| P2093 | author name string | Pieters J | |
| P2860 | cites work | HLA-DR molecules from an antigen-processing mutant cell line are associated with invariant chain peptides | Q24294751 |
| | Structure of the human class I histocompatibility antigen, HLA-A2 | Q24297966 |
| | The structure of an intermediate in class II MHC maturation: CLIP bound to HLA-DR3 | Q24303524 |
| | An essential role for HLA-DM in antigen presentation by class II major histocompatibility molecules | Q24309308 |
| | A dendritic-cell-derived C-C chemokine that preferentially attracts naive T cells | Q24311809 |
| | AP-3: an adaptor-like protein complex with ubiquitous expression | Q24315945 |
| | Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome) | Q24317711 |
| | HLA-DM induces clip dissociation from MHC class II αβ dimers and facilitates peptide loading | Q24318038 |
| | Characterization of the adaptor-related protein complex, AP-3 | Q24321479 |
| | Sec61-mediated transfer of a membrane protein from the endoplasmic reticulum to the proteasome for destruction | Q24324602 |
| | Essential role for cathepsin S in MHC class II-associated invariant chain processing and peptide loading | Q24328923 |
| | The epitopes of influenza nucleoprotein recognized by cytotoxic T lymphocytes can be defined with short synthetic peptides | Q24339477 |
| | Clathrin coats at 21 A resolution: a cellular assembly designed to recycle multiple membrane receptors | Q24533303 |
| | Pool sequencing of natural HLA-DR, DQ, and DP ligands reveals detailed peptide motifs, constraints of processing, and general rules | Q72271969 |
| | Molecular requirements for the interaction of class II major histocompatibility complex molecules and invariant chain with calnexin | Q72536368 |
| | The B-cell antigen receptor complex: structure and signal transduction | Q72768322 |
| | Proteases, processing, and thymic selection | Q74516573 |
| | Genetic susceptibility to systemic lupus erythematosus | Q74578130 |
| | Impaired invariant chain degradation and antigen presentation and diminished collagen-induced arthritis in cathepsin S null mice | Q74595052 |
| | Signal transduction of phagocytosis | Q75294630 |
| | Phagocytosis of microbes: insights and prospects | Q75294681 |
| | Mechanisms of protein sorting and coat assembly: insights from the clathrin-coated vesicle pathway | Q77159594 |
| | Transport vesicles: coats of many colours | Q77316060 |
| | MHC class II and invariant chain biosynthesis and transport during maturation of human precursor dendritic cells | Q77658986 |
| | Mice lacking the transcription factor CIITA--a second look | Q77786394 |
| | Autoimmunity | Q95444134 |
| | HLA-DR associates with specific stress proteins and is retained in the endoplasmic reticulum in invariant chain negative cells | Q24675139 |
| | Major histocompatibility complex class II-associated p41 invariant chain fragment is a strong inhibitor of lysosomal cathepsin L | Q24678337 |
| | B lymphocytes secrete antigen-presenting vesicles | Q24678522 |
| | Invariant chain trimers are sequestered in the rough endoplasmic reticulum in the absence of association with HLA class II antigens | Q24678747 |
| | Dendritic cells use macropinocytosis and the mannose receptor to concentrate macromolecules in the major histocompatibility complex class II compartment: downregulation by cytokines and bacterial products | Q24678867 |
| | Identification of a novel cell type in peripheral lymphoid organs of mice. I. Morphology, quantitation, tissue distribution | Q24679240 |
| | Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma | Q24681545 |
| | Crystal structures of two viral peptides in complex with murine MHC class I H-2Kb | Q27642080 |
| | Specificity pockets for the side chains of peptide antigens in HLA-Aw68 | Q27700642 |
| | Crystal structure of the human class II MHC protein HLA-DR1 complexed with an influenza virus peptide | Q27731272 |
| | Atomic structure of clathrin: a beta propeller terminal domain joins an alpha zigzag linker | Q27766075 |
| | Dendritic cells and the control of immunity | Q27860918 |
| | A novel di-leucine motif and a tyrosine-based motif independently mediate lysosomal targeting and endocytosis of CD3 chains | Q27913878 |
| | A new human HLA class II-related locus, DM | Q28235428 |
| | MHC class II-deficient combined immunodeficiency: a disease of gene regulation | Q28247076 |
| | HLA-DMA and -DMB genes are both required for MHC class II/peptide complex formation in antigen-presenting cells | Q28251133 |
| | Limited polymorphism in HLA-DM does not involve the peptide binding groove | Q28255697 |
| | The serum mannose-binding protein and the macrophage mannose receptor are pattern recognition molecules that link innate and adaptive immunity | Q28287631 |
| | Interaction of tyrosine-based sorting signals with clathrin-associated proteins | Q28290076 |
| | DM enhances peptide binding to class II MHC by release of invariant chain-derived peptide | Q28295795 |
| | A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome) | Q28301107 |
| | Uptake of Pneumocystis carinii mediated by the macrophage mannose receptor | Q28301754 |
| | Sequence analysis of peptides bound to MHC class II molecules | Q28303686 |
| | Altered antigen presentation in mice lacking H2-O | Q28504672 |
| | H2-M mutant mice are defective in the peptide loading of class II molecules, antigen presentation, and T cell repertoire selection | Q28504958 |
| | Mice lacking H2-M complexes, enigmatic elements of the MHC class II peptide-loading pathway | Q28507891 |
| | The MHC class II molecule H2-M is targeted to an endosomal compartment by a tyrosine-based targeting motif | Q28585954 |
| | Antigen presentation and T cell development in H2-M-deficient mice | Q28587240 |
| | Antigen processing for presentation by class II major histocompatibility complex requires cleavage by cathepsin E | Q28589161 |
| | Cathepsin S required for normal MHC class II peptide loading and germinal center development | Q28611850 |
| | MHC class II-associated invariant chain contains a sorting signal for endosomal compartments | Q28612553 |
| | Negative regulation by HLA-DO of MHC class II-restricted antigen processing | Q28613199 |
| | Cathepsin L: critical role in Ii degradation and CD4 T cell selection in the thymus | Q28613227 |
| | Inhibition of invariant chain (Ii)-calnexin interaction results in enhanced degradation of Ii but does not prevent the assembly of alpha beta Ii complexes | Q36365643 |
| | Related leucine-based cytoplasmic targeting signals in invariant chain and major histocompatibility complex class II molecules control endocytic presentation of distinct determinants in a single protein | Q36376527 |
| | Dendritic cells are recruited into the airway epithelium during the inflammatory response to a broad spectrum of stimuli | Q36377468 |
| | Degradation of mouse invariant chain: roles of cathepsins S and D and the influence of major histocompatibility complex polymorphism | Q36380525 |
| | A lysosomal targeting signal in the cytoplasmic tail of the beta chain directs HLA-DM to MHC class II compartments. | Q36382769 |
| | Sorting signals in the MHC class II invariant chain cytoplasmic tail and transmembrane region determine trafficking to an endocytic processing compartment | Q36382892 |
| | Type II and III receptors for immunoglobulin G (IgG) control the presentation of different T cell epitopes from single IgG-complexed antigens | Q36400334 |
| | Complement receptors and phagocytosis | Q36499115 |
| | Bacterial entry into eukaryotic cells | Q37342351 |
| | MHC class-II molecules and autoimmunity | Q37357888 |
| | Receptor-mediated antigen uptake and its effect on antigen presentation to class II-restricted T lymphocytes | Q37925555 |
| | Protein degradation in the endoplasmic reticulum | Q37947738 |
| | The role of N-linked oligosaccharides of MHC class II antigens in T cell stimulation | Q38307334 |
| | New class II-like genes in the murine MHC. | Q38332928 |
| | MHC class II invariant chains in antigen processing and presentation | Q38735747 |
| | Protein oligomerization in the endoplasmic reticulum | Q38737584 |
| | Predominant naturally processed peptides bound to HLA-DR1 are derived from MHC-related molecules and are heterogeneous in size | Q39229154 |
| | Acidification of the endocytic and exocytic pathways | Q39459758 |
| | The immune response genes of the major histocompatibility complex | Q39475236 |
| | Constitutive and regulated secretion of proteins | Q39683816 |
| | Genetics and expression of mouse Ia antigens | Q39849787 |
| | Histocompatibility-linked immune response genes | Q39866999 |
| | Role of MHC gene products in immune regulation | Q40100288 |
| | The class II molecules of the human and murine major histocompatibility complex. | Q40108949 |
| | Quality control in the secretory pathway | Q40380586 |
| | The cell biology of CTL killing | Q40404856 |
| | HLA-DM: an in vivo facilitator of MHC class II peptide loading | Q40410057 |
| | The endocytic activity of dendritic cells. | Q40457008 |
| | MHC molecules as peptide receptors | Q40485460 |
| | Dominance and crypticity of T cell antigenic determinants | Q40486347 |
| | Immunoglobulin E-binding structures on antigen-presenting cells present in skin and blood | Q40518123 |
| | Phagocytosis | Q40523944 |
| | Chemistry of peptides associated with MHC class I and class II molecules | Q40540085 |
| | Molecular basis of Fc receptor function | Q40602173 |
| | The role of clathrin, adaptors and dynamin in endocytosis | Q40647427 |
| | Biology of animal lectins | Q40800560 |
| | Positive selection of lymphocytes | Q40807424 |
| | MHC-dependent antigen processing and peptide presentation: providing ligands for T lymphocyte activation | Q40807437 |
| | The mouse B-cell antigen receptor: definition and assembly of the core receptor of the five immunoglobulin isotypes | Q40833862 |
| | Peptides naturally presented by MHC class I molecules | Q40898177 |
| | Origin, maturation and antigen presenting function of dendritic cells. | Q40906220 |
| | Regulation of MHC class II gene expression. | Q40928426 |
| | Invariant chain structure and MHC class II function | Q40968427 |
| | The cell biology of infection by intracellular bacterial pathogens. | Q41020962 |
| | How MHC class II molecules acquire peptide cargo: biosynthesis and trafficking through the endocytic pathway | Q41020969 |
| | Detection of a common polypeptide chain in I-A and I-E sub-region immunoprecipitates | Q41048783 |
| | Developing and shedding inhibitions: how MHC class II molecules reach maturity | Q41053707 |
| | HLA-DO is a negative modulator of HLA-DM-mediated MHC class II peptide loading | Q41064461 |
| | Distinct antigen MHC class II complexes generated by separate processing pathways. | Q41079003 |
| | Developmental regulation of MHC class II transport in mouse dendritic cells. | Q41093187 |
| | Antigen endocytosis and presentation mediated by human membrane IgG1 in the absence of the Ig(alpha)/Ig(beta) dimer | Q41101974 |
| | The alpha chain gene of H-2O has an unexpected location in the major histocompatibility complex | Q36231627 |
| | Phagocytic chimeric receptors require both transmembrane and cytoplasmic domains from the mannose receptor | Q36232139 |
| | Efficient endosomal localization of major histocompatibility complex class II-invariant chain complexes requires multimerization of the invariant chain targeting sequence | Q36235619 |
| | Isoforms of the invariant chain regulate transport of MHC class II molecules to antigen processing compartments | Q36236708 |
| | Protein targeting by tyrosine- and di-leucine-based signals: evidence for distinct saturable components | Q36237576 |
| | Demonstration of structural polymorphism among HLA-DR light chains by two-dimensional gel electrophoresis | Q36343209 |
| | Dendritic cells are accessory cells for the development of anti-trinitrophenyl cytotoxic T lymphocytes | Q36344044 |
| | Antigen presentation by hapten-specific B lymphocytes. I. Role of surface immunoglobulin receptors | Q36349536 |
| | Cell surface expression of class II histocompatibility antigens occurs in the absence of the invariant chain | Q36353070 |
| | Tyrosine phosphorylation is required for Fc receptor-mediated phagocytosis in mouse macrophages | Q36361230 |
| | Specificity and promiscuity among naturally processed peptides bound to HLA-DR alleles | Q36361966 |
| | Dendritic cell progenitors phagocytose particulates, including bacillus Calmette-Guerin organisms, and sensitize mice to mycobacterial antigens in vivo | Q36362128 |
| | Determinant capture as a possible mechanism of protection afforded by major histocompatibility complex class II molecules in autoimmune disease | Q36362580 |
| | The requirement for DM in class II-restricted antigen presentation and SDS-stable dimer formation is allele and species dependent. | Q36364225 |
| | Binding of major histocompatibility complex class II to the invariant chain-derived peptide, CLIP, is regulated by allelic polymorphism in class II. | Q36364390 |
| | Confrontation between intracellular bacteria and the immune system. | Q43459073 |
| | Fc receptors | Q44298973 |
| | Two-dimensional gel analysis of the polypeptides precipitated by a polymorphic HLA-DR1,2,w6 monoclonal antibody: evidence for a third locus | Q44827228 |
| | Isolation and analysis of naturally processed viral peptides as recognized by cytotoxic T cells | Q45007765 |
| | Two forms of the Ia antigen-associated invariant chain result from alternative initiations at two in-phase AUGs | Q45200339 |
| | Sequestration from immune CD4+ T cells of mycobacteria growing in human macrophages | Q45222064 |
| | Intracellular transport of class II MHC molecules directed by invariant chain. | Q45941447 |
| | A novel class II MHC molecule with unusual tissue distribution | Q45998244 |
| | Invariant chain distinguishes between the exogenous and endogenous antigen presentation pathways | Q46424023 |
| | Clathrin coats--threads laid bare | Q46487428 |
| | Characterization of a naturally processed MHC class II-restricted T-cell determinant of hen egg lysozyme | Q46739108 |
| | Developmental regulation of invariant chain proteolysis controls MHC class II trafficking in mouse dendritic cells. | Q47872621 |
| | Secretory lysosomes - a special mechanism of regulated secretion in haemopoietic cells | Q47986701 |
| | Nomenclature for factors of the HLA system, 1996. | Q48775755 |
| | Transient aggregation of major histocompatibility complex class II chains during assembly in normal spleen cells. | Q49164800 |
| | Antigen presentation by memory B cells: the sting is in the tail. | Q52043159 |
| | Some recollections of Peter Gorer and his work on this fiftieth anniversary of his discovery of H-2. | Q52404001 |
| | The repertoire of T cells shaped by a single MHC/peptide ligand. | Q52887226 |
| | The role of complement and complement receptors in induction and regulation of immunity. | Q53992218 |
| | Allele-specific motifs revealed by sequencing of self-peptides eluted from MHC molecules | Q55042699 |
| | Antigen receptor tail clue. | Q55060334 |
| | Restriction of in vitro T cell-mediated cytotoxicity in lymphocytic choriomeningitis within a syngeneic or semiallogeneic system. | Q55061347 |
| | The mannose receptor functions as a high capacity and broad specificity antigen receptor in human dendritic cells | Q57275938 |
| | Inflammatory stimuli induce accumulation of MHC class II complexes on dendritic cells | Q57275942 |
| | Mannose receptor mediated antigen uptake and presentation in human dendritic cells | Q57275947 |
| | The mannose 6-phosphate receptor and the biogenesis of lysosomes | Q57960197 |
| | Immunology Inside the gearbox of the dendritic cell | Q58323381 |
| | Antigen processing and class II MHC peptide-loading compartments in human B-lymphoblastoid cells | Q58323390 |
| | Lymphocytes recognize human vascular endothelial and dermal fibroblast Ia antigens induced by recombinant immune interferon | Q59063739 |
| | Antigen-specific interaction between T and B cells | Q59063745 |
| | Binding of immunogenic peptides to Ia histocompatibility molecules | Q59070314 |
| | Association of class I major histocompatibility heavy and light chains induced by viral peptides | Q59072754 |
| | Reversal of fortune for nascent proteins | Q59072797 |
| | Transient accumulation of new class II MHC molecules in a novel endocytic compartment in B lymphocytes | Q59098594 |
| | Cytotoxic T cells recognize fragments of the influenza nucleoprotein | Q61761274 |
| | Emerging principles for the recognition of peptide antigens by MHC class I molecules | Q67494475 |
| | Exact prediction of a natural T cell epitope | Q67702861 |
| | Map of the human MHC | Q67848204 |
| | HL-A, immune-response genes, and disease | Q70017187 |
| | Biochemical characterization of an invariant polypeptide associated with Ia antigens in human and mouse | Q70903774 |
| | Mice lacking the MHC class II transactivator (CIITA) show tissue-specific impairment of MHC class II expression | Q71066478 |
| | The gene encoding the human class II antigen-associated gamma chain is located on chromosome 5 | Q71429361 |
| | Receptor-mediated pinocytosis of mannose glycoconjugates by macrophages: characterization and evidence for receptor recycling | Q71494370 |
| | Potent effects of low levels of MHC class II-associated invariant chain on CD4+ T cell development | Q71727590 |
| | Reconstitution of invariant chain function in transgenic mice in vivo by individual p31 and p41 isoforms | Q71727595 |
| | Major histocompatibility class II peptide occupancy, antigen presentation, and CD4+ T cell function in mice lacking the p41 isoform of invariant chain | Q71727600 |
| | Destructive proteolysis by cysteine proteases in antigen presentation of ovalbumin | Q71918543 |
| | Cathepsin D, but not cathepsin B, releases T cell stimulatory fragments from lysozyme that are functional in the context of multiple murine class II MHC molecules | Q72194431 |
| | Peptide motifs of HLA-B51, -B52 and -B78 molecules, and implications for Behćet's disease | Q72201949 |
| | Identification of two distinct mechanisms of phagocytosis controlled by different Rho GTPases | Q29614245 |
| | The proteasome: paradigm of a self-compartmentalizing protease | Q29615187 |
| | Intracellular Aspects of the Process of Protein Synthesis | Q29615237 |
| | Endocytosis and molecular sorting | Q29616706 |
| | Lack of acidification in Mycobacterium phagosomes produced by exclusion of the vesicular proton-ATPase | Q29617355 |
| | The biogenesis of lysosomes | Q29617860 |
| | The ubiquitin system | Q29618565 |
| | The human cytomegalovirus US11 gene product dislocates MHC class I heavy chains from the endoplasmic reticulum to the cytosol | Q29618773 |
| | Response of cultured macrophages to Mycobacterium tuberculosis, with observations on fusion of lysosomes with phagosomes | Q31154479 |
| | Mechanism of Shigella entry into epithelial cells | Q33536573 |
| | Impact of intracellular location of and antigen display by intracellular bacteria: implications for vaccine development | Q33538300 |
| | A coat protein on phagosomes involved in the intracellular survival of mycobacteria | Q33862936 |
| | Dileucine-based sorting signals bind to the beta chain of AP-1 at a site distinct and regulated differently from the tyrosine-based motif-binding site | Q33888654 |
| | The mannose receptor mediates uptake of pathogenic and nonpathogenic mycobacteria and bypasses bactericidal responses in human macrophages | Q34000130 |
| | Localization of the HLA class II-associated invariant chain gene to human chromosome band 5q32. | Q34167283 |
| | Molecular characterization of the human macrophage mannose receptor: demonstration of multiple carbohydrate recognition-like domains and phagocytosis of yeasts in Cos-1 cells | Q34269349 |
| | Membrane insertion and oligomeric assembly of HLA-DR histocompatibility antigens | Q34273916 |
| | The receptor DEC-205 expressed by dendritic cells and thymic epithelial cells is involved in antigen processing | Q34310837 |
| | Assembly, transport, and function of MHC class II molecules | Q34328789 |
| | Isolation and characterization of the intracellular MHC class II compartment. | Q34340778 |
| | Three-dimensional structure of the human class II histocompatibility antigen HLA-DR1. | Q34350288 |
| | The chondroitin sulfate form of invariant chain can enhance stimulation of T cell responses through interaction with CD44. | Q34352008 |
| | Initiation and processing of signals from the B cell antigen receptor | Q34425416 |
| | Host-pathogen interactions during entry and actin-based movement of Listeria monocytogenes | Q34453738 |
| | Mechanisms of MHC class I--restricted antigen processing | Q34468834 |
| | An asparaginyl endopeptidase processes a microbial antigen for class II MHC presentation. | Q34485526 |
| | The trans Golgi network: sorting at the exit site of the Golgi complex. | Q34562583 |
| | L. monocytogenes-induced actin assembly requires the actA gene product, a surface protein | Q34614282 |
| | Immunological surveillance against altered self components by sensitised T lymphocytes in lymphocytes choriomeningitis | Q34699212 |
| | The mannose receptor and other macrophage lectins | Q35228669 |
| | Chemistry and functional role of the invariant chain | Q35228677 |
| | Immunological aspects of demyelinating diseases | Q35319665 |
| | The immunogenetics of rheumatoid arthritis | Q35532736 |
| | Protein antigens of Chlamydia psittaci present in infected cells but not detected in the infectious elementary body | Q35771161 |
| | Complexity in the major histocompatibility complex | Q36022934 |
| | Transfer of proteins across membranes. II. Reconstitution of functional rough microsomes from heterologous components | Q36204254 |
| | Tails from the hall of infection: actin-based motility of pathogens. | Q41104075 |
| | Role of B cell receptor Ig alpha and Ig beta subunits in MHC class II-restricted antigen presentation | Q41306022 |
| | The two novel MHC class II transactivators RFX5 and CIITA both control expression of HLA-DM genes | Q41322316 |
| | Mediation by HLA-DM of dissociation of peptides from HLA-DR | Q41333614 |
| | Antigen presentation mediated by recycling of surface HLA-DR molecules. | Q41335304 |
| | Regulation of transcription of MHC class II genes | Q41353021 |
| | MHC class II restricted antigen presentation | Q41353041 |
| | Inter-relationship among macrophages, natural killer cells and neutrophils in early stages of Listeria resistance | Q41353064 |
| | How HLA-DM edits the MHC class II peptide repertoire: survival of the fittest? | Q41370585 |
| | Assembly and intracellular transport of HLA-DM and correction of the class II antigen-processing defect in T2 cells | Q41440525 |
| | Regulation of MHC class II expression by interferon-gamma mediated by the transactivator gene CIITA. | Q41457392 |
| | A segment of the MHC class II beta chain plays a critical role in targeting class II molecules to the endocytic pathway | Q41458842 |
| | Fc receptor biology | Q41464279 |
| | Capture and processing of exogenous antigens for presentation on MHC molecules. | Q41464375 |
| | Biogenesis of phagolysosomes proceeds through a sequential series of interactions with the endocytic apparatus | Q41483433 |
| | Signal transduction in the mammalian cell during bacterial attachment and entry | Q41502909 |
| | Linking cargo to vesicle formation: receptor tail interactions with coat proteins. | Q41566699 |
| | Structure of the murine Ia-associated invariant (Ii) chain as deduced from a cDNA clone. | Q41569267 |
| | Invariant chain peptides in most HLA-DR molecules of an antigen-processing mutant | Q41589934 |
| | Antigen presentation enhanced by the alternatively spliced invariant chain gene product p41. | Q41619054 |
| | Endosomal proteases and antigen processing | Q41633118 |
| | Formation of a nine-subunit complex by HLA class II glycoproteins and the invariant chain | Q41653246 |
| | Intracellular transport and localization of major histocompatibility complex class II molecules and associated invariant chain | Q41653697 |
| | Peptide selection by MHC class I molecules | Q41687117 |
| | Microbial immunology: a new mechanism for immune subversion | Q41690560 |
| | Segregation of MHC class II molecules from MHC class I molecules in the Golgi complex for transport to lysosomal compartments | Q41695026 |
| | Isolation of an endogenously processed immunodominant viral peptide from the class I H–2Kb molecule | Q41714857 |
| | Antigen processing: HLA-DO--a hitchhiking inhibitor of HLA-DM. | Q41720786 |
| | Toxoplasma gondii: fusion competence of parasitophorous vacuoles in Fc receptor-transfected fibroblasts | Q41725157 |
| | Empty MHC class I molecules come out in the cold | Q41725383 |
| | Role of B-cell and Fc receptors in the selection of T-cell epitopes | Q41729828 |
| | Endosomal proteolysis and MHC class II function | Q41729834 |
| | Invariant chain association with HLA-DR molecules inhibits immunogenic peptide binding | Q41731115 |
| | Viral strategies of immune evasion | Q41735903 |
| | Defective processing and presentation of exogenous antigens in mutants with normal HLA class II genes | Q41944480 |
| | Class II transactivator regulates the expression of multiple genes involved in antigen presentation | Q41944761 |
| | A role of Ia-associated invariant chains in antigen processing and presentation. | Q41946241 |
| | Antigen capture and major histocompatibility class II compartments of freshly isolated and cultured human blood dendritic cells | Q41946843 |
| | Keratinocyte-Derived Monocyte Chemoattractant Protein 1 (MCP-1): Analysis in a Transgenic Model Demonstrates MCP-1 Can Recruit Dendritic and Langerhans Cells to Skin | Q42479824 |
| | Immunocytochemical characterization of the endocytic and phagolysosomal compartments in peritoneal macrophages | Q42545057 |
| | Acceleration of intracellular targeting of antigen by the B-cell antigen receptor: importance depends on the nature of the antigen-antibody interaction. | Q42594655 |
| | Transport properties of free and MHC class II-associated oligomers containing different isoforms of human invariant chain | Q42605882 |
| | A macrophage invasion mechanism of pathogenic mycobacteria | Q42662108 |
| | Distinct intracellular compartments involved in invariant chain degradation and antigenic peptide loading of major histocompatibility complex (MHC) class II molecules | Q42796320 |
| | Colocalization of F-actin and talin during Fc receptor-mediated phagocytosis in mouse macrophages | Q42938886 |
| | A 15 amino acid fragment of influenza nucleoprotein synthesized in the cytoplasm is presented to class I-restricted cytotoxic T lymphocytes | Q42939778 |
| | Suppressive effect of antibody on processing of T cell epitopes | Q42941954 |
| | Characterization of the Mycobacterium tuberculosis phagosome and evidence that phagosomal maturation is inhibited | Q42942760 |
| | T cell responses affected by aminopeptidase N (CD13)-mediated trimming of major histocompatibility complex class II-bound peptides | Q42943610 |
| P304 | page(s) | 159-208 | |
| P577 | publication date | 2000-01-01 | |
| P1433 | published in | Advances in Immunology | Q15752932 |
| P1476 | title | MHC class II-restricted antigen processing and presentation | |
| P478 | volume | 75 | |