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Blocking LLT1-NKRP1A (zeige KLRB1 Proteine) interaction will make prostate cancer cells susceptible to killing by NK cells, suggesting a therapeutic option for treatment of prostate cancer.
these data suggest that LLT1-CD161 (zeige KLRB1 Proteine) interactions play a novel and important role in B cell maturation (zeige TNFRSF17 Proteine) within the Germinal center in humans.
In RA joints, LLT1 is expressed by cells of the monocyte/macrophage lineage.
The hexamer of glycosylated LLT1 consists of three classical dimers. The hexameric packing may indicate a possible mode of interaction of C-type lectin (zeige MBL2 Proteine)-like proteins in the glycosylated form.
One polymorphism in LLT1 was found to be associated with our Crohn's Disease population (P<0.034).Our Ulcerative Colitis cohort was not associated with the variation in LLT1 (P=0.33)
LLT1 and CD161 (zeige KLRB1 Proteine) have roles in modulating immune responses to pathogens; and interferon-gamma (zeige IFNG Proteine) contributes to modulate immune responses
Molecular basis for LLT1 protein recognition by human CD161 (zeige KLRB1 Proteine) protein (NKRP1A/KLRB1 (zeige KLRB1 Proteine)).
Data show that only CLEC2D isoform 1 (LLT1) is expressed on the cell surface.
LLT1 used Src (zeige SRC Proteine)-PTK, p38 (zeige CRK Proteine) and ERK (zeige EPHB2 Proteine) signalling pathways, but not PKC (zeige PRRT2 Proteine), PI3K (zeige PIK3CA Proteine) or calcineurin pathways, to increase production of IFN-gamma (zeige IFNG Proteine) by human natural killer cells.
LLT1 induces Interferon (zeige IFNA Proteine) Type II production by natural killer cells.
these findings demonstrate that Clr-b is an IFN-stimulated gene on healthy bystander cells, in addition to a missing-self marker on MCMV-infected cells, and thereby enhances the dynamic range of innate self-nonself discrimination by NK cells
Data suggest that killer cell lectin-like receptors NKR (zeige TACR3 Proteine)-P1B:Clr-b (Klrb1 (zeige KLRB1 Proteine):Clec2d) interactions may provide a model for human hematopoietic cell transplants.
Reductions of Clr-b may be involved in sensitizing poxvirus-infected cells to natural killer (NK) cells.
LLT1 and CD161 have roles in modulating immune responses to pathogens; and interferon-gamma (zeige IFNG Proteine) contributes to modulate immune responses
cloning and characterization of a cognate ligand, Ocil, for the inhibitory NK receptors (NKR)-P1B and NKR-P1D. Ocil/Clr-b is displayed at high levels on nearly all hematopoietic cells, in a pattern that is similar to that of class I MHC molecules.
Data show that osteoclast inhibitory lectin (OCIL) binds a range of physiologically important glycosaminoglycans, and this property may modulate OCIL actions upon other cells.
Limited divergence of the BALB/c Nkrp1-Ocil/Clr region helps explain a longstanding confusion regarding the strain-specific NK1.1 alloantigen reactivity of mouse natural killer cells.
OCIL is a physiological negative regulator of bone.
PTHrp(1-34) regulates OCIL expression in vitro through cAMP/PKA, Ca(2 (zeige CA2 Proteine)+)/CaMK II (zeige CAMK2B Proteine), and MAPK (zeige MAPK1 Proteine) signaling pathways.
Identification of a novel family of genes, named Clr (zeige CALCR Proteine), encoding C-type lectin-like molecules, which maps in the natural killer (NK) gene complex (NKC) on mouse Chromosome 6.
This gene encodes a member of the natural killer cell receptor C-type lectin family. The encoded protein inhibits osteoclast formation and contains a transmembrane domain near the N-terminus as well as the C-type lectin-like extracellular domain. Several alternatively spliced transcript variants have been identified for this gene.
C-type lectin domain family 2 member D
, C-type lectin related f
, C-type lectin superfamily 2, member D
, lectin-like NK cell receptor
, lectin-like transcript 1
, osteoclast inhibitory lectin
, C-type lectin-domain family 2 member D
, C-type lectin-related protein B
, lectin-like transmembrane protein
, C-type lectin domain family 2 member D5
, C-type lectin domain family 2, member D
, C-type lectin domain family 2 member H-like