| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2004PNAS..101.4942K |
| P356 | DOI | 10.1073/PNAS.0401279101 |
| P8608 | Fatcat ID | release_e6sw5exd7nhprh5y6yzizdatv4 |
| P932 | PMC publication ID | 387353 |
| P698 | PubMed publication ID | 15037737 |
| P5875 | ResearchGate publication ID | 8662479 |
| P50 | author | Peter C. Doherty | Q309814 |
| Katherine Kedzierska | Q28355204 | ||
| Stephen J. Turner | Q47502192 | ||
| P2860 | cites work | The epitopes of influenza nucleoprotein recognized by cytotoxic T lymphocytes can be defined with short synthetic peptides | Q24339477 |
| Conserved T cell receptor repertoire in primary and memory CD8 T cell responses to an acute viral infection | Q24657414 | ||
| A structural basis for the selection of dominant alphabeta T cell receptors in antiviral immunity | Q27640322 | ||
| A structural basis for immunodominant human T cell receptor recognition | Q27641421 | ||
| The three-dimensional structure of H-2Db at 2.4 A resolution: implications for antigen-determinant selection | Q27729346 | ||
| Structure of the complex between human T-cell receptor, viral peptide and HLA-A2 | Q27733853 | ||
| Immunodominance in major histocompatibility complex class I-restricted T lymphocyte responses | Q33652450 | ||
| A previously unrecognized H-2D(b)-restricted peptide prominent in the primary influenza A virus-specific CD8(+) T-cell response is much less apparent following secondary challenge | Q33801952 | ||
| A direct estimate of the human alphabeta T cell receptor diversity | Q33878476 | ||
| Protection and compensation in the influenza virus-specific CD8+ T cell response | Q35163418 | ||
| In vivo proliferation of naïve and memory influenza-specific CD8(+) T cells | Q35557069 | ||
| Preferential usage of the T-cell receptor by influenza virus hemagglutinin-specific human CD4+ T lymphocytes: in vitro life span of clonotypic T cells | Q35852655 | ||
| Measuring the diaspora for virus-specific CD8+ T cells. | Q35941203 | ||
| The sizes of the CDR3 hypervariable regions of the murine T-cell receptor beta chains vary as a function of the recombined germ-line segments | Q36291877 | ||
| Public and private V beta T cell receptor repertoires against hen egg white lysozyme (HEL) in nontransgenic versus HEL transgenic mice | Q36363704 | ||
| Dominant selection of an invariant T cell antigen receptor in response to persistent infection by Epstein-Barr virus. | Q36364099 | ||
| Recurrent T cell receptor rearrangements in the cytotoxic T lymphocyte response in vivo against the p815 murine tumor | Q36366282 | ||
| Evolution of antigen-specific T cell receptors in vivo: preimmune and antigen-driven selection of preferred complementarity-determining region 3 (CDR3) motifs | Q36368219 | ||
| Differential antigen presentation regulates the changing patterns of CD8+ T cell immunodominance in primary and secondary influenza virus infections | Q36371363 | ||
| Stability and diversity of T cell receptor repertoire usage during lymphocytic choriomeningitis virus infection of mice | Q36401170 | ||
| Future influenza vaccines and the use of genetic recombinants | Q36551515 | ||
| Restricted V-segment usage in T-cell receptors from cytotoxic T lymphocytes specific for a major epitope of lymphocytic choriomeningitis virus | Q36796002 | ||
| Differential tumor necrosis factor receptor 2-mediated editing of virus-specific CD8+ effector T cells | Q37074146 | ||
| Comparative T cell receptor repertoire selection by antigen after adoptive transfer: a glimpse at an antigen-specific preimmune repertoire | Q37229529 | ||
| Restricted use of T cell receptor V genes in murine autoimmune encephalomyelitis raises possibilities for antibody therapy | Q39272381 | ||
| T-cell receptor V-region usage and antigen specificity. The cytochrome c model system. | Q40465707 | ||
| Contemporary analysis of MHC-related immunodominance hierarchies in the CD8+ T cell response to influenza A viruses | Q40860957 | ||
| The outline structure of the T-cell alpha beta receptor. | Q41094902 | ||
| Very diverse CD8 T cell clonotypic responses after virus infections | Q45673893 | ||
| Analysis of clonotype distribution and persistence for an influenza virus-specific CD8+ T cell response | Q45724232 | ||
| Virus-specific CD8+ T cells in primary and secondary influenza pneumonia | Q45755057 | ||
| Prominent usage of V beta 8.3 T cells in the H-2Db-restricted response to an influenza A virus nucleoprotein epitope | Q45786754 | ||
| Virus-specific CD8+ T-cell memory determined by clonal burst size | Q45789854 | ||
| Limited heterogeneity of T cell receptors from lymphocytes mediating autoimmune encephalomyelitis allows specific immune intervention | Q46499427 | ||
| Size estimate of the alpha beta TCR repertoire of naive mouse splenocytes | Q47238652 | ||
| Diversity of T cell receptors specific for the VSV antigenic peptide (N52-59) bound by the H-2Kb class I molecule | Q48076085 | ||
| Genomic organization and sequence of T-cell receptor beta-chain constant- and joining-region genes | Q48388339 | ||
| Mouse T cell antigen receptor: structure and organization of constant and joining gene segments encoding the beta polypeptide | Q48389171 | ||
| Single-cell PCR analysis of TCR repertoires selected by antigen in vivo: a high magnitude CD8 response is comprised of very few clones. | Q52050424 | ||
| Antigen-specific development of primary and memory T cells in vivo. | Q52053475 | ||
| Junctional biases in the naive TCR repertoire control the CTL response to an immunodominant determinant of HSV-1. | Q52922603 | ||
| Cellular events in the lymph node and lung of mice with influenza. Consequences of depleting CD4+ T cells | Q67657695 | ||
| Memory TCR repertoires analyzed long-term reflect those selected during the primary response | Q71398160 | ||
| Antigen-driven selection of TCR In vivo: related TCR alpha-chains pair with diverse TCR beta-chains | Q73201976 | ||
| Shapes of MHC restriction | Q74451838 | ||
| P433 | issue | 14 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | virus | Q808 |
| P304 | page(s) | 4942-4947 | |
| P577 | publication date | 2004-03-22 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Conserved T cell receptor usage in primary and recall responses to an immunodominant influenza virus nucleoprotein epitope | |
| P478 | volume | 101 |
| Q24622687 | A requisite role for induced regulatory T cells in tolerance based on expanding antigen receptor diversity |
| Q27670418 | A semi-invariant Vα10+ T cell antigen receptor defines a population of natural killer T cells with distinct glycolipid antigen-recognition properties |
| Q34304888 | A virus-specific CD8+ T cell immunodominance hierarchy determined by antigen dose and precursor frequencies |
| Q45413199 | Addition of a prominent epitope affects influenza A virus-specific CD8+ T cell immunodominance hierarchies when antigen is limiting |
| Q36509892 | Age-associated decline in T cell repertoire diversity leads to holes in the repertoire and impaired immunity to influenza virus |
| Q28284174 | An in vivo cytotoxicity threshold for influenza A virus-specific effector and memory CD8(+) T cells |
| Q40973238 | Antigen Specificity of Type I NKT Cells Is Governed by TCR β-Chain Diversity. |
| Q36739772 | Antigen-specific immunotherapy for autoimmune diseases |
| Q26765927 | Avian Influenza Viruses, Inflammation, and CD8(+) T Cell Immunity |
| Q37837483 | Bias in the αβ T-cell repertoire: implications for disease pathogenesis and vaccination |
| Q48535407 | Burnet, chick embryos, viruses, clones and quantitative biology |
| Q27686847 | CD1d-lipid antigen recognition by the γδ TCR |
| Q41668932 | CD3bright signals on γδ T cells identify IL-17A-producing Vγ6Vδ1+ T cells |
| Q37840341 | CD8 T cell responses to influenza virus infection in aged mice |
| Q43620861 | Characterization of conserved CDR3 sequence of TCR alpha- and beta-chain genes in peripheral blood T-cells from patients with diffuse large B-cell lymphoma |
| Q59800421 | Cheating the Hunger Games; Mechanisms Controlling Clonal Diversity of CD8 Effector and Memory Populations |
| Q54266162 | Clonally diverse CD38+HLA-DR+CD8+ T cells persist during fatal H7N9 disease. |
| Q35091189 | Clonally related CD8+ T cells responsible for rapid population of both diffuse nasal-associated lymphoid tissue and lung after respiratory virus infection |
| Q27653021 | Complete modification of TCR specificity and repertoire selection does not perturb a CD8+ T cell immunodominance hierarchy |
| Q30402467 | Consequences of suboptimal priming are apparent for low-avidity T-cell responses |
| Q33914114 | Contribution of T cell receptor affinity to overall avidity for virus-specific CD8+ T cell responses |
| Q37088595 | Dietary gluten triggers concomitant activation of CD4+ and CD8+ αβ T cells and γδ T cells in celiac disease |
| Q54452411 | Diversity and clonotypic composition of influenza-specific CD8+ TCR repertoires remain unaltered in the absence of Aire. |
| Q34165211 | Diversity of the CD8+ T cell repertoire elicited against an immunodominant epitope does not depend on the context of infection |
| Q34975847 | Diversity of the T-cell response to pulmonary Cryptococcus neoformans infection. |
| Q40996539 | Double-negative T resident memory cells of the lung react to influenza virus infection via CD11c(hi) dendritic cells |
| Q34694947 | Early establishment of diverse T cell receptor profiles for influenza-specific CD8(+)CD62L(hi) memory T cells |
| Q27347326 | Early priming minimizes the age-related immune compromise of CD8⁺ T cell diversity and function |
| Q28709263 | Ecological analysis of antigen-specific CTL repertoires defines the relationship between naive and immune T-cell populations |
| Q35012614 | Effect of MHC class I diversification on influenza epitope-specific CD8+ T cell precursor frequency and subsequent effector function |
| Q33771135 | Effector CD8+ T cells recovered from an influenza pneumonia differentiate to a state of focused gene expression |
| Q27649750 | Epitope-specific TCR repertoire diversity imparts no functional advantage on the CD8+ T cell response to cognate viral peptides |
| Q36528969 | Establishment and recall of CD8+ T-cell memory in a model of localized transient infection |
| Q37754754 | Factors influencing immunodominance hierarchies in TCD8+ -mediated antiviral responses |
| Q39028500 | Feature selection using a one dimensional naïve Bayes' classifier increases the accuracy of support vector machine classification of CDR3 repertoires |
| Q38925984 | Fixed expression of single influenza virus-specific TCR chains demonstrates the capacity for TCR α- and β-chain diversity in the face of peptide-MHC class I specificity |
| Q45373917 | Fixing an irrelevant TCR alpha chain reveals the importance of TCR beta diversity for optimal TCR alpha beta pairing and function of virus-specific CD8+ T cells. |
| Q93382455 | GITRL on inflammatory antigen presenting cells in the lung parenchyma provides signal 4 for T-cell accumulation and tissue-resident memory T-cell formation |
| Q36563266 | Heightened self-reactivity associated with selective survival, but not expansion, of naïve virus-specific CD8+ T cells in aged mice |
| Q45402819 | Heterogeneity of effector phenotype for acute phase and memory influenza A virus-specific CTL. |
| Q40431345 | High resolution structures of highly bulged viral epitopes bound to major histocompatibility complex class I. Implications for T-cell receptor engagement and T-cell immunodominance |
| Q39026323 | High-throughput sequencing of the T-cell receptor repertoire: pitfalls and opportunities |
| Q39975684 | Homogenization of TCR repertoires within secondary CD62Lhigh and CD62Llow virus-specific CD8+ T cell populations |
| Q34077312 | Immune memory and aging: an infinite or finite resource? |
| Q51982189 | Immunity and age: living in the past? |
| Q36452600 | Influenza and the challenge for immunology |
| Q43657076 | Influenza epitope-specific CD8+ T cell avidity, but not cytokine polyfunctionality, can be determined by TCRβ clonotype |
| Q45286056 | Lack of prominent peptide-major histocompatibility complex features limits repertoire diversity in virus-specific CD8+ T cell populations |
| Q59357739 | Lifelong CMV infection improves immune defense in old mice by broadening the mobilized TCR repertoire against third-party infection |
| Q36417221 | Lifelong persistent viral infection alters the naive T cell pool, impairing CD8 T cell immunity in late life |
| Q35834524 | Location rather than CD62L phenotype is critical in the early establishment of influenza-specific CD8+ T cell memory |
| Q37778284 | Mapping the life histories of T cells. |
| Q51022188 | Memory precursor phenotype of CD8+ T cells reflects early antigenic experience rather than memory numbers in a model of localized acute influenza infection. |
| Q51969816 | Method for assessing the similarity between subsets of the T cell receptor repertoire. |
| Q55877020 | Methods for comparing the diversity of samples of the T cell receptor repertoire |
| Q35635344 | Mutually exclusive T-cell receptor induction and differential susceptibility to human immunodeficiency virus type 1 mutational escape associated with a two-amino-acid difference between HLA class I subtypes |
| Q45381583 | Narrowed TCR diversity for immunised mice challenged with recombinant influenza A-HIV Env(311-320) virus |
| Q34537506 | Narrowed TCR repertoire and viral escape as a consequence of heterologous immunity |
| Q37782409 | Nature and nurture: T-cell receptor-dependent and T-cell receptor-independent differentiation cues in the selection of the memory T-cell pool. |
| Q33902414 | One naive T cell, multiple fates in CD8+ T cell differentiation. |
| Q36200039 | Paired TCRαβ analysis of virus-specific CD8(+) T cells exposes diversity in a previously defined 'narrow' repertoire |
| Q34429027 | Paired analysis of TCRα and TCRβ chains at the single-cell level in mice |
| Q27676834 | Preemptive priming readily overcomes structure-based mechanisms of virus escape |
| Q33882912 | Primary CTL response magnitude in mice is determined by the extent of naive T cell recruitment and subsequent clonal expansion |
| Q34338725 | Profile of a Serial Killer: Cellular and Molecular Approaches to Study Individual Cytotoxic T‐Cells following Therapeutic Vaccination |
| Q27664060 | Protective Efficacy of Cross-Reactive CD8+ T Cells Recognising Mutant Viral Epitopes Depends on Peptide-MHC-I Structural Interactions and T Cell Activation Threshold |
| Q40212609 | Quantification of repertoire diversity of influenza-specific epitopes with predominant public or private TCR usage |
| Q41858955 | Random T-cell receptor recruitment in human immunodeficiency virus type 1 (HIV-1)-specific CD8+ T cells from genetically identical twins infected with the same HIV-1 strain |
| Q36655719 | Rapid Evolution of the CD8+ TCR Repertoire in Neonatal Mice |
| Q37544031 | Reproducible selection of high avidity CD8+ T-cell clones following secondary acute virus infection |
| Q35785225 | Selective depletion of high-avidity human immunodeficiency virus type 1 (HIV-1)-specific CD8+ T cells after early HIV-1 infection |
| Q35214734 | Sharing of T cell receptors in antigen-specific responses is driven by convergent recombination |
| Q27329554 | Significant impact of sequence variations in the nucleoprotein on CD8 T cell-mediated cross-protection against influenza A virus infections |
| Q55640449 | Single-Cell Approach to Influenza-Specific CD8+ T Cell Receptor Repertoires Across Different Age Groups, Tissues, and Following Influenza Virus Infection. |
| Q36323551 | Structural Basis for Clonal Diversity of the Public T Cell Response to a Dominant Human Cytomegalovirus Epitope |
| Q27667972 | Structural basis for enabling T-cell receptor diversity within biased virus-specific CD8+ T-cell responses |
| Q36655911 | Structural determinants of T-cell receptor bias in immunity |
| Q42374922 | T Cell Receptor Profiling in Type 1 Diabetes |
| Q37389695 | T cell islet accumulation in type 1 diabetes is a tightly regulated, cell-autonomous event |
| Q40168065 | T cell receptor gene therapy for autoimmune diseases |
| Q37001455 | Terminal deoxynucleotidyltransferase is required for the establishment of private virus-specific CD8+ TCR repertoires and facilitates optimal CTL responses |
| Q56917578 | The CDR3 regions of an immunodominant T cell receptor dictate the 'energetic landscape' of peptide-MHC recognition |
| Q40307772 | The T Cell Response to the Contact Sensitizer Paraphenylenediamine Is Characterized by a Polyclonal Diverse Repertoire of Antigen-Specific Receptors. |
| Q45401359 | The context of epitope presentation can influence functional quality of recalled influenza A virus-specific memory CD8+ T cells |
| Q37830730 | The descent of memory T cells. |
| Q37800308 | The future of lupus therapy modulating autoantigen recognition |
| Q33988743 | The magnitude of CD4(+) T-cell activation rather than TCR diversity determines the outcome of Leishmania infection in mice |
| Q37095250 | The molecular basis for public T-cell responses? |
| Q36919171 | Tracking phenotypically and functionally distinct T cell subsets via T cell repertoire diversity |
| Q36148883 | Validation of RNA-based molecular clonotype analysis for virus-specific CD8+ T-cells in formaldehyde-fixed specimens isolated from peripheral blood |
| Q46167518 | Visualizing CTL activity for different CD8+ effector T cells supports the idea that lower TCR/epitope avidity may be advantageous for target cell killing. |
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