| scholarly article | Q13442814 |
| P50 | author | Ralph Steinman | Q105494 |
| P2093 | author name string | K Inaba | |
| E Puré | |||
| M T Crowley | |||
| G Ruberti | |||
| M D Witmer-Pack | |||
| G Fathman | |||
| L Tardelli | |||
| P2860 | cites work | The epitopes of influenza nucleoprotein recognized by cytotoxic T lymphocytes can be defined with short synthetic peptides | Q24339477 |
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| Structure of the gene of tum- transplantation antigen P91A: the mutated exon encodes a peptide recognized with Ld by cytolytic T cells | Q28512984 | ||
| Microtubule-dependent retrograde transport of proteins into the ER in the presence of brefeldin A suggests an ER recycling pathway | Q29620187 | ||
| T-independent and T-dependent steps in the murine B cell response to antiimmunoglobulin | Q30442744 | ||
| Contribution of dendritic cells to stimulation of the murine syngeneic mixed leukocyte reaction | Q34260675 | ||
| Protein degradation in cultured cells. II. The uptake of chloroquine by rat fibroblasts and the inhibition of cellular protein degradation and cathepsin B1. | Q36202418 | ||
| Processing of lysozyme by macrophages: identification of the determinant recognized by two T-cell hybridomas | Q36257785 | ||
| Decrease in macrophage antigen catabolism caused by ammonia and chloroquine is associated with inhibition of antigen presentation to T cells | Q36275163 | ||
| Lymphocyte specificity to protein antigens. II. Fine specificity of T-cell activation with cytochrome c and derived peptides as antigenic probes | Q36341212 | ||
| Lymphokine enhances the expression and synthesis of Ia antigens on cultured mouse peritoneal macrophages | Q36344137 | ||
| Precursor frequency analysis of lymphokine-secreting alloreactive T lymphocytes. Dissociation of subsets producing interleukin 2, macrophage-activating factor, and granulocyte-macrophage colony-stimulating factor on the basis of Lyt-2 phenotype | Q36347100 | ||
| Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing | Q36348935 | ||
| Murine epidermal Langerhans cells mature into potent immunostimulatory dendritic cells in vitro | Q36349915 | ||
| Chloroquine affects biosynthesis of Ia molecules by inhibiting dissociation of invariant (gamma) chains from alpha-beta dimers in B cells | Q36350981 | ||
| Regulation of antigen presentation by acidic pH. | Q36351024 | ||
| The presumptive CDR3 regions of both T cell receptor alpha and beta chains determine T cell specificity for myoglobin peptides | Q36351944 | ||
| Dendritic cells pulsed with protein antigens in vitro can prime antigen-specific, MHC-restricted T cells in situ | Q36352646 | ||
| Granulocyte/macrophage colony-stimulating factor and interleukin 1 mediate the maturation of murine epidermal Langerhans cells into potent immunostimulatory dendritic cells | Q36354420 | ||
| Enhanced T cell responses to antigenic peptides targeted to B cell surface Ig, Ia, or class I molecules | Q36355067 | ||
| Presentation of exogenous protein antigens by dendritic cells to T cell clones. Intact protein is presented best by immature, epidermal Langerhans cells | Q36356239 | ||
| Granulocyte/macrophage colony-stimulating factor is essential for the viability and function of cultured murine epidermal Langerhans cells | Q36357544 | ||
| Increased expression of Ia antigens on resting B cells: an additional role for B-cell growth factor | Q37571189 | ||
| Localization of antigen on lymph node dendritic cells after exposure to the contact sensitizer fluorescein isothiocyanate. Functional and morphological studies | Q38518849 | ||
| Immunologic functions of Ia-bearing epidermal Langerhans cells | Q39515233 | ||
| Brefeldin A implicates egress from endoplasmic reticulum in class I restricted antigen presentation | Q41325460 | ||
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| A role of Ia-associated invariant chains in antigen processing and presentation. | Q41946241 | ||
| Protein synthesis in antigen processing. | Q41947029 | ||
| Synthetic peptides as antigens and competitors in recognition by H-2-restricted cytolytic T cells specific for HLA. | Q41964127 | ||
| Identification of a novel cell type in peripheral lymphoid organs of mice. II. Functional properties in vitro | Q42022012 | ||
| The relation between major histocompatibility complex (MHC) restriction and the capacity of Ia to bind immunogenic peptides | Q42074920 | ||
| Langerhans' cells, veiled cells, and interdigitating cells in the mouse recognized by a monoclonal antibody | Q42937985 | ||
| A small number of anti-CD3 molecules on dendritic cells stimulate DNA synthesis in mouse T lymphocytes | Q42939565 | ||
| Cells with dendritic morphology and bright interleukin-1 alpha staining circulate in the blood of patients with rheumatoid arthritis | Q44014770 | ||
| Interaction of peptide antigens and class II major histocompatibility complex antigens | Q45044764 | ||
| Two better cell lines for making hybridomas expressing specific T cell receptors. | Q48287125 | ||
| In vitro evidence that Langerhans cells can adopt two functionally distinct forms capable of antigen presentation to T lymphocytes. | Q52112187 | ||
| Antigen processing and intracellular Ia. Possible roles of endocytosis and protein synthesis in Ia function. | Q54362556 | ||
| Antigen recognition by H-2-restricted T cells. II. A tryptic ovalbumin peptide that substitutes for processed antigen | Q56922571 | ||
| Association of class I major histocompatibility heavy and light chains induced by viral peptides | Q59072754 | ||
| The foreign antigen binding site and T cell recognition regions of class I histocompatibility antigens | Q59092174 | ||
| Time dependence of B cell processing and presentation of peptide and native protein antigens | Q60673559 | ||
| Antigen-bearing langerhans cells in skin, dermal lymphatics and in lymph nodes | Q67487391 | ||
| Quantitation of surface antigens on cultured murine epidermal Langerhans cells: rapid and selective increase in the level of surface MHC products | Q68128520 | ||
| Enhanced antigen-presenting capacity of cultured Langerhans' cells is associated with markedly increased expression of Ia antigen | Q68829466 | ||
| Molecular mapping of a histocompatibility-restricted immunodominant T cell epitope with synthetic and natural peptides: implications for T cell antigenic structure | Q68955504 | ||
| Uptake, Intracellular Transport and Degradation of Exogenous Protein by Langerhans Cells An Electron Microscopic-Cytochemical Study Using Peroxidase as Tracer Substance | Q71427279 | ||
| A shared alloantigenic determinant on Ia antigens encoded by the I-A and I-E subregions: evidence for I region gene duplication | Q72650068 | ||
| Ia invariant chain detected on lymphocyte surfaces by monoclonal antibody | Q72677142 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1459-1469 | |
| P577 | publication date | 1990-11-01 | |
| P1433 | published in | Journal of Experimental Medicine | Q3186912 |
| P1476 | title | Antigen processing by epidermal Langerhans cells correlates with the level of biosynthesis of major histocompatibility complex class II molecules and expression of invariant chain | |
| P478 | volume | 172 |
| Q41154338 | A conditionally immortalized dendritic cell line which differentiates in contact with T cells or T cell-derived cytokines. |
| Q34987424 | A potential role of macrophage activation in the treatment of cancer |
| Q40514971 | An analysis of the role of skin Langerhans cells (LC) in the cytoplasmic processing of HIV-1 peptides after "peplotion" transepidermal transfer and HLA class I presentation to CD8+ CTLs--an approach to immunization of humans |
| Q35378182 | Analysis of immunization route-related variation in the immune response to heat-killed Salmonella typhimurium in mice |
| Q41946843 | Antigen capture and major histocompatibility class II compartments of freshly isolated and cultured human blood dendritic cells |
| Q33699321 | Antigen capture, processing, and presentation by dendritic cells: recent cell biological studies. |
| Q44555210 | Antigen presentation on MHC molecules as a diversity filter that enhances immune efficacy |
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| Q36934685 | Circulating HLA-DR(+) natural killer cells have potent lytic ability and weak antigen-presenting cell function |
| Q37472931 | Class II major histocompatibility complex molecules of murine dendritic cells: synthesis, sialylation of invariant chain, and antigen processing capacity are down-regulated upon culture |
| Q52066859 | Comparison of antigen presentation by lymph node cells from protein and peptide-primed mice. |
| Q36371218 | Constitutive presentation of a natural tissue autoantigen exclusively by dendritic cells in the draining lymph node |
| Q67487832 | Contact Allergens Modulate the Expression of MHC Class II Molecules on Murine Epidermal Langerhans Cells by Endocytotic Mechanisms |
| Q36266484 | Control of MHC class II antigen presentation in dendritic cells: a balance between creative and destructive forces. |
| Q41232464 | Cultured human Langerhans' cells are superior to fresh cells at presenting native HIV-1 protein antigens to specific CD4+ T-cell lines |
| Q41115176 | Cutaneous leishmaniasis: a model for analysis of the immunoregulation by accessory cells |
| Q41353587 | Cytokine-dependent regulation of growth and maturation in murine epidermal dendritic cell lines |
| Q33874509 | Cytokines and chemokines in the initiation and regulation of epidermal Langerhans cell mobilization |
| Q53986332 | Defect of protective immunity to Schistosoma mansoni infection in Mongolian gerbils involves limited recruitment of dendritic cells in the vaccinated skin. |
| Q28585705 | Defective major histocompatibility complex class II assembly, transport, peptide acquisition, and CD4+ T cell selection in mice lacking invariant chain expression |
| Q35789511 | Dendritic cell maturation and antigen presentation in the absence of invariant chain. |
| Q36362128 | Dendritic cell progenitors phagocytose particulates, including bacillus Calmette-Guerin organisms, and sensitize mice to mycobacterial antigens in vivo |
| Q24706826 | Dendritic cells as a tool for the predictive identification of skin sensitisation hazard - The report and recommendations of ECVAM workshop 51 |
| Q49137643 | Dendritic cells in Leishmania major-immune mice harbor persistent parasites and mediate an antigen-specific T cell immune response |
| Q73840347 | Dendritic cells lose ability to present protein antigen after stimulating antigen-specific T cell responses, despite upregulation of MHC class II expression |
| Q34078105 | Dendritic cells, implications on function from studies of the afferent lymph veiled cell. |
| Q41225268 | Different cytokines regulate antigen uptake and presentation of a precursor dendritic cell line |
| Q54321603 | Differential regulation of MHC II and invariant chain expression during maturation of monocyte-derived dendritic cells. |
| Q42938806 | Disappearance of certain acidic organelles (endosomes and Langerhans cell granules) accompanies loss of antigen processing capacity upon culture of epidermal Langerhans cells |
| Q72589395 | Distribution of HLA class II molecules in epidermal Langerhans cells in situ |
| Q70768270 | Donor-derived chimerism in recipients of organ transplants |
| Q36361336 | Downregulation of the antigen presenting cell function(s) of pulmonary dendritic cells in vivo by resident alveolar macrophages |
| Q28251443 | Efficient presentation of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and downregulated by tumor necrosis factor alpha |
| Q37190099 | Endocytosis by antigen presenting cells: dendritic cells are as endocytically active as other antigen presenting cells |
| Q42811453 | Endosomally stored MHC class II does not contribute to antigen presentation by dendritic cells at inflammatory conditions. |
| Q71458387 | Epidermal Langerhans' cell induction of immunity against an ultraviolet-induced skin tumour |
| Q47997792 | Expression of major histocompatibility complex class II antigen in neoplastic cells of canine cutaneous histiocytoma |
| Q72650446 | Half-life of antigen/major histocompatibility complex class II complexes in vivo: intra- and interorgan variations |
| Q74578843 | Human epidermal Langerhans cells lack functional mannose receptors and a fully developed endosomal/lysosomal compartment for loading of HLA class II molecules |
| Q36231236 | Identification of proliferating dendritic cell precursors in mouse blood |
| Q24803671 | Identification of proteases employed by dendritic cells in the processing of protein purified derivative (PPD) |
| Q26827675 | Immunological cells and functions in Gaucher disease |
| Q28377124 | In vitro evaluation of the sensitization potential of weak contact allergens using langerhans-like dendritic cells and autologous T cells |
| Q52060733 | In vitro primary sensitization and restimulation of hapten-specific T cells by fresh and cultured human epidermal Langerhans' cells. |
| Q57275942 | Inflammatory stimuli induce accumulation of MHC class II complexes on dendritic cells |
| Q35810853 | Interaction of antigen presenting cells with mycobacteria. |
| Q72112185 | Internalization of surface HLA-DR molecules by human epidermal Langerhans cells: analysis by flow cytometry and confocal microscopy |
| Q72525379 | Interstitial lung macrophages interact with dendritic cells to present antigenic peptides derived from particulate antigens to T cells |
| Q41623807 | Irreversible association of peptides with class II MHC molecules in living cells. |
| Q40680757 | Isolation and function of human dendritic cells. |
| Q49155579 | Langerhans cells transport Leishmania major from the infected skin to the draining lymph node for presentation to antigen-specific T cells |
| Q43803094 | Localization of Class II Molecules in Storage Vesicles, Endosomes and Lysosomes in Human Dendritic Cells |
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| Q72102720 | Macrophages, but not dendritic cells, accumulate colloidal carbon following administration in situ |
| Q52876821 | Macrophages, but not dendritic cells, present collagen to T cells. |
| Q36365201 | Mechanisms of acquired thymic tolerance in experimental autoimmune encephalomyelitis: thymic dendritic-enriched cells induce specific peripheral T cell unresponsiveness in vivo |
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| Q42641902 | Molecular cloning and expression of two chicken invariant chain isoforms produced by alternative splicing |
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| Q68147110 | Murine epidermal Langerhans cells are potent stimulators of an antigen-specific T cell response to Leishmania major, the cause of cutaneous leishmaniasis |
| Q54422953 | Myocutaneous flaps in patients with head and neck cancer retain their immunological capacities in an activated functional state. |
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| Q40269946 | Presentation of mycobacterial antigens by human dendritic cells: lack of transfer from infected macrophages |
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| Q72238550 | Role of epidermal Langerhans' cells in the induction of protective immunity to Schistosoma mansoni in guinea-pigs |
| Q42971765 | Selective recruitment of immature and mature dendritic cells by distinct chemokines expressed in different anatomic sites |
| Q67526841 | Spleen dendritic cells exhibit altered morphology and increased allostimulatory capacity after short-term culture |
| Q68056304 | Studies on the surface phenotype and functions of dendritic cells in parenchymal lung tissue of the rat |
| Q35553745 | Synthesis, stability, and subcellular distribution of major histocompatibility complex class II molecules in Langerhans cells infected with Leishmania major. |
| Q41060280 | The defective antigen-presenting activity of murine fetal macrophage cell lines |
| Q40457008 | The endocytic activity of dendritic cells. |
| Q36368355 | The formation of immunogenic major histocompatibility complex class II-peptide ligands in lysosomal compartments of dendritic cells is regulated by inflammatory stimuli |
| Q35427248 | The immunologic properties of epidermal Langerhans cells as a part of the dendritic cell system. |
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