| scholarly article | Q13442814 |
| P50 | author | Jeffrey L. Browning | Q42486462 |
| David D. Chaplin | Q42780504 | ||
| Yang-Xin Fu | Q57177963 | ||
| P2093 | author name string | R A Flavell | |
| S Jayaraman | |||
| P S Hochman | |||
| P D Rennert | |||
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| T cell-independent antigens type 2. | Q34300069 | ||
| 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 | ||
| STUDIES ON THE SENSITIZATION OF ANIMALS WITH SIMPLE CHEMICAL COMPOUNDS. II. | Q34613286 | ||
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| Independent signals regulate development of primary and secondary follicle structure in spleen and mesenteric lymph node | Q36157845 | ||
| Studies on the sensitization of animals with simple chemical compounds. XII. The influence of excision of allergenic depots on onset of delayed hypersensitivity and tolerance | Q36269511 | ||
| Initiation of autoimmune diabetes by developmentally regulated presentation of islet cell antigens in the pancreatic lymph nodes | Q36367942 | ||
| Mice lacking expression of the chemokines CCL21-ser and CCL19 (plt mice) demonstrate delayed but enhanced T cell immune responses | Q36369047 | ||
| The requirement of membrane lymphotoxin for the presence of dendritic cells in lymphoid tissues | Q36375299 | ||
| On the key role of secondary lymphoid organs in antiviral immune responses studied in alymphoplastic (aly/aly) and spleenless (Hox11(-)/-) mutant mice. | Q36377346 | ||
| The route of antigen entry determines the requirement for L-selectin during immune responses | Q36377474 | ||
| A critical role for lymphotoxin in experimental allergic encephalomyelitis | Q36380767 | ||
| Analysis of dose response of trinitrochlorobenzene contact hypersensitivity induction in mice: pretreatment with cyclophosphamide reveals an optimal sensitizing dose | Q38516212 | ||
| Localization of antigen on lymph node dendritic cells after exposure to the contact sensitizer fluorescein isothiocyanate. Functional and morphological studies | Q38518849 | ||
| Maturation and migration of cutaneous dendritic cells. | Q40447773 | ||
| The role of Langerhans cells in allergic contact hypersensitivity. A review of findings in man and guinea pigs | Q40525519 | ||
| Chance encounters and organized rendezvous. | Q40898585 | ||
| Origin, maturation and antigen presenting function of dendritic cells. | Q40906220 | ||
| Antigen localisation regulates immune responses in a dose- and time-dependent fashion: a geographical view of immune reactivity | Q41492285 | ||
| Lymphotoxin-beta-deficient mice show defective antiviral immunity. | Q41679119 | ||
| Lymph node germinal centers form in the absence of follicular dendritic cell networks | Q41853947 | ||
| Characterization of nonlymphoid cells derived from rat peripheral lymph | Q41869071 | ||
| Mice lacking expression of secondary lymphoid organ chemokine have defects in lymphocyte homing and dendritic cell localization | Q42064511 | ||
| Surface lymphotoxin alpha/beta complex is required for the development of peripheral lymphoid organs | Q42196937 | ||
| 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 | ||
| Ox40-ligand has a critical costimulatory role in dendritic cell:T cell interactions | Q42806821 | ||
| The role of afferent lymphatics in the rejection of skin homografts | Q42833013 | ||
| Some misconceptions about understanding autoimmunity through experiments with knockouts | Q42931515 | ||
| Reversal of virus-induced systemic shock and respiratory failure by blockade of the lymphotoxin pathway | Q45745997 | ||
| Experimental studies on the pathogenesis of contact eczema in the guinea-pig. | Q46190618 | ||
| Langerhans cells form a reticuloepithelial trap for external contact antigens | Q46267315 | ||
| 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 interferon-gamma in contact hypersensitivity assessed in interferon-gamma receptor-deficient mice. | Q52507054 | ||
| Selective disruption of lymphotoxin ligands reveals a novel set of mucosal lymph nodes and unique effects on lymph node cellular organization. | Q52528591 | ||
| Turning off follicular dendritic cells | Q59068710 | ||
| Effector and regulatory T cells in allergic contact dermatitis | Q61703544 | ||
| TNF and lymphotoxin beta cooperate in the maintenance of secondary lymphoid tissue microarchitecture but not in the development of lymph nodes | Q63968518 | ||
| Classification of chemical allergens according to cytokine secretion profiles of murine lymph node cells | Q73106077 | ||
| Generation of primary antigen-specific human T- and B-cell responses in immunocompetent SCID-hu mice | Q73308236 | ||
| Alternate mucosal immune system: organized Peyer's patches are not required for IgA responses in the gastrointestinal tract | Q73755884 | ||
| Inhibition of functional T cell priming and contact hypersensitivity responses by treatment with anti-secondary lymphoid chemokine antibody during hapten sensitization | Q73755891 | ||
| Immunologic 'ignorance' of vascularized organ transplants in the absence of secondary lymphoid tissue | Q73844688 | ||
| Distinct roles for B7-1 and B7-2 determinants during priming of effector CD8+ Tc1 and regulatory CD4+ Th2 cells for contact hypersensitivity | Q73900245 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | lymph node | Q170758 |
| P304 | page(s) | 1227-1238 | |
| P577 | publication date | 2001-06-01 | |
| P1433 | published in | Journal of Experimental Medicine | Q3186912 |
| P1476 | title | Essential role of lymph nodes in contact hypersensitivity revealed in lymphotoxin-alpha-deficient mice | |
| P478 | volume | 193 |
| Q35679191 | A role for surface lymphotoxin in experimental autoimmune encephalomyelitis independent of LIGHT. |
| Q53640513 | An indispensable role of type-1 IFNs for inducing CTL-mediated complete eradication of established tumor tissue by CpG-liposome co-encapsulated with model tumor antigen. |
| Q27329088 | Comparative Analysis of Immune Activation Markers of CD8(+) T Cells in Lymph Nodes of Different Origins in SIV-Infected Chinese Rhesus Macaques |
| Q42944784 | Compartmentalized production of CCL17 in vivo: strong inducibility in peripheral dendritic cells contrasts selective absence from the spleen. |
| Q36370664 | Complementary role of CD4+ T cells and secondary lymphoid tissues for cross-presentation of tumor antigen to CD8+ T cells. |
| Q38464800 | Contact sensitizer potassium dichromate alters lymphocyte populations in draining lymph nodes and blood in mice |
| Q35209138 | Cytokine knockouts in contact hypersensitivity research |
| Q35064876 | Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBα. |
| Q37142696 | Dose metrics in the acquisition of skin sensitization: thresholds and importance of dose per unit area |
| Q45236202 | Follicular dendritic cell dedifferentiation reduces scrapie susceptibility following inoculation via the skin |
| Q30440584 | Immunity to melanoma antigens: from self-tolerance to immunotherapy |
| Q54328516 | Implications of nasopharynx-associated lymphoid tissue (NALT) in the development of allergic responses in an allergic rhinitis mouse model. |
| Q35748193 | 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 |
| Q31156611 | Lymphoid organ development and cell migration |
| Q35219029 | Lymphotoxin/light, lymphoid microenvironments and autoimmune disease |
| Q34815328 | Manipulation of lymphoid microenvironments in nonhuman primates by an inhibitor of the lymphotoxin pathway |
| Q33452541 | Neo-lymphoid aggregates in the adult liver can initiate potent cell-mediated immunity |
| Q35216947 | Organogenesis of peripheral lymphoid organs. |
| Q34610191 | Regulatory T cells interfere with the development of bronchus-associated lymphoid tissue |
| Q45018410 | Role of inducible bronchus associated lymphoid tissue (iBALT) in respiratory immunity |
| Q30311891 | Route of immunization with peptide-pulsed dendritic cells controls the distribution of memory and effector T cells in lymphoid tissues and determines the pattern of regional tumor control |
| Q33539882 | Secondary lymphoid organs are dispensable for the development of T-cell-mediated immunity during tuberculosis |
| Q73072574 | Secondary lymphoid organs are important but not absolutely required for allograft responses |
| Q51983250 | T cell- and B cell-independent adaptive immunity mediated by natural killer cells. |
| Q34418103 | T-cell subpopulations in the development of atopic and contact allergy. |
| Q38288045 | Targeted disruption of LIGHT causes defects in costimulatory T cell activation and reveals cooperation with lymphotoxin beta in mesenteric lymph node genesis |
| Q35568430 | The Role of Chemokines in Inflammatory Skin Diseases |
| Q36845128 | The absence of cutaneous lymph nodes results in a Th2 response and increased susceptibility to Leishmania major infection in mice |
| Q35139185 | What makes a chemical an allergen? |
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