| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Nancy Ruddle | Q63662154 |
| P2093 | author name string | Eitan M Akirav | |
| P2860 | cites work | RANK is essential for osteoclast and lymph node development | Q24598872 |
| Lymphoid tissue inducer-like cells are an innate source of IL-17 and IL-22 | Q24648620 | ||
| Cytotoxicity mediated by soluble antigen and lymphocytes in delayed hypersensitivity. 3. Analysis of mechanism | Q24679391 | ||
| Specific remodeling of splenic architecture by cytomegalovirus. | Q25257147 | ||
| The orphan nuclear receptor RORgammat directs the differentiation program of proinflammatory IL-17+ T helper cells | Q27860620 | ||
| A chemokine-driven positive feedback loop organizes lymphoid follicles | Q28142202 | ||
| The role of the nuclear hormone receptor RORγt in the development of lymph nodes and Peyer's patches | Q28206376 | ||
| An essential function for the nuclear receptor RORgamma(t) in the generation of fetal lymphoid tissue inducer cells | Q28235728 | ||
| Structure and function of the spleen | Q28264813 | ||
| A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen | Q28300225 | ||
| 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 | ||
| Tyrosine kinase receptor RET is a key regulator of Peyer's patch organogenesis | Q28511182 | ||
| Lymphatic endothelial cell identity is reversible and its maintenance requires Prox1 activity | Q28584887 | ||
| Overlapping roles of CXCL13, interleukin 7 receptor alpha, and CCR7 ligands in lymph node development | Q28585776 | ||
| 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 | ||
| OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis | Q28589430 | ||
| Prox1 induces lymphatic endothelial differentiation via integrin alpha9 and other signaling cascades | Q30479201 | ||
| Chemokines and cell migration in secondary lymphoid organs | Q33807114 | ||
| Development of peripheral lymphoid organs and natural killer cells depends on the helix-loop-helix inhibitor Id2. | Q33854381 | ||
| Anatomical basis of tolerance and immunity to intestinal antigens | Q33965210 | ||
| Lymphocyte homing to bronchus-associated lymphoid tissue (BALT) is mediated by L-selectin/PNAd, alpha4beta1 integrin/VCAM-1, and LFA-1 adhesion pathways | Q34198405 | ||
| Defective lymphoid development in mice lacking expression of the common cytokine receptor gamma chain. | Q34307135 | ||
| 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 | ||
| Isolated lymphoid follicles can function as sites for induction of mucosal immune responses | Q34554635 | ||
| Development of secondary lymphoid organs | Q34764895 | ||
| 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 | ||
| Organogenesis of lymphoid tissues | Q35096187 | ||
| Dendritic Cell Function in Vivo during the Steady State: A Role in Peripheral Tolerance | Q35119879 | ||
| Regulation of secondary lymphoid organ development by the nuclear factor-kappaB signal transduction pathway | Q35216951 | ||
| Lymphatic vasculature development | Q35620076 | ||
| Studies on the structure and permeability of the microvasculature in normal rat lymph nodes | Q35878286 | ||
| Two sides of a cellular coin: CD4(+)CD3- cells regulate memory responses and lymph-node organization | Q36202186 | ||
| Organizing a mucosal defense | Q36209682 | ||
| A new mutation, aly, that induces a generalized lack of lymph nodes accompanied by immunodeficiency in mice | Q72753495 | ||
| Three distinctive steps in Peyer's patch formation of murine embryo | Q73312318 | ||
| Isolated lymphoid follicle formation is inducible and dependent upon lymphotoxin-sufficient B lymphocytes, lymphotoxin beta receptor, and TNF receptor I function | Q73419615 | ||
| Lymphoid precursors in intestinal cryptopatches express CCR6 and undergo dysregulated development in the absence of CCR6 | Q73827790 | ||
| 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 | ||
| Essential role of IL-7 receptor alpha in the formation of Peyer's patch anlage | Q74261728 | ||
| 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 | ||
| Different cytokines induce surface lymphotoxin-alphabeta on IL-7 receptor-alpha cells that differentially engender lymph nodes and Peyer's patches | Q78651212 | ||
| Lymphotoxin-independent expression of TNF-related activation-induced cytokine by stromal cells in cryptopatches, isolated lymphoid follicles, and Peyer's patches | Q80178390 | ||
| Intestinal cryptopatch formation in mice requires lymphotoxin alpha and the lymphotoxin beta receptor | Q81111365 | ||
| Conduit for privileged communications in the lymph node | Q81304835 | ||
| Novel tumor necrosis factor-knockout mice that lack Peyer's patches | Q81653276 | ||
| Regulation of peripheral lymph node genesis by the tumor necrosis factor family member TRANCE | Q36368551 | ||
| Lymph-borne chemokines and other low molecular weight molecules reach high endothelial venules via specialized conduits while a functional barrier limits access to the lymphocyte microenvironments in lymph node cortex | Q36368559 | ||
| The CCR7 ligand elc (CCL19) is transcytosed in high endothelial venules and mediates T cell recruitment | Q36369301 | ||
| Ectopic LTαβ Directs Lymphoid Organ Neogenesis with Concomitant Expression of Peripheral Node Addressin and a HEV-restricted Sulfotransferase | Q36370988 | ||
| Lymphoid organ development: from ontogeny to neogenesis | Q36426808 | ||
| Development and function of the mammalian spleen. | Q36709430 | ||
| Th17 cell differentiation: the long and winding road | Q37133442 | ||
| A developmental switch in lymphocyte homing receptor and endothelial vascular addressin expression regulates lymphocyte homing and permits CD4+ CD3- cells to colonize lymph nodes | Q37307203 | ||
| Targeted disruption of LIGHT causes defects in costimulatory T cell activation and reveals cooperation with lymphotoxin beta in mesenteric lymph node genesis | Q38288045 | ||
| The conduit system transports soluble antigens from the afferent lymph to resident dendritic cells in the T cell area of the lymph node | Q38459394 | ||
| Organizer-like reticular stromal cell layer common to adult secondary lymphoid organs | Q39926763 | ||
| LTbetaR signaling induces cytokine expression and up-regulates lymphangiogenic factors in lymph node anlagen | Q39986041 | ||
| Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kappa b-inducing kinase | Q40954925 | ||
| Lymphotoxin alpha3 induces chemokines and adhesion molecules: insight into the role of LT alpha in inflammation and lymphoid organ development | Q40986515 | ||
| Lymphotoxin beta receptor triggering induces activation of the nuclear factor kappaB transcription factor in some cell types | Q41159609 | ||
| RANK signals from CD4(+)3(-) inducer cells regulate development of Aire-expressing epithelial cells in the thymic medulla | Q41868543 | ||
| Lymphotoxin-beta receptor signaling is required for the homeostatic control of HEV differentiation and function | Q42486404 | ||
| Cytotoxicity mediated by soluble antigen and lymphocytes in delayed hypersensitivity. II. Correlation of the in vitro response with skin reactivity | Q42775143 | ||
| The histogenesis of lymph nodes in rat and rabbit | Q43713709 | ||
| 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 | ||
| Differential roles of interleukin-17A and -17F in host defense against mucoepithelial bacterial infection and allergic responses. | Q44894318 | ||
| MAdCAM-1 expressing sacral lymph node in the lymphotoxin beta-deficient mouse provides a site for immune generation following vaginal herpes simplex virus-2 infection | Q45611482 | ||
| Human fetal lymphoid tissue-inducer cells are interleukin 17-producing precursors to RORC+ CD127+ natural killer-like cells | Q46231038 | ||
| 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 | ||
| Synchrony of high endothelial venules and lymphatic vessels revealed by immunization. | Q50476530 | ||
| 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 | ||
| Distinct activities of stromal cells involved in the organogenesis of lymph nodes and Peyer's patches. | Q51981354 | ||
| Lymphotoxin a-dependent and -independent signals regulate stromal organizer cell homeostasis during lymph node organogenesis. | Q51984858 | ||
| Ectopic lymphoid-organ development occurs through interleukin 7-mediated enhanced survival of lymphoid-tissue-inducer cells. | Q51985115 | ||
| Inducible lymphoid tissues in the adult gut: recapitulation of a fetal developmental pathway? | Q52051919 | ||
| Induction of secondary and tertiary lymphoid structures in the skin. | Q52085787 | ||
| 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 defects of lymphoid cells in Jak3 kinase-deficient mice. | Q52204302 | ||
| Restoration of lymphoid organ integrity through the interaction of lymphoid tissue-inducer cells with stroma of the T cell zone. | Q52586488 | ||
| Cutting edge: Uniqueness of lymphoid chemokine requirement for the initiation and maturation of nasopharynx-associated lymphoid tissue organogenesis. | Q53588599 | ||
| Lymphocyte Cytotoxicity in vitro: Activation and Release of a Cytotoxic Factor | Q59095839 | ||
| Phenotypic differences between Th1 and Th17 cells and negative regulation of Th1 cell differentiation by IL-17 | Q62735747 | ||
| Function of CD4+CD3- cells in relation to B- and T-zone stroma in spleen | Q63346578 | ||
| TNF and lymphotoxin beta cooperate in the maintenance of secondary lymphoid tissue microarchitecture but not in the development of lymph nodes | Q63968518 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 2205-2212 | |
| P577 | publication date | 2009-08-01 | |
| P1433 | published in | Journal of Immunology | Q3521441 |
| P1476 | title | Secondary lymphoid organs: responding to genetic and environmental cues in ontogeny and the immune response | |
| P478 | volume | 183 |
| Q26851559 | A role for Th17 cells in the regulation of tertiary lymphoid follicles |
| Q34997755 | An important role of lymphatic vessel activation in limiting acute inflammation |
| Q64056538 | Assessment of the Live Attenuated and Wild-Type -Induced Immune Gene Expression and Langerhans-Like Cell Profiles in the Immune-Related Organs of Catfish |
| Q36431033 | Autotaxin through lysophosphatidic acid stimulates polarization, motility, and transendothelial migration of naive T cells |
| Q91974136 | B cell memory: building two walls of protection against pathogens |
| Q92283518 | Biological characteristics of transcription factor RelB in different immune cell types: implications for the treatment of multiple sclerosis |
| Q39595063 | CCR5 blockade combined with cyclosporine A attenuates liver GVHD by impairing T cells function |
| Q34790016 | CCR7 expressing mesenchymal stem cells potently inhibit graft-versus-host disease by spoiling the fourth supplemental Billingham's tenet |
| Q39027200 | CCR7 guides migration of mesenchymal stem cell to secondary lymphoid organs: a novel approach to separate GvHD from GvL effect |
| Q39675353 | CLEC-2 is required for development and maintenance of lymph nodes. |
| Q35163486 | CXCL13 responsiveness but not CXCR5 expression by late transitional B cells initiates splenic white pulp formation |
| Q41024037 | Cathepsin S Is Involved in Th17 Differentiation Through the Upregulation of IL-6 by Activating PAR-2 after Systemic Exposure to Lipopolysaccharide from Porphyromonas gingivalis |
| Q35156132 | Characterization of Toll-like receptor-4 (TLR-4) in the spleen and thymus of Swiss albino mice and its modulation in experimental endotoxemia |
| Q30497147 | Characterization of mononuclear phagocytic cells in medaka fish transgenic for a cxcr3a:gfp reporter |
| Q99630951 | Chronic lung allograft dysfunction post-lung transplantation: The era of bronchiolitis obliterans syndrome and restrictive allograft syndrome |
| Q90620255 | Detection of amastigotes and histopathological alterations in the thymus of Leishmania infantum-infected dogs |
| Q35235833 | Distinct developmental requirements for isolated lymphoid follicle formation in the small and large intestine: RANKL is essential only in the small intestine. |
| Q47412765 | Effects of carbon monoxide on early dysfunction and microangiopathy following GalT-KO porcine pulmonary xenotransplantation in cynomolgus monkeys |
| Q38036894 | Engineering approaches to immunotherapy. |
| Q39075966 | Fat-Associated Lymphoid Clusters in Inflammation and Immunity |
| Q42392661 | Follicular dendritic cells, conduits, lymphatic vessels, and high endothelial venules in tertiary lymphoid organs: Parallels with lymph node stroma |
| Q90212551 | Friend or Foe: The Protective and Pathological Roles of Inducible Bronchus-Associated Lymphoid Tissue in Pulmonary Diseases |
| Q35533807 | Gene, environment, microbiome and mucosal immune tolerance in rheumatoid arthritis |
| Q38297557 | Harnessing biomaterials to engineer the lymph node microenvironment for immunity or tolerance. |
| Q37812388 | Helicobacter pyloriand its effect on innate and adaptive immunity: new insights and vaccination strategies |
| Q85331942 | High endothelial venules through a transcriptomics lens |
| Q82262627 | Human immune system mice: current potential and limitations for translational research on human antibody responses |
| Q39021513 | IL-17, a new kid on the block of tertiary lymphoid organs |
| Q90696181 | IL-4 promotes stromal cell expansion and is critical for development of a type-2, but not a type 1 immune response |
| Q34025272 | Immunoglobulin responses at the mucosal interface. |
| Q36038434 | Impaired sense of smell and altered olfactory system in RAG-1(-∕-) immunodeficient mice |
| Q40693590 | Implications of NOVA1 suppression within the microenvironment of gastric cancer: association with immune cell dysregulation |
| Q35882546 | Inflammation-induced formation of fat-associated lymphoid clusters |
| Q37948123 | LTβR and CD40: working together in dendritic cells to optimize immune responses. |
| Q35685422 | Lymph node hypertrophy following Leishmania major infection is dependent on TLR9. |
| Q37602241 | Lymphatic vessels and tertiary lymphoid organs |
| Q36823937 | Lymphotoxin network pathways shape the tumor microenvironment |
| Q41902336 | Lymphotoxin-sensitive microenvironments in homeostasis and inflammation. |
| Q37257195 | Lymphotoxin-β receptor signaling through NF-κB2-RelB pathway reprograms adipocyte precursors as lymph node stromal cells |
| Q38673425 | Mechanisms involved in triggering rheumatoid arthritis |
| Q38068182 | Mesenchymal cell differentiation during lymph node organogenesis |
| Q34149280 | Murine visceral leishmaniasis: IgM and polyclonal B-cell activation lead to disease exacerbation |
| Q35348282 | NF-κB in immunobiology. |
| Q92377800 | NOVA1 induction by inflammation and NOVA1 suppression by epigenetic regulation in head and neck squamous cell carcinoma |
| Q36771836 | NOVA1 inhibition by miR-146b-5p in the remnant tissue microenvironment defines occult residual disease after gastric cancer removal. |
| Q30463993 | Nutritionally mediated programming of the developing immune system |
| Q33823116 | Ontogeny of stromal organizer cells during lymph node development. |
| Q28512141 | PI3K p110δ is expressed by gp38(-)CD31(+) and gp38(+)CD31(+) spleen stromal cells and regulates their CCL19, CCL21, and LTβR mRNA levels |
| Q28533558 | Postnatal leptin promotes organ maturation and development in IUGR piglets |
| Q36412789 | RANKL-RANK interaction in immune regulatory systems |
| Q36076923 | RORγt Expression and Lymphoid Neogenesis in the Brain of Patients with Secondary Progressive Multiple Sclerosis |
| Q38957043 | Regulation of Lymph Node Vascular-Stromal Compartment by Dendritic Cells |
| Q64910442 | Repetitive ischemic injuries to the kidneys result in lymph node fibrosis and impaired healing. |
| Q37787865 | Role of lymphatic vessels in tumor immunity: passive conduits or active participants? |
| Q33800318 | Roles of the NF-kappaB pathway in lymphocyte development and function |
| Q42477680 | Salmonid T cells assemble in the thymus, spleen and in novel interbranchial lymphoid tissue |
| Q21131218 | Stromal cells control soluble material and cellular transport in lymph nodes |
| Q99594459 | Targeting NF-κB pathway for the therapy of diseases: mechanism and clinical study |
| Q47194123 | Tertiary Lymphoid Structures in Cancer: Drivers of Antitumor Immunity, Immunosuppression, or Bystander Sentinels in Disease? |
| Q38810926 | Tertiary lymphoid structures, drivers of the anti-tumor responses in human cancers |
| Q91669779 | The Lymphatic System in Obesity, Insulin Resistance, and Cardiovascular Diseases |
| Q37540859 | The inhibitory receptor BTLA controls γδ T cell homeostasis and inflammatory responses. |
| Q34031207 | The noncanonical NF-κB pathway |
| Q36826546 | Transmembrane TNF-TNFR2 Impairs Th17 Differentiation by Promoting Il2 Expression |
| Q36719083 | Upregulated Neuro-oncological Ventral Antigen 1 (NOVA1) Expression Is Specific to Mature and Immature T- and NK-Cell Lymphomas. |
| Q37572802 | Upregulation of CC Chemokine Receptor 7 (CCR7) Enables Migration of Xenogeneic Human Adipose-Derived Mesenchymal Stem Cells to Rat Secondary Lymphoid Organs |
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