Quantum dot/peptide-MHC biosensors reveal strong CD8-dependent cooperation between self and viral antigens that augment the T cell response. - Wikidata - wikimedia - TriplyDB

Quantum dot/peptide-MHC biosensors reveal strong CD8-dependent cooperation between self and viral antigens that augment the T cell response.

Quantum dot/peptide-MHC biosensors reveal strong CD8-dependent cooperation between self and viral antigens that augment the T cell response.

http://www.wikidata.org/entity/Q35130764

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The multiple roles of the CD8 coreceptor in T cell biology: opportunities for the selective modulation of self-reactive cytotoxic T cells Integrins Influence the Size and Dynamics of Signaling Microclusters in a Pyk2-dependent Manner How a T Cell Receptor-like Antibody Recognizes Major Histocompatibility Complex-bound Peptide Evaluating frequency and quality of pathogen-specific T cells.Strategies for interfacing inorganic nanocrystals with biological systems based on polymer-coating.T-cell artificial focal triggering tools: linking surface interactions with cell response.A novel composite immunotoxin that suppresses rabies virus production by the infected cells.Bioimaging of nucleolin aptamer-containing 5-(N-benzylcarboxyamide)-2'-deoxyuridine more capable of specific binding to targets in cancer cells The impact of TCR-binding properties and antigen presentation format on T cell responsiveness.Nanoscale artificial antigen presenting cells for T cell immunotherapy Evidence that the density of self peptide-MHC ligands regulates T-cell receptor signaling.Opposite effects of endogenous peptide-MHC class I on T cell activity in the presence and absence of CD8.Snapin, positive regulator of stimulation- induced Ca²⁺ release through RyR, is necessary for HIV-1 replication in T cells.Stage-dependent reactivity of thymocytes to self-peptide--MHC complexes.Sensitivity of T cells to antigen and antagonism emerges from differential regulation of the same molecular signaling module.T cell activation enhancement by endogenous pMHC acts for both weak and strong agonists but varies with differentiation state Endogenous viral antigen processing generates peptide-specific MHC class I cell-surface clusters.The MHC class I peptide repertoire is molded by the transcriptome.NSOM/QD-based nanoscale immunofluorescence imaging of antigen-specific T-cell receptor responses during an in vivo clonal Vγ2Vδ2 T-cell expansion.Quantum dot conjugates of GABA and muscimol: binding to α1β2γ2 and ρ1 GABA(A) receptors.Regulation of cytotoxic T lymphocyte triggering by PIR-B on dendritic cells.Tapping out a mechanical code for T cell triggering Viral infection causes a shift in the self peptide repertoire presented by human MHC class I molecules.Class II major histocompatibility complex tetramer staining: progress, problems, and prospects.Role of T cell receptor affinity in the efficacy and specificity of adoptive T cell therapies.Coreceptor affinity for MHC defines peptide specificity requirements for TCR interaction with coagonist peptide-MHC.Compact biocompatible quantum dots functionalized for cellular imaging.Cutting edge: TLR ligands increase TCR triggering by slowing peptide-MHC class I decay rates Quantum dots: a powerful tool for understanding the intricacies of nanoparticle-mediated drug delivery.Co-receptors and recognition of self at the immunological synapse.Current approaches to measuring human islet-antigen specific T cell function in type 1 diabetes.Signaling microdomains in T cells.T cell receptor signaling kinetics takes the stage.Normal T cell homeostasis: the conversion of naive cells into memory-phenotype cells New insights into the T cell synapse from single molecule techniques.Mechanisms controlling granule-mediated cytolytic activity of cytotoxic T lymphocytes.Dendritic cells enhance the antigen sensitivity of T cells.Polymer-coated quantum dots.A review of reagents for fluorescence microscopy of cellular compartments and structures, Part III: reagents for actin, tubulin, cellular membranes, and whole cell and cytoplasm.Adoptive T Cell Therapies: A Comparison of T Cell Receptors and Chimeric Antigen Receptors

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Quantum dot/peptide-MHC biosensors reveal strong CD8-dependent cooperation between self and viral antigens that augment the T cell response.

http://www.wikidata.org/entity/Q35130764

description

2006 nî lūn-bûn

@nan

2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Quantum dot/peptide-MHC biosen ...... t augment the T cell response.

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Quantum dot/peptide-MHC biosen ...... t augment the T cell response.

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type

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Quantum dot/peptide-MHC biosen ...... t augment the T cell response.

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Quantum dot/peptide-MHC biosen ...... t augment the T cell response.

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Quantum dot/peptide-MHC biosen ...... t augment the T cell response.

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Proceedings of the National Academy of Sciences of the United States of America

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Quantum dot/peptide-MHC biosen ...... t augment the T cell response.

@en

P2093

Aaron R Clapp

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Ellen R Goldman

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Nadia Anikeeva

http://www.w3.org/2001/XMLSchema#string

Tatiana Lebedeva

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Yuri Sykulev

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P2860

Classical and nonclassical class I major histocompatibility complex molecules exhibit subtle conformational differences that affect binding to CD8alphaalpha

ICAM-1 co-stimulates target cells to facilitate antigen presentation

Identification of a peptide recognized by five melanoma-specific human cytotoxic T cell lines.

Molecular interactions of coreceptor CD8 and MHC class I: the molecular basis for functional coordination with the T-cell receptor.

Differences in antigen recognition and cytolytic activity of CD8(+) and CD8(-) T cells that express the same antigen-specific receptor.

Vesicle trafficking and cell surface membrane patchiness.

Quantum dot bioconjugates for imaging, labelling and sensing.

Cytotoxic T lymphocytes form an antigen-independent ring junction

The specificity of TCR/pMHC interaction.

Molecular coordination of alphabeta T-cell receptors and coreceptors CD8 and CD4 in their recognition of peptide-MHC ligands.

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103

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Michael L Dustin

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2006-10-31T00:00:00Z

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6719701

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17077145

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1636542

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