scholarly article | Q13442814 |
P2093 | author name string | M D Cooper | |
J G Cyster | |||
J L Browning | |||
M D Gunn | |||
D S Riminton | |||
J D Sedgwick | |||
K N Schmidt | |||
V N Ngo | |||
H Korner | |||
P2860 | cites work | LIGHT, a new member of the TNF superfamily, and lymphotoxin alpha are ligands for herpesvirus entry mediator | Q24308657 |
B cell-attracting chemokine 1, a human CXC chemokine expressed in lymphoid tissues, selectively attracts B lymphocytes via BLR1/CXCR5 | Q24309316 | ||
Secondary lymphoid-tissue chemokine is a functional ligand for the CC chemokine receptor CCR7 | Q24318384 | ||
Molecular cloning of a novel human CC chemokine secondary lymphoid-tissue chemokine that is a potent chemoattractant for lymphocytes and mapped to chromosome 9p13 | Q24319684 | ||
Molecular cloning of a novel human CC chemokine EBI1-ligand chemokine that is a specific functional ligand for EBI1, CCR7 | Q24322056 | ||
A highly efficacious lymphocyte chemoattractant, stromal cell-derived factor 1 (SDF-1) | Q24677007 | ||
A chemokine expressed in lymphoid high endothelial venules promotes the adhesion and chemotaxis of naive T lymphocytes | Q24681916 | ||
Identification and characterization of a novel beta chemokine containing six conserved cysteines | Q28246202 | ||
Isolation and characterization of Exodus-2, a novel C-C chemokine with a unique 37-amino acid carboxyl-terminal extension | Q28249290 | ||
Characterization of lymphotoxin-alpha beta complexes on the surface of mouse lymphocytes | Q28250284 | ||
Turning off follicular dendritic cells | Q59068710 | ||
Crucial role of 55-kilodalton TNF receptor in TNF-induced adhesion molecule expression and leukocyte organ infiltration | Q63968529 | ||
The origin of the dendritic reticulum cell. An experimental enzyme-histochemical and electron microscopic study on the rabbit spleen | Q71262106 | ||
Role of colony stimulating factor-1 in the establishment and regulation of tissue macrophages during postnatal development of the mouse | Q72106554 | ||
Expression of the G-protein--coupled receptor BLR1 defines mature, recirculating B cells and a subset of T-helper memory cells | Q72686189 | ||
Lymphotoxin but not tumor necrosis factor functions to maintain splenic architecture and humoral responsiveness in adult mice | Q73691802 | ||
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 | ||
Transgenic expression of lymphotoxin restores lymph nodes to lymphotoxin-alpha-deficient mice | Q73900251 | ||
A B-cell-homing chemokine made in lymphoid follicles activates Burkitt's lymphoma receptor-1 | Q28263524 | ||
CK beta-11/macrophage inflammatory protein-3 beta/EBI1-ligand chemokine is an efficacious chemoattractant for T and B cells | Q28264381 | ||
A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen | Q28300225 | ||
Identification through bioinformatics of two new macrophage proinflammatory human chemokines: MIP-3alpha and MIP-3beta | Q28302521 | ||
Challenging cytokine redundancy: inflammatory cell movement and clinical course of experimental autoimmune encephalomyelitis are normal in lymphotoxin-deficient, but not tumor necrosis factor-deficient, mice | Q28506176 | ||
Abnormal development of peripheral lymphoid organs in mice deficient in lymphotoxin | Q28507630 | ||
Characterization of tumor necrosis factor-deficient mice | Q28512785 | ||
TNF receptor-deficient mice reveal divergent roles for p55 and p75 in several models of inflammation | Q28513332 | ||
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 | ||
Identification of a new mouse beta-chemokine, thymus-derived chemotactic agent 4, with activity on T lymphocytes and mesangial cells | Q28591058 | ||
Immune and inflammatory responses in TNF alpha-deficient mice: a critical requirement for TNF alpha in the formation of primary B cell follicles, follicular dendritic cell networks and germinal centers, and in the maturation of the humoral immune re | Q28594116 | ||
Gene targeting in C57BL/6 ES cells. Successful germ line transmission using recipient BALB/c blastocysts developmentally matured in vitro | Q34626094 | ||
Molecular cloning and structure of a pre-B-cell growth-stimulating factor | Q35106000 | ||
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 | ||
Chronic inflammation caused by lymphotoxin is lymphoid neogenesis | Q36366337 | ||
Lymphotoxin-alpha (LTalpha) supports development of splenic follicular structure that is required for IgG responses | Q36377326 | ||
Spontaneous follicular exclusion of SHP1-deficient B cells is conditional on the presence of competitor wild-type B cells | Q36400509 | ||
B lymphocytes induce the formation of follicular dendritic cell clusters in a lymphotoxin alpha-dependent fashion. | Q36400576 | ||
The sequential role of lymphotoxin and B cells in the development of splenic follicles. | Q36400592 | ||
Generation of splenic follicular structure and B cell movement in tumor necrosis factor-deficient mice. | Q36404217 | ||
Disrupted splenic architecture, but normal lymph node development in mice expressing a soluble lymphotoxin-beta receptor-IgG1 fusion protein. | Q36688075 | ||
Signal sequence trap: a cloning strategy for secreted proteins and type I membrane proteins | Q36766113 | ||
Epstein-Barr virus-induced molecule 1 ligand chemokine is expressed by dendritic cells in lymphoid tissues and strongly attracts naive T cells and activated B cells | Q36851758 | ||
Depressed Langerhans cell migration and reduced contact hypersensitivity response in mice lacking TNF receptor p75. | Q38502888 | ||
The ligands and receptors of the lymphotoxin system | Q40541150 | ||
The murine BP-3 gene encodes a relative of the CD38/NAD glycohydrolase family | Q41445963 | ||
Lymphocyte homing: the scent of a follicle. | Q41480493 | ||
Lymphotoxin-alpha-deficient and TNF receptor-I-deficient mice define developmental and functional characteristics of germinal centers | Q41492256 | ||
Mouse lymphotoxin-beta receptor. Molecular genetics, ligand binding, and expression | Q41673342 | ||
Surface lymphotoxin alpha/beta complex is required for the development of peripheral lymphoid organs | Q42196937 | ||
Selective recruitment of immature and mature dendritic cells by distinct chemokines expressed in different anatomic sites | Q42971765 | ||
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 | ||
Identification of macrophages and dendritic cells in the osteopetrotic (op/op) mouse. | Q48315503 | ||
Reticular cells in peripheral lymphoid tissues express the phosphatidylinositol-linked BP-3 antigen | Q52237971 | ||
Selective disruption of lymphotoxin ligands reveals a novel set of mucosal lymph nodes and unique effects on lymph node cellular organization. | Q52528591 | ||
Cytotoxic activities of recombinant soluble murine lymphotoxin-alpha and lymphotoxin-alpha beta complexes. | Q52559033 | ||
P4510 | describes a project that uses | ImageQuant | Q112270642 |
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 403-412 | |
P577 | publication date | 1999-01-01 | |
P1433 | published in | Journal of Experimental Medicine | Q3186912 |
P1476 | title | 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 | |
P478 | volume | 189 |
Q24291798 | A DAP12-mediated pathway regulates expression of CC chemokine receptor 7 and maturation of human dendritic cells |
Q47614119 | A TNF-p100 pathway subverts noncanonical NF-κB signaling in inflamed secondary lymphoid organs. |
Q28142202 | A chemokine-driven positive feedback loop organizes lymphoid follicles |
Q42109460 | A conduit system distributes chemokines and small blood-borne molecules through the splenic white pulp |
Q36369352 | A coordinated change in chemokine responsiveness guides plasma cell movements |
Q35679191 | A role for surface lymphotoxin in experimental autoimmune encephalomyelitis independent of LIGHT. |
Q40735725 | A role for the alveolar epithelium in recruitment of mononuclear cells into the lung |
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Q42972702 | Alymphoplasia (aly)-type nuclear factor kappaB-inducing kinase (NIK) causes defects in secondary lymphoid tissue chemokine receptor signaling and homing of peritoneal cells to the gut-associated lymphatic tissue system |
Q28235728 | An essential function for the nuclear receptor RORgamma(t) in the generation of fetal lymphoid tissue inducer cells |
Q33552492 | Analysis of cytokines in the early development of gastric secondary lymphoid follicles in Helicobacter pylori-infected BALB/c mice with neonatal thymectomy. |
Q54763105 | Analysis of the maturation process of dendritic cells deficient for TNF and lymphotoxin-alpha reveals an essential role for TNF. |
Q84564792 | Antigen-dependent rescue of nose-associated lymphoid tissue (NALT) development independent of LTbetaR and CXCR5 signaling |
Q37761494 | Artificial engineering of secondary lymphoid organs. |
Q36073815 | Association of CXCL10 and CXCL13 levels with disease activity and cutaneous manifestation in active adult-onset Still's disease |
Q34296482 | Attractions and migrations of lymphoid cells in the organization of humoral immune responses |
Q38665740 | B cells and their cytokine activities implications in human diseases |
Q37603296 | B cells as therapeutic targets in SLE. |
Q36504635 | B-cell selection and the development of autoantibodies |
Q57041869 | B-cell subsets: cellular interactions and relevance in multiple sclerosis |
Q38167667 | B-lymphocyte tolerance and effector function in immunity and autoimmunity |
Q36762885 | BCA-1 is highly expressed in Helicobacter pylori-induced mucosa-associated lymphoid tissue and gastric lymphoma |
Q41740089 | BLC expression in pancreatic islets causes B cell recruitment and lymphotoxin-dependent lymphoid neogenesis. |
Q35145609 | Biological functions of tumor necrosis factor cytokines and their receptors |
Q47927327 | 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 |
Q37805001 | Bronchus-associated lymphoid tissue (BALT) structure and function |
Q28588634 | CC chemokine receptor (CCR)2 is required for langerhans cell migration and localization of T helper cell type 1 (Th1)-inducing dendritic cells. Absence of CCR2 shifts the Leishmania major-resistant phenotype to a susceptible state dominated by Th2 c |
Q36095617 | CCL21 expression pattern of human secondary lymphoid organ stroma is conserved in inflammatory lesions with lymphoid neogenesis. |
Q28594485 | CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs |
Q35874330 | CCR7/CCL19 controls expression of EDG-1 in T cells |
Q34157703 | CD157, the Janus of CD38 but with a unique personality |
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Q92857870 | CD8+ T-Cell Response to HIV Infection in the Era of Antiretroviral Therapy |
Q36368291 | CXC chemokine receptor 5 expression defines follicular homing T cells with B cell helper function |
Q37238275 | CXCL13 is elevated in Sjögren's syndrome in mice and humans and is implicated in disease pathogenesis |
Q28217241 | CXCL13 is required for B1 cell homing, natural antibody production, and body cavity immunity |
Q35163486 | CXCL13 responsiveness but not CXCR5 expression by late transitional B cells initiates splenic white pulp formation |
Q38536579 | CXCR5, the Defining Marker for Follicular B Helper T (TFH) Cells. |
Q38869034 | Catalytic subunits of the phosphatase calcineurin interact with NF-κB-inducing kinase (NIK) and attenuate NIK-dependent gene expression |
Q24805154 | Cell-cell interactions in synovitis. Interactions between T cells and B cells in rheumatoid arthritis |
Q34052870 | Changes in B- and T-lymphocyte and chemokine levels with rituximab treatment in multiple sclerosis. |
Q28293692 | Characterizing follicular dendritic cells: A progress report |
Q35947260 | Chemokine signatures in the skin disorders of Lyme borreliosis in Europe: predominance of CXCL9 and CXCL10 in erythema migrans and acrodermatitis and CXCL13 in lymphocytoma |
Q34002668 | Chemokines and dendritic cell traffic. |
Q34296506 | Chemokines in immunity |
Q34167947 | Chemokines in lymphopoiesis and lymphoid organ development |
Q34139595 | Chemokines: immunology's high impact factors |
Q63976622 | Comparative Transcriptomic Analysis Identifies a Range of Immunologically Related Functional Elaborations of Lymph Node Associated Lymphatic and Blood Endothelial Cells |
Q35084291 | Concerted action of the chemokine and lymphotoxin system in secondary lymphoid-organ development |
Q40590092 | Cooperating mechanisms of CXCR5 and CCR7 in development and organization of secondary lymphoid organs |
Q24685416 | Coordination between NF-kappaB family members p50 and p52 is essential for mediating LTbetaR signals in the development and organization of secondary lymphoid tissues |
Q36206426 | Critical role of CD4 T cells in maintaining lymphoid tissue structure for immune cell homeostasis and reconstitution. |
Q28511726 | Critical roles for IFN-β in lymphoid development, myelopoiesis, and tumor development: Links to tumor necrosis factor α |
Q53468958 | Decreased expression of intestinal chemokine TECK/CCL25 in experimental obstructive jaundice and its reversal following internal biliary drainage. |
Q38883160 | Defective CCR7 expression on dendritic cells contributes to the development of visceral leishmaniasis |
Q34129744 | Dendritic cell biology and regulation of dendritic cell trafficking by chemokines |
Q47357498 | Detection of ectopic B-cell follicles with germinal centers in the meninges of patients with secondary progressive multiple sclerosis. |
Q52572835 | Development of nephritis but not sialadenitis in autoimmune-prone BAFF transgenic mice lacking marginal zone B cells. |
Q34764895 | Development of secondary lymphoid organs |
Q40468715 | Differential lymphotoxin-beta and interferon gamma signaling during mouse liver regeneration induced by chronic and acute injury. |
Q36991047 | Differential regulation of CCL21 in lymphoid/nonlymphoid tissues for effectively attracting T cells to peripheral tissues |
Q35216954 | Dissecting the role of lymphotoxin in lymphoid organs by conditional targeting |
Q44158648 | Distinct role of surface lymphotoxin expressed by B cells in the organization of secondary lymphoid tissues |
Q37899957 | Disturbance of cytokine networks in Sjögren's syndrome |
Q28251850 | EBI2 mediates B cell segregation between the outer and centre follicle |
Q35119934 | Ectopic Germinal Center Formation in Rheumatoid Synovitis |
Q36370988 | Ectopic LTαβ Directs Lymphoid Organ Neogenesis with Concomitant Expression of Peripheral Node Addressin and a HEV-restricted Sulfotransferase |
Q34363840 | Ectopic lymphoid organogenesis: a fast track for autoimmunity |
Q37075235 | Ectopic lymphoid tissues and local immunity |
Q30299955 | Effector lymphocyte-induced lymph node-like vasculature enables naive T-cell entry into tumours and enhanced anti-tumour immunity |
Q36908953 | Effects of chronic ethanol feeding on murine dendritic cell numbers, turnover rate, and dendropoiesis |
Q34006525 | Effects of tumor necrosis factor alpha on host immune response in chronic persistent tuberculosis: possible role for limiting pathology |
Q42275091 | Emergence and Evolution of Secondary Lymphoid Organs |
Q33576226 | Eosinophils control the resolution of inflammation and draining lymph node hypertrophy through the proresolving mediators and CXCL13 pathway in mice |
Q40453661 | Epitope spreading initiates in the CNS in two mouse models of multiple sclerosis. |
Q36369156 | Essential role of lymph nodes in contact hypersensitivity revealed in lymphotoxin-alpha-deficient mice. |
Q36466170 | Exosomes from HIV-1-infected Cells Stimulate Production of Pro-inflammatory Cytokines through Trans-activating Response (TAR) RNA |
Q44010556 | Expression of lymphotoxin beta governs immunity at two distinct levels |
Q41905092 | Expression of lymphotoxin-alphabeta on antigen-specific T cells is required for DC function |
Q34225157 | Expression profiling in knockout mice: lymphotoxin versus tumor necrosis factor in the maintenance of splenic microarchitecture |
Q39075966 | Fat-Associated Lymphoid Clusters in Inflammation and Immunity |
Q37215955 | Fetal exposure to ethanol has long-term effects on the severity of influenza virus infections |
Q50144852 | Fibroblastic reticular cells in lymph nodes regulate the homeostasis of naive T cells. |
Q38001203 | Fine-tuning of dendritic cell biology by the TNF superfamily |
Q24676570 | Follicular B helper T cells express CXC chemokine receptor 5, localize to B cell follicles, and support immunoglobulin production |
Q36991851 | Follicular dendritic cells emerge from ubiquitous perivascular precursors |
Q35669109 | Follicular dendritic cells help establish follicle identity and promote B cell retention in germinal centers |
Q30441344 | Follicular shuttling of marginal zone B cells facilitates antigen transport |
Q33182386 | Formation of Peyer's patches |
Q40487229 | Generation of a synthetic lymphoid tissue-like organoid in mice |
Q36761972 | Graft Site Microenvironment Determines Dendritic Cell Trafficking Through the CCR7-CCL19/21 Axis |
Q36217780 | Growth of Murine Splenic Tissue Is Suppressed by Lymphotoxin β-Receptor Signaling (LTβR) Originating from Splenic and Non-Splenic Tissues |
Q41492683 | HIV-1 single-stranded RNA induces CXCL13 secretion in human monocytes via TLR7 activation and plasmacytoid dendritic cell-derived type I IFN. |
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Q35170914 | Homing of antibody secreting cells |
Q37326558 | ICOS, CD40, and lymphotoxin beta receptors signal sequentially and interdependently to initiate a germinal center reaction |
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Q35017978 | Identification of a new stromal cell type involved in the regulation of inflamed B cell follicles |
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Q36253046 | Inducible tertiary lymphoid structures, autoimmunity, and exocrine dysfunction in a novel model of salivary gland inflammation in C57BL/6 mice |
Q42683418 | Infection with Toxoplasma gondii alters lymphotoxin expression associated with changes in splenic architecture |
Q35882546 | Inflammation-induced formation of fat-associated lymphoid clusters |
Q34397537 | Interactions between the intestinal microbiota and innate lymphoid cells. |
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Q64447653 | Isolated lymphoid follicle maturation induces the development of follicular dendritic cells |
Q34126584 | Low CXCL13 expression, splenic lymphoid tissue atrophy and germinal center disruption in severe canine visceral leishmaniasis |
Q37875904 | Lymphatics: at the interface of immunity, tolerance, and tumor metastasis |
Q34139610 | Lymphocyte traffic control by chemokines |
Q37186200 | Lymphoid chemokines in chronic neuroinflammation |
Q35216967 | Lymphoid microenvironment in the gut for immunoglobulin A and inflammation. |
Q33735993 | Lymphoid neo-organogenesis: lymphotoxin's role in inflammation and development |
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Q36986700 | Lymphoid organogenesis in brief |
Q36290311 | Lymphoid organogenesis in the intestine. |
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Q35951798 | Lymphotoxin and LIGHT signaling pathways and target genes |
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Q35083503 | Lymphotoxin plays a crucial role in the development and function of nasal-associated lymphoid tissue through regulation of chemokines and peripheral node addressin |
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Q36369047 | Mice lacking expression of the chemokines CCL21-ser and CCL19 (plt mice) demonstrate delayed but enhanced T cell immune responses |
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Q34717984 | Novel lymphotoxin alpha (LTalpha) knockout mice with unperturbed tumor necrosis factor expression: reassessing LTalpha biological functions. |
Q37948124 | OX40 and CD30 signals in CD4(+) T-cell effector and memory function: a distinct role for lymphoid tissue inducer cells in maintaining CD4(+) T-cell memory but not effector function |
Q37246687 | Orchestrating the orchestrators: chemokines in control of T cell traffic |
Q35096187 | Organogenesis of lymphoid tissues |
Q36691073 | Overexpression of lymphotoxin in T cells induces fulminant thymic involution |
Q28512141 | PI3K p110δ is expressed by gp38(-)CD31(+) and gp38(+)CD31(+) spleen stromal cells and regulates their CCL19, CCL21, and LTβR mRNA levels |
Q34275978 | Pathogenesis of rheumatoid arthritis. The role of T cells and other beasts. |
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Q37285430 | Recapitulation of B cell differentiation in the central nervous system of patients with multiple sclerosis. |
Q35104223 | Recipient B cells are not required for graft-versus-host disease induction |
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Q44223059 | Reduced competitiveness of autoantigen-engaged B cells due to increased dependence on BAFF. |
Q52582787 | Reduced lymphotoxin-beta production by tumour cells is associated with loss of follicular dendritic cell phenotype and diffuse growth in follicular lymphoma. |
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Q36543544 | Regulation of T(H)2 development by CXCR5+ dendritic cells and lymphotoxin-expressing B cells |
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Q35216951 | Regulation of secondary lymphoid organ development by the nuclear factor-kappaB signal transduction pathway |
Q34610191 | Regulatory T cells interfere with the development of bronchus-associated lymphoid tissue |
Q35168331 | Resident B cells regulate thymic expression of myelin oligodendrocyte glycoprotein |
Q36369174 | Reversal of spontaneous autoimmune insulitis in nonobese diabetic mice by soluble lymphotoxin receptor |
Q47906614 | Role of 4-1BB in Allograft Rejection Mediated by CD8+ T Cells |
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Q45018410 | Role of inducible bronchus associated lymphoid tissue (iBALT) in respiratory immunity |
Q37765477 | Role of lymphotoxin and homeostatic chemokines in the development and function of local lymphoid tissues in the respiratory tract. |
Q34111943 | Role of lymphotoxin in experimental models of infectious diseases: potential benefits and risks of a therapeutic inhibition of the lymphotoxin-beta receptor pathway |
Q37619093 | Role of secondary lymphoid tissues in primary and memory T-cell responses to a transplanted organ |
Q37576573 | Role of the Lymphotoxin/LIGHT System in the Development and Maintenance of Reticular Networks and Vasculature in Lymphoid Tissues |
Q37200730 | Roles of embryonic and adult lymphoid tissue inducer cells in primary and secondary lymphoid tissues |
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Q78952383 | Secondary lymphoid organ chemokines are elevated in the cerebrospinal fluid during central nervous system inflammation |
Q37397090 | Secondary lymphoid organs: responding to genetic and environmental cues in ontogeny and the immune response |
Q36369043 | Secreted lymphotoxin-alpha is essential for the control of an intracellular bacterial infection. |
Q56603390 | Shaping Up Adaptive Immunity: The Impact of CCR7 and CXCR5 on Lymphocyte Trafficking |
Q74082070 | Signaling via LTbetaR on the lamina propria stromal cells of the gut is required for IgA production |
Q36951063 | Sjögren's syndrome--a plethora of clinical and immunological phenotypes with a complex genetic background |
Q25257147 | Specific remodeling of splenic architecture by cytomegalovirus. |
Q35925046 | Splenic CD19-CD35+B220+ cells function as an inducer of follicular dendritic cell network formation |
Q36369671 | Splenic T zone development is B cell dependent |
Q47110972 | Spoiling for a Fight: B Lymphocytes As Initiator and Effector Populations within Tertiary Lymphoid Organs in Autoimmunity and Transplantation. |
Q28068106 | Stromal Fibroblasts in Tertiary Lymphoid Structures: A Novel Target in Chronic Inflammation |
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Q83679980 | Stromal cells directly mediate the re-establishment of the lymph node compartments after transplantation by CXCR5 or CCL19/21 signalling |
Q82715309 | Stromal cells put the brakes on T-cell responses |
Q28264813 | Structure and function of the spleen |
Q58712847 | T Cells That Help B Cells in Chronically Inflamed Tissues |
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Q30743828 | TNF ligands and receptors in autoimmunity: an update |
Q54561449 | TNF-dependent overexpression of CCL21 is an underlying cause of progressive lymphoaccumulation in generalized lymphoproliferative disorder. |
Q90388642 | TNF-α Contributes to Lymphoid Tissue Disorganization and Germinal Center B Cell Suppression during Intracellular Bacterial Infection |
Q36551188 | Targeting CXCL13 During Neuroinflammation |
Q27009348 | Targeting and utilizing primary tumors as live vaccines: changing strategies |
Q37175025 | Targeting tumors with LIGHT to generate metastasis-clearing immunity |
Q39683541 | Temporary blockade of the tumor necrosis factor receptor signaling pathway impedes the spread of scrapie to the brain |
Q35110486 | Tertiary Lymphoid Structure-Associated B Cells are Key Players in Anti-Tumor Immunity |
Q33833203 | Th1/Th2 subsets: distinct differences in homing and chemokine receptor expression? |
Q27025082 | The Lymphotoxin Network: orchestrating a type I interferon response to optimize adaptive immunity |
Q36393411 | The adjuvant LT-K63 can restore delayed maturation of follicular dendritic cells and poor persistence of both protein- and polysaccharide-specific antibody-secreting cells in neonatal mice |
Q50882792 | The chronicity of tonsillitis is significantly correlated with an increase in an LTi cell portion. |
Q34191942 | The development of inducible bronchus-associated lymphoid tissue depends on IL-17. |
Q50658648 | The identification and developmental requirements of colonic CD169⁺ macrophages. |
Q35216957 | The impact of CCR7 and CXCR5 on lymphoid organ development and systemic immunity |
Q35104199 | The lymphoid chemokine, CXCL13, is dispensable for the initial recruitment of B cells to the acutely inflamed central nervous system |
Q30494620 | The lymphotoxin LTalpha(1)beta(2) controls postnatal and adult spleen marginal sinus vascular structure and function |
Q37382924 | The lymphotoxin pathway regulates Aire-independent expression of ectopic genes and chemokines in thymic stromal cells |
Q36604759 | The lymphotoxin pathway: beyond lymph node development. |
Q40696432 | The lymphotoxin-beta receptor induces different patterns of gene expression via two NF-kappaB pathways |
Q36375299 | The requirement of membrane lymphotoxin for the presence of dendritic cells in lymphoid tissues |
Q35005856 | The role of CD45+CD4+CD3- cells in lymphoid organ development |
Q37863514 | The role of chemokines and their receptors in angiogenesis |
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