about
sameAs
Heat shock proteins 70 and 60 share common receptors which are expressed on human monocyte-derived but not epidermal dendritic cellsBirbeck granules are subdomains of endosomal recycling compartment in human epidermal Langerhans cells, which form where Langerin accumulatesTime-Dependent Decay of mRNA and Ribosomal RNA during Platelet Aging and Its Correlation with Translation ActivityBirbeck granule-like "organized smooth endoplasmic reticulum" resulting from the expression of a cytoplasmic YFP-tagged langerinCrystal structure of human CD1e reveals a groove suited for lipid-exchange processesHomozygous human TAP peptide transporter mutation in HLA class I deficiencyHuman factor B. Complete cDNA sequence of the BF*S allelePhenotypic studies of natural killer cell subsets in human transporter associated with antigen processing deficiency.Platelets are dispensable for antibody-mediated transfusion-related acute lung injury in the mouse.HLA class I deficiencies due to mutations in subunit 1 of the peptide transporter TAP1.Characterization of CD1e, a third type of CD1 molecule expressed in dendritic cells.Common characteristics of the human and rhesus macaque CD1e molecules: conservation of biochemical and biological properties during primate evolution.Lysosomal-associated transmembrane protein 5 (LAPTM5) is a molecular partner of CD1e.The cellular pathway of CD1e in immature and maturing dendritic cells.Assistance of microbial glycolipid antigen processing by CD1e.Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX geneAntigen-presenting cells and tolerance induction.Endogenous phosphatidylcholine and a long spacer ligand stabilize the lipid-binding groove of CD1b.Fine tuning by human CD1e of lipid-specific immune responses.Structural reorganization of the antigen-binding groove of human CD1b for presentation of mycobacterial sulfoglycolipidsRab11A controls the biogenesis of Birbeck granules by regulating Langerin recycling and stability.Clinical and immunological aspects of HLA class I deficiency.Deciphering the role of CD1e protein in mycobacterial phosphatidyl-myo-inositol mannosides (PIM) processing for presentation by CD1b to T lymphocytes.Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).Activity and phenotype of natural killer cells in peptide transporter (TAP)-deficient patients (type I bare lymphocyte syndrome)Shared reactivity of V{delta}2(neg) {gamma}{delta} T cells against cytomegalovirus-infected cells and tumor intestinal epithelial cellsDescription of HLA class I- and CD8-deficient patients: Insights into the function of cytotoxic T lymphocytes and NK cells in host defense.A Rab11A/myosin Vb/Rab11-FIP2 complex frames two late recycling steps of langerin from the ERC to the plasma membrane.HLA-DQA2 and HLA-DQB2 genes are specifically expressed in human Langerhans cells and encode a new HLA class II molecule.The assembly of CD1e is controlled by an N-terminal propeptide which is processed in endosomal compartments.Cutting edge: a naturally occurring mutation in CD1e impairs lipid antigen presentation.Synthesis and regulation of complement components by human monocytes/macrophages and by acute monocytic leukemia.The P2X1 receptor is required for neutrophil extravasation during lipopolysaccharide-induced lethal endotoxemia in mice.Dual role of IL-21 in megakaryopoiesis and platelet homeostasis.Unilateral necrotising toxoplasmic retinochoroiditis as the main clinical manifestation of a peptide transporter (TAP) deficiency.A novel mutation for TAP deficiency and its possible association with Toxoplasmosis.FcepsilonRI induces the tryptophan degradation pathway involved in regulating T cell responses.An essential role for tripeptidyl peptidase in the generation of an MHC class I epitope.Quantification of indoleamine 2,3-dioxygenase gene induction in atopic and non-atopic monocytes after ligation of the high-affinity receptor for IgE, Fc(epsilon)RI and interferon-gamma stimulation.Characterisation of two differently processed forms of human recombinant factor IX synthesised in CHO cells transformed with a polycistronic vector.
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description
hulumtues
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wetenschapper
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հետազոտող
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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prefLabel
Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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Henri de la Salle
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P214
P1053
H-9353-2016
P106
P21
P214
P31
P3829
P496
0000-0001-5136-0776
P569
2000-01-01T00:00:00Z
P735
P7859
viaf-207054912