellular and Molecular Microenvironment Is Present in Tertiary Lymphoid Organs of Patients with Spontaneous Prostate Cancer Regression |
| Q33618911 | Bronchus-associated lymphoid tissue (BALT) and survival in a vaccine mouse model of tularemia |
| Q38953303 | Lymphotoxin in physiology of lymphoid tissues - Implication for antiviral defense |
| Q36246200 | The NS1 protein of influenza A virus blocks RIG-I-mediated activation of the noncanonical NF-κB pathway and p52/RelB-dependent gene expression in lung epithelial cells |
| Q38903995 | The formation and function of tertiary lymphoid follicles in chronic pulmonary inflammation |
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