| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S12026-009-8095-8 |
| P698 | PubMed publication ID | 19198764 |
| P2093 | author name string | Andrea J Sant | |
| Jason M Weaver | |||
| P2860 | cites work | Cleavage of the papillomavirus minor capsid protein, L2, at a furin consensus site is necessary for infection | Q24537437 |
| Antiviral CD4+ memory T cells are IL-15 dependent | Q24676283 | ||
| The mechanism by which influenza A virus nucleoprotein forms oligomers and binds RNA | Q27640425 | ||
| Crystal structure of MHC class II I-Ab in complex with a human CLIP peptide: prediction of an I-Ab peptide-binding motif | Q27640503 | ||
| Structures of an MHC class II molecule with covalently bound single peptides | Q27732720 | ||
| Functional association between viral and cellular transcription during influenza virus infection | Q27863933 | ||
| Nuclear traffic of influenza virus proteins and ribonucleoprotein complexes | Q27864127 | ||
| Nuclear import and export of influenza virus nucleoprotein | Q27867703 | ||
| Gamma-interferon-inducible lysosomal thiol reductase (GILT). Maturation, activity, and mechanism of action | Q28138259 | ||
| Occurrence of an HIV-1 gp160 endoproteolytic activity in low-density vesicles and evidence for a distinct density distribution from endogenously expressed furin and PC7/LPC convertases | Q28142392 | ||
| The impact of the non-classical MHC proteins HLA-DM and HLA-DO on loading of MHC class II molecules | Q28142443 | ||
| Two subsets of memory T lymphocytes with distinct homing potentials and effector functions | Q28146072 | ||
| Dynamics of CD8+ T cell priming by dendritic cells in intact lymph nodes | Q28202515 | ||
| T-cell priming by dendritic cells in lymph nodes occurs in three distinct phases | Q28237805 | ||
| Achieving stability through editing and chaperoning: regulation of MHC class II peptide binding and expression | Q28273723 | ||
| The Impact of H2-DM on Humoral Immune Responses | Q28506169 | ||
| Clustering of Th Cell Epitopes on Exposed Regions of HIV Envelope Despite Defects in Antibody Activity | Q79125450 | ||
| Functional specialization of memory Th cells revealed by expression of integrin CD49b | Q79834615 | ||
| The kinetic stability of MHC class II:peptide complexes is a key parameter that dictates immunodominance | Q80416551 | ||
| Immunodominance in TCD8+ responses to viruses: cell biology, cellular immunology, and mathematical models | Q80444901 | ||
| Endoproteolysis in health and diseases--implications of proprotein convertases (PCs) | Q81190073 | ||
| Real-time manipulation of T cell-dendritic cell interactions in vivo reveals the importance of prolonged contacts for CD4+ T cell activation | Q81469542 | ||
| Modulation of peptide-dependent allospecific epitopes on HLA-DR4 molecules by HLA-DM. | Q41052024 | ||
| Determinant selection for T-cell tolerance in HEL-transgenic mice: dissociation between immunogenicity and tolerogenicity | Q41116405 | ||
| Human histocompatibility leukocyte antigen (HLA)-DM edits peptides presented by HLA-DR according to their ligand binding motifs | Q41154435 | ||
| The endogenous pathway of MHC class II antigen presentation. | Q41168212 | ||
| Mediation by HLA-DM of dissociation of peptides from HLA-DR | Q41333614 | ||
| How HLA-DM edits the MHC class II peptide repertoire: survival of the fittest? | Q41370585 | ||
| Peptide binding to the most frequent HLA-A class I alleles measured by quantitative molecular binding assays | Q41450491 | ||
| How HLA-DM Affects the Peptide Repertoire Bound to HLA-DR Molecules | Q41594025 | ||
| Selection of the MHC Class II-associated peptide repertoire by HLA-DM | Q41649540 | ||
| Interference with the binding of a naturally processed peptide to class II alters the immunodominance of T cell epitopes in vivo | Q41662292 | ||
| Antigen-presenting cells and the selection of immunodominant epitopes | Q41674613 | ||
| MHC class II-restricted presentation of intracellular antigen | Q41694984 | ||
| Protein sorting within the mhc class II antigen-processing pathway | Q41710771 | ||
| The generation of immunogenic peptides can be selectively increased or decreased by proteolytic enzyme inhibitors | Q42472217 | ||
| The majority of immunogenic epitopes generate CD4+ T cells that are dependent on MHC class II-bound peptide-flanking residues | Q42679630 | ||
| Immunodominance of CD4 T cells to foreign antigens is peptide intrinsic and independent of molecular context: implications for vaccine design | Q42925957 | ||
| Primary and memory T cell responses induced by hepatitis C virus multiepitope long peptides | Q42998313 | ||
| Immunization with a synthetic multiepitope antigen induces humoral and cellular immune responses to hepatitis C virus in mice | Q43037078 | ||
| Heterogeneity of the T cell response to immunodominant determinants within hen eggwhite lysozyme of individual syngeneic hybrid F1 mice: implications for autoimmunity and infection. | Q43464025 | ||
| Kinetics of precursor cleavage at the dibasic sites. Involvement of peptide dynamics | Q43962943 | ||
| Interleukin 7 and T cell receptor signals regulate homeostasis of CD4 memory cells | Q44479232 | ||
| Structural basis for helper T-cell and antibody epitope immunodominance in bacteriophage T4 Hsp10. Role of disordered loops | Q44619152 | ||
| Antigen processing and T cell repertoires as crucial aleatory features in induction of autoimmunity | Q44750798 | ||
| Impairment of immunological memory in the absence of MHC despite survival of memory T cells | Q45072920 | ||
| Imaging of plasmacytoid dendritic cell interactions with T cells | Q45817701 | ||
| A Bayesian regression approach to the prediction of MHC-II binding affinity | Q45828576 | ||
| Efficient synthesis of influenza virus hemagglutinin in mammalian cells with an extrachromosomal Epstein-Barr virus vector. | Q45845331 | ||
| Rapid expansion and IL-4 expression by Leishmania-specific naive helper T cells in vivo | Q46150935 | ||
| From protein microarrays to diagnostic antigen discovery: a study of the pathogen Francisella tularensis | Q46315736 | ||
| Lymphoid reservoirs of antigen-specific memory T helper cells | Q46609740 | ||
| Measurement of peptide dissociation from MHC class II molecules | Q46629980 | ||
| Insertion of the dibasic motif in the flanking region of a cryptic self-determinant leads to activation of the epitope-specific T cells | Q46635947 | ||
| The relative energetic contributions of dominant P1 pocket versus hydrogen bonding interactions to peptide:class II stability: implications for the mechanism of DM function | Q46916435 | ||
| Modulation of the immunogenicity of antigenic determinants by their flanking residues | Q48013126 | ||
| Peptide-binding motifs for the I-Ad MHC class II molecule: alternate pH-dependent binding behavior | Q51807705 | ||
| Static energy analysis of MHC class I and class II peptide-binding affinity | Q51887363 | ||
| Class II-independent generation of CD4 memory T cells from effectors | Q52031200 | ||
| T cell recognition of myoglobin. Localization of the sites stimulating T cell proliferative responses by synthetic overlapping peptides encompassing the entire molecule | Q52209814 | ||
| Control of Leishmania major by a monoclonal alpha beta T cell repertoire | Q52530262 | ||
| Enhanced catalytic action of HLA-DM on the exchange of peptides lacking backbone hydrogen bonds between their N-terminal region and the MHC class II alpha-chain | Q52552855 | ||
| Proliferating CD4+ T cells undergo immediate growth arrest upon cessation of TCR signaling in vivo | Q53509518 | ||
| Antigen three-dimensional structure guides the processing and presentation of helper T-cell epitopes | Q54458197 | ||
| Induction of T cell responses by chimeric bacterial proteins expressing several copies of a viral T cell epitope. | Q54648972 | ||
| Antigen recognition by H-2-restricted T cells. II. A tryptic ovalbumin peptide that substitutes for processed antigen | Q56922571 | ||
| Intercellular Adhesion Molecule-1-Dependent Stable Interactions between T Cells and Dendritic Cells Determine CD8+ T Cell Memory | Q58862007 | ||
| Distinct T cell dynamics in lymph nodes during the induction of tolerance and immunity | Q58862024 | ||
| In vivo competition between self peptides and foreign antigens in T-cell activation | Q59065328 | ||
| Helper T-cell Epitope Immunodominance Associated with Structurally Stable Segments of Hen Egg Lysozyme and HIV gp120 | Q59600025 | ||
| Expression of heterologous peptides at two permissive sites of the MalE protein: antigenicity and immunogenicity of foreign B-cell and T-cell epitopes | Q67541840 | ||
| Mechanisms of T cell epitope immunodominance analyzed in murine listeriosis | Q71829469 | ||
| Immunodominance: a single amino acid substitution within an antigenic site alters intramolecular selection of T cell determinants | Q72090150 | ||
| Role of amino acid sequences flanking dibasic cleavage sites in precursor proteolytic processing. The importance of the first residue C-terminal of the cleavage site | Q72572370 | ||
| Identification of distinct predominant epitopes recognized by myoglobin-specific T cells under the control of different Ir genes and characterization of representative T cell clones | Q72722984 | ||
| Ovalbumin(323-339) peptide binds to the major histocompatibility complex class II I-A(d) protein using two functionally distinct registers | Q73277342 | ||
| Immunodominance is independent of structural constraints: each region within hen eggwhite lysozyme is potentially available upon processing of native antigen | Q73705562 | ||
| T Cell Receptor Recognition of MHC Class II–Bound Peptide Flanking Residues Enhances Immunogenicity and Results in Altered TCR V Region Usage | Q73767636 | ||
| Cutting edge: H-2DM is responsible for the large differences in presentation among peptides selected by I-Ak during antigen processing | Q73827781 | ||
| Cutting edge: introduction of an endopeptidase cleavage motif into a determinant flanking region of hen egg lysozyme results in enhanced T cell determinant display | Q73910685 | ||
| Dynamic imaging of T cell-dendritic cell interactions in lymph nodes | Q74253957 | ||
| The proprotein convertases | Q28609903 | ||
| Enhanced dissociation of HLA-DR-bound peptides in the presence of HLA-DM | Q28613111 | ||
| Editing of the HLA-DR-peptide repertoire by HLA-DM | Q28613148 | ||
| Accelerated migration of respiratory dendritic cells to the regional lymph nodes is limited to the early phase of pulmonary infection | Q30310545 | ||
| Multiple anti-interferon actions of the influenza A virus NS1 protein | Q30361157 | ||
| Direct ex vivo analyses of HLA-DR1 transgenic mice reveal an exceptionally broad pattern of immunodominance in the primary HLA-DR1-restricted CD4 T-cell response to influenza virus hemagglutinin | Q30361736 | ||
| Visualizing regulatory T cell control of autoimmune responses in nonobese diabetic mice | Q30498716 | ||
| Identification of destabilizing residues in HLA class II-selected bacteriophage display libraries edited by HLA-DM. | Q30652859 | ||
| Integrating epitope data into the emerging web of biomedical knowledge resources | Q31111568 | ||
| Regulatory T cells inhibit stable contacts between CD4+ T cells and dendritic cells in vivo | Q33236315 | ||
| Influenza A virus non-structural protein 1 (NS1) interacts with cellular multifunctional protein nucleolin during infection | Q33296558 | ||
| Human CD4+ T cell epitopes from vaccinia virus induced by vaccination or infection | Q33302672 | ||
| Quantitative predictions of peptide binding to any HLA-DR molecule of known sequence: NetMHCIIpan | Q33349439 | ||
| Immunodominance in major histocompatibility complex class I-restricted T lymphocyte responses | Q33652450 | ||
| Reversal of immunodominance among autoantigenic T-cell epitopes | Q33753125 | ||
| Individual hydrogen bonds play a critical role in MHC class II: peptide interactions: implications for the dynamic aspects of class II trafficking and DM-mediated peptide exchange | Q33815440 | ||
| HLA-DM and the MHC class II antigen presentation pathway | Q33878174 | ||
| Energetic asymmetry among hydrogen bonds in MHC class II*peptide complexes | Q33930509 | ||
| HLA-DM, HLA-DO and tapasin: functional similarities and differences | Q34492989 | ||
| Polyclonal adaptive regulatory CD4 cells that can reverse type I diabetes become oligoclonal long-term protective memory cells | Q34512471 | ||
| Stable T cell-dendritic cell interactions precede the development of both tolerance and immunity in vivo | Q34558048 | ||
| Endosomal trafficking and proprotein convertase cleavage of cis Golgi protein GP73 produces marker for hepatocellular carcinoma | Q34657401 | ||
| Epitope identification and vaccine design for cancer immunotherapy | Q34675496 | ||
| The convergent roles of tapasin and HLA-DM in antigen presentation. | Q34784992 | ||
| Optimizing vaccine design for cellular processing, MHC binding and TCR recognition | Q35005969 | ||
| Epitope-based vaccines: an update on epitope identification, vaccine design and delivery | Q35192612 | ||
| T cell repertoire scanning is promoted by dynamic dendritic cell behavior and random T cell motility in the lymph node | Q35731136 | ||
| Virus-specific antigen presentation by different subsets of cells from lung and mediastinal lymph node tissues of influenza virus-infected mice | Q35848499 | ||
| MODPROPEP: a program for knowledge-based modeling of protein-peptide complexes | Q35914254 | ||
| In the absence of the invariant chain, HLA-DR molecules display a distinct array of peptides which is influenced by the presence or absence of HLA-DM | Q36158655 | ||
| CD4+ T cells that enter the draining lymph nodes after antigen injection participate in the primary response and become central-memory cells | Q36228572 | ||
| T cell determinant structure: cores and determinant envelopes in three mouse major histocompatibility complex haplotypes | Q36229970 | ||
| The impact of DM on MHC class II-restricted antigen presentation can be altered by manipulation of MHC-peptide kinetic stability | Q36238108 | ||
| The relationship between immunodominance, DM editing, and the kinetic stability of MHC class II:peptide complexes | Q36266503 | ||
| Influences of antigen processing on the expression of the T cell repertoire. Evidence for MHC-specific hindering structures on the products of processing | Q36355124 | ||
| Mechanisms influencing the immunodominance of T cell determinants | Q36355734 | ||
| Major histocompatibility complex class II-restricted presentation of an internally synthesized antigen displays cell-type variability and segregates from the exogenous class II and endogenous class I presentation pathways | Q36361976 | ||
| Invariant chain and DM edit self-peptide presentation by major histocompatibility complex (MHC) class II molecules | Q36367514 | ||
| DM determines the cryptic and immunodominant fate of T cell epitopes | Q36368876 | ||
| Quantitation of CD8+ T cell responses to newly identified HLA-A*0201-restricted T cell epitopes conserved among vaccinia and variola (smallpox) viruses | Q36370707 | ||
| HLA-DM recognizes the flexible conformation of major histocompatibility complex class II. | Q36404572 | ||
| Immunopathogenesis of hepatitis C virus infection: multifaceted strategies subverting innate and adaptive immunity | Q36423743 | ||
| Immunodominance and immunodomination: critical factors in developing effective CD8+ T-cell-based cancer vaccines | Q36543806 | ||
| Time Course of Synthesis and Assembly of Influenza Virus Proteins | Q36565531 | ||
| Confronting complexity: real-world immunodominance in antiviral CD8+ T cell responses | Q36626160 | ||
| Novel features of the respiratory tract T-cell response to influenza virus infection: lung T cells increase expression of gamma interferon mRNA in vivo and maintain high levels of mRNA expression for interleukin-5 (IL-5) and IL-10. | Q36637398 | ||
| Immune epitope mapping in the post-genomic era: lessons for vaccine development | Q36656929 | ||
| Direct class I HLA antigen discovery to distinguish virus-infected and cancerous cells | Q36689109 | ||
| The function of local lymphoid tissues in pulmonary immune responses | Q36693484 | ||
| Clearance of influenza virus from the lung depends on migratory langerin+CD11b- but not plasmacytoid dendritic cells | Q36742276 | ||
| Harnessing bioinformatics to discover new vaccines | Q36805723 | ||
| Immunodominance in CD4 T-cell responses: implications for immune responses to influenza virus and for vaccine design | Q36837134 | ||
| Three dimensional structure directs T-cell epitope dominance associated with allergy | Q36908976 | ||
| The influenza virus NS1 protein: inhibitor of innate and adaptive immunity | Q37066762 | ||
| SAP-controlled T-B cell interactions underlie germinal centre formation | Q37119530 | ||
| T cell sensing of antigen dose governs interactive behavior with dendritic cells and sets a threshold for T cell activation | Q37233655 | ||
| Kinetic analysis of peptide loading onto HLA-DR molecules mediated by HLA-DM. | Q37361625 | ||
| Antigen structure influences helper T-cell epitope dominance in the human immune response to HIV envelope glycoprotein gp120. | Q37373708 | ||
| Synthesis and function of influenza A virus glycoproteins | Q37419117 | ||
| Antigenicity and immunogenicity of a synthetic human immunodeficiency virus type 1 group m consensus envelope glycoprotein | Q37742876 | ||
| Modulating the immunological properties of a linear B-cell epitope by insertion into permissive sites of the MalE protein. | Q38350738 | ||
| Antigen presentation in extracellular matrix: interactions of T cells with dendritic cells are dynamic, short lived, and sequential | Q39549098 | ||
| Differential immunogenicity of various heterologous prime-boost vaccine regimens using DNA and viral vectors in healthy volunteers | Q39566146 | ||
| Specific antitumor immune response induced by a novel DNA vaccine composed of multiple CTL and T helper cell epitopes of prostate cancer associated antigens | Q40422465 | ||
| Endogenous antigen presentation by MHC class II molecules. | Q40447881 | ||
| Dominance and crypticity of T cell antigenic determinants | Q40486347 | ||
| Sorting of furin in polarized epithelial and endothelial cells: expression beyond the Golgi apparatus | Q40564413 | ||
| Formation of two peptide/MHC II isomers is catalyzed differentially by HLA-DM. | Q40676502 | ||
| The involvement of antigen processing in determinant selection by class II MHC and its relationship to immunodominance | Q40780290 | ||
| Several protein regions contribute to determine the nuclear and cytoplasmic localization of the influenza A virus nucleoprotein | Q40905176 | ||
| Role of APC in the selection of immunodominant T cell epitopes. | Q40913991 | ||
| Assessment of the role of determinant selection in genetic control of the immune response to insulin in H-2b mice | Q40933813 | ||
| The Distinctive Features of Influenza Virus Infection of Dendritic Cells | Q41048210 | ||
| P433 | issue | 2-3 | |
| P304 | page(s) | 123-143 | |
| P577 | publication date | 2009-02-07 | |
| P13046 | publication type of scholarly work | review article | Q7318358 |
| P1433 | published in | Immunologic Research | Q15754981 |
| P1476 | title | Understanding the focused CD4 T cell response to antigen and pathogenic organisms | |
| P478 | volume | 45 |
| Q42149041 | CD4 T-cell memory responses to viral infections of humans show pronounced immunodominance independent of duration or viral persistence. |
| Q30363065 | Computationally driven deletion of broadly distributed T cell epitopes in a biotherapeutic candidate. |
| Q34460478 | Flanking Residues Are Central to DO11.10 T Cell Hybridoma Stimulation by Ovalbumin 323–339 |
| Q42754778 | Immune System as a Sensory System |
| Q41961320 | Immunology at the university of Rochester |
| Q64248501 | Imprinting and Editing of the Human CD4 T Cell Response to Influenza Virus |
| Q84498369 | Loss in CD4 T-cell responses to multiple epitopes in influenza due to expression of one additional MHC class II molecule in the host |
| Q91868521 | Myalgic Encephalomyelitis/Chronic Fatigue Syndrome as a Hyper-Regulated Immune System Driven by an Interplay Between Regulatory T Cells and Chronic Human Herpesvirus Infections |
| Q41534356 | Population mechanics: A mathematical framework to study T cell homeostasis |
| Q30371474 | Protein deimmunization via structure-based design enables efficient epitope deletion at high mutational loads |
| Q28384290 | Spectrum of HLA associations: the case of medically refractory pediatric acute lymphoblastic leukemia |
| Q37453545 | T cell immunodominance is dictated by the positively selecting self-peptide |
| Q37249406 | The control of the specificity of CD4 T cell responses: thresholds, breakpoints, and ceilings |
| Q27335659 | The growth threshold conjecture: a theoretical framework for understanding T-cell tolerance |
| Q37208000 | Thermodynamics of Peptide-MHC Class II Interactions: Not all Complexes are Created Equal |
| Q50089598 | βarrestin-2-dependent Signaling Promotes CCR4-mediated Chemotaxis of Murine T Helper Type 2 Cells |
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