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2 single nucleotide polymorphisms in toll like receptor 1 were significantly associated with Treponema denticola.
We found lower expression levels of TLR1, TLR3 (show TLR3 Proteins), TLR4 (show TLR4 Proteins), TLR7 (show TLR7 Proteins) and TLR9 (show TLR9 Proteins) in PBMCs from patients with ALL compared with those from control patients. We also observed that the PBMCs from patients with Pre-B and B ALL had lower TLR4 (show TLR4 Proteins) expression than controls
These data suggest that the TLR1 N248S polymorphism might play a role in Th1/Th2 differentiation, and the determination of serum IgE levels.
a case-control study of 504 Papua New Guinean children with severe malaria showed that a genetic variant in TLR1 may contribute to the low severe malaria case fatality rates in this region through a reduced pro-inflammatory cellular phenotype.
The data suggest that genetic variation in TLR1 has effects on the host response to Plasmodium falciparum malaria in Asian populations.
a novel mechanism of action for TLR1 SNP rs5743618 in modulating polymorphonuclear leukocytes priming responses.
concluded that TLR-1 rs4833095 and TLR10 (show TLR10 Proteins) rs10004195 confer susceptibility to development of gastroduodenal disease, especially GC in H.pylori disease
Activation of MyD88-dependent TLR1/2 signaling by misfolded alpha-synuclein, a protein linked to neurodegenerative disorders.
SNP TLR1-248N is associated with TB protection in an Indian population and exhibits an increased immune response to Mycobacterium tuberculosis lysate in vitro.
The expression of TLR1 was the lowest and expression of TLR4 (show TLR4 Proteins) was the highest on leukocytes in acute otitis media children.
B cell TLR1/2, TLR4 (show TLR4 Proteins), TLR7 (show TLR7 Proteins) and TLR9 (show TLR9 Proteins) interact in induction of class switch DNA recombination, modulated by BCR (show BCR Proteins) and CD40 (show CD40 Proteins) in mounting of T-cell independent antibody responses.
TLR9 (show TLR9 Proteins) modulates TLR1 expression in Leishmania major-infected macrophages.
Postradiotherapeutic NO production was dependent on TLR1 gene expression. Although iNOS (show NOS2 Proteins) activity was reduced by inhibiting TLR1 expression with TLR1-siRNA, it was enhanced by TLR1 overexpression.
lipopeptides elicit TLR1/2 and TLR2/6 signaling in the endolysosomes, but not on the cell surface.
We found that CEP specifically synergizes with low-dose TLR2-agonists (but not agonists for other TLRs) to induce production of inflammatory cytokines. Moreover, CEP selectively augments TLR2/TLR1-signaling instead of TLR2/TLR6 (show TLR6 Proteins)-signaling
IkappaB-zeta regulates TLR-mediated CSR by inducing AID
aortic angiogenesis is preceded by an immune reaction with overexpression of Toll (show TLR4 Proteins)-like receptors (TLRs) and TLR-inducible genes.
Identify TLR1 as a critical innate receptor for protective intestinal T(H)17 immunity.
Graphene significantly stimulates the secretion of cytokines/chemokines via TLR- and NF-kappaB (show NFKB1 Proteins)-related signaling pathways
TLR2, TLR1, and TLR6 (show TLR6 Proteins) haev roles in innate immunity and initiate inflammatory responses to bacterial lipopeptides by epithelial and stromal cells of bovine endometrium
variants in the TLR1 gene are associated with susceptibility to bovine tuberculosis, whereas no significant association can be inferred from the polymorphisms in the TLR9 (show TLR9 Proteins) gene
Whereas previous results regarding the TLR1 gene were not corroborated, a risk haplotype was detected in TLR2; however, its low frequency indicates that this detected association should be interpreted with caution.
This study showed that TLR1 and TLR2 together are necessary for the recognition of triacylated lipopeptides.
The expression analysis showed similar expression profiles for TLR1 and TLR6 (show TLR6 Proteins), which indicate a co-regulation of these two genes, TLR10 (show TLR10 Proteins) had a different expression profile, pointing toward a stronger functional diversification compared to TLR1 and TLR6 (show TLR6 Proteins).
The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This gene is ubiquitously expressed, and at higher levels than other TLR genes. Different length transcripts presumably resulting from use of alternative polyadenylation site, and/or from alternative splicing, have been noted for this gene.
toll/interleukin-1 receptor-like protein
, Toll-like receptor 1 long form